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'en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)'
(id=8232273 ; fe=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=89048 creation date=2017-07-23 touchdate=2025-07-28 08:33:54.000)
≈ 3371 relations sortantes

  1. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in a disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 10 gene (adamts10, 608990.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in a disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 10 gene (adamts10, 608990.0001) | rel=r_associated | relid=0 | w=43
  2. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the adult folate receptor 1 gene (folr1, 136430.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adult folate receptor 1 gene (folr1, 136430.0001) | rel=r_associated | relid=0 | w=43
  3. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the alpha-1 subunit of the thyroid hormone receptor gene (thra, 190120.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1 subunit of the thyroid hormone receptor gene (thra, 190120.0001) | rel=r_associated | relid=0 | w=43
  4. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the alpha-11 guanine nucleotide-binding protein gene (gna11, 139313.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-11 guanine nucleotide-binding protein gene (gna11, 139313.0003) | rel=r_associated | relid=0 | w=43
  5. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the androgen receptor gene (ar, 313700.0020)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the androgen receptor gene (ar, 313700.0020) | rel=r_associated | relid=0 | w=43
  6. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the cdgsh iron sulfur domain protein 2 gene (cisd2, 611507.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cdgsh iron sulfur domain protein 2 gene (cisd2, 611507.0001) | rel=r_associated | relid=0 | w=43
  7. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the complex i, subunit nd4l gene (mtnd4l, 516004.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complex i, subunit nd4l gene (mtnd4l, 516004.0002) | rel=r_associated | relid=0 | w=43
  8. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the cyclin-dependent kinase inhibitor-1b gene (cdkn1b, 600778.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclin-dependent kinase inhibitor-1b gene (cdkn1b, 600778.0001) | rel=r_associated | relid=0 | w=43
  9. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the cyld gene (605018.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyld gene (605018.0001) | rel=r_associated | relid=0 | w=43
  10. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the diacylglycerol kinase, epsilon, 64-kd gene (dgke, 601440.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the diacylglycerol kinase, epsilon, 64-kd gene (dgke, 601440.0001) | rel=r_associated | relid=0 | w=43
  11. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the dna ligase-4 gene (lig4, 601837.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna ligase-4 gene (lig4, 601837.0007) | rel=r_associated | relid=0 | w=43
  12. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0013) | rel=r_associated | relid=0 | w=43
  13. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the fas ligand gene (fasl, 134638.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fas ligand gene (fasl, 134638.0001) | rel=r_associated | relid=0 | w=43
  14. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the homeo box-a11 gene (hoxa11, 142958.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeo box-a11 gene (hoxa11, 142958.0001) | rel=r_associated | relid=0 | w=43
  15. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the homolog of the mouse noggin gene (nog, 602991.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse noggin gene (nog, 602991.0001) | rel=r_associated | relid=0 | w=43
  16. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the interleukin-36 receptor antagonist gene (il36rn, 605507.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interleukin-36 receptor antagonist gene (il36rn, 605507.0001) | rel=r_associated | relid=0 | w=43
  17. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the junction plakoglobin gene (jup, 173325.0002).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the junction plakoglobin gene (jup, 173325.0002). | rel=r_associated | relid=0 | w=43
  18. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the mitochondrial complex i, subunit nd4 gene (mtnd4, 516003.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial complex i, subunit nd4 gene (mtnd4, 516003.0003) | rel=r_associated | relid=0 | w=43
  19. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the mitochondrial trna lysine 1 gene (mttl1, 590050.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial trna lysine 1 gene (mttl1, 590050.0001) | rel=r_associated | relid=0 | w=43
  20. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0029)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0029) | rel=r_associated | relid=0 | w=43
  21. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the neurofibromin gene (nf1, 613113.0033)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neurofibromin gene (nf1, 613113.0033) | rel=r_associated | relid=0 | w=43
  22. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the nlr family, caspase recruitment domain-containing 4 gene (nlrc4, 606831.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nlr family, caspase recruitment domain-containing 4 gene (nlrc4, 606831.0001) | rel=r_associated | relid=0 | w=43
  23. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the phosphodiesterase 6h, cgmp-specific, cone, gamma gene (pde6h, 601190.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphodiesterase 6h, cgmp-specific, cone, gamma gene (pde6h, 601190.0001) | rel=r_associated | relid=0 | w=43
  24. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the polyribonucleotide nucleotidyltransferase 1 gene (pnpt1, 610316.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polyribonucleotide nucleotidyltransferase 1 gene (pnpt1, 610316.0001) | rel=r_associated | relid=0 | w=43
  25. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the smad nuclear interacting protein-1 gene (snip1, 608241.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the smad nuclear interacting protein-1 gene (snip1, 608241.0001) | rel=r_associated | relid=0 | w=43
  26. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the t-cell receptor alpha chain constant region gene (trac, 186880.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the t-cell receptor alpha chain constant region gene (trac, 186880.0001) | rel=r_associated | relid=0 | w=43
  27. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the transmembrane protein 126a gene (tmem126a, 612988.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 126a gene (tmem126a, 612988.0001) | rel=r_associated | relid=0 | w=43
  28. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the transmembrane protein 231 gene (tmem231, 614949.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 231 gene (tmem231, 614949.0001) | rel=r_associated | relid=0 | w=43
  29. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the tubulin-gamma complex-associated protein 6 gene (tubgcp6, 610053.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin-gamma complex-associated protein 6 gene (tubgcp6, 610053.0001) | rel=r_associated | relid=0 | w=43
  30. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the type v collagen, alpha-2 gene (col5a2, 120190.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the type v collagen, alpha-2 gene (col5a2, 120190.0003) | rel=r_associated | relid=0 | w=43
  31. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by mutation in the zrs regulatory element located in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zrs regulatory element located in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0018) | rel=r_associated | relid=0 | w=43
  32. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:caused by the glycogenin 1 gene (gyg1, 603942.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by the glycogenin 1 gene (gyg1, 603942.0001) | rel=r_associated | relid=0 | w=43
  33. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 43 / 1 -> en:due to hemizygous deletion of 4p16.3
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:due to hemizygous deletion of 4p16.3 | rel=r_associated | relid=0 | w=43
  34. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by deletion in the nephrocystin gene (nphp1, 607100.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion in the nephrocystin gene (nphp1, 607100.0005) | rel=r_associated | relid=0 | w=42
  35. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in lactase (lct, 603202.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in lactase (lct, 603202.0001) | rel=r_associated | relid=0 | w=42
  36. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the adenosine deaminase, rna-specific gene (adar, 601059.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenosine deaminase, rna-specific gene (adar, 601059.0001) | rel=r_associated | relid=0 | w=42
  37. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the aldehyde dehydrogenase 18 family, member a1 gene (aldh18a1, 138250.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aldehyde dehydrogenase 18 family, member a1 gene (aldh18a1, 138250.0001) | rel=r_associated | relid=0 | w=42
  38. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the calcium-binding protein 2 gene (cabp2, 607314.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calcium-binding protein 2 gene (cabp2, 607314.0001) | rel=r_associated | relid=0 | w=42
  39. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the caspase recruitment domain-containing protein 14 gene (card14, 607211.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the caspase recruitment domain-containing protein 14 gene (card14, 607211.0006) | rel=r_associated | relid=0 | w=42
  40. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the cell death-inducing dffa-like effector c gene (cidec, 612120.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cell death-inducing dffa-like effector c gene (cidec, 612120.0001) | rel=r_associated | relid=0 | w=42
  41. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the cgmp-dependent regulatory protein kinase, type 1 gene (prkg1, 176894.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cgmp-dependent regulatory protein kinase, type 1 gene (prkg1, 176894.0001) | rel=r_associated | relid=0 | w=42
  42. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0004) | rel=r_associated | relid=0 | w=42
  43. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the coiled-coil-helix-coiled-coil helix domain-containing protein 10 gene (chchd10, 615903.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil-helix-coiled-coil helix domain-containing protein 10 gene (chchd10, 615903.0001) | rel=r_associated | relid=0 | w=42
  44. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the cytochrome c oxidase iii gene (mtco3, 516050.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase iii gene (mtco3, 516050.0005) | rel=r_associated | relid=0 | w=42
  45. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the desmin gene (des, 125660.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the desmin gene (des, 125660.0018) | rel=r_associated | relid=0 | w=42
  46. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the dna methyltransferase 1 gene (dnmt1, 126375.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna methyltransferase 1 gene (dnmt1, 126375.0001) | rel=r_associated | relid=0 | w=42
  47. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 1 gene (eif2b1, 606686.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 1 gene (eif2b1, 606686.0001) | rel=r_associated | relid=0 | w=42
  48. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the eukaryotic translation initiation factor 4-gamma, 1 gene (eif4g1, 600495.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation initiation factor 4-gamma, 1 gene (eif4g1, 600495.0001) | rel=r_associated | relid=0 | w=42
  49. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the ferritin heavy chain-1 gene (fth1, 134770.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ferritin heavy chain-1 gene (fth1, 134770.0001) | rel=r_associated | relid=0 | w=42
  50. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0002).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0002). | rel=r_associated | relid=0 | w=42
  51. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the gamma-aminobutyric acid receptor, gamma-2 gene (gabrg2, 137164.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma-aminobutyric acid receptor, gamma-2 gene (gabrg2, 137164.0002) | rel=r_associated | relid=0 | w=42
  52. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the gene encoding peripheral myelin protein-22 (pmp22, 601097.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding peripheral myelin protein-22 (pmp22, 601097.0004) | rel=r_associated | relid=0 | w=42
  53. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the h19 gene (h19, 103280.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the h19 gene (h19, 103280.0001) | rel=r_associated | relid=0 | w=42
  54. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the homolog of the mouse monogenic, audiogenic seizure susceptibility 1 gene (mass1, 602851.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse monogenic, audiogenic seizure susceptibility 1 gene (mass1, 602851.0001) | rel=r_associated | relid=0 | w=42
  55. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the homolog of the mouse pink-eyed dilution gene (oca2, 611409.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse pink-eyed dilution gene (oca2, 611409.0001) | rel=r_associated | relid=0 | w=42
  56. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the interferon-induced helicase c domain-containing protein 1 gene (ifih1, 606951.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interferon-induced helicase c domain-containing protein 1 gene (ifih1, 606951.0001) | rel=r_associated | relid=0 | w=42
  57. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the mitochondrial apoptogenic protein 1 gene (apopt1, 616003.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial apoptogenic protein 1 gene (apopt1, 616003.0001) | rel=r_associated | relid=0 | w=42
  58. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the nephrocystin 1 gene (nphp1, 607100.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nephrocystin 1 gene (nphp1, 607100.0001) | rel=r_associated | relid=0 | w=42
  59. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the nucleolar protein family a, member 3 gene (nola3, 606471.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nucleolar protein family a, member 3 gene (nola3, 606471.0001) | rel=r_associated | relid=0 | w=42
  60. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the potassium voltage-gated channel, shaker-related subfamily, member 1 gene (kcna1, 176260.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, shaker-related subfamily, member 1 gene (kcna1, 176260.0001) | rel=r_associated | relid=0 | w=42
  61. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the pou domain, class 1, transcription factor 1 gene (pou1f1, 173110.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pou domain, class 1, transcription factor 1 gene (pou1f1, 173110.0001) | rel=r_associated | relid=0 | w=42
  62. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the rab3 gtpase-activating protein subunit 1 gene (rab3gap1, 602536.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rab3 gtpase-activating protein subunit 1 gene (rab3gap1, 602536.0001) | rel=r_associated | relid=0 | w=42
  63. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the serine active site-containing protein 1 (serac1, 614725.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the serine active site-containing protein 1 (serac1, 614725.0001) | rel=r_associated | relid=0 | w=42
  64. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the serine protease inhibitor, kazal-type-1 gene (spink1, 167790.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the serine protease inhibitor, kazal-type-1 gene (spink1, 167790.0001) | rel=r_associated | relid=0 | w=42
  65. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the tafazzin gene (taz, 300394.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tafazzin gene (taz, 300394.0001) | rel=r_associated | relid=0 | w=42
  66. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the tar dna-binding protein (tardbp, 605078.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tar dna-binding protein (tardbp, 605078.0001) | rel=r_associated | relid=0 | w=42
  67. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the transmembrane protein 173 gene (tmem173, 612374.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 173 gene (tmem173, 612374.0001) | rel=r_associated | relid=0 | w=42
  68. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the tumor-associated calcium signal transducer 2 gene (tacstd2, 137290.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tumor-associated calcium signal transducer 2 gene (tacstd2, 137290.0001) | rel=r_associated | relid=0 | w=42
  69. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutation in the wd repeat-containing protein antisense to tp53 gene (wrap53, 612661.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein antisense to tp53 gene (wrap53, 612661.0001) | rel=r_associated | relid=0 | w=42
  70. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutations in the beta-2 integrin gene (itgb2, 600065.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the beta-2 integrin gene (itgb2, 600065.0001) | rel=r_associated | relid=0 | w=42
  71. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 42 / 0.977 -> en:caused by mutations in the excision-repair cross-complementing group 8 gene (ercc8, 609412.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the excision-repair cross-complementing group 8 gene (ercc8, 609412.0001) | rel=r_associated | relid=0 | w=42
  72. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the actin, alpha, cardiac muscle gene (actc1, 102540.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the actin, alpha, cardiac muscle gene (actc1, 102540.0001) | rel=r_associated | relid=0 | w=41
  73. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the atpase, h+ transporting, lysosomal, v0 subunit a2 gene (atp6v0a2, 611716.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, h+ transporting, lysosomal, v0 subunit a2 gene (atp6v0a2, 611716.0001) | rel=r_associated | relid=0 | w=41
  74. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the bbs5 gene (bbs5, 603650.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bbs5 gene (bbs5, 603650.0001) | rel=r_associated | relid=0 | w=41
  75. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the bone morphogenetic protein receptor, type 1b gene (bmpr1b, 603248.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bone morphogenetic protein receptor, type 1b gene (bmpr1b, 603248.0001) | rel=r_associated | relid=0 | w=41
  76. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the carbohydrate sulfotransferase-14 gene (chst14, 608429.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carbohydrate sulfotransferase-14 gene (chst14, 608429.0001) | rel=r_associated | relid=0 | w=41
  77. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the cytochrome c oxidase iii gene (mtco3, 516050.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase iii gene (mtco3, 516050.0001) | rel=r_associated | relid=0 | w=41
  78. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the cytochrome p450, subfamily iid6 gene (cyp2d6, 124030.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450, subfamily iid6 gene (cyp2d6, 124030.0001) | rel=r_associated | relid=0 | w=41
  79. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the filamin a gene (flna, 300017.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the filamin a gene (flna, 300017.0001) | rel=r_associated | relid=0 | w=41
  80. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the glutaredoxin, cysteine-rich, 2 gene (grxcr2, 615762.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutaredoxin, cysteine-rich, 2 gene (grxcr2, 615762.0001) | rel=r_associated | relid=0 | w=41
  81. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the katanin, p80 subunit, b1 gene (katnb1, 602703.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the katanin, p80 subunit, b1 gene (katnb1, 602703.0001) | rel=r_associated | relid=0 | w=41
  82. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the laminin beta-3 gene (lamb3, 150310.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the laminin beta-3 gene (lamb3, 150310.0001) | rel=r_associated | relid=0 | w=41
  83. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the male germ cell-associated kinase gene (mak, 154235.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the male germ cell-associated kinase gene (mak, 154235.0001) | rel=r_associated | relid=0 | w=41
  84. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the myeloid/lymphoid or mixed lineage leukemia gene (mll, 159555.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myeloid/lymphoid or mixed lineage leukemia gene (mll, 159555.0001) | rel=r_associated | relid=0 | w=41
  85. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 6 gene (ndufs6, 603848.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 6 gene (ndufs6, 603848.0001) | rel=r_associated | relid=0 | w=41
  86. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the rab3 gtpase-activating protein subunit 2 gene (rab3gap2, 609275.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rab3 gtpase-activating protein subunit 2 gene (rab3gap2, 609275.0001) | rel=r_associated | relid=0 | w=41
  87. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the sar1, s. cerevisiae, homolog b gene (sar1b, 607690.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sar1, s. cerevisiae, homolog b gene (sar1b, 607690.0001) | rel=r_associated | relid=0 | w=41
  88. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the sodium channel, nonvoltage-gated 1, alpha gene (scnn1a, 600228.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sodium channel, nonvoltage-gated 1, alpha gene (scnn1a, 600228.0006) | rel=r_associated | relid=0 | w=41
  89. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the solute carrier family 26, member 3 gene (slc26a3, 126650.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 26, member 3 gene (slc26a3, 126650.0001) | rel=r_associated | relid=0 | w=41
  90. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily b, member 1 gene (smarcb1, 601607.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily b, member 1 gene (smarcb1, 601607.0001) | rel=r_associated | relid=0 | w=41
  91. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutation in the udp-n-acetyl-alpha-d-galactosamine:polypeptide n-acetylgalactosaminyltransferase 3 gene (galnt3, 601756.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the udp-n-acetyl-alpha-d-galactosamine:polypeptide n-acetylgalactosaminyltransferase 3 gene (galnt3, 601756.0001) | rel=r_associated | relid=0 | w=41
  92. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutations in the emopamil-binding protein gene (ebp, 300205.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the emopamil-binding protein gene (ebp, 300205.0006) | rel=r_associated | relid=0 | w=41
  93. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutations in the low density lipoprotein receptor gene (ldlr, 143890.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the low density lipoprotein receptor gene (ldlr, 143890.0001) | rel=r_associated | relid=0 | w=41
  94. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:caused by mutations in the ret protoncogene (ret, 1645761.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the ret protoncogene (ret, 1645761.0001) | rel=r_associated | relid=0 | w=41
  95. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:conferred by mutation in the dual serine/threonine and tyrosine protein kinase gene (dstyk, 612666.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:conferred by mutation in the dual serine/threonine and tyrosine protein kinase gene (dstyk, 612666.0001) | rel=r_associated | relid=0 | w=41
  96. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 41 / 0.953 -> en:contiguous gene syndrome caused by homozygous deletion of approximately 122kb on chromosome 11p15-p14
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by homozygous deletion of approximately 122kb on chromosome 11p15-p14 | rel=r_associated | relid=0 | w=41
  97. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:a contiguous gene syndrome caused by deletion of the friend leukemia virus integration 1 gene (fli1, 193067) and perhaps other genes in 11q23
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome caused by deletion of the friend leukemia virus integration 1 gene (fli1, 193067) and perhaps other genes in 11q23 | rel=r_associated | relid=0 | w=40
  98. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by deletion of 3.0-30.0mb on 14q11-q22
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion of 3.0-30.0mb on 14q11-q22 | rel=r_associated | relid=0 | w=40
  99. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the 73-kd pdz-domain-containing protein (ush1c, 605242.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 73-kd pdz-domain-containing protein (ush1c, 605242.0001) | rel=r_associated | relid=0 | w=40
  100. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the alpha-3 laminin gene (lama3, 600805.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-3 laminin gene (lama3, 600805.0003) | rel=r_associated | relid=0 | w=40
  101. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the aminomethyltransferase gene (amt, 238310.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aminomethyltransferase gene (amt, 238310.0001) | rel=r_associated | relid=0 | w=40
  102. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the cholinergic receptor, nicotinic, beta-1 subunit (chrnb1, 100710.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, beta-1 subunit (chrnb1, 100710.0003) | rel=r_associated | relid=0 | w=40
  103. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the cytochrome c oxidase subunit iii gene (mtco3, 516050.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase subunit iii gene (mtco3, 516050.0004) | rel=r_associated | relid=0 | w=40
  104. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0003) | rel=r_associated | relid=0 | w=40
  105. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the deoxyribonuclease i-like 3 gene (dnase1l3, 602244.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the deoxyribonuclease i-like 3 gene (dnase1l3, 602244.0001) | rel=r_associated | relid=0 | w=40
  106. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the eukaryotic translation initiation factor 2-alpha kinase 3 (eif2ak3, 604032.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation initiation factor 2-alpha kinase 3 (eif2ak3, 604032.0001) | rel=r_associated | relid=0 | w=40
  107. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the factor xiii beta subunit (f13b, 134580.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the factor xiii beta subunit (f13b, 134580.0001) | rel=r_associated | relid=0 | w=40
  108. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the ferrochelatase gene (fech, 177000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ferrochelatase gene (fech, 177000.0001) | rel=r_associated | relid=0 | w=40
  109. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the fibroblast growth factor 3 gene (fgf3, 164950.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor 3 gene (fgf3, 164950.0001) | rel=r_associated | relid=0 | w=40
  110. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the filamin a gene (flna, 300017.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the filamin a gene (flna, 300017.0011) | rel=r_associated | relid=0 | w=40
  111. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the g protein signaling modulator 2 gene (gpsm2, 609245.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the g protein signaling modulator 2 gene (gpsm2, 609245.0001) | rel=r_associated | relid=0 | w=40
  112. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the g-protein, alpha-stimulating 1 gene (gnas1, 139320.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the g-protein, alpha-stimulating 1 gene (gnas1, 139320.0001) | rel=r_associated | relid=0 | w=40
  113. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the gamma g hemoglobin gene (hbg2, 142250.0025)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma g hemoglobin gene (hbg2, 142250.0025) | rel=r_associated | relid=0 | w=40
  114. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the gamma-b crystallin gene (crygb, 123670.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma-b crystallin gene (crygb, 123670.0001) | rel=r_associated | relid=0 | w=40
  115. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the gap junction protein, beta-2 gene (gjb2, 121011.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gap junction protein, beta-2 gene (gjb2, 121011.0002) | rel=r_associated | relid=0 | w=40
  116. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0018) | rel=r_associated | relid=0 | w=40
  117. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the inositol monophosphatase domain-containing protein 1 gene (impad1, 614010.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inositol monophosphatase domain-containing protein 1 gene (impad1, 614010.0001) | rel=r_associated | relid=0 | w=40
  118. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the mannosidase, alpha, class 1b, member 1 gene (man1b1, 604346.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mannosidase, alpha, class 1b, member 1 gene (man1b1, 604346.0001). | rel=r_associated | relid=0 | w=40
  119. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the methyl-cpg-binding protein 2 gene (mecp2, 300005.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methyl-cpg-binding protein 2 gene (mecp2, 300005.0003) | rel=r_associated | relid=0 | w=40
  120. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) 1 alpha subcomplex, 1 gene (ndufa1, 300078.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) 1 alpha subcomplex, 1 gene (ndufa1, 300078.0001) | rel=r_associated | relid=0 | w=40
  121. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the neutrophil-expressed elastase gene (elane, 130130.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neutrophil-expressed elastase gene (elane, 130130.0006) | rel=r_associated | relid=0 | w=40
  122. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the olfactory receptor, family 2, subfamily j, member 3 gene (or2j3, 615016.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the olfactory receptor, family 2, subfamily j, member 3 gene (or2j3, 615016.0001) | rel=r_associated | relid=0 | w=40
  123. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the sclerostin gene (sost, 605740.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sclerostin gene (sost, 605740.0005) | rel=r_associated | relid=0 | w=40
  124. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the short stature homeo box gene (shox, 312865.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the short stature homeo box gene (shox, 312865.0003) | rel=r_associated | relid=0 | w=40
  125. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the shugoshin-like-1 gene (sgol1, 609168.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the shugoshin-like-1 gene (sgol1, 609168.0001) | rel=r_associated | relid=0 | w=40
  126. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the sodium channel, nonvoltage-gated 1, beta gene (scnn1b, 600760.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sodium channel, nonvoltage-gated 1, beta gene (scnn1b, 600760.0009) | rel=r_associated | relid=0 | w=40
  127. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the spermine synthase gene (sms, 300105.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the spermine synthase gene (sms, 300105.0001) | rel=r_associated | relid=0 | w=40
  128. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the synaptojanin-1 gene (synj1, 604297.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the synaptojanin-1 gene (synj1, 604297.0001) | rel=r_associated | relid=0 | w=40
  129. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the t7 gene 4-like protein with intramitochondrial nucleoid localization gene (c10orf2, 606075.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the t7 gene 4-like protein with intramitochondrial nucleoid localization gene (c10orf2, 606075.0012) | rel=r_associated | relid=0 | w=40
  130. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0012) | rel=r_associated | relid=0 | w=40
  131. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutation in the wd repeat-containing protein 45 gene (wdr45, 300526.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein 45 gene (wdr45, 300526.0001) | rel=r_associated | relid=0 | w=40
  132. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutations in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0002) | rel=r_associated | relid=0 | w=40
  133. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutations in the cln8 gene (cln8, 607837.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cln8 gene (cln8, 607837.0002) | rel=r_associated | relid=0 | w=40
  134. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutations in the hexosaminidase a, alpha polypeptide gene (hexa, 272800.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the hexosaminidase a, alpha polypeptide gene (hexa, 272800.0001) | rel=r_associated | relid=0 | w=40
  135. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by mutations in the sh2 domain protein 1a gene (sh2d1a, 300490.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the sh2 domain protein 1a gene (sh2d1a, 300490.0001) | rel=r_associated | relid=0 | w=40
  136. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:caused by triplication of the alpha-synuclein gene (snca, 163890.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by triplication of the alpha-synuclein gene (snca, 163890.0003) | rel=r_associated | relid=0 | w=40
  137. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:contiguous gene deletion syndrome caused by deletion (650kb-3.7mb) of 17p11.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene deletion syndrome caused by deletion (650kb-3.7mb) of 17p11.2 | rel=r_associated | relid=0 | w=40
  138. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 40 / 0.93 -> en:contiguous gene syndrome caused by deletion of 18p11.21-p11.1
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by deletion of 18p11.21-p11.1 | rel=r_associated | relid=0 | w=40
  139. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:2p21del syndrome is a contiguous gene syndrome caused by 179kb deletion containing the slc3a1 (104614), prepl (609557), ppm1b (603770), and c2orf34 (609559) genes
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:2p21del syndrome is a contiguous gene syndrome caused by 179kb deletion containing the slc3a1 (104614), prepl (609557), ppm1b (603770), and c2orf34 (609559) genes | rel=r_associated | relid=0 | w=39
  140. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the aldolase b, fructose-bisphosphate gene (aldob, 612724.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aldolase b, fructose-bisphosphate gene (aldob, 612724.0001) | rel=r_associated | relid=0 | w=39
  141. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the alpha-1,4-glucosidase gene (gaa, 606800.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1,4-glucosidase gene (gaa, 606800.0002) | rel=r_associated | relid=0 | w=39
  142. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the alpha-4 laminin gene (lama4, 600133.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-4 laminin gene (lama4, 600133.0001) | rel=r_associated | relid=0 | w=39
  143. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the androgen receptor gene (ar, 313700.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the androgen receptor gene (ar, 313700.0001) | rel=r_associated | relid=0 | w=39
  144. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the atp-binding cassette, subfamily b, member 11 gene (abcb11, 603201.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily b, member 11 gene (abcb11, 603201.0001) | rel=r_associated | relid=0 | w=39
  145. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the fxyd domain-containing ion transport regulator 2 gene (fxyd2, 601814.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fxyd domain-containing ion transport regulator 2 gene (fxyd2, 601814.0001) | rel=r_associated | relid=0 | w=39
  146. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the gene encoding a disintegrin and metalloproteinase domain-10 (adam10, 602192.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding a disintegrin and metalloproteinase domain-10 (adam10, 602192.0001) | rel=r_associated | relid=0 | w=39
  147. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the glutamate-cysteine ligase, catalytic subunit gene (gclc, 606857.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutamate-cysteine ligase, catalytic subunit gene (gclc, 606857.0001) | rel=r_associated | relid=0 | w=39
  148. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the homolog of the yeast vacuolar protein sorting 35 gene (vps35, 601501.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the yeast vacuolar protein sorting 35 gene (vps35, 601501.0001) | rel=r_associated | relid=0 | w=39
  149. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the leucine-rich repeat, immunoglobulin-like, and transmembrane domains-containing protein-3 gene (lrit3, 615004.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucine-rich repeat, immunoglobulin-like, and transmembrane domains-containing protein-3 gene (lrit3, 615004.0001) | rel=r_associated | relid=0 | w=39
  150. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the mitochondrial trna (valine) gene (mttv, 590105.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial trna (valine) gene (mttv, 590105.0002) | rel=r_associated | relid=0 | w=39
  151. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the nonerythrocytic beta 2 spectrin gene (sptbn2, 604985.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nonerythrocytic beta 2 spectrin gene (sptbn2, 604985.0001) | rel=r_associated | relid=0 | w=39
  152. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the nuclear factor i/x gene (nfix, 164005.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear factor i/x gene (nfix, 164005.0002) | rel=r_associated | relid=0 | w=39
  153. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the phosphodiesterase-6c, cgmp-specific, cone, alpha prime gene (pde6c, 600827.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphodiesterase-6c, cgmp-specific, cone, alpha prime gene (pde6c, 600827.0001) | rel=r_associated | relid=0 | w=39
  154. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the phosphomannomutase 2 gene (pmm2, 601785.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphomannomutase 2 gene (pmm2, 601785.0001) | rel=r_associated | relid=0 | w=39
  155. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the plakophilin-2 gene (602861.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the plakophilin-2 gene (602861.0001) | rel=r_associated | relid=0 | w=39
  156. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the rho guanine nucleotide exchange factor 9 gene (arhgef9, 300429.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rho guanine nucleotide exchange factor 9 gene (arhgef9, 300429.0001) | rel=r_associated | relid=0 | w=39
  157. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the senataxin gene (setx, 608465.00006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the senataxin gene (setx, 608465.00006) | rel=r_associated | relid=0 | w=39
  158. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the sh3 domain-binding protein-2 gene (sh3bp2, 602104.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sh3 domain-binding protein-2 gene (sh3bp2, 602104.0001) | rel=r_associated | relid=0 | w=39
  159. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the sialyltransferase-9 gene (siat9, 604402.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sialyltransferase-9 gene (siat9, 604402.0001) | rel=r_associated | relid=0 | w=39
  160. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, aralar), member 12 gene (slc25a12, 603667.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, aralar), member 12 gene (slc25a12, 603667.0001) | rel=r_associated | relid=0 | w=39
  161. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the telethonin gene (tcap, 604488.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the telethonin gene (tcap, 604488.0001). | rel=r_associated | relid=0 | w=39
  162. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0006) | rel=r_associated | relid=0 | w=39
  163. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0006) | rel=r_associated | relid=0 | w=39
  164. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutation in the wd repeat-containing protein 62 (wdr62, 613583.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein 62 (wdr62, 613583.0001) | rel=r_associated | relid=0 | w=39
  165. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0006) | rel=r_associated | relid=0 | w=39
  166. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutations in the helicase-2 gene (xh2, 300032.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the helicase-2 gene (xh2, 300032.0011) | rel=r_associated | relid=0 | w=39
  167. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutations in the sclerostin gene (sost, 605740.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the sclerostin gene (sost, 605740.0001) | rel=r_associated | relid=0 | w=39
  168. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:caused by mutations in the solute carrier family 4, sodium bicarbonate cotransporter, member 4 gene (slc4a4, 603345.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the solute carrier family 4, sodium bicarbonate cotransporter, member 4 gene (slc4a4, 603345.0001) | rel=r_associated | relid=0 | w=39
  169. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 39 / 0.907 -> en:contiguous gene deletion syndrome caused by microdeletion (43-490kb) of chromosome 11q13
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene deletion syndrome caused by microdeletion (43-490kb) of chromosome 11q13 | rel=r_associated | relid=0 | w=39
  170. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by duplication of 186-260kb on 16p13.3
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of 186-260kb on 16p13.3 | rel=r_associated | relid=0 | w=38
  171. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by expanded cag trinucleotide repeats in the ataxin-1 gene (atx1, 601556.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by expanded cag trinucleotide repeats in the ataxin-1 gene (atx1, 601556.0001) | rel=r_associated | relid=0 | w=38
  172. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in chromosome 6 open reading frame 221 gene (c6orf221, 611687.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in chromosome 6 open reading frame 221 gene (c6orf221, 611687.0001) | rel=r_associated | relid=0 | w=38
  173. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the activation-induced cytidine deaminase gene (aicda, 605257.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the activation-induced cytidine deaminase gene (aicda, 605257.0001) | rel=r_associated | relid=0 | w=38
  174. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the alanyl-trna synthetase 2 gene (aars2, 612035.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alanyl-trna synthetase 2 gene (aars2, 612035.0004) | rel=r_associated | relid=0 | w=38
  175. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the arginine vasopressin receptor 2 gene (avpr2, 300538.0021)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the arginine vasopressin receptor 2 gene (avpr2, 300538.0021) | rel=r_associated | relid=0 | w=38
  176. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the coiled-coil domain-containing protein 11 gene (ccdc11, 614759.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil domain-containing protein 11 gene (ccdc11, 614759.0001) | rel=r_associated | relid=0 | w=38
  177. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the dna polymerase-gamma gene (polg, 174763.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna polymerase-gamma gene (polg, 174763.0002) | rel=r_associated | relid=0 | w=38
  178. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the dyskerin gene (dkc1, 300126.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dyskerin gene (dkc1, 300126.0001) | rel=r_associated | relid=0 | w=38
  179. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the family with sequence similarity 111, member b gene (fam111b, 615584.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the family with sequence similarity 111, member b gene (fam111b, 615584.0001) | rel=r_associated | relid=0 | w=38
  180. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the gamma subunit of the nonvoltage-gated sodium channel 1 gene (scnn1g, 600761.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma subunit of the nonvoltage-gated sodium channel 1 gene (scnn1g, 600761.0002) | rel=r_associated | relid=0 | w=38
  181. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the gnas complex locus, antisense transcript (gnasas, 610540.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gnas complex locus, antisense transcript (gnasas, 610540.0001) | rel=r_associated | relid=0 | w=38
  182. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the homeo box c13 gene (hoxc13, 142976.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeo box c13 gene (hoxc13, 142976.0001) | rel=r_associated | relid=0 | w=38
  183. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the homolog of the s. cerevisiae alg6 gene (alg6, 604566.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae alg6 gene (alg6, 604566.0001) | rel=r_associated | relid=0 | w=38
  184. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the interferon regulatory factor 8 gene (irf8, 601565.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interferon regulatory factor 8 gene (irf8, 601565.0001) | rel=r_associated | relid=0 | w=38
  185. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the keratin 10 gene (krt10, 148080.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 10 gene (krt10, 148080.0014) | rel=r_associated | relid=0 | w=38
  186. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the lim homeo box gene 4 (lhx4, 602146.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lim homeo box gene 4 (lhx4, 602146.0001) | rel=r_associated | relid=0 | w=38
  187. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the matrix metalloproteinase-13 gene (mmp13, 600108.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the matrix metalloproteinase-13 gene (mmp13, 600108.0001). | rel=r_associated | relid=0 | w=38
  188. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the mitochondrial lon peptidase-1 gene (lonp1, 605490.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial lon peptidase-1 gene (lonp1, 605490.0001) | rel=r_associated | relid=0 | w=38
  189. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the mitochondrial trna (leucine)-1 gene (mttl1, 590050.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial trna (leucine)-1 gene (mttl1, 590050.0011) | rel=r_associated | relid=0 | w=38
  190. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the myosin viia gene (myo7a, 276903.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin viia gene (myo7a, 276903.0001) | rel=r_associated | relid=0 | w=38
  191. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the neurotrophic tyrosine kinase receptor, type 1, gene (ntrk1, 191315.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neurotrophic tyrosine kinase receptor, type 1, gene (ntrk1, 191315.0001) | rel=r_associated | relid=0 | w=38
  192. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the nuclear receptor binding set domain protein 1 (nsd1, 606681.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear receptor binding set domain protein 1 (nsd1, 606681.0011) | rel=r_associated | relid=0 | w=38
  193. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the nuclear-encoded mitochondrial deoxyguanosine kinase gene (dguok, 601465.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear-encoded mitochondrial deoxyguanosine kinase gene (dguok, 601465.0001). | rel=r_associated | relid=0 | w=38
  194. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 2 gene (kcnq2, 602235.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 2 gene (kcnq2, 602235.0001) | rel=r_associated | relid=0 | w=38
  195. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the protein tyrosine phosphatase, nonreceptor-type, 11 gene (ptpn11, 176876.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein tyrosine phosphatase, nonreceptor-type, 11 gene (ptpn11, 176876.0001) | rel=r_associated | relid=0 | w=38
  196. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the rab3 gtpase-activating protein (noncatalytic) subunit 2 gene (rab3gap2, 609275.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rab3 gtpase-activating protein (noncatalytic) subunit 2 gene (rab3gap2, 609275.0002) | rel=r_associated | relid=0 | w=38
  197. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the ras-associated protein rab39b gene (rab39b, 300774.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ras-associated protein rab39b gene (rab39b, 300774.0003) | rel=r_associated | relid=0 | w=38
  198. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the ribonuclease h2, subunit a gene (rnaseh2a, 606034.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribonuclease h2, subunit a gene (rnaseh2a, 606034.0001) | rel=r_associated | relid=0 | w=38
  199. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the sulfatase-modifying factor 1 gene (sumf1, 607939.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sulfatase-modifying factor 1 gene (sumf1, 607939.0001) | rel=r_associated | relid=0 | w=38
  200. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the synaptonemal complex protein-3 gene (sycp3, 604759.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the synaptonemal complex protein-3 gene (sycp3, 604759.0001) | rel=r_associated | relid=0 | w=38
  201. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutation in the ubiquinol-cytochrome c reductase core protein ii gene (uqcr2, 191329.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquinol-cytochrome c reductase core protein ii gene (uqcr2, 191329.0001) | rel=r_associated | relid=0 | w=38
  202. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutations in the marvel domain-containing protein 2 gene (marveld2, 610572.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the marvel domain-containing protein 2 gene (marveld2, 610572.0001) | rel=r_associated | relid=0 | w=38
  203. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutations in the n(5,10)-methylenetetrahydrofolate reductase gene (mthfr, 607093.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the n(5,10)-methylenetetrahydrofolate reductase gene (mthfr, 607093.0001) | rel=r_associated | relid=0 | w=38
  204. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutations in the nad(p)h steroid dehydrogenase-like protein gene (nsdhl, 300275.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the nad(p)h steroid dehydrogenase-like protein gene (nsdhl, 300275.0001) | rel=r_associated | relid=0 | w=38
  205. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:caused by mutations in the thyroid peroxidase gene (tpo, 606765.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the thyroid peroxidase gene (tpo, 606765.0001) | rel=r_associated | relid=0 | w=38
  206. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 38 / 0.884 -> en:full trisomy 21, 94%
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:full trisomy 21, 94% | rel=r_associated | relid=0 | w=38
  207. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:a contiguous gene syndrome caused by deletion of 180kb encompassing 18 genes on chromosome 17p13.1
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome caused by deletion of 180kb encompassing 18 genes on chromosome 17p13.1 | rel=r_associated | relid=0 | w=37
  208. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by duplications or deletions on xq26 involving the sry-box 3 gene (sox3, 313430)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplications or deletions on xq26 involving the sry-box 3 gene (sox3, 313430) | rel=r_associated | relid=0 | w=37
  209. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in paired box gene-1 (pax1, 167411.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in paired box gene-1 (pax1, 167411.0001) | rel=r_associated | relid=0 | w=37
  210. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the 41-kd centrosomal protein gene (cep41, 610523.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 41-kd centrosomal protein gene (cep41, 610523.0001) | rel=r_associated | relid=0 | w=37
  211. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the alpha-sarcoglycan gene (sgca, 600119.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-sarcoglycan gene (sgca, 600119.0001) | rel=r_associated | relid=0 | w=37
  212. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the beta-actin gene (actb, 102630.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-actin gene (actb, 102630.0001). | rel=r_associated | relid=0 | w=37
  213. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the bmp binding endothelial regulator gene (bmper, 608699.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bmp binding endothelial regulator gene (bmper, 608699.0001) | rel=r_associated | relid=0 | w=37
  214. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the dolichyl-phosphate n-acetylglucosamine phosphotransferase gene (dpagt1, 191350.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dolichyl-phosphate n-acetylglucosamine phosphotransferase gene (dpagt1, 191350.0001) | rel=r_associated | relid=0 | w=37
  215. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the exosome component 8 gene (exosc8, 606019.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the exosome component 8 gene (exosc8, 606019.0001) | rel=r_associated | relid=0 | w=37
  216. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the fez family zinc finger protein-1 gene (fezf1, 613301.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fez family zinc finger protein-1 gene (fezf1, 613301.0001) | rel=r_associated | relid=0 | w=37
  217. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the fibroblast growth factor 10 gene (fgf10, 602115.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor 10 gene (fgf10, 602115.0003) | rel=r_associated | relid=0 | w=37
  218. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the filamin a gene (flna, 300017.0025)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the filamin a gene (flna, 300017.0025) | rel=r_associated | relid=0 | w=37
  219. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0001) | rel=r_associated | relid=0 | w=37
  220. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the gata-binding protein 2 gene (gata2, 137295.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein 2 gene (gata2, 137295.0001) | rel=r_associated | relid=0 | w=37
  221. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the grhl2 gene (608576.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the grhl2 gene (608576.0001) | rel=r_associated | relid=0 | w=37
  222. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the heparan sulfate 6-o-sulfotransferase-1 gene (hs6st1, 604846.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heparan sulfate 6-o-sulfotransferase-1 gene (hs6st1, 604846.0001) | rel=r_associated | relid=0 | w=37
  223. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the lysyl-trna synthetase gene (kars, 601421.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lysyl-trna synthetase gene (kars, 601421.0001) | rel=r_associated | relid=0 | w=37
  224. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the mads box transcription enhancer factor 2, polypeptide c gene (mef2c, 600662.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mads box transcription enhancer factor 2, polypeptide c gene (mef2c, 600662.0001) | rel=r_associated | relid=0 | w=37
  225. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the matrix metalloproteinase-20 gene (mmp20, 604629.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the matrix metalloproteinase-20 gene (mmp20, 604629.0001) | rel=r_associated | relid=0 | w=37
  226. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the methionine sulfoxide reductase b3 gene (msrb3, 613719.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methionine sulfoxide reductase b3 gene (msrb3, 613719.0001) | rel=r_associated | relid=0 | w=37
  227. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the myosin va gene (myo5a, 160777.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin va gene (myo5a, 160777.0002) | rel=r_associated | relid=0 | w=37
  228. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the n-acylsphingosine amidohydrolase 1 gene (asah1, 613468.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the n-acylsphingosine amidohydrolase 1 gene (asah1, 613468.0006) | rel=r_associated | relid=0 | w=37
  229. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 2 gene (ndufs2, 602985.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 2 gene (ndufs2, 602985.0001) | rel=r_associated | relid=0 | w=37
  230. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the nuclear receptor subfamily 2, group f, member 2 gene (nr2f2, 107773.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear receptor subfamily 2, group f, member 2 gene (nr2f2, 107773.0001) | rel=r_associated | relid=0 | w=37
  231. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the nuclear receptor subfamily 3, group c, member 1 gene (nr3c1, 138040.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear receptor subfamily 3, group c, member 1 gene (nr3c1, 138040.0001) | rel=r_associated | relid=0 | w=37
  232. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the peptidase d gene (pepd, 613230.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peptidase d gene (pepd, 613230.0001) | rel=r_associated | relid=0 | w=37
  233. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the phosphatidylinositol glycan, class v gene (pigv, 610274.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol glycan, class v gene (pigv, 610274.0001) | rel=r_associated | relid=0 | w=37
  234. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 192500.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 192500.0013) | rel=r_associated | relid=0 | w=37
  235. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the set-binding factor-2 gene (sbf2, 607697.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the set-binding factor-2 gene (sbf2, 607697.0001) | rel=r_associated | relid=0 | w=37
  236. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the sry-box-10 gene (sox10, 602229.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sry-box-10 gene (sox10, 602229.0001) | rel=r_associated | relid=0 | w=37
  237. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the tbc1 domain family, member 20 gene (tbc1d20, 611663.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tbc1 domain family, member 20 gene (tbc1d20, 611663.0001) | rel=r_associated | relid=0 | w=37
  238. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the testis/liver gamma-2 subunit of phosphorylase kinase gene (phkg2, 172471.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the testis/liver gamma-2 subunit of phosphorylase kinase gene (phkg2, 172471.0001) | rel=r_associated | relid=0 | w=37
  239. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the thyroid transcription factor 1 gene (titf1, 600635.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thyroid transcription factor 1 gene (titf1, 600635.0005) | rel=r_associated | relid=0 | w=37
  240. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the transmembrane 43 gene (tmem43, 612048.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane 43 gene (tmem43, 612048.0002) | rel=r_associated | relid=0 | w=37
  241. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the twist transcription factor gene (twist, 601622.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the twist transcription factor gene (twist, 601622.0001) | rel=r_associated | relid=0 | w=37
  242. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:caused by mutation in the wnk lysine deficient protein kinase 4 gene (wnk4, 601844.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wnk lysine deficient protein kinase 4 gene (wnk4, 601844.0001) | rel=r_associated | relid=0 | w=37
  243. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:features other than acd/mpv are variably present
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:features other than acd/mpv are variably present | rel=r_associated | relid=0 | w=37
  244. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:linked to a locus at 16q.
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:linked to a locus at 16q. | rel=r_associated | relid=0 | w=37
  245. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:susceptibility conferred by mutation in the inwardly rectifying potassium channel, subfamily j, member 18 gene (kcnj18, 613236.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the inwardly rectifying potassium channel, subfamily j, member 18 gene (kcnj18, 613236.0001) | rel=r_associated | relid=0 | w=37
  246. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 37 / 0.86 -> en:susceptibility conferred by mutation in the toll-like receptor-2 gene (tlr2, 603028.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the toll-like receptor-2 gene (tlr2, 603028.0001) | rel=r_associated | relid=0 | w=37
  247. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:a contiguous gene deletion syndrome caused by a deletion (3.9 mb) of chromosome 2p16.1-p15
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene deletion syndrome caused by a deletion (3.9 mb) of chromosome 2p16.1-p15 | rel=r_associated | relid=0 | w=36
  248. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:a contiguous gene syndrome caused by deletion of the lissencephaly 1 gene (lis1, 601545) and the tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon isoform gene (ywhae, 605066)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome caused by deletion of the lissencephaly 1 gene (lis1, 601545) and the tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon isoform gene (ywhae, 605066) | rel=r_associated | relid=0 | w=36
  249. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:a contiguous gene syndrome caused by mutations in the zinc finger transcription factor trps1 (trps1, 604386) and the exostosin 1 gene (ext1, 133700)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome caused by mutations in the zinc finger transcription factor trps1 (trps1, 604386) and the exostosin 1 gene (ext1, 133700) | rel=r_associated | relid=0 | w=36
  250. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:associated with mutation in the p53 tumor protein gene (tp53, 191170.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:associated with mutation in the p53 tumor protein gene (tp53, 191170.0006) | rel=r_associated | relid=0 | w=36
  251. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:bcl2 gene on chromosome 18q21 is juxtaposed to igh gene at 14q32, resulting chimeric bcl2-igh mrna is expressed blocking apoptosis
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:bcl2 gene on chromosome 18q21 is juxtaposed to igh gene at 14q32, resulting chimeric bcl2-igh mrna is expressed blocking apoptosis | rel=r_associated | relid=0 | w=36
  252. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by deletion of 6-12mb on 3pter-p25
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion of 6-12mb on 3pter-p25 | rel=r_associated | relid=0 | w=36
  253. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by duplication of 0.9 - 1.2 mb on 8q22.1
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of 0.9 - 1.2 mb on 8q22.1 | rel=r_associated | relid=0 | w=36
  254. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by duplication of the methyl-cp6-binding protein 2 gene (mecp2, 300005.0030)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of the methyl-cp6-binding protein 2 gene (mecp2, 300005.0030) | rel=r_associated | relid=0 | w=36
  255. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by hexanucleotide repeat expansion (ggcctg)n in the homolog of the s. cerevisiae nop56 gene (nop56, 614154.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by hexanucleotide repeat expansion (ggcctg)n in the homolog of the s. cerevisiae nop56 gene (nop56, 614154.0001) | rel=r_associated | relid=0 | w=36
  256. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by interstitial or terminal deletion of chromosome 18q
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by interstitial or terminal deletion of chromosome 18q | rel=r_associated | relid=0 | w=36
  257. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0014) and the gap junction protein, beta-3 gene (gjb3, 603324.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0014) and the gap junction protein, beta-3 gene (gjb3, 603324.0011) | rel=r_associated | relid=0 | w=36
  258. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in glycogen synthase 1 gene (gys1, 138570.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in glycogen synthase 1 gene (gys1, 138570.0001) | rel=r_associated | relid=0 | w=36
  259. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in phosphorylase kinase, beta subunit (phkb, 172490.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in phosphorylase kinase, beta subunit (phkb, 172490.0001) | rel=r_associated | relid=0 | w=36
  260. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase 4 gene (hsd17b4, 601860.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase 4 gene (hsd17b4, 601860.0008) | rel=r_associated | relid=0 | w=36
  261. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase x gene (hsd17b10, 300256.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase x gene (hsd17b10, 300256.0001) | rel=r_associated | relid=0 | w=36
  262. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the 290-kd centrosomal protein (cep290, 610142.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 290-kd centrosomal protein (cep290, 610142.0013) | rel=r_associated | relid=0 | w=36
  263. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the 3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2 gene (papss2, 603005.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2 gene (papss2, 603005.0001) | rel=r_associated | relid=0 | w=36
  264. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the 4-aminobutyrate aminotransferase gene (abat, 137150.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 4-aminobutyrate aminotransferase gene (abat, 137150.0001) | rel=r_associated | relid=0 | w=36
  265. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the 57-kd centrosomal protein gene (cep57, 607951.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 57-kd centrosomal protein gene (cep57, 607951.0001) | rel=r_associated | relid=0 | w=36
  266. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the acid beta-glucosidase gene (gba, 606463.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the acid beta-glucosidase gene (gba, 606463.0006) | rel=r_associated | relid=0 | w=36
  267. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the actin, alpha-2, smooth muscle, aorta gene (acta2, 102620.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the actin, alpha-2, smooth muscle, aorta gene (acta2, 102620.0004) | rel=r_associated | relid=0 | w=36
  268. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the adp-ribosylation factor guanine nucleotide exchange factor 2 gene (arfgef2, 605371.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adp-ribosylation factor guanine nucleotide exchange factor 2 gene (arfgef2, 605371.0001) | rel=r_associated | relid=0 | w=36
  269. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the alkaline phosphatase gene (alpl, 171760.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alkaline phosphatase gene (alpl, 171760.0001) | rel=r_associated | relid=0 | w=36
  270. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the alpha-1-subunit of the voltage-gated type ii sodium channel gene (scn2a, 182390.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1-subunit of the voltage-gated type ii sodium channel gene (scn2a, 182390.0002) | rel=r_associated | relid=0 | w=36
  271. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the alpha-3 catenin gene (ctnna3, 607667.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-3 catenin gene (ctnna3, 607667.0001) | rel=r_associated | relid=0 | w=36
  272. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the alpha-5 gap junction protein gene (gja5, 121013.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-5 gap junction protein gene (gja5, 121013.0001) | rel=r_associated | relid=0 | w=36
  273. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the alpha-actin-1 gene (acta1, 102610.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-actin-1 gene (acta1, 102610.0001) | rel=r_associated | relid=0 | w=36
  274. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the alpha-b-crystallin gene (cryab, 123590.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-b-crystallin gene (cryab, 123590.0001) | rel=r_associated | relid=0 | w=36
  275. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0004) | rel=r_associated | relid=0 | w=36
  276. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the alpha-tectorin gene (tecta, 602574.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-tectorin gene (tecta, 602574.0001) | rel=r_associated | relid=0 | w=36
  277. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the alsin gene (als2, 606352.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alsin gene (als2, 606352.0005) | rel=r_associated | relid=0 | w=36
  278. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the angiotensin-converting enzyme gene (ace, 106180.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the angiotensin-converting enzyme gene (ace, 106180.0003) | rel=r_associated | relid=0 | w=36
  279. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ankyrin 2 gene (ank2, 106410.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ankyrin 2 gene (ank2, 106410.0001) | rel=r_associated | relid=0 | w=36
  280. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ankyrin repeat domain-containing protein 11 gene (ankrd11, 611192.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ankyrin repeat domain-containing protein 11 gene (ankrd11, 611192.0001) | rel=r_associated | relid=0 | w=36
  281. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the anoctamin 5 gene gene (ano5, 608662.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the anoctamin 5 gene gene (ano5, 608662.0001) | rel=r_associated | relid=0 | w=36
  282. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the arginase gene (arg1, 207800.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the arginase gene (arg1, 207800.0001) | rel=r_associated | relid=0 | w=36
  283. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the aristaless-like homeobox 3 gene (alx3, 606014.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aristaless-like homeobox 3 gene (alx3, 606014.0001) | rel=r_associated | relid=0 | w=36
  284. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the artemis gene (artemis, 605988.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the artemis gene (artemis, 605988.0001) | rel=r_associated | relid=0 | w=36
  285. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the arylsulfatase e gene (arse, 300180.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the arylsulfatase e gene (arse, 300180.0001) | rel=r_associated | relid=0 | w=36
  286. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the aspartyl-trna synthetase 2 gene (dars2, 610956.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aspartyl-trna synthetase 2 gene (dars2, 610956.0001) | rel=r_associated | relid=0 | w=36
  287. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the atlastin gtpase 3 gene (atl3, 609369.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atlastin gtpase 3 gene (atl3, 609369.0001) | rel=r_associated | relid=0 | w=36
  288. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the atp-binding cassette, subfamily g, member 5 gene (abcg5, 605459.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily g, member 5 gene (abcg5, 605459.0001) | rel=r_associated | relid=0 | w=36
  289. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the atpase, cu++ transporting, alpha polypeptide gene (atp7a, 300011.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, cu++ transporting, alpha polypeptide gene (atp7a, 300011.0001) | rel=r_associated | relid=0 | w=36
  290. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the atpase, h+ transporting, lysosomal, beta polypeptide, 58kd gene (atp6b1, 192132.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, h+ transporting, lysosomal, beta polypeptide, 58kd gene (atp6b1, 192132.0001) | rel=r_associated | relid=0 | w=36
  291. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the avian sarcoma viral (v-ski) oncogene homolog gene (ski, 164780.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the avian sarcoma viral (v-ski) oncogene homolog gene (ski, 164780.0001) | rel=r_associated | relid=0 | w=36
  292. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the axonemal dynein assembly factor 3 gene (dnaaf3, 614566.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the axonemal dynein assembly factor 3 gene (dnaaf3, 614566.0001) | rel=r_associated | relid=0 | w=36
  293. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the bcl2-associated athanogene 3 gene (bag3, 603883.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bcl2-associated athanogene 3 gene (bag3, 603883.0002) | rel=r_associated | relid=0 | w=36
  294. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the beta acid glucosidase 2 gene (gba2, 609471.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta acid glucosidase 2 gene (gba2, 609471.0001) | rel=r_associated | relid=0 | w=36
  295. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the beta subunit of the hydroxyacyl-coa dehydrogenase/3-ketoacyl-coa thiolase/enoyl-coa hydratase (hadhb, 143450.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta subunit of the hydroxyacyl-coa dehydrogenase/3-ketoacyl-coa thiolase/enoyl-coa hydratase (hadhb, 143450.0001) | rel=r_associated | relid=0 | w=36
  296. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the beta-1,3-glucosyltransferase gene (b3galtl, 610308.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1,3-glucosyltransferase gene (b3galtl, 610308.0001) | rel=r_associated | relid=0 | w=36
  297. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the beta-1,3-n-acetylgalactosaminyltransferase 2 gene (b3galnt2, 610194.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1,3-n-acetylgalactosaminyltransferase 2 gene (b3galnt2, 610194.0001) | rel=r_associated | relid=0 | w=36
  298. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the beta-2b tubulin gene (tubb2b, 612850.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-2b tubulin gene (tubb2b, 612850.0001) | rel=r_associated | relid=0 | w=36
  299. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the beta-3 transforming growth factor gene (tgfb3, 190230.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-3 transforming growth factor gene (tgfb3, 190230.0003) | rel=r_associated | relid=0 | w=36
  300. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the bone morphogenetic protein-1 gene (bmp1, 112264.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bone morphogenetic protein-1 gene (bmp1, 112264.0001) | rel=r_associated | relid=0 | w=36
  301. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the bruton tyrosine kinase gene (btk, 300300.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bruton tyrosine kinase gene (btk, 300300.0004) | rel=r_associated | relid=0 | w=36
  302. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the c1q- and tumor necrosis factor-related protein 5 gene (c1qtnf5, 608752.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the c1q- and tumor necrosis factor-related protein 5 gene (c1qtnf5, 608752.0001) | rel=r_associated | relid=0 | w=36
  303. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the c20orf7 gene (612360.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the c20orf7 gene (612360.0001) | rel=r_associated | relid=0 | w=36
  304. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cadherin 23 gene (cdh23, 605516.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cadherin 23 gene (cdh23, 605516.0001) | rel=r_associated | relid=0 | w=36
  305. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cancer susceptibility candidate 5 gene (casc5, 609173.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cancer susceptibility candidate 5 gene (casc5, 609173.0001) | rel=r_associated | relid=0 | w=36
  306. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the carbonic anhydrase va gene (ca5a, 114761.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carbonic anhydrase va gene (ca5a, 114761.0001) | rel=r_associated | relid=0 | w=36
  307. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the carboxypeptidase a6 gene (cpa6, 609562.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carboxypeptidase a6 gene (cpa6, 609562.0002) | rel=r_associated | relid=0 | w=36
  308. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cardiac muscle alpha actin gene (actc1, 102540.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cardiac muscle alpha actin gene (actc1, 102540.0003) | rel=r_associated | relid=0 | w=36
  309. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cathepsin c gene (ctsc, 602365.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cathepsin c gene (ctsc, 602365.0006) | rel=r_associated | relid=0 | w=36
  310. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ccm2 gene (ccm2, 607929.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ccm2 gene (ccm2, 607929.0001) | rel=r_associated | relid=0 | w=36
  311. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cd3 antigen, epsilon subunit gene (cd3e, 186830.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd3 antigen, epsilon subunit gene (cd3e, 186830.0003) | rel=r_associated | relid=0 | w=36
  312. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the centrosome spindle pole-associated protein 1 gene (cspp1, 611654.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the centrosome spindle pole-associated protein 1 gene (cspp1, 611654.0001) | rel=r_associated | relid=0 | w=36
  313. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ceramide synthase 1 gene (cers1, 606919.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ceramide synthase 1 gene (cers1, 606919.0001) | rel=r_associated | relid=0 | w=36
  314. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the chloride channel 2 gene (clcn2, 600570.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chloride channel 2 gene (clcn2, 600570.0006) | rel=r_associated | relid=0 | w=36
  315. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the chloride intracellular channel 2 gene (clic2, 300138.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chloride intracellular channel 2 gene (clic2, 300138.0001) | rel=r_associated | relid=0 | w=36
  316. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cholinergic receptor, nicotinic, alpha polypeptide-1, muscle gene (chrna1, 100690.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, alpha polypeptide-1, muscle gene (chrna1, 100690.0013) | rel=r_associated | relid=0 | w=36
  317. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the chromosome 12 open reading frame 62 gene (c12orf62, 614478.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 12 open reading frame 62 gene (c12orf62, 614478.0001) | rel=r_associated | relid=0 | w=36
  318. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the chromosome 16 open reading frame 57 gene (c16orf57, 613276.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 16 open reading frame 57 gene (c16orf57, 613276.0001) | rel=r_associated | relid=0 | w=36
  319. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the chromosome 2 open reading frame 25 gene (c2orf25, 611935.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 2 open reading frame 25 gene (c2orf25, 611935.0001) | rel=r_associated | relid=0 | w=36
  320. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the claudin 19 (cldn19, 610036.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the claudin 19 (cldn19, 610036.0001) | rel=r_associated | relid=0 | w=36
  321. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the coagulation factor ii gene (f2, 176930.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coagulation factor ii gene (f2, 176930.0001) | rel=r_associated | relid=0 | w=36
  322. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the coagulation factor ix gene (f9, 300746.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coagulation factor ix gene (f9, 300746.0001) | rel=r_associated | relid=0 | w=36
  323. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the coagulation factor v gene (f5, 612309.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coagulation factor v gene (f5, 612309.0004) | rel=r_associated | relid=0 | w=36
  324. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the coenzyme a synthase gene (coasy, 609855.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coenzyme a synthase gene (coasy, 609855.0001) | rel=r_associated | relid=0 | w=36
  325. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the coiled-coil and c2 domain-containing 1a gene (cc2d1a, 610055.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil and c2 domain-containing 1a gene (cc2d1a, 610055.0001) | rel=r_associated | relid=0 | w=36
  326. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the coiled-coil and c2 domains-containing protein 2a (cc2d2a, 612013.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil and c2 domains-containing protein 2a (cc2d2a, 612013.0001) | rel=r_associated | relid=0 | w=36
  327. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the coiled-coil domain-containing protein 78 gene (ccdc78, 614666.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil domain-containing protein 78 gene (ccdc78, 614666.0001) | rel=r_associated | relid=0 | w=36
  328. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0030)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0030) | rel=r_associated | relid=0 | w=36
  329. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the collagen ix, alpha-1 polypeptide gene (col9a1, 120210.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ix, alpha-1 polypeptide gene (col9a1, 120210.0001) | rel=r_associated | relid=0 | w=36
  330. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the collagen ix, alpha-3 polypeptide gene (col9a3, 120270.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ix, alpha-3 polypeptide gene (col9a3, 120270.0001) | rel=r_associated | relid=0 | w=36
  331. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0001) | rel=r_associated | relid=0 | w=36
  332. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the complement component receptor 2 gene (cr2, 120650.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement component receptor 2 gene (cr2, 120650.0002) | rel=r_associated | relid=0 | w=36
  333. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the complement component-8, alpha polypeptide gene (c8a, 120950.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement component-8, alpha polypeptide gene (c8a, 120950.0002) | rel=r_associated | relid=0 | w=36
  334. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the complement component-8, beta polypeptide gene (c8b, 120960.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement component-8, beta polypeptide gene (c8b, 120960.0001) | rel=r_associated | relid=0 | w=36
  335. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the complement factor d gene (cfd, 134350.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement factor d gene (cfd, 134350.0001) | rel=r_associated | relid=0 | w=36
  336. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the component x gene of the pyruvate dehydrogenase complex (pdhx, 608769.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the component x gene of the pyruvate dehydrogenase complex (pdhx, 608769.0001) | rel=r_associated | relid=0 | w=36
  337. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the connexin 26 gene (gjb2, 121011.0020)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the connexin 26 gene (gjb2, 121011.0020) | rel=r_associated | relid=0 | w=36
  338. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the connexin-32 gene (gjb1, 304040.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the connexin-32 gene (gjb1, 304040.0001) | rel=r_associated | relid=0 | w=36
  339. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the coproporphyrinogen oxidase gene (cpo, 612732.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coproporphyrinogen oxidase gene (cpo, 612732.0001) | rel=r_associated | relid=0 | w=36
  340. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cystathionine beta-synthase gene (cbs, 613381.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cystathionine beta-synthase gene (cbs, 613381.0001) | rel=r_associated | relid=0 | w=36
  341. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cystinosin gene (ctns, 219800.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cystinosin gene (ctns, 219800.0001) | rel=r_associated | relid=0 | w=36
  342. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cytochrome b-245, beta polypeptide gene (cybb, 300481.0022)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome b-245, beta polypeptide gene (cybb, 300481.0022) | rel=r_associated | relid=0 | w=36
  343. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cytochrome b(-245) alpha subunit gene (cyba, 608508.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome b(-245) alpha subunit gene (cyba, 608508.0001) | rel=r_associated | relid=0 | w=36
  344. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the cytochrome b(-245) beta subunit gene (cybb, 300481.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome b(-245) beta subunit gene (cybb, 300481.0001) | rel=r_associated | relid=0 | w=36
  345. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dihydrolipoamide branched chain transacylase gene (dbt, 248610.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dihydrolipoamide branched chain transacylase gene (dbt, 248610.0001) | rel=r_associated | relid=0 | w=36
  346. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dihydrolipoamide dehydrogenase gene (dld, 238331.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dihydrolipoamide dehydrogenase gene (dld, 238331.0001) | rel=r_associated | relid=0 | w=36
  347. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dna methyl-transferase 3b gene (dnmt3b, 602900.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna methyl-transferase 3b gene (dnmt3b, 602900.0001) | rel=r_associated | relid=0 | w=36
  348. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dna methyltransferase 3a gene (dnmt3a, 602769.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna methyltransferase 3a gene (dnmt3a, 602769.0001) | rel=r_associated | relid=0 | w=36
  349. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 6 gene (dnajb6, 611332.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 6 gene (dnajb6, 611332.0001) | rel=r_associated | relid=0 | w=36
  350. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 3 gene (dnajc3, 601184.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 3 gene (dnajc3, 601184.0001) | rel=r_associated | relid=0 | w=36
  351. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 6 gene (dnajc6, 608375.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 6 gene (dnajc6, 608375.0001) | rel=r_associated | relid=0 | w=36
  352. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0001) | rel=r_associated | relid=0 | w=36
  353. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dynein axonemal heavy chain 11 gene (dnah11, 603339.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynein axonemal heavy chain 11 gene (dnah11, 603339.0001) | rel=r_associated | relid=0 | w=36
  354. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dysferlin gene (dysf, 603009.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dysferlin gene (dysf, 603009.0003) | rel=r_associated | relid=0 | w=36
  355. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the dystonin gene (dst, 113810.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dystonin gene (dst, 113810.0002) | rel=r_associated | relid=0 | w=36
  356. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ef-hand domain (c-terminal)-containing 1 gene efhc1, (608815.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ef-hand domain (c-terminal)-containing 1 gene efhc1, (608815.0006) | rel=r_associated | relid=0 | w=36
  357. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the embryonic skeletal muscle myosin heavy chain 3 gene (myh3, 160720.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the embryonic skeletal muscle myosin heavy chain 3 gene (myh3, 160720.0001) | rel=r_associated | relid=0 | w=36
  358. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the endothelin 1 gene (edn1, 131240.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endothelin 1 gene (edn1, 131240.0004) | rel=r_associated | relid=0 | w=36
  359. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the endothelin-3 gene (edn3, 131242.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endothelin-3 gene (edn3, 131242.0001) | rel=r_associated | relid=0 | w=36
  360. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the enoyl-coenzyme a, hydratase/3-hydroxyacyl coenzyme a dehydrogenase gene (ehhadh, 607037.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the enoyl-coenzyme a, hydratase/3-hydroxyacyl coenzyme a dehydrogenase gene (ehhadh, 607037.0001) | rel=r_associated | relid=0 | w=36
  361. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the excision-repair cross-complementing group 6 gene (ercc6, 609413.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the excision-repair cross-complementing group 6 gene (ercc6, 609413.0001) | rel=r_associated | relid=0 | w=36
  362. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the excision-repair, complementing defective, in chinese hamster, number 5 gene (ercc5, 133530.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the excision-repair, complementing defective, in chinese hamster, number 5 gene (ercc5, 133530.0001) | rel=r_associated | relid=0 | w=36
  363. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the f receptor-type protein-tyrosine phosphatase gene (ptprf, 179590.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the f receptor-type protein-tyrosine phosphatase gene (ptprf, 179590.0001) | rel=r_associated | relid=0 | w=36
  364. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the family with sequence similarity 111, member a gene (fam111a, 615292.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the family with sequence similarity 111, member a gene (fam111a, 615292.0001) | rel=r_associated | relid=0 | w=36
  365. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the family with sequence similarity 111, member a, gene (fam111a, 615292.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the family with sequence similarity 111, member a, gene (fam111a, 615292.0002) | rel=r_associated | relid=0 | w=36
  366. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the family with sequence similarity 123, member b gene (fam123b, 300647.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the family with sequence similarity 123, member b gene (fam123b, 300647.0001) | rel=r_associated | relid=0 | w=36
  367. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the family with sequence similarity 126 gene, member a gene (fam126a, 610531.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the family with sequence similarity 126 gene, member a gene (fam126a, 610531.0001) | rel=r_associated | relid=0 | w=36
  368. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fas antigen gene (fas, 134637.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fas antigen gene (fas, 134637.0001) | rel=r_associated | relid=0 | w=36
  369. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fat mass- and obesity-associated gene (fto, 610966.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fat mass- and obesity-associated gene (fto, 610966.0001) | rel=r_associated | relid=0 | w=36
  370. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ferritin light chain gene (ftl, 134790.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ferritin light chain gene (ftl, 134790.0001) | rel=r_associated | relid=0 | w=36
  371. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0001) | rel=r_associated | relid=0 | w=36
  372. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fibrillin 2 gene (fbn2, 121050.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibrillin 2 gene (fbn2, 121050.0001) | rel=r_associated | relid=0 | w=36
  373. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fibroblast growth factor 23 gene (fgf23, 605380.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor 23 gene (fgf23, 605380.0001) | rel=r_associated | relid=0 | w=36
  374. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0007) | rel=r_associated | relid=0 | w=36
  375. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0043)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0043) | rel=r_associated | relid=0 | w=36
  376. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fibroblast growth factor-10 gene (fgf10, 602115.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor-10 gene (fgf10, 602115.0001) | rel=r_associated | relid=0 | w=36
  377. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fibronectin-like domain-containing leucine-rich transmembrane protein 3 gene (flrt3, 604808.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibronectin-like domain-containing leucine-rich transmembrane protein 3 gene (flrt3, 604808.0001) | rel=r_associated | relid=0 | w=36
  378. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the forkhead box c2 gene (foxc2, 602402.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead box c2 gene (foxc2, 602402.0007) | rel=r_associated | relid=0 | w=36
  379. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fras1-related extracellular matrix protein 1 gene (frem1, 608944.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fras1-related extracellular matrix protein 1 gene (frem1, 608944.0004) | rel=r_associated | relid=0 | w=36
  380. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fumarylacetoacetase gene (fah, 613871.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fumarylacetoacetase gene (fah, 613871.0001) | rel=r_associated | relid=0 | w=36
  381. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the fyve, rhogef, and ph domain-containing protein-4 gene (fgd4, 611104.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fyve, rhogef, and ph domain-containing protein-4 gene (fgd4, 611104.0001) | rel=r_associated | relid=0 | w=36
  382. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the g protein-coupled receptor 56 gene (gpr56, 604110.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the g protein-coupled receptor 56 gene (gpr56, 604110.0001) | rel=r_associated | relid=0 | w=36
  383. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the gamma sarcoglycan gene (sgcg, 253700.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma sarcoglycan gene (sgcg, 253700.0001) | rel=r_associated | relid=0 | w=36
  384. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the gamma-aminobutyric acid (gaba) a receptor, gamma-2 gene (gabrg2, 137164.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma-aminobutyric acid (gaba) a receptor, gamma-2 gene (gabrg2, 137164.0001) | rel=r_associated | relid=0 | w=36
  385. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606589.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606589.0001) | rel=r_associated | relid=0 | w=36
  386. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the gata-binding protein-1 gene (gata1, 305371.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein-1 gene (gata1, 305371.0001) | rel=r_associated | relid=0 | w=36
  387. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the gli-kruppel family member 2 gene (gli2, 165230.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gli-kruppel family member 2 gene (gli2, 165230.0008) | rel=r_associated | relid=0 | w=36
  388. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the glial cell line-derived neurotrophic factor gene (gdnf, 600837.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glial cell line-derived neurotrophic factor gene (gdnf, 600837.0001) | rel=r_associated | relid=0 | w=36
  389. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the glioma-inactivated leucine-rich 1 gene (lgi1, 604619.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glioma-inactivated leucine-rich 1 gene (lgi1, 604619.0001) | rel=r_associated | relid=0 | w=36
  390. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the glutathione peroxidase-4 gene (gpx4, 138322.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutathione peroxidase-4 gene (gpx4, 138322.0001) | rel=r_associated | relid=0 | w=36
  391. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the glycerol-3-phosphate dehydrogenase 1 gene (gpd1, 138420.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycerol-3-phosphate dehydrogenase 1 gene (gpd1, 138420.0001) | rel=r_associated | relid=0 | w=36
  392. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the glypican 6 gene (gpc6, 604404.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glypican 6 gene (gpc6, 604404.0001) | rel=r_associated | relid=0 | w=36
  393. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the gtp cyclohydrolase 1 gene (gch1, 600225.0017)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gtp cyclohydrolase 1 gene (gch1, 600225.0017) | rel=r_associated | relid=0 | w=36
  394. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the gtp-binding protein 3 gene (gtpbp3, 608536.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gtp-binding protein 3 gene (gtpbp3, 608536.0001) | rel=r_associated | relid=0 | w=36
  395. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the heat-shock 27-kd protein 3 gene (hspb3, 604624.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heat-shock 27-kd protein 3 gene (hspb3, 604624.0001). | rel=r_associated | relid=0 | w=36
  396. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the hemoglobin beta gene (hbb, 141900.0437)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hemoglobin beta gene (hbb, 141900.0437) | rel=r_associated | relid=0 | w=36
  397. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the hemoglobin gamma a gene (hbg1, 142200.0026)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hemoglobin gamma a gene (hbg1, 142200.0026) | rel=r_associated | relid=0 | w=36
  398. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the heparanase-2 gene (hpse2, 613469.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heparanase-2 gene (hpse2, 613469.0001) | rel=r_associated | relid=0 | w=36
  399. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the hepatocyte nuclear factor-1-beta gene (tcf2, 189907.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hepatocyte nuclear factor-1-beta gene (tcf2, 189907.0001) | rel=r_associated | relid=0 | w=36
  400. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the histidine ammonia lyase gene (hal, 609457.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the histidine ammonia lyase gene (hal, 609457.0001) | rel=r_associated | relid=0 | w=36
  401. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the histidyl-trna synthetase gene (hars, 142810.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the histidyl-trna synthetase gene (hars, 142810.0001) | rel=r_associated | relid=0 | w=36
  402. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of chlamydomonas poc1 centriolar protein a gene (poc1a, 614783.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of chlamydomonas poc1 centriolar protein a gene (poc1a, 614783.0001) | rel=r_associated | relid=0 | w=36
  403. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of s. cerevisiae cell division cycle 6 gene (cdc6, 602627.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of s. cerevisiae cell division cycle 6 gene (cdc6, 602627.0001) | rel=r_associated | relid=0 | w=36
  404. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the a. nidulans nude 1 gene (nde1, 609449.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the a. nidulans nude 1 gene (nde1, 609449.0004) | rel=r_associated | relid=0 | w=36
  405. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the drosophila aristaless homeobox gene (arix, 602753.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila aristaless homeobox gene (arix, 602753.0001) | rel=r_associated | relid=0 | w=36
  406. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the drosophila dachsous 1 gene (dchs1, 603057.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila dachsous 1 gene (dchs1, 603057.0001) | rel=r_associated | relid=0 | w=36
  407. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the drosophila dicer 1 gene (dicer1, 606241.0007).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila dicer 1 gene (dicer1, 606241.0007). | rel=r_associated | relid=0 | w=36
  408. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the drosophila discs large 3 gene (dlg3, 300189.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila discs large 3 gene (dlg3, 300189.0001) | rel=r_associated | relid=0 | w=36
  409. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the drosophila fat tumor suppressor gene 4 (fat4, 612411.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila fat tumor suppressor gene 4 (fat4, 612411.0003) | rel=r_associated | relid=0 | w=36
  410. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the drosophila muscle segment homeo box-2 gene (msx2, 123101.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila muscle segment homeo box-2 gene (msx2, 123101.0002) | rel=r_associated | relid=0 | w=36
  411. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the drosophila orthodenticle 2 gene (otx2, 600038.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila orthodenticle 2 gene (otx2, 600038.0001) | rel=r_associated | relid=0 | w=36
  412. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the drosophila suppressor of fused gene (sufu, 607035.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila suppressor of fused gene (sufu, 607035.0007) | rel=r_associated | relid=0 | w=36
  413. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the mouse itchy gene (itch, 606409.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse itchy gene (itch, 606409.0001) | rel=r_associated | relid=0 | w=36
  414. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the mouse seizure threshold 2 gene (szt2, 615463.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse seizure threshold 2 gene (szt2, 615463.0001) | rel=r_associated | relid=0 | w=36
  415. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the mouse stimulated by retinoic acid-6 gene (stra6, 610745.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse stimulated by retinoic acid-6 gene (stra6, 610745.0007) | rel=r_associated | relid=0 | w=36
  416. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the mouse tubby gene (tub, 601197.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse tubby gene (tub, 601197.0001) | rel=r_associated | relid=0 | w=36
  417. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the s. cerevisiae coq2 gene (coq2, 609825.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae coq2 gene (coq2, 609825.0001) | rel=r_associated | relid=0 | w=36
  418. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the s. cerevisiae mitochondrial translation optimization 1 gene (mto1, 614667.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae mitochondrial translation optimization 1 gene (mto1, 614667.0001) | rel=r_associated | relid=0 | w=36
  419. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the s. cerevisiae postmeiotic segregation increased 2 gene (pms2, 600259.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae postmeiotic segregation increased 2 gene (pms2, 600259.0001) | rel=r_associated | relid=0 | w=36
  420. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the s. cerevisiae sco1 gene (sco1, 603644.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae sco1 gene (sco1, 603644.0001) | rel=r_associated | relid=0 | w=36
  421. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the homolog of the s. cerevisiae trna splicing endonuclease 54 gene (tsen54, 608755.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae trna splicing endonuclease 54 gene (tsen54, 608755.0001) | rel=r_associated | relid=0 | w=36
  422. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the human homolog of the drosophila 'patched' gene 2 (ptch2, 603673.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the human homolog of the drosophila 'patched' gene 2 (ptch2, 603673.0003) | rel=r_associated | relid=0 | w=36
  423. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the hyperpolarization-activated cyclic nucleotide-gated potassium channel 4 gene (hcn4, 605206.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hyperpolarization-activated cyclic nucleotide-gated potassium channel 4 gene (hcn4, 605206.0001) | rel=r_associated | relid=0 | w=36
  424. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the hypocretin gene (hcrt, 602358.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hypocretin gene (hcrt, 602358.0001) | rel=r_associated | relid=0 | w=36
  425. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the inositol 1,4,5-triphosphate receptor, type 1 gene (itpr1, 147265)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inositol 1,4,5-triphosphate receptor, type 1 gene (itpr1, 147265) | rel=r_associated | relid=0 | w=36
  426. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the inositol polyphosphate-5-phosphatase, 72-kd gene (inpp5e, 613037.0002).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inositol polyphosphate-5-phosphatase, 72-kd gene (inpp5e, 613037.0002). | rel=r_associated | relid=0 | w=36
  427. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the integral membrane protein-2b gene (itm2b, 603904.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the integral membrane protein-2b gene (itm2b, 603904.0003) | rel=r_associated | relid=0 | w=36
  428. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the integrin, beta-3 gene (itgb3, 173470.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the integrin, beta-3 gene (itgb3, 173470.0001) | rel=r_associated | relid=0 | w=36
  429. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the integrin, beta-3 gene (itgb3, 173470.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the integrin, beta-3 gene (itgb3, 173470.0018) | rel=r_associated | relid=0 | w=36
  430. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the intestinal sodium/glucose transporter gene (slc5a1, 182380.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the intestinal sodium/glucose transporter gene (slc5a1, 182380.0001) | rel=r_associated | relid=0 | w=36
  431. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the iq motif-containing protein b1 gene (iqcb1, 609237.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the iq motif-containing protein b1 gene (iqcb1, 609237.0001) | rel=r_associated | relid=0 | w=36
  432. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the jagged 1 gene (jag1, 601920.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the jagged 1 gene (jag1, 601920.0001) | rel=r_associated | relid=0 | w=36
  433. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the junctional adhesion molecule 3 gene (jam3, 606871.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the junctional adhesion molecule 3 gene (jam3, 606871.0001) | rel=r_associated | relid=0 | w=36
  434. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the keratin 14 gene (krt14, 148066.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 14 gene (krt14, 148066.0005) | rel=r_associated | relid=0 | w=36
  435. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the keratin 5 gene (krt5, 148040.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 5 gene (krt5, 148040.0001) | rel=r_associated | relid=0 | w=36
  436. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the keratin 5 gene (krt5, 148040.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 5 gene (krt5, 148040.0018) | rel=r_associated | relid=0 | w=36
  437. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the keratin 6a gene (krt6a, 148041.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 6a gene (krt6a, 148041.0001) | rel=r_associated | relid=0 | w=36
  438. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the keratin-13 gene (krt13, 148065.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin-13 gene (krt13, 148065.0001) | rel=r_associated | relid=0 | w=36
  439. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the kiaa0196 gene (kiaa0196, 610657.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kiaa0196 gene (kiaa0196, 610657.0001) | rel=r_associated | relid=0 | w=36
  440. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the kiaa0196 gene (kiaa0196, 610657.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kiaa0196 gene (kiaa0196, 610657.0004) | rel=r_associated | relid=0 | w=36
  441. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the kiaa2022 gene (300524.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kiaa2022 gene (300524.0001) | rel=r_associated | relid=0 | w=36
  442. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the kinesin family member 22 gene (kif22, 603213.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 22 gene (kif22, 603213.0001) | rel=r_associated | relid=0 | w=36
  443. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the kinesin family member 5c gene (kif5c, 604593.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 5c gene (kif5c, 604593.0001) | rel=r_associated | relid=0 | w=36
  444. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the lamin a/c gene (lmna, 150330.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin a/c gene (lmna, 150330.0001) | rel=r_associated | relid=0 | w=36
  445. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the lamin a/c gene (lmna, 150330.0020)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin a/c gene (lmna, 150330.0020) | rel=r_associated | relid=0 | w=36
  446. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the latent transforming growth factor-beta-binding protein 2 gene (ltbp2, 602091.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the latent transforming growth factor-beta-binding protein 2 gene (ltbp2, 602091.0012) | rel=r_associated | relid=0 | w=36
  447. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the leucine-rich repeat- and sterile alpha motif-containing 1 gene (lrsam1, 610933.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucine-rich repeat- and sterile alpha motif-containing 1 gene (lrsam1, 610933.0001) | rel=r_associated | relid=0 | w=36
  448. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the liver glycogen phosphorylase gene (pygl, 613741.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the liver glycogen phosphorylase gene (pygl, 613741.0001) | rel=r_associated | relid=0 | w=36
  449. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the major facilitator superfamily domain-containing protein-8 gene (mfsd8, 611124.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the major facilitator superfamily domain-containing protein-8 gene (mfsd8, 611124.0001) | rel=r_associated | relid=0 | w=36
  450. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the manan-binding lectin serine protease-1 gene (masp1, 600521.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the manan-binding lectin serine protease-1 gene (masp1, 600521.0001) | rel=r_associated | relid=0 | w=36
  451. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the matrix metalloproteinase 2 gene (mmp2, 120360.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the matrix metalloproteinase 2 gene (mmp2, 120360.0001) | rel=r_associated | relid=0 | w=36
  452. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mediator complex subunit 13-like gene (med13l, 608771.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mediator complex subunit 13-like gene (med13l, 608771.0001) | rel=r_associated | relid=0 | w=36
  453. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the melanocortin-2 receptor accessory protein gene (mrap, 609196.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the melanocortin-2 receptor accessory protein gene (mrap, 609196.0001) | rel=r_associated | relid=0 | w=36
  454. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the membrane-spanning 4 domains, subfamily a, member 1 gene (ms4a1, 112210.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the membrane-spanning 4 domains, subfamily a, member 1 gene (ms4a1, 112210.0001) | rel=r_associated | relid=0 | w=36
  455. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mitochondrial elongation factor g1 gene (gfm1, 606639.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial elongation factor g1 gene (gfm1, 606639.0001) | rel=r_associated | relid=0 | w=36
  456. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mitochondrial methionyl-trna formyltransferase gene (mtfmt, 611766.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial methionyl-trna formyltransferase gene (mtfmt, 611766.0001) | rel=r_associated | relid=0 | w=36
  457. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mitochondrial ribosomal protein l44 gene (mrpl44, 611849.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial ribosomal protein l44 gene (mrpl44, 611849.0001) | rel=r_associated | relid=0 | w=36
  458. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mitochondrial transfer rna, mitochondrial, serine, 1 gene (mtts1, 590080.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial transfer rna, mitochondrial, serine, 1 gene (mtts1, 590080.0002) | rel=r_associated | relid=0 | w=36
  459. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mitochondrial trna-glutamic acid gene (mtte, 590025.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial trna-glutamic acid gene (mtte, 590025.0001) | rel=r_associated | relid=0 | w=36
  460. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mitochondrial trna-lysine gene (mttk, 590060.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial trna-lysine gene (mttk, 590060.0005) | rel=r_associated | relid=0 | w=36
  461. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mitochondrion-associated apoptosis-inducing factor 1 gene (aifm1, 300169.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrion-associated apoptosis-inducing factor 1 gene (aifm1, 300169.0001) | rel=r_associated | relid=0 | w=36
  462. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mkks gene (mkks, 604896.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mkks gene (mkks, 604896.0003) | rel=r_associated | relid=0 | w=36
  463. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mks1 gene (mks1, 609883.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mks1 gene (mks1, 609883.0006) | rel=r_associated | relid=0 | w=36
  464. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mmaa gene (mmaa, 607481.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mmaa gene (mmaa, 607481.0001) | rel=r_associated | relid=0 | w=36
  465. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the monocarboxylate transporter 8 gene (mct8, 300095.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the monocarboxylate transporter 8 gene (mct8, 300095.0001) | rel=r_associated | relid=0 | w=36
  466. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the mouse homolog of the nodal gene (nodal, 601265.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mouse homolog of the nodal gene (nodal, 601265.0001) | rel=r_associated | relid=0 | w=36
  467. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the myofibrillogenesis regulator 1 gene (mr1, 609023.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myofibrillogenesis regulator 1 gene (mr1, 609023.0001) | rel=r_associated | relid=0 | w=36
  468. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the n-deacetylase/n-sulfotransferase 1 gene (ndst1, 600853.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the n-deacetylase/n-sulfotransferase 1 gene (ndst1, 600853.0001) | rel=r_associated | relid=0 | w=36
  469. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 1 gene (ndufs1, 157655.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 1 gene (ndufs1, 157655.0001) | rel=r_associated | relid=0 | w=36
  470. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 4 gene (ndufs4, 602694.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 4 gene (ndufs4, 602694.0001) | rel=r_associated | relid=0 | w=36
  471. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 8 gene (ndufs8, 602141.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 8 gene (ndufs8, 602141.0001) | rel=r_associated | relid=0 | w=36
  472. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the nadh dehydrogenase, subunit 5 gene (mtnd5, 516005.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase, subunit 5 gene (mtnd5, 516005.0003) | rel=r_associated | relid=0 | w=36
  473. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the nata catalytic subunit of n-alpha-acetyltransferase-10 gene (naa10, 300013.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nata catalytic subunit of n-alpha-acetyltransferase-10 gene (naa10, 300013.0002) | rel=r_associated | relid=0 | w=36
  474. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the neurofibromin-2 gene (nf2, 607379.0017)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neurofibromin-2 gene (nf2, 607379.0017) | rel=r_associated | relid=0 | w=36
  475. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the neurofilament light chain gene (nefl, 162280.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neurofilament light chain gene (nefl, 162280.0003) | rel=r_associated | relid=0 | w=36
  476. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the never-in-mitosis gene a-related kinase-2 gene (nek2, 604043.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the never-in-mitosis gene a-related kinase-2 gene (nek2, 604043.0001) | rel=r_associated | relid=0 | w=36
  477. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the nicotinamide nucleotide adenylyltransferase-1 gene (nmnat1, 608700.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nicotinamide nucleotide adenylyltransferase-1 gene (nmnat1, 608700.0001) | rel=r_associated | relid=0 | w=36
  478. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the nlr family, pyrin-domain containing 3 gene (nlrp3, 606416.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nlr family, pyrin-domain containing 3 gene (nlrp3, 606416.0004) | rel=r_associated | relid=0 | w=36
  479. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the nonmuscle myosin heavy chain 14 gene (myh14, 608568.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nonmuscle myosin heavy chain 14 gene (myh14, 608568.0006) | rel=r_associated | relid=0 | w=36
  480. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the norrin gene (ndp, 300658.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the norrin gene (ndp, 300658.0001) | rel=r_associated | relid=0 | w=36
  481. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the origin recognition complex, subunit 4, gene (orc4, 603056.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the origin recognition complex, subunit 4, gene (orc4, 603056.0001) | rel=r_associated | relid=0 | w=36
  482. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ornithine transcarbamylase gene (otc, 311250.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ornithine transcarbamylase gene (otc, 311250.0001) | rel=r_associated | relid=0 | w=36
  483. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the otoancorin gene (otoa, 607038.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the otoancorin gene (otoa, 607038.0001) | rel=r_associated | relid=0 | w=36
  484. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the paired-like homeodomain transcription factor-1 gene (pitx1, 602149.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the paired-like homeodomain transcription factor-1 gene (pitx1, 602149.0001) | rel=r_associated | relid=0 | w=36
  485. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the paired-related homeobox gene 1 (prrx1, 167420.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the paired-related homeobox gene 1 (prrx1, 167420.0001) | rel=r_associated | relid=0 | w=36
  486. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the perforin 1 gene (prf1, 170280.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the perforin 1 gene (prf1, 170280.0001) | rel=r_associated | relid=0 | w=36
  487. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the peroxisome biogenesis factor-12 gene (pex12, 601758.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor-12 gene (pex12, 601758.0001) | rel=r_associated | relid=0 | w=36
  488. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0007) | rel=r_associated | relid=0 | w=36
  489. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 2 gene (pik3r2, 603157.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 2 gene (pik3r2, 603157.0001) | rel=r_associated | relid=0 | w=36
  490. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the phosphatidylinositol glycan, class a gene (piga, 311770.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol glycan, class a gene (piga, 311770.0011) | rel=r_associated | relid=0 | w=36
  491. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the phosphatidylinositol glycan, class m gene (pigm, 610273.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol glycan, class m gene (pigm, 610273.0001) | rel=r_associated | relid=0 | w=36
  492. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the phosphatidylinositol glycan, class o gene (pigo, 614730.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol glycan, class o gene (pigo, 614730.0001) | rel=r_associated | relid=0 | w=36
  493. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the phosphodiesterase 11a gene (pde11a, 604961.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphodiesterase 11a gene (pde11a, 604961.0001) | rel=r_associated | relid=0 | w=36
  494. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the phospholipase c, gamma-2 gene (plcg2, 600220.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phospholipase c, gamma-2 gene (plcg2, 600220.0001) | rel=r_associated | relid=0 | w=36
  495. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the phosphoribosylpyrophosphate synthetase 1 gene (prps1, 311850.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoribosylpyrophosphate synthetase 1 gene (prps1, 311850.0009) | rel=r_associated | relid=0 | w=36
  496. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the phosphoserine aminotransferase-1 gene (psat1, 610936.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoserine aminotransferase-1 gene (psat1, 610936.0001) | rel=r_associated | relid=0 | w=36
  497. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the phytanoyl-coa hydroxylase gene (phyh, 602026.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phytanoyl-coa hydroxylase gene (phyh, 602026.0001) | rel=r_associated | relid=0 | w=36
  498. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the piezo-type mechanosensitive ion channel component 2 gene (piezo2, 613629.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the piezo-type mechanosensitive ion channel component 2 gene (piezo2, 613629.0004) | rel=r_associated | relid=0 | w=36
  499. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the plastin 3 gene (pls3, 300131.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the plastin 3 gene (pls3, 300131.0001) | rel=r_associated | relid=0 | w=36
  500. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the platelet glycoprotein ix gene (gp9, 173515.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the platelet glycoprotein ix gene (gp9, 173515.0001) | rel=r_associated | relid=0 | w=36
  501. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the platelet-derived growth factor, beta polypeptide gene (pdgfb, 190040.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the platelet-derived growth factor, beta polypeptide gene (pdgfb, 190040.0003) | rel=r_associated | relid=0 | w=36
  502. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the plectin 1 gene (plec1, 601282.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the plectin 1 gene (plec1, 601282.0010) | rel=r_associated | relid=0 | w=36
  503. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the poliovirus receptor-like 1 gene (pvrl1, 600644.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the poliovirus receptor-like 1 gene (pvrl1, 600644.0002) | rel=r_associated | relid=0 | w=36
  504. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the poly-u-binding splicing factor, 60kd gene (puf60, 604819.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the poly-u-binding splicing factor, 60kd gene (puf60, 604819.0001) | rel=r_associated | relid=0 | w=36
  505. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the polycystin 1 gene (pkd1, 601313.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polycystin 1 gene (pkd1, 601313.0001) | rel=r_associated | relid=0 | w=36
  506. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the pou domain, class 3, transcription factor 4 gene (pou3f4, 300039.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pou domain, class 3, transcription factor 4 gene (pou3f4, 300039.0001) | rel=r_associated | relid=0 | w=36
  507. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the pr-domain containing protein-5 gene (prdm5, 614161.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pr-domain containing protein-5 gene (prdm5, 614161.0001) | rel=r_associated | relid=0 | w=36
  508. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase gene (plod, 153454.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase gene (plod, 153454.0001) | rel=r_associated | relid=0 | w=36
  509. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the prolyl hydroxylase domain-containing protein 2 gene (egln1, 606425.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prolyl hydroxylase domain-containing protein 2 gene (egln1, 606425.0001) | rel=r_associated | relid=0 | w=36
  510. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the protein c gene (proc, 612283.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein c gene (proc, 612283.0003) | rel=r_associated | relid=0 | w=36
  511. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the protein kinase, interferon-inducible double-stranded rna-dependent activator gene (prkra, 603424.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein kinase, interferon-inducible double-stranded rna-dependent activator gene (prkra, 603424.0001) | rel=r_associated | relid=0 | w=36
  512. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the pseudouridine synthase-1 gene (pus1, 608109.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pseudouridine synthase-1 gene (pus1, 608109.0001) | rel=r_associated | relid=0 | w=36
  513. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the pterin-4-alpha-carbinolamine dehydratase 1 gene (pcbd1, 126090.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pterin-4-alpha-carbinolamine dehydratase 1 gene (pcbd1, 126090.0001) | rel=r_associated | relid=0 | w=36
  514. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the purinergic receptor p2x, ligand-gated ion channel, 2 gene (p2rx2, 600844.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the purinergic receptor p2x, ligand-gated ion channel, 2 gene (p2rx2, 600844.0001) | rel=r_associated | relid=0 | w=36
  515. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the pyrroline-5-carboxylate reductase 1 gene (pycr1, 179035.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pyrroline-5-carboxylate reductase 1 gene (pycr1, 179035.0001) | rel=r_associated | relid=0 | w=36
  516. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the recombination-activating gene 2 (rag2, 179616.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the recombination-activating gene 2 (rag2, 179616.0009) | rel=r_associated | relid=0 | w=36
  517. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ret protooncogene (ret, 164761.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ret protooncogene (ret, 164761.0014) | rel=r_associated | relid=0 | w=36
  518. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the reticulon 2 gene (rtn2, 603183.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the reticulon 2 gene (rtn2, 603183.0001). | rel=r_associated | relid=0 | w=36
  519. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the retinol dehydrogenase 11 gene (rdh11, 607849.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the retinol dehydrogenase 11 gene (rdh11, 607849.0001) | rel=r_associated | relid=0 | w=36
  520. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ribosomal protein s29 gene (rps29, 603633.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribosomal protein s29 gene (rps29, 603633.0001) | rel=r_associated | relid=0 | w=36
  521. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the rna, u4, small nuclear, at-ac form gene (rnu4atac, 601428.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rna, u4, small nuclear, at-ac form gene (rnu4atac, 601428.0001) | rel=r_associated | relid=0 | w=36
  522. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the s. cerevisiae homolog of mediator of rna polymerase ii transcription, subunit 12 gene (med12, 300188.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the s. cerevisiae homolog of mediator of rna polymerase ii transcription, subunit 12 gene (med12, 300188.0002) | rel=r_associated | relid=0 | w=36
  523. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the scaffold protein containing ankyrin repeats and sam domain gene (sans, 607696.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the scaffold protein containing ankyrin repeats and sam domain gene (sans, 607696.0001) | rel=r_associated | relid=0 | w=36
  524. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the septin 9 gene (sept9, 604061.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the septin 9 gene (sept9, 604061.0001) | rel=r_associated | relid=0 | w=36
  525. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the set-binding factor 1 gene (sbf1, 603560.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the set-binding factor 1 gene (sbf1, 603560.0001) | rel=r_associated | relid=0 | w=36
  526. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the slit- and ntrk-like family, member 1 gene (slitrk1, 609678.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the slit- and ntrk-like family, member 1 gene (slitrk1, 609678.0001) | rel=r_associated | relid=0 | w=36
  527. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the slit- and ntrk-like family, member-6 gene (slitrk6, 609681.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the slit- and ntrk-like family, member-6 gene (slitrk6, 609681.0001) | rel=r_associated | relid=0 | w=36
  528. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the small nuclear ribonucleoprotein polypeptide e gene (snrpe, 128160.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the small nuclear ribonucleoprotein polypeptide e gene (snrpe, 128160.0001) | rel=r_associated | relid=0 | w=36
  529. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the sodium channel, nonvoltage-gated 1, gamma gene (scnn1g, 600761.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sodium channel, nonvoltage-gated 1, gamma gene (scnn1g, 600761.0005) | rel=r_associated | relid=0 | w=36
  530. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the solute carrier family 12 (sodium/chloride transporter), member 6 gene (slc12a6, 604878.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 12 (sodium/chloride transporter), member 6 gene (slc12a6, 604878.0001) | rel=r_associated | relid=0 | w=36
  531. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the solute carrier family 19, folate transporter, member 3 gene (slc19a3, 606152.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 19, folate transporter, member 3 gene (slc19a3, 606152.0001) | rel=r_associated | relid=0 | w=36
  532. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0008) | rel=r_associated | relid=0 | w=36
  533. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the solute carrier family 22 (organic cation transporter), member 5 gene (slc22a5, 603377.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 22 (organic cation transporter), member 5 gene (slc22a5, 603377.0001). | rel=r_associated | relid=0 | w=36
  534. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, glutamate), member 22 gene (slc25a22, 609302.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, glutamate), member 22 gene (slc25a22, 609302.0001) | rel=r_associated | relid=0 | w=36
  535. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the solute carrier family 25 (mitochondrial carrier) member 4 gene (slc25a4, 103220.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier) member 4 gene (slc25a4, 103220.0001) | rel=r_associated | relid=0 | w=36
  536. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 8 gene (slc26a8, 608480.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 8 gene (slc26a8, 608480.0001) | rel=r_associated | relid=0 | w=36
  537. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the solute carrier family 26, member 4 gene (slc26a4, 605646.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 26, member 4 gene (slc26a4, 605646.0004) | rel=r_associated | relid=0 | w=36
  538. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the solute carrier family 35, cmp-sialic acid transporter, member 1 gene (slc35a1, 605634.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 35, cmp-sialic acid transporter, member 1 gene (slc35a1, 605634.0001) | rel=r_associated | relid=0 | w=36
  539. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the sonic hedgehog gene (shh, 600725.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sonic hedgehog gene (shh, 600725.0014) | rel=r_associated | relid=0 | w=36
  540. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the stip1 homologous and u box-containing protein 1 gene (stub1, 607207.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the stip1 homologous and u box-containing protein 1 gene (stub1, 607207.0001) | rel=r_associated | relid=0 | w=36
  541. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0002) | rel=r_associated | relid=0 | w=36
  542. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a, member 4 gene (smarca4, 603254.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a, member 4 gene (smarca4, 603254.0001) | rel=r_associated | relid=0 | w=36
  543. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the synaptic nuclear envelope protein 1 gene (syne1, 608441.0008).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the synaptic nuclear envelope protein 1 gene (syne1, 608441.0008). | rel=r_associated | relid=0 | w=36
  544. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the synaptic ras gtpase activating protein 1 gene (syngap1, 603384.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the synaptic ras gtpase activating protein 1 gene (syngap1, 603384.0001) | rel=r_associated | relid=0 | w=36
  545. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the synaptophysin gene (syp, 313475.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the synaptophysin gene (syp, 313475.0001) | rel=r_associated | relid=0 | w=36
  546. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the syntaxin 1b gene (stx1b, 601485.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the syntaxin 1b gene (stx1b, 601485.0001) | rel=r_associated | relid=0 | w=36
  547. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the system b(0) neutral amino acid transporter-1 gene (slc6a19, 608893.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the system b(0) neutral amino acid transporter-1 gene (slc6a19, 608893.0001) | rel=r_associated | relid=0 | w=36
  548. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the tectonic family, member 1 gene (tctn1, 609863.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tectonic family, member 1 gene (tctn1, 609863.0001) | rel=r_associated | relid=0 | w=36
  549. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the tetratricopeptide repeat domain-containing protein 8 gene (ttc8, 608132.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tetratricopeptide repeat domain-containing protein 8 gene (ttc8, 608132.0001) | rel=r_associated | relid=0 | w=36
  550. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the thap domain-containing protein 1 gene (thap1, 609520.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thap domain-containing protein 1 gene (thap1, 609520.0001) | rel=r_associated | relid=0 | w=36
  551. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the thiamine pyrophosphokinase gene (tpk1, 606370.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thiamine pyrophosphokinase gene (tpk1, 606370.0001) | rel=r_associated | relid=0 | w=36
  552. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the thrombopoietin gene (thpo, 600044.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thrombopoietin gene (thpo, 600044.0001) | rel=r_associated | relid=0 | w=36
  553. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the thymidine phosphorylase gene (tymp, 131222.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thymidine phosphorylase gene (tymp, 131222.0001) | rel=r_associated | relid=0 | w=36
  554. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the titin gene (ttn, 188840.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the titin gene (ttn, 188840.0004) | rel=r_associated | relid=0 | w=36
  555. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the tolloid-like 1 gene (tll1, 606742.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tolloid-like 1 gene (tll1, 606742.0001) | rel=r_associated | relid=0 | w=36
  556. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the trafficking protein particle complex, subunit 11 gene (trappc11, 614138.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the trafficking protein particle complex, subunit 11 gene (trappc11, 614138.0001) | rel=r_associated | relid=0 | w=36
  557. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the transcription factor-4 gene (tcf4, 602272.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transcription factor-4 gene (tcf4, 602272.0001) | rel=r_associated | relid=0 | w=36
  558. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the transglutaminase-5 gene (tgm5, 603805.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transglutaminase-5 gene (tgm5, 603805.0001) | rel=r_associated | relid=0 | w=36
  559. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0001). | rel=r_associated | relid=0 | w=36
  560. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the transmembrane mucin 1 gene (muc1, 158340.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane mucin 1 gene (muc1, 158340.0001). | rel=r_associated | relid=0 | w=36
  561. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the transmembrane protein 16e gene (tmem16e, 608662.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 16e gene (tmem16e, 608662.0003) | rel=r_associated | relid=0 | w=36
  562. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the transmembrane protein 98 gene (tmem98, 615949.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 98 gene (tmem98, 615949.0001) | rel=r_associated | relid=0 | w=36
  563. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the tropomyosin 2 gene (tpm2, 190990.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tropomyosin 2 gene (tpm2, 190990.0004) | rel=r_associated | relid=0 | w=36
  564. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the tumor necrosis factor receptor superfamily member 1a gene (tnfrsf1a, 191190.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tumor necrosis factor receptor superfamily member 1a gene (tnfrsf1a, 191190.0001). | rel=r_associated | relid=0 | w=36
  565. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the tyrosine kinase 2 gene (tyk2, 176941.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tyrosine kinase 2 gene (tyk2, 176941.0001) | rel=r_associated | relid=0 | w=36
  566. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ubiquinol-cytochrome c reductase-protein gene (uqcrb, 191330.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquinol-cytochrome c reductase-protein gene (uqcrb, 191330.0001). | rel=r_associated | relid=0 | w=36
  567. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ubiquitin-like modifier-activating enzyme 1 gene (uba1, 314370.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquitin-like modifier-activating enzyme 1 gene (uba1, 314370.0001) | rel=r_associated | relid=0 | w=36
  568. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the ubiquitin-specific protease 9, x chromosome gene (usp9x, 300072.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquitin-specific protease 9, x chromosome gene (usp9x, 300072.0001) | rel=r_associated | relid=0 | w=36
  569. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the uridine monophosphate synthetase gene (umps, 613891.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the uridine monophosphate synthetase gene (umps, 613891.0001) | rel=r_associated | relid=0 | w=36
  570. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the urocanase domain-containing protein 1 gene (uroc1, 613012.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the urocanase domain-containing protein 1 gene (uroc1, 613012.0001) | rel=r_associated | relid=0 | w=36
  571. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the usherin gene (ush2a, 608400.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the usherin gene (ush2a, 608400.0001). | rel=r_associated | relid=0 | w=36
  572. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the v-raf-1 murine leukemia viral oncogene homolog-1 gene (raf1, 164760.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-raf-1 murine leukemia viral oncogene homolog-1 gene (raf1, 164760.0005) | rel=r_associated | relid=0 | w=36
  573. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the voltage-gated potassium channel, kqt-like subfamily, member 4 gene (kcnq4, 603537.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated potassium channel, kqt-like subfamily, member 4 gene (kcnq4, 603537.0001) | rel=r_associated | relid=0 | w=36
  574. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the voltage-gated, type ii sodium channel, alpha subunit (scn2a, 182390.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated, type ii sodium channel, alpha subunit (scn2a, 182390.0008) | rel=r_associated | relid=0 | w=36
  575. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the was gene (was, 300392.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the was gene (was, 300392.0004) | rel=r_associated | relid=0 | w=36
  576. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the wd repeat-containing protein 60 gene (wdr60, 615462.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein 60 gene (wdr60, 615462.0001) | rel=r_associated | relid=0 | w=36
  577. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the wingless-type mmtv integration site family, member 1 gene (wnt1, 164820.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wingless-type mmtv integration site family, member 1 gene (wnt1, 164820.0001) | rel=r_associated | relid=0 | w=36
  578. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the wingless-type mmtv integration site family, member 3 gene (wnt3, 165330.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wingless-type mmtv integration site family, member 3 gene (wnt3, 165330.0001) | rel=r_associated | relid=0 | w=36
  579. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the wolframin gene (wfs1, 222300.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wolframin gene (wfs1, 222300.0001) | rel=r_associated | relid=0 | w=36
  580. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the wolframin gene (wfs1, 606201.0020)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wolframin gene (wfs1, 606201.0020) | rel=r_associated | relid=0 | w=36
  581. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the x-linked small muscle protein gene (smpx, 300226.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the x-linked small muscle protein gene (smpx, 300226.0001) | rel=r_associated | relid=0 | w=36
  582. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation in the zinc metalloproteinase ste24 gene (zmpste24, 606480.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc metalloproteinase ste24 gene (zmpste24, 606480.0003) | rel=r_associated | relid=0 | w=36
  583. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutation of the dpy19-like 2 gene (dpy19l2, 613893.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation of the dpy19-like 2 gene (dpy19l2, 613893.0001) | rel=r_associated | relid=0 | w=36
  584. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in cartilage oligomeric matrix protein (comp, 600310.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in cartilage oligomeric matrix protein (comp, 600310.0001) | rel=r_associated | relid=0 | w=36
  585. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the butrylcholinesterase gene (bche, 177400.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the butrylcholinesterase gene (bche, 177400.0001) | rel=r_associated | relid=0 | w=36
  586. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the chemokine (c-x-c motif) receptor 4 gene (cxcr4, 162643.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the chemokine (c-x-c motif) receptor 4 gene (cxcr4, 162643.0001) | rel=r_associated | relid=0 | w=36
  587. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the claudin-1 gene (cldn1, 603718.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the claudin-1 gene (cldn1, 603718.0001) | rel=r_associated | relid=0 | w=36
  588. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the coagulation factor viii gene (f8, 306700.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the coagulation factor viii gene (f8, 306700.0001) | rel=r_associated | relid=0 | w=36
  589. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the cystinosin gene (ctns, 219800.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cystinosin gene (ctns, 219800.0009) | rel=r_associated | relid=0 | w=36
  590. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the delta-7-dehydrocholesterol reductase gene (dhcr7, 602858.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the delta-7-dehydrocholesterol reductase gene (dhcr7, 602858.0001) | rel=r_associated | relid=0 | w=36
  591. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the follicle-stimulating hormone receptor gene (fshr, 136435.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the follicle-stimulating hormone receptor gene (fshr, 136435.0008) | rel=r_associated | relid=0 | w=36
  592. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the galactosamine-6-sulfatase gene (galns, 612222.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the galactosamine-6-sulfatase gene (galns, 612222.0001). | rel=r_associated | relid=0 | w=36
  593. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the mitochondrial rna-processing endoribonuclease gene (rmrp, 157660.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the mitochondrial rna-processing endoribonuclease gene (rmrp, 157660.0001) | rel=r_associated | relid=0 | w=36
  594. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the neuroblastoma-derived v-myc avian myelocytomatosis viral-related oncogene (mycn, 164840.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the neuroblastoma-derived v-myc avian myelocytomatosis viral-related oncogene (mycn, 164840.0001) | rel=r_associated | relid=0 | w=36
  595. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the prion protein gene (prnp, 176640.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the prion protein gene (prnp, 176640.0018) | rel=r_associated | relid=0 | w=36
  596. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the selenoprotein n-1 gene (sepn1, 606210.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the selenoprotein n-1 gene (sepn1, 606210.0001) | rel=r_associated | relid=0 | w=36
  597. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 606718.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 606718.0001) | rel=r_associated | relid=0 | w=36
  598. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the succinate dehydrogenase complex subunit c gene (sdhc, 602413.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the succinate dehydrogenase complex subunit c gene (sdhc, 602413.0001) | rel=r_associated | relid=0 | w=36
  599. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the torsion dystonia-1 gene (dyt1, 605204.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the torsion dystonia-1 gene (dyt1, 605204.0001). | rel=r_associated | relid=0 | w=36
  600. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by mutations in the uridine diphosphate glycosyltransferase 1 gene (ugt1a1, 191740.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the uridine diphosphate glycosyltransferase 1 gene (ugt1a1, 191740.0010) | rel=r_associated | relid=0 | w=36
  601. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by simultaneous homozygous mutation in both the solute carrier organic anion transporter family, member 1b1 gene (slco1b1, 604843.0001) and the solute carrier organic anion transporter family, member 1b3 gene (slco1b3, 605495.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by simultaneous homozygous mutation in both the solute carrier organic anion transporter family, member 1b1 gene (slco1b1, 604843.0001) and the solute carrier organic anion transporter family, member 1b3 gene (slco1b3, 605495.0001) | rel=r_associated | relid=0 | w=36
  602. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by somatic deletion of 1 allele of the ribosomal protein s14 gene (rps14, 130620)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic deletion of 1 allele of the ribosomal protein s14 gene (rps14, 130620) | rel=r_associated | relid=0 | w=36
  603. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by somatic mutation in the phosphatidylinositol 3-kinase, catalytic, alpha polypeptide gene (pik3ca, 171834.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the phosphatidylinositol 3-kinase, catalytic, alpha polypeptide gene (pik3ca, 171834.0003) | rel=r_associated | relid=0 | w=36
  604. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:caused by somatic mutation in the v-ki-ras2 kirsten rat sarcoma viral oncogene homolog gene (kras, 190070.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the v-ki-ras2 kirsten rat sarcoma viral oncogene homolog gene (kras, 190070.0005) | rel=r_associated | relid=0 | w=36
  605. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:contiguous gene deletion syndrome caused by deletion (3.5mb) of 1q32-q44
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene deletion syndrome caused by deletion (3.5mb) of 1q32-q44 | rel=r_associated | relid=0 | w=36
  606. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:contiguous gene syndrome caused by microdeletion (600-800kb) of chromosome 17q21.31 encompassing genes crhr1 (122561), mapt (157140), sth (607067), imp5 (608284), and kansl1 (612452)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by microdeletion (600-800kb) of chromosome 17q21.31 encompassing genes crhr1 (122561), mapt (157140), sth (607067), imp5 (608284), and kansl1 (612452) | rel=r_associated | relid=0 | w=36
  607. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:microdeletion of 15q11 in 70% of patients confirmed by fluorescent in situ hybridization
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:microdeletion of 15q11 in 70% of patients confirmed by fluorescent in situ hybridization | rel=r_associated | relid=0 | w=36
  608. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:mosaic trisomy 21, 2.4%
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:mosaic trisomy 21, 2.4% | rel=r_associated | relid=0 | w=36
  609. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:rare cases secondary to chromosome translocation
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:rare cases secondary to chromosome translocation | rel=r_associated | relid=0 | w=36
  610. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:susceptibility conferred by mutation in the cd46 antigen gene (cd46, 120920.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the cd46 antigen gene (cd46, 120920.0001) | rel=r_associated | relid=0 | w=36
  611. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:susceptibility conferred by mutation in the cyclin-dependent kinase-4 gene (cdk4, 123829.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the cyclin-dependent kinase-4 gene (cdk4, 123829.0001) | rel=r_associated | relid=0 | w=36
  612. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:susceptibility conferred by mutation in the gamma-aminobutyric acid receptor, delta gene (gabrd, 137163.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the gamma-aminobutyric acid receptor, delta gene (gabrd, 137163.0001) | rel=r_associated | relid=0 | w=36
  613. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:susceptibility conferred by mutation in the major histocompatibility complex, class i, b gene (hla-b, 142830.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the major histocompatibility complex, class i, b gene (hla-b, 142830.0001) | rel=r_associated | relid=0 | w=36
  614. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:susceptibility conferred by mutation in the major histocompatibility complex, class i, c gene (hla-c, 142840.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the major histocompatibility complex, class i, c gene (hla-c, 142840.0001) | rel=r_associated | relid=0 | w=36
  615. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:susceptibility conferred by mutation in the neurofilament, heavy polypeptide gene (nefh, 162230.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the neurofilament, heavy polypeptide gene (nefh, 162230.0001) | rel=r_associated | relid=0 | w=36
  616. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:susceptibility conferred by mutation in the thrombomodulin gene (thbd, 188040.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the thrombomodulin gene (thbd, 188040.0005) | rel=r_associated | relid=0 | w=36
  617. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:susceptibility conferred by mutation in the voltage-dependent calcium channel, l type, alpha-1s subunit gene (cacna1s, 114208.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the voltage-dependent calcium channel, l type, alpha-1s subunit gene (cacna1s, 114208.0005) | rel=r_associated | relid=0 | w=36
  618. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 36 / 0.837 -> en:translocation 21, 3.3%
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:translocation 21, 3.3% | rel=r_associated | relid=0 | w=36
  619. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:a contiguous gene syndrome caused by deletion (1.5mb - 3.0mb) of 22q11.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome caused by deletion (1.5mb - 3.0mb) of 22q11.2 | rel=r_associated | relid=0 | w=35
  620. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:cause by mutation in the anthrax toxin receptor 1 gene (antxr1, 606410.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:cause by mutation in the anthrax toxin receptor 1 gene (antxr1, 606410.0002) | rel=r_associated | relid=0 | w=35
  621. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:cause by mutation in the homolog of the s. cerevisiae alg2 gene (alg2, 607905.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:cause by mutation in the homolog of the s. cerevisiae alg2 gene (alg2, 607905.0001) | rel=r_associated | relid=0 | w=35
  622. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by a deletion of chromosome 9p
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a deletion of chromosome 9p | rel=r_associated | relid=0 | w=35
  623. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by a trinucleotide repeat expansion (cag)n in the huntingtin gene (htt, 613004.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a trinucleotide repeat expansion (cag)n in the huntingtin gene (htt, 613004.0001) | rel=r_associated | relid=0 | w=35
  624. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by contiguous gene duplication (chrx:135.6-136.1, grch37) on xq26.3
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by contiguous gene duplication (chrx:135.6-136.1, grch37) on xq26.3 | rel=r_associated | relid=0 | w=35
  625. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by duplication of 0.25 to 1.08 mb on chromosome 5p13
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of 0.25 to 1.08 mb on chromosome 5p13 | rel=r_associated | relid=0 | w=35
  626. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by duplication of 1.0-2.5mb on chromosome 17q12
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of 1.0-2.5mb on chromosome 17q12 | rel=r_associated | relid=0 | w=35
  627. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by fusion of the fip1-like 1 gene (fip1l1, 607686) and the platelet-derived growth factor receptor-alpha gene (pdgfra, 173490)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by fusion of the fip1-like 1 gene (fip1l1, 607686) and the platelet-derived growth factor receptor-alpha gene (pdgfra, 173490) | rel=r_associated | relid=0 | w=35
  628. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by microdeletions of 11p13
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by microdeletions of 11p13 | rel=r_associated | relid=0 | w=35
  629. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in cytochrome p450, family 24, subfamily a, polypeptide-1 gene (cyp24a1, 126065.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in cytochrome p450, family 24, subfamily a, polypeptide-1 gene (cyp24a1, 126065.0001) | rel=r_associated | relid=0 | w=35
  630. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in establishment of cohesion 1, s. cerevisiae, homolog of, 2 gene ( esco2, 609353.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in establishment of cohesion 1, s. cerevisiae, homolog of, 2 gene ( esco2, 609353.0004) | rel=r_associated | relid=0 | w=35
  631. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in galactose-1-phosphate uridyltransferase gene (galt, 230400.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in galactose-1-phosphate uridyltransferase gene (galt, 230400.0001) | rel=r_associated | relid=0 | w=35
  632. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in serine protease 56 gene (prss56, 613858.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in serine protease 56 gene (prss56, 613858.0001) | rel=r_associated | relid=0 | w=35
  633. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in subunit a of the neuronal voltage-gated sodium channel gene (scn1a, 182389.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in subunit a of the neuronal voltage-gated sodium channel gene (scn1a, 182389.0012) | rel=r_associated | relid=0 | w=35
  634. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase x gene (hsd17b10, 300256.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase x gene (hsd17b10, 300256.0004) | rel=r_associated | relid=0 | w=35
  635. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the 3-beta-hydroxy-delta-5-c27-steroid oxidoreductase gene (hsd3b7, 607764.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 3-beta-hydroxy-delta-5-c27-steroid oxidoreductase gene (hsd3b7, 607764.0001) | rel=r_associated | relid=0 | w=35
  636. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the 4-hydroxyphenylpyruvate dioxygenase gene (hpd, 609695.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 4-hydroxyphenylpyruvate dioxygenase gene (hpd, 609695.0005) | rel=r_associated | relid=0 | w=35
  637. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the 5-prime nucleotidase, cytosolic ii gene (nt5c2, 600417.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 5-prime nucleotidase, cytosolic ii gene (nt5c2, 600417.0001) | rel=r_associated | relid=0 | w=35
  638. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the 62-kd nucleoporin gene (nup62, 605815.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 62-kd nucleoporin gene (nup62, 605815.0001) | rel=r_associated | relid=0 | w=35
  639. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the aarf domain-containing kinase 4 gene (adck4, 615567.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aarf domain-containing kinase 4 gene (adck4, 615567.0001) | rel=r_associated | relid=0 | w=35
  640. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the abelson helper integration site 1 gene (ahi1, 608894.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the abelson helper integration site 1 gene (ahi1, 608894.0001) | rel=r_associated | relid=0 | w=35
  641. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the acid beta glucosidase gene (gba, 606463.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the acid beta glucosidase gene (gba, 606463.0001) | rel=r_associated | relid=0 | w=35
  642. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the adaptor-related protein complex 4, beta-1 subunit gene (ap4b1, 607245.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adaptor-related protein complex 4, beta-1 subunit gene (ap4b1, 607245.0001) | rel=r_associated | relid=0 | w=35
  643. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the adenomatous polyposis coli gene (apc, 611731.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenomatous polyposis coli gene (apc, 611731.0001) | rel=r_associated | relid=0 | w=35
  644. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the adenosine deaminase gene (ada, 102700.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenosine deaminase gene (ada, 102700.0001) | rel=r_associated | relid=0 | w=35
  645. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the adp-ribosylation factor-like 6 gene (arl6, 608845.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adp-ribosylation factor-like 6 gene (arl6, 608845.0001) | rel=r_associated | relid=0 | w=35
  646. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the agrin gene (agrn, 103320.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the agrin gene (agrn, 103320.0001) | rel=r_associated | relid=0 | w=35
  647. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the aldehyde dehydrogenase 1 family, member a3 gene (aldh1a3, 600463.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aldehyde dehydrogenase 1 family, member a3 gene (aldh1a3, 600463.0001) | rel=r_associated | relid=0 | w=35
  648. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the alpha subunit of the 3-methylcrotonyl-coa carboxylase gene (mccc1, 609010.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha subunit of the 3-methylcrotonyl-coa carboxylase gene (mccc1, 609010.0001) | rel=r_associated | relid=0 | w=35
  649. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the alpha-1d subunit of the l-type voltage-dependent calcium channel gene (cacna1d, 114206.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1d subunit of the l-type voltage-dependent calcium channel gene (cacna1d, 114206.0001) | rel=r_associated | relid=0 | w=35
  650. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0001) | rel=r_associated | relid=0 | w=35
  651. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the alpha-subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0003) | rel=r_associated | relid=0 | w=35
  652. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the alpha-tubulin 1a gene (tuba1a, 602529.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-tubulin 1a gene (tuba1a, 602529.0001) | rel=r_associated | relid=0 | w=35
  653. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the aminoacylase-1 gene (acy1, 104620.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aminoacylase-1 gene (acy1, 104620.0001). | rel=r_associated | relid=0 | w=35
  654. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the androgen receptor gene (ar, 313700.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the androgen receptor gene (ar, 313700.0008) | rel=r_associated | relid=0 | w=35
  655. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ankyrin repeat and sterile alpha motif domains-containing protein gene 6 (anks6, 615370.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ankyrin repeat and sterile alpha motif domains-containing protein gene 6 (anks6, 615370.0001) | rel=r_associated | relid=0 | w=35
  656. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the anthrax toxin receptor 2 gene (antxr2, 608041.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the anthrax toxin receptor 2 gene (antxr2, 608041.0001) | rel=r_associated | relid=0 | w=35
  657. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the apoptosis-inducing factor, mitochondrion-associated, 1 gene (aifm1, 300169.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the apoptosis-inducing factor, mitochondrion-associated, 1 gene (aifm1, 300169.0002) | rel=r_associated | relid=0 | w=35
  658. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the argininosuccinate lyase gene (asl, 608310.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the argininosuccinate lyase gene (asl, 608310.0001) | rel=r_associated | relid=0 | w=35
  659. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ataxia-telangiectasia mutated gene (atm, 607585.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ataxia-telangiectasia mutated gene (atm, 607585.0001) | rel=r_associated | relid=0 | w=35
  660. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the atlastin-1 gene (atl1, 606439.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atlastin-1 gene (atl1, 606439.0010) | rel=r_associated | relid=0 | w=35
  661. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the atp synthase 6 gene (mtap6, 516060.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp synthase 6 gene (mtap6, 516060.0003) | rel=r_associated | relid=0 | w=35
  662. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0001) | rel=r_associated | relid=0 | w=35
  663. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0012) | rel=r_associated | relid=0 | w=35
  664. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the atp/gtp-binding protein-like-1 gene (agbl1, 615496.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp/gtp-binding protein-like-1 gene (agbl1, 615496.0001) | rel=r_associated | relid=0 | w=35
  665. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the atpase, h+ transporting, lysosomal, accessory protein-2 gene (atp6ap2, 300556.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, h+ transporting, lysosomal, accessory protein-2 gene (atp6ap2, 300556.0002) | rel=r_associated | relid=0 | w=35
  666. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the atpase, na+k+ transporting, alpha-2 polypeptide gene (atp1a2, 182340.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, na+k+ transporting, alpha-2 polypeptide gene (atp1a2, 182340.0001) | rel=r_associated | relid=0 | w=35
  667. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the atpase, na+k+ transporting, alpha-3 polypeptide gene (atp1a3, 182350.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, na+k+ transporting, alpha-3 polypeptide gene (atp1a3, 182350.0009) | rel=r_associated | relid=0 | w=35
  668. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the avian myelocytomatosis viral (v-myc) oncogene homolog (myc, 190080.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the avian myelocytomatosis viral (v-myc) oncogene homolog (myc, 190080.0001) | rel=r_associated | relid=0 | w=35
  669. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the b-cell receptor-associated protein 31 gene (bcap31, 300398.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the b-cell receptor-associated protein 31 gene (bcap31, 300398.0001) | rel=r_associated | relid=0 | w=35
  670. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the bbs10 gene (bbs10, 610148.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bbs10 gene (bbs10, 610148.0001) | rel=r_associated | relid=0 | w=35
  671. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the bbs7 gene (bbs7, 607590.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bbs7 gene (bbs7, 607590.0001) | rel=r_associated | relid=0 | w=35
  672. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0001) | rel=r_associated | relid=0 | w=35
  673. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the beta actin gene (actb, 102630.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta actin gene (actb, 102630.0002) | rel=r_associated | relid=0 | w=35
  674. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the beta-1 galactosidase gene (glb1, 611458.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1 galactosidase gene (glb1, 611458.0001) | rel=r_associated | relid=0 | w=35
  675. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the beta-1 laminin gene (lamb1, 150240.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1 laminin gene (lamb1, 150240.0001) | rel=r_associated | relid=0 | w=35
  676. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the beta-1,4-mannosyltransferase gene (alg1, 605907.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1,4-mannosyltransferase gene (alg1, 605907.0001) | rel=r_associated | relid=0 | w=35
  677. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the beta-carotene 15,15-prime-monooxygenase 1 gene (bcmo1, 605748.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-carotene 15,15-prime-monooxygenase 1 gene (bcmo1, 605748.0001). | rel=r_associated | relid=0 | w=35
  678. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the biogenesis of lysosome-related organelles complex 1, subunit 3 gene (bloc1s3, 609762.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the biogenesis of lysosome-related organelles complex 1, subunit 3 gene (bloc1s3, 609762.0001) | rel=r_associated | relid=0 | w=35
  679. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the biotinidase gene (btd, 253260.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the biotinidase gene (btd, 253260.0001) | rel=r_associated | relid=0 | w=35
  680. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the bone morphogenetic protein 4 (bmp4, 112262.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bone morphogenetic protein 4 (bmp4, 112262.0001) | rel=r_associated | relid=0 | w=35
  681. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the bruton agammaglobulinemia tyrosine kinase gene (btk, 300300.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bruton agammaglobulinemia tyrosine kinase gene (btk, 300300.0001) | rel=r_associated | relid=0 | w=35
  682. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the budding uninhibited by benzimidazoles 1 beta gene (bub1b, 602860.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the budding uninhibited by benzimidazoles 1 beta gene (bub1b, 602860.0003) | rel=r_associated | relid=0 | w=35
  683. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the c homolog of the s. cerevisiae rad51 gene (rad51c, 602774.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the c homolog of the s. cerevisiae rad51 gene (rad51c, 602774.0001) | rel=r_associated | relid=0 | w=35
  684. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the c20orf7 gene (c20orf7, 612360.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the c20orf7 gene (c20orf7, 612360.0002) | rel=r_associated | relid=0 | w=35
  685. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cadherin 3 gene (cdh3, 114021.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cadherin 3 gene (cdh3, 114021.0001) | rel=r_associated | relid=0 | w=35
  686. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the calcium channel, voltage-dependent, l type, alpha 1d subunit gene (cacna1d, 114206.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calcium channel, voltage-dependent, l type, alpha 1d subunit gene (cacna1d, 114206.0002) | rel=r_associated | relid=0 | w=35
  687. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the calcium-activated nucleotidase 1 gene (cant1, 613165.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calcium-activated nucleotidase 1 gene (cant1, 613165.0001) | rel=r_associated | relid=0 | w=35
  688. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the calmodulin-1 gene (calm1, 114180.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calmodulin-1 gene (calm1, 114180.0001) | rel=r_associated | relid=0 | w=35
  689. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the carboxypeptidase a6 gene (cpa6, 609562.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carboxypeptidase a6 gene (cpa6, 609562.0001) | rel=r_associated | relid=0 | w=35
  690. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cardiac troponin t2 gene (tnnt2, 191045.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cardiac troponin t2 gene (tnnt2, 191045.0011) | rel=r_associated | relid=0 | w=35
  691. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0009) | rel=r_associated | relid=0 | w=35
  692. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the caspase 8 gene (casp8, 601763.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the caspase 8 gene (casp8, 601763.0001) | rel=r_associated | relid=0 | w=35
  693. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cathepsin c gene (ctsc, 602365.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cathepsin c gene (ctsc, 602365.0001) | rel=r_associated | relid=0 | w=35
  694. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the caveolin 1 gene (cav1, 601047.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the caveolin 1 gene (cav1, 601047.0004) | rel=r_associated | relid=0 | w=35
  695. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the caveolin 3 gene (cav3, 601253.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the caveolin 3 gene (cav3, 601253.0007) | rel=r_associated | relid=0 | w=35
  696. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ccctc-binding factor gene (ctcf, 604167.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ccctc-binding factor gene (ctcf, 604167.0001) | rel=r_associated | relid=0 | w=35
  697. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cd19 antigen gene (cd191, 107265.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd19 antigen gene (cd191, 107265.0001) | rel=r_associated | relid=0 | w=35
  698. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cd3 antigen, gamma subunit gene (cd3g, 186740.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd3 antigen, gamma subunit gene (cd3g, 186740.0001) | rel=r_associated | relid=0 | w=35
  699. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the centromeric protein e gene (cenpe, 117143.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the centromeric protein e gene (cenpe, 117143.0001) | rel=r_associated | relid=0 | w=35
  700. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ceramide synthase 3 gene (cers3, 615276.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ceramide synthase 3 gene (cers3, 615276.0001) | rel=r_associated | relid=0 | w=35
  701. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the chaperonin-containing t-complex peptide-1 subunit 5 gene (cct5, 610150.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chaperonin-containing t-complex peptide-1 subunit 5 gene (cct5, 610150.0001) | rel=r_associated | relid=0 | w=35
  702. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the chloride channel 7 gene (clcn7, 602727.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chloride channel 7 gene (clcn7, 602727.0004) | rel=r_associated | relid=0 | w=35
  703. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cholinergic receptor, nicotinic, alpha polypeptide-1 gene (chrna1, 100690.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, alpha polypeptide-1 gene (chrna1, 100690.0001) | rel=r_associated | relid=0 | w=35
  704. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cholinergic receptor, nicotinic, beta polypeptide-1 gene (chrnb1, 100710.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, beta polypeptide-1 gene (chrnb1, 100710.0001) | rel=r_associated | relid=0 | w=35
  705. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the chromosome 19 open reading frame 12 gene (c19orf12, 614297.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 19 open reading frame 12 gene (c19orf12, 614297.0006) | rel=r_associated | relid=0 | w=35
  706. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cln6 gene (cln6, 606725.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cln6 gene (cln6, 606725.0001) | rel=r_associated | relid=0 | w=35
  707. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the coagulation factor vii gene (f7, 613878.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coagulation factor vii gene (f7, 613878.0001) | rel=r_associated | relid=0 | w=35
  708. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the coagulation factor x gene (f10, 613872.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coagulation factor x gene (f10, 613872.0001). | rel=r_associated | relid=0 | w=35
  709. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cochlin gene (coch, 603196.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cochlin gene (coch, 603196.0001) | rel=r_associated | relid=0 | w=35
  710. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the coiled-coil domain-containing protein 88c (ccdc88c, 611204.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil domain-containing protein 88c (ccdc88c, 611204.0001) | rel=r_associated | relid=0 | w=35
  711. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0001) | rel=r_associated | relid=0 | w=35
  712. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0045)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0045) | rel=r_associated | relid=0 | w=35
  713. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0014).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0014). | rel=r_associated | relid=0 | w=35
  714. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the collagen type viii alpha-2 gene (col8a2, 120252.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen type viii alpha-2 gene (col8a2, 120252.0001) | rel=r_associated | relid=0 | w=35
  715. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0008) | rel=r_associated | relid=0 | w=35
  716. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the complement component 1, q subcomponent, b chain gene (c1qb, 120570.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement component 1, q subcomponent, b chain gene (c1qb, 120570.0001) | rel=r_associated | relid=0 | w=35
  717. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the complex i, subunit nd4 gene (mtnd4, 516003.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complex i, subunit nd4 gene (mtnd4, 516003.0001) | rel=r_associated | relid=0 | w=35
  718. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cyclin d2 gene (ccnd2, 123833.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclin d2 gene (ccnd2, 123833.0001) | rel=r_associated | relid=0 | w=35
  719. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cyclin m4 gene (cnnm4, 607805.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclin m4 gene (cnnm4, 607805.0001) | rel=r_associated | relid=0 | w=35
  720. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cyclin o gene (ccno, 607752.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclin o gene (ccno, 607752.0001) | rel=r_associated | relid=0 | w=35
  721. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cyclin-dependent kinase 6 gene (cdk6, 603368.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclin-dependent kinase 6 gene (cdk6, 603368.0001) | rel=r_associated | relid=0 | w=35
  722. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cyld gene (605018.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyld gene (605018.0003) | rel=r_associated | relid=0 | w=35
  723. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the cytochrome c oxidase, subunit 15 gene (cox15, 603646.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase, subunit 15 gene (cox15, 603646.0001) | rel=r_associated | relid=0 | w=35
  724. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ddhd domain-containing protein 2 gene (ddhd2, 615003.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ddhd domain-containing protein 2 gene (ddhd2, 615003.0001) | rel=r_associated | relid=0 | w=35
  725. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dedicator of cytokinesis 7 gene (dock7, 615730.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dedicator of cytokinesis 7 gene (dock7, 615730.0001) | rel=r_associated | relid=0 | w=35
  726. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dehydrogenase e1 and transketolase domains-containing protein 1 gene (dhtkd1, 614984.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dehydrogenase e1 and transketolase domains-containing protein 1 gene (dhtkd1, 614984.0001) | rel=r_associated | relid=0 | w=35
  727. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the delta-1 phospholipase c gene (plcd1, 602142.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the delta-1 phospholipase c gene (plcd1, 602142.0001) | rel=r_associated | relid=0 | w=35
  728. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0001) | rel=r_associated | relid=0 | w=35
  729. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dfna5 gene (608798.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dfna5 gene (608798.0001) | rel=r_associated | relid=0 | w=35
  730. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dicarbonyl/l-xylulose reductase gene (dcxr, 608347.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dicarbonyl/l-xylulose reductase gene (dcxr, 608347.0001) | rel=r_associated | relid=0 | w=35
  731. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the disintegrin-like and metalloproteinase with thrombospondin type 1 motif 18 gene (adamts18, 607512.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the disintegrin-like and metalloproteinase with thrombospondin type 1 motif 18 gene (adamts18, 607512.0002) | rel=r_associated | relid=0 | w=35
  732. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dna methyltransferase 1 gene (dnmt1, 126375.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna methyltransferase 1 gene (dnmt1, 126375.0003) | rel=r_associated | relid=0 | w=35
  733. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dna polymerase, epsilon gene (pole, 174762.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna polymerase, epsilon gene (pole, 174762.0002) | rel=r_associated | relid=0 | w=35
  734. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 2 gene (dnajb2, 604139.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 2 gene (dnajb2, 604139.0003) | rel=r_associated | relid=0 | w=35
  735. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dopamine beta-hydroxylase gene (dbh, 609312.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dopamine beta-hydroxylase gene (dbh, 609312.0002) | rel=r_associated | relid=0 | w=35
  736. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dual-specificity phosphatase-6 gene (dusp6, 602748.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dual-specificity phosphatase-6 gene (dusp6, 602748.0001) | rel=r_associated | relid=0 | w=35
  737. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the dysferlin gene (dys, 603009.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dysferlin gene (dys, 603009.0001) | rel=r_associated | relid=0 | w=35
  738. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the edar-associated death domain gene (edaradd, 606603.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the edar-associated death domain gene (edaradd, 606603.0002) | rel=r_associated | relid=0 | w=35
  739. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the elmo/ced12 domain-containing protein 3 gene (elmod3, 615427.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the elmo/ced12 domain-containing protein 3 gene (elmod3, 615427.0001) | rel=r_associated | relid=0 | w=35
  740. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the endoglin gene (eng, 131195.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endoglin gene (eng, 131195.0001) | rel=r_associated | relid=0 | w=35
  741. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the endothelin receptor type b gene (ednrb, 131244.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endothelin receptor type b gene (ednrb, 131244.0001) | rel=r_associated | relid=0 | w=35
  742. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the endothelin-1 gene (edn1, 131240.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endothelin-1 gene (edn1, 131240.0002) | rel=r_associated | relid=0 | w=35
  743. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the enteric smooth muscle actin gamma-2 gene (actg2, 102545.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the enteric smooth muscle actin gamma-2 gene (actg2, 102545.0001) | rel=r_associated | relid=0 | w=35
  744. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the epithelial cellular adhesion molecule gene (epcam, 185535.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the epithelial cellular adhesion molecule gene (epcam, 185535.0001) | rel=r_associated | relid=0 | w=35
  745. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the estrogen receptor-1 gene (esr1, 133430.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the estrogen receptor-1 gene (esr1, 133430.0002) | rel=r_associated | relid=0 | w=35
  746. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ets variant gene 6 (etv, 600618.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ets variant gene 6 (etv, 600618.0003) | rel=r_associated | relid=0 | w=35
  747. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 5 gene (eif2b5, 603945.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 5 gene (eif2b5, 603945.0001) | rel=r_associated | relid=0 | w=35
  748. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the excision repair cross complementing rodent repair deficiency, complementation group 6 gene (ercc6, 133540.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the excision repair cross complementing rodent repair deficiency, complementation group 6 gene (ercc6, 133540.0007) | rel=r_associated | relid=0 | w=35
  749. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the excision-repair cross-complementing group 3 gene (ercc3, 133510.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the excision-repair cross-complementing group 3 gene (ercc3, 133510.0001) | rel=r_associated | relid=0 | w=35
  750. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the excision-repair cross-complementing group 4 gene (ercc4, 133520.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the excision-repair cross-complementing group 4 gene (ercc4, 133520.0001) | rel=r_associated | relid=0 | w=35
  751. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the f-box only protein 31 gene (fbxo31, 609102.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the f-box only protein 31 gene (fbxo31, 609102.0001) | rel=r_associated | relid=0 | w=35
  752. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the f-box only protein 38 gene (fbxo38, 608533.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the f-box only protein 38 gene (fbxo38, 608533.0001) | rel=r_associated | relid=0 | w=35
  753. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the family with sequence similarity 20, member a gene (fam20a, 611062.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the family with sequence similarity 20, member a gene (fam20a, 611062.0001) | rel=r_associated | relid=0 | w=35
  754. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fancd2/fanci-associated nuclease 1 gene (fan1, 613534.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fancd2/fanci-associated nuclease 1 gene (fan1, 613534.0001) | rel=r_associated | relid=0 | w=35
  755. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fas-associated via death domain gene (fadd, 602457.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fas-associated via death domain gene (fadd, 602457.0001) | rel=r_associated | relid=0 | w=35
  756. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ferm domain-containing 7 gene (frmd7, 300628.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ferm domain-containing 7 gene (frmd7, 300628.0001) | rel=r_associated | relid=0 | w=35
  757. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0015) | rel=r_associated | relid=0 | w=35
  758. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fibroblast growth factor 23 gene (fgf23, 605380.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor 23 gene (fgf23, 605380.0003) | rel=r_associated | relid=0 | w=35
  759. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0002) | rel=r_associated | relid=0 | w=35
  760. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0035)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0035) | rel=r_associated | relid=0 | w=35
  761. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0001) | rel=r_associated | relid=0 | w=35
  762. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the filamin c gene (flnc, 102565.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the filamin c gene (flnc, 102565.0003) | rel=r_associated | relid=0 | w=35
  763. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the folliculin gene (flcn, 607273.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the folliculin gene (flcn, 607273.0001) | rel=r_associated | relid=0 | w=35
  764. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the forkhead transcription factor foxl2 gene (foxl2, 605597.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead transcription factor foxl2 gene (foxl2, 605597.0001) | rel=r_associated | relid=0 | w=35
  765. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0001) | rel=r_associated | relid=0 | w=35
  766. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fukutin gene (fktn, 607440.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fukutin gene (fktn, 607440.0001) | rel=r_associated | relid=0 | w=35
  767. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fukutin gene (fktn, 607440.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fukutin gene (fktn, 607440.0005) | rel=r_associated | relid=0 | w=35
  768. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fumarate hydratase gene (fh, 136850.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fumarate hydratase gene (fh, 136850.0001) | rel=r_associated | relid=0 | w=35
  769. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fumarate hydratase gene (fh, 136850.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fumarate hydratase gene (fh, 136850.0003) | rel=r_associated | relid=0 | w=35
  770. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the fyve and coiled-coil domain containing-1 gene (fyco1, 607182.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fyve and coiled-coil domain containing-1 gene (fyco1, 607182.0001) | rel=r_associated | relid=0 | w=35
  771. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the gamma type 1 phosphatidylinositol 4-phosphate 5-kinase gene (pip5k1c, 606102.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma type 1 phosphatidylinositol 4-phosphate 5-kinase gene (pip5k1c, 606102.0001) | rel=r_associated | relid=0 | w=35
  772. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the gap junction alpha-12 gene (gja12, 608803.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gap junction alpha-12 gene (gja12, 608803.0001) | rel=r_associated | relid=0 | w=35
  773. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the gap junction protein, beta 2 gene (gjb2, 121011.0020)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gap junction protein, beta 2 gene (gjb2, 121011.0020) | rel=r_associated | relid=0 | w=35
  774. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the gap junction protein, gamma-2 gene (gjc2, 608803.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gap junction protein, gamma-2 gene (gjc2, 608803.0009) | rel=r_associated | relid=0 | w=35
  775. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the gastric intrinsic factor gene (gif, 609342.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gastric intrinsic factor gene (gif, 609342.0001). | rel=r_associated | relid=0 | w=35
  776. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0001) | rel=r_associated | relid=0 | w=35
  777. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the gene atp-binding cassette, subfamily a, member 5 gene (abca5, 612503.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene atp-binding cassette, subfamily a, member 5 gene (abca5, 612503.0001) | rel=r_associated | relid=0 | w=35
  778. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the gene encoding growth/differentiation factor-2 (gdf2, 605120.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding growth/differentiation factor-2 (gdf2, 605120.0001) | rel=r_associated | relid=0 | w=35
  779. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the gigaxonin gene (gan, 605379.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gigaxonin gene (gan, 605379.0001) | rel=r_associated | relid=0 | w=35
  780. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the glycogen branching enzyme gene (gbe1, 607839.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycogen branching enzyme gene (gbe1, 607839.0001) | rel=r_associated | relid=0 | w=35
  781. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the grainyhead-like-3 gene (grhl3, 608317.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the grainyhead-like-3 gene (grhl3, 608317.0001) | rel=r_associated | relid=0 | w=35
  782. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the granulin gene (grn, 138945.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the granulin gene (grn, 138945.0001) | rel=r_associated | relid=0 | w=35
  783. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the growth/differentiation factor 1 gene (gdf1, 602880.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the growth/differentiation factor 1 gene (gdf1, 602880.0001) | rel=r_associated | relid=0 | w=35
  784. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the guanine nucleotide-binding protein, alpha-stimulating activity polypeptide gene (gnas, 139320.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the guanine nucleotide-binding protein, alpha-stimulating activity polypeptide gene (gnas, 139320.0002) | rel=r_associated | relid=0 | w=35
  785. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the guanylate cyclase 2c gene (gucy2c, 601330.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the guanylate cyclase 2c gene (gucy2c, 601330.0001) | rel=r_associated | relid=0 | w=35
  786. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the hect domain and rcc1-like domain 2 (herc2, 605837.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hect domain and rcc1-like domain 2 (herc2, 605837.0004) | rel=r_associated | relid=0 | w=35
  787. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the heparin cofactor ii gene (hcf2, 142360.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heparin cofactor ii gene (hcf2, 142360.0001) | rel=r_associated | relid=0 | w=35
  788. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homeobox a2 gene (hoxa2, 604685.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeobox a2 gene (hoxa2, 604685.0001) | rel=r_associated | relid=0 | w=35
  789. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog 1 of drosophila notch gene (notch1, 190198.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog 1 of drosophila notch gene (notch1, 190198.0003) | rel=r_associated | relid=0 | w=35
  790. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of chlamydomonas poc1 centriolar protein-b gene (poc1b, 614784.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of chlamydomonas poc1 centriolar protein-b gene (poc1b, 614784.0001) | rel=r_associated | relid=0 | w=35
  791. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the drosophila fat tumor suppressor 4 gene (fat4, 612411.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila fat tumor suppressor 4 gene (fat4, 612411.0001) | rel=r_associated | relid=0 | w=35
  792. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the e. coli dnaj subfamily c member 19 gene (dnajc19, 608977.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the e. coli dnaj subfamily c member 19 gene (dnajc19, 608977.0001) | rel=r_associated | relid=0 | w=35
  793. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the e. coli mutl 1 gene (mlh1, 120436.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the e. coli mutl 1 gene (mlh1, 120436.0006) | rel=r_associated | relid=0 | w=35
  794. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0001) | rel=r_associated | relid=0 | w=35
  795. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the mouse noggin gene (nog, 602991.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse noggin gene (nog, 602991.0003) | rel=r_associated | relid=0 | w=35
  796. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the s. cerevisiae brf1 gene (brf1, 604902.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae brf1 gene (brf1, 604902.0001) | rel=r_associated | relid=0 | w=35
  797. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the s. cerevisiae fig4 gene (fig4, 609390.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae fig4 gene (fig4, 609390.0001) | rel=r_associated | relid=0 | w=35
  798. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the s. cerevisiae iba57 gene (iba57, 615316.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae iba57 gene (iba57, 615316.0001) | rel=r_associated | relid=0 | w=35
  799. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the s. cerevisiae meiotic recombination 11 a gene (mre11a, 600814.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae meiotic recombination 11 a gene (mre11a, 600814.0001) | rel=r_associated | relid=0 | w=35
  800. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the s. pombe rad21 gene (rad21, 606462.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. pombe rad21 gene (rad21, 606462.0001) | rel=r_associated | relid=0 | w=35
  801. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the homolog of the yeast vacuolar protein sorting 45 gene (vps45, 610035.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the yeast vacuolar protein sorting 45 gene (vps45, 610035.0001) | rel=r_associated | relid=0 | w=35
  802. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the hsn2 isoform of the protein kinase, lysine-deficient 1 gene (wnk1, 605232.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hsn2 isoform of the protein kinase, lysine-deficient 1 gene (wnk1, 605232.0003) | rel=r_associated | relid=0 | w=35
  803. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the human homolog of the iron-sulfur cluster scaffold gene (iscu, 611911.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the human homolog of the iron-sulfur cluster scaffold gene (iscu, 611911.0001) | rel=r_associated | relid=0 | w=35
  804. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the hyperpolarization-activated cyclic nucleotide-gated potassium channel (hcn1, 602780.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hyperpolarization-activated cyclic nucleotide-gated potassium channel (hcn1, 602780.0001) | rel=r_associated | relid=0 | w=35
  805. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the immunoglobulin lambda-like polypeptide 1 gene (igll1, 146770.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the immunoglobulin lambda-like polypeptide 1 gene (igll1, 146770.0001) | rel=r_associated | relid=0 | w=35
  806. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the immunoglobulin-binding protein-1 gene (igbp1, 300139.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the immunoglobulin-binding protein-1 gene (igbp1, 300139.0001) | rel=r_associated | relid=0 | w=35
  807. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the insulin receptor gene (insr, 147670.0037)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the insulin receptor gene (insr, 147670.0037) | rel=r_associated | relid=0 | w=35
  808. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the kat8 regulatory nsl complex subunit 1 gene (kansl1, 612452.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kat8 regulatory nsl complex subunit 1 gene (kansl1, 612452.0001) | rel=r_associated | relid=0 | w=35
  809. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the kelch-like 10 gene (klhl10, 608778.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kelch-like 10 gene (klhl10, 608778.0001) | rel=r_associated | relid=0 | w=35
  810. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the kelch-like 41 gene (klhl41, 607701.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kelch-like 41 gene (klhl41, 607701.0001) | rel=r_associated | relid=0 | w=35
  811. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the kelch-like 7 gene (klhl7, 611119.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kelch-like 7 gene (klhl7, 611119.0001) | rel=r_associated | relid=0 | w=35
  812. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the kinesin family member 1b gene (kif1b, 605995.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 1b gene (kif1b, 605995.0001) | rel=r_associated | relid=0 | w=35
  813. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the kinesin family member 21a gene (kif21a, 608283.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 21a gene (kif21a, 608283.0001) | rel=r_associated | relid=0 | w=35
  814. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the kizuna centrosomal protein gene (kiz, 615757.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kizuna centrosomal protein gene (kiz, 615757.0001) | rel=r_associated | relid=0 | w=35
  815. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the krev interaction trapped 1 gene (krit1 604214.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the krev interaction trapped 1 gene (krit1 604214.0001). | rel=r_associated | relid=0 | w=35
  816. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the lamin a/c gene (lmna, 150330.0017)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin a/c gene (lmna, 150330.0017) | rel=r_associated | relid=0 | w=35
  817. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the lamin a/c gene (lmna, 150330.0045)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin a/c gene (lmna, 150330.0045) | rel=r_associated | relid=0 | w=35
  818. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the laminin gamma-2 gene (lamc2, 150292.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the laminin gamma-2 gene (lamc2, 150292.0001) | rel=r_associated | relid=0 | w=35
  819. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the low density lipoprotein receptor-related protein 2 gene (lrp2, 600073.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the low density lipoprotein receptor-related protein 2 gene (lrp2, 600073.0001) | rel=r_associated | relid=0 | w=35
  820. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the low-density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the low-density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0014) | rel=r_associated | relid=0 | w=35
  821. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the lymphocyte-specific protein-tyrosine kinase gene (lck, 153390.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lymphocyte-specific protein-tyrosine kinase gene (lck, 153390.0001) | rel=r_associated | relid=0 | w=35
  822. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the major facilitator superfamily domain-containing protein-8 gene (mfsd8, 611124.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the major facilitator superfamily domain-containing protein-8 gene (mfsd8, 611124.0008) | rel=r_associated | relid=0 | w=35
  823. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the malonyl-coa decarboxylase gene (mlycd, 606761.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the malonyl-coa decarboxylase gene (mlycd, 606761.0001) | rel=r_associated | relid=0 | w=35
  824. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the matrilin 3 gene (matn3, 602109.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the matrilin 3 gene (matn3, 602109.0001) | rel=r_associated | relid=0 | w=35
  825. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the membrane-type frizzled-related protein gene (mfrp, 606227.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the membrane-type frizzled-related protein gene (mfrp, 606227.0005) | rel=r_associated | relid=0 | w=35
  826. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the methionine adenosyltransferase 1 gene (mat1a, 610550.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methionine adenosyltransferase 1 gene (mat1a, 610550.0001) | rel=r_associated | relid=0 | w=35
  827. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the methionine synthase gene (mtr, 156570.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methionine synthase gene (mtr, 156570.0001) | rel=r_associated | relid=0 | w=35
  828. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0001) | rel=r_associated | relid=0 | w=35
  829. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the mitochondrial aconitase gene (aco2, 100850.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial aconitase gene (aco2, 100850.0001) | rel=r_associated | relid=0 | w=35
  830. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the mitochondrial arginyl-trna synthetase gene (rars2, 611524.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial arginyl-trna synthetase gene (rars2, 611524.0001) | rel=r_associated | relid=0 | w=35
  831. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the mitochondrial poly(a) polymerase gene (mtpap, 613669.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial poly(a) polymerase gene (mtpap, 613669.0001) | rel=r_associated | relid=0 | w=35
  832. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the mitochondrial rna-processing endoribonuclease gene (rmrp, 157660.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial rna-processing endoribonuclease gene (rmrp, 157660.0009) | rel=r_associated | relid=0 | w=35
  833. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the mitochondrial trna serine 1 gene (mtts1, 590080.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial trna serine 1 gene (mtts1, 590080.0003) | rel=r_associated | relid=0 | w=35
  834. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the mitochondrial-encoded atp synthase 6 gene (mtatp6, 516060.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial-encoded atp synthase 6 gene (mtatp6, 516060.0005) | rel=r_associated | relid=0 | w=35
  835. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the mitofusin 2 gene (mfn2, 608507.00001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitofusin 2 gene (mfn2, 608507.00001) | rel=r_associated | relid=0 | w=35
  836. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the mothers against decapentaplegic, drosophila homolog of, 4 gene (smad4, 600993.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mothers against decapentaplegic, drosophila homolog of, 4 gene (smad4, 600993.0007) | rel=r_associated | relid=0 | w=35
  837. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the mothers against decapentaplegic, drosophila, homolog of, 3 gene (smad3, 603109.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mothers against decapentaplegic, drosophila, homolog of, 3 gene (smad3, 603109.0001) | rel=r_associated | relid=0 | w=35
  838. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the multiple epidermal growth factor-like domains-8 gene (megf8, 604267.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the multiple epidermal growth factor-like domains-8 gene (megf8, 604267.0001) | rel=r_associated | relid=0 | w=35
  839. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the myelin protein zero gene (mpz, 159440.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0001) | rel=r_associated | relid=0 | w=35
  840. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the myelin protein zero gene (mpz, 159440.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0004) | rel=r_associated | relid=0 | w=35
  841. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, gamma subunit gene (gnptg, 607838.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, gamma subunit gene (gnptg, 607838.0001) | rel=r_associated | relid=0 | w=35
  842. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex 9 gene (ndufa9, 603834.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex 9 gene (ndufa9, 603834.0001) | rel=r_associated | relid=0 | w=35
  843. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the natriuretic peptide receptor 2 gene (npr2, 108961)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the natriuretic peptide receptor 2 gene (npr2, 108961) | rel=r_associated | relid=0 | w=35
  844. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the neural retina leucine zipper gene (nrl, 162080.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neural retina leucine zipper gene (nrl, 162080.0001) | rel=r_associated | relid=0 | w=35
  845. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the neuronal nicotinic cholinergic receptor, alpha polypeptide 4 gene (chrna4, 118504.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neuronal nicotinic cholinergic receptor, alpha polypeptide 4 gene (chrna4, 118504.0002) | rel=r_associated | relid=0 | w=35
  846. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the neutrophil cytosolic factor-1 gene, p47-phox (ncf1, 608512.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neutrophil cytosolic factor-1 gene, p47-phox (ncf1, 608512.0001) | rel=r_associated | relid=0 | w=35
  847. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the nonerythrocytic alpha-spectrin 1 gene (sptan1, 182810.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nonerythrocytic alpha-spectrin 1 gene (sptan1, 182810.0001) | rel=r_associated | relid=0 | w=35
  848. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the nonimprinted gene in prader-willi syndrome/angelman syndrome chromosome region-1 (nipa1, 608145.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nonimprinted gene in prader-willi syndrome/angelman syndrome chromosome region-1 (nipa1, 608145.0001) | rel=r_associated | relid=0 | w=35
  849. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the nuclear factor of kappa light chain gene enhancer in b cells inhibitor alpha gene (nfkbia, 164008.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear factor of kappa light chain gene enhancer in b cells inhibitor alpha gene (nfkbia, 164008.0001). | rel=r_associated | relid=0 | w=35
  850. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the nuclear receptor subfamily 2, group e, member 3 gene (nr2e3, 604485.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear receptor subfamily 2, group e, member 3 gene (nr2e3, 604485.0006) | rel=r_associated | relid=0 | w=35
  851. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the nucleolar protein-3 gene (nol3, 605235.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nucleolar protein-3 gene (nol3, 605235.0001) | rel=r_associated | relid=0 | w=35
  852. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ofd1 gene (ofd1, 300170.0007).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ofd1 gene (ofd1, 300170.0007). | rel=r_associated | relid=0 | w=35
  853. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ofd1 gene (ofd1, 300170.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ofd1 gene (ofd1, 300170.0011) | rel=r_associated | relid=0 | w=35
  854. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the paired box 3 gene (pax3, 606597.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the paired box 3 gene (pax3, 606597.0001) | rel=r_associated | relid=0 | w=35
  855. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the paraplegin gene (spg7, 602783.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the paraplegin gene (spg7, 602783.0001) | rel=r_associated | relid=0 | w=35
  856. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the parathyroid hormone-like hormone gene (pthlh, 168470.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the parathyroid hormone-like hormone gene (pthlh, 168470.0001) | rel=r_associated | relid=0 | w=35
  857. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0001) | rel=r_associated | relid=0 | w=35
  858. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0006) | rel=r_associated | relid=0 | w=35
  859. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the peroxisome biogenesis factor 10 gene (pex10, 602859.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor 10 gene (pex10, 602859.0002) | rel=r_associated | relid=0 | w=35
  860. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the peroxisome proliferator-activated receptor-gamma gene (pparg, 601487.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome proliferator-activated receptor-gamma gene (pparg, 601487.0007) | rel=r_associated | relid=0 | w=35
  861. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0001) | rel=r_associated | relid=0 | w=35
  862. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 1 gene (pik3r1, 171833.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 1 gene (pik3r1, 171833.0001) | rel=r_associated | relid=0 | w=35
  863. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the phosphodiesterase-6g, cgmp-specific, rod, gamma gene (pde6g, 180073.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphodiesterase-6g, cgmp-specific, rod, gamma gene (pde6g, 180073.0001) | rel=r_associated | relid=0 | w=35
  864. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the phosphoglucomutase-1 gene (pgm1, 171900.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoglucomutase-1 gene (pgm1, 171900.0001) | rel=r_associated | relid=0 | w=35
  865. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the phosphoglycerate dehydrogenase gene (phgdh, 606879.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoglycerate dehydrogenase gene (phgdh, 606879.0001) | rel=r_associated | relid=0 | w=35
  866. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the phosphoglycerate mutase 2 gene (pgam2, 612931.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoglycerate mutase 2 gene (pgam2, 612931.0001) | rel=r_associated | relid=0 | w=35
  867. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the phosphoribosylpyrophosphate synthetase 1 gene (prps1, 311850.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoribosylpyrophosphate synthetase 1 gene (prps1, 311850.0011) | rel=r_associated | relid=0 | w=35
  868. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the piezo-type mechanosensitive ion channel component 2 gene (piezo2, 613629.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the piezo-type mechanosensitive ion channel component 2 gene (piezo2, 613629.0001) | rel=r_associated | relid=0 | w=35
  869. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the piezo1 ion channel gene (piezo1, 611184.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the piezo1 ion channel gene (piezo1, 611184.0001) | rel=r_associated | relid=0 | w=35
  870. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the polyglutamine-binding protein-1 gene (pqbp1, 300463.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polyglutamine-binding protein-1 gene (pqbp1, 300463.0001) | rel=r_associated | relid=0 | w=35
  871. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the polyribonucleotide nucleotidyltransferase 1 gene (pnpt1, 610316.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polyribonucleotide nucleotidyltransferase 1 gene (pnpt1, 610316.0002) | rel=r_associated | relid=0 | w=35
  872. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the porcupine, drosophila, homolog of gene (porcn, 300651.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the porcupine, drosophila, homolog of gene (porcn, 300651.0001) | rel=r_associated | relid=0 | w=35
  873. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 2 gene (kcnj1, 600681.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 2 gene (kcnj1, 600681.0014) | rel=r_associated | relid=0 | w=35
  874. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the potassium channel, voltage-gated, shaker-related subfamily, member 5 gene (kcna5, 176267.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium channel, voltage-gated, shaker-related subfamily, member 5 gene (kcna5, 176267.0001) | rel=r_associated | relid=0 | w=35
  875. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the potassium channel, voltage-gated, subfamily v, member 2 gene (kcnv2, 607604.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium channel, voltage-gated, subfamily v, member 2 gene (kcnv2, 607604.0001) | rel=r_associated | relid=0 | w=35
  876. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the presenilin 2 gene (psen2, 600759.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the presenilin 2 gene (psen2, 600759.0001) | rel=r_associated | relid=0 | w=35
  877. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase (lysine hydroxylase) 2 gene (plod2, 601865.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase (lysine hydroxylase) 2 gene (plod2, 601865.0001) | rel=r_associated | relid=0 | w=35
  878. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene (plod3, 603066.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene (plod3, 603066.0001) | rel=r_associated | relid=0 | w=35
  879. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the prokineticin receptor-2 gene (prokr2, 607123.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prokineticin receptor-2 gene (prokr2, 607123.0001) | rel=r_associated | relid=0 | w=35
  880. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the prolactin receptor gene (prlr, 176761.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prolactin receptor gene (prlr, 176761.0002) | rel=r_associated | relid=0 | w=35
  881. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the propionyl coenzyme a carboxylase, beta polypeptide gene (pccb, 232050.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the propionyl coenzyme a carboxylase, beta polypeptide gene (pccb, 232050.0001) | rel=r_associated | relid=0 | w=35
  882. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the protein o-fucosyltransferase-1 gene (pofut1, 607491.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein o-fucosyltransferase-1 gene (pofut1, 607491.0001) | rel=r_associated | relid=0 | w=35
  883. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the protein o-glucosyltransferase-1 gene (poglut1, 615618.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein o-glucosyltransferase-1 gene (poglut1, 615618.0001) | rel=r_associated | relid=0 | w=35
  884. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase gene (pomgnt1, 606822.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase gene (pomgnt1, 606822.0001) | rel=r_associated | relid=0 | w=35
  885. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the protocadherin 19 gene (pcdh19, 300460.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protocadherin 19 gene (pcdh19, 300460.0001). | rel=r_associated | relid=0 | w=35
  886. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the receptor for the fc fragment of igg, low affinity iiia (fcgr3a, 146740.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the receptor for the fc fragment of igg, low affinity iiia (fcgr3a, 146740.0002) | rel=r_associated | relid=0 | w=35
  887. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the recq protein-like 2 gene (recql2, 604611.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the recq protein-like 2 gene (recql2, 604611.0001) | rel=r_associated | relid=0 | w=35
  888. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the recq protein-like 3 gene (recql3, 604610.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the recq protein-like 3 gene (recql3, 604610.0001) | rel=r_associated | relid=0 | w=35
  889. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the red cell membrane band 3 gene (bnd3, 109270.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the red cell membrane band 3 gene (bnd3, 109270.0003) | rel=r_associated | relid=0 | w=35
  890. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the regulatory factor x, 6 gene (rfx6, 612659.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the regulatory factor x, 6 gene (rfx6, 612659.0001) | rel=r_associated | relid=0 | w=35
  891. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ric-like protein without caax motif 1 gene (rit1, 609591.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ric-like protein without caax motif 1 gene (rit1, 609591.0001) | rel=r_associated | relid=0 | w=35
  892. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the rna-binding motif protein 28 gene (rbm28, 612074.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rna-binding motif protein 28 gene (rbm28, 612074.0001) | rel=r_associated | relid=0 | w=35
  893. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the romboid 5, drosophila, homolog of, 2 gene (rhbdf2, 614404.0001 )
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the romboid 5, drosophila, homolog of, 2 gene (rhbdf2, 614404.0001 ) | rel=r_associated | relid=0 | w=35
  894. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the rp1-like protein 1 gene (rp1l1, 608581.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rp1-like protein 1 gene (rp1l1, 608581.0001) | rel=r_associated | relid=0 | w=35
  895. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the sam domain- and hd domain-containing protein 1 gene (samhd1, 606754.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sam domain- and hd domain-containing protein 1 gene (samhd1, 606754.0011) | rel=r_associated | relid=0 | w=35
  896. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the sedlin gene (sedl, 300202.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sedlin gene (sedl, 300202.0001) | rel=r_associated | relid=0 | w=35
  897. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the serine palmitoyltransferase, long-chain base subunit 2 gene (sptlc2, 605713.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the serine palmitoyltransferase, long-chain base subunit 2 gene (sptlc2, 605713.0001) | rel=r_associated | relid=0 | w=35
  898. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the set domain-containing protein 5 gene (setd5, 615743.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the set domain-containing protein 5 gene (setd5, 615743.0001) | rel=r_associated | relid=0 | w=35
  899. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the shh (600725) regulatory element in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the shh (600725) regulatory element in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0010) | rel=r_associated | relid=0 | w=35
  900. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the six-transmembrane epithelial antigen of prostate 3 gene (steap3, 609671.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the six-transmembrane epithelial antigen of prostate 3 gene (steap3, 609671.0001) | rel=r_associated | relid=0 | w=35
  901. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0025)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0025) | rel=r_associated | relid=0 | w=35
  902. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the soluble guanylate cyclase 1, alpha 3 gene (gucy1a3, 139396.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the soluble guanylate cyclase 1, alpha 3 gene (gucy1a3, 139396.0001) | rel=r_associated | relid=0 | w=35
  903. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene (slc13a5, 608305.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene (slc13a5, 608305.0001) | rel=r_associated | relid=0 | w=35
  904. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the solute carrier family 17 (sodium phosphate cotransporter), member 3 gene (slc17a3, 611034.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 17 (sodium phosphate cotransporter), member 3 gene (slc17a3, 611034.0001) | rel=r_associated | relid=0 | w=35
  905. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene (slc25a19, 606521.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene (slc25a19, 606521.0002) | rel=r_associated | relid=0 | w=35
  906. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the solute carrier family 46 (folate transporter), member 1 gene (slc46a1, 611672.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 46 (folate transporter), member 1 gene (slc46a1, 611672.0001) | rel=r_associated | relid=0 | w=35
  907. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the solute carrier family 52 (riboflavin transporter), member 3 gene (slc52a3, 613350.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 52 (riboflavin transporter), member 3 gene (slc52a3, 613350.0001) | rel=r_associated | relid=0 | w=35
  908. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the solute carrier family 9, isoform a6 gene (slc9a6, 300231.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 9, isoform a6 gene (slc9a6, 300231.0001) | rel=r_associated | relid=0 | w=35
  909. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the somatic cytochrome c gene (cycs, 123970.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the somatic cytochrome c gene (cycs, 123970.0001) | rel=r_associated | relid=0 | w=35
  910. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the sparc-related modular calcium-binding 1 gene (smoc1, 608488.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sparc-related modular calcium-binding 1 gene (smoc1, 608488.0001) | rel=r_associated | relid=0 | w=35
  911. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the spastin gene (spg4, 604277.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the spastin gene (spg4, 604277.0001) | rel=r_associated | relid=0 | w=35
  912. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the sry-box-10 gene (sox10, 602229.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sry-box-10 gene (sox10, 602229.0005) | rel=r_associated | relid=0 | w=35
  913. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the stam-binding protein gene (stambp, 606247.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the stam-binding protein gene (stambp, 606247.0001) | rel=r_associated | relid=0 | w=35
  914. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the sterol 3-beta-hydroxysteroid-delta-5-desaturase gene (sc5dl, 602286.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sterol 3-beta-hydroxysteroid-delta-5-desaturase gene (sc5dl, 602286.0001) | rel=r_associated | relid=0 | w=35
  915. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605921.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605921.0004) | rel=r_associated | relid=0 | w=35
  916. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the surfeit 1 gene (surf1, 185620.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the surfeit 1 gene (surf1, 185620.0001) | rel=r_associated | relid=0 | w=35
  917. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0001) | rel=r_associated | relid=0 | w=35
  918. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the swi/snf-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, dead/h box-containing, 1 gene (smarcad1, 612761.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the swi/snf-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, dead/h box-containing, 1 gene (smarcad1, 612761.0001) | rel=r_associated | relid=0 | w=35
  919. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily 1, member 1 gene (smarce1, 603111.0002).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily 1, member 1 gene (smarce1, 603111.0002). | rel=r_associated | relid=0 | w=35
  920. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily b, member 1 gene (smarcb1, 601607.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily b, member 1 gene (smarcb1, 601607.0005) | rel=r_associated | relid=0 | w=35
  921. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the synapsin-1 gene (syn1, 313440.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the synapsin-1 gene (syn1, 313440.0001) | rel=r_associated | relid=0 | w=35
  922. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the t-box 15 gene (tbx15, 604127.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the t-box 15 gene (tbx15, 604127.0001) | rel=r_associated | relid=0 | w=35
  923. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the tachykinin-3 gene (tac3, 162330.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tachykinin-3 gene (tac3, 162330.0001) | rel=r_associated | relid=0 | w=35
  924. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the telo2-interacting protein 2 gene (tti2, 614426.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the telo2-interacting protein 2 gene (tti2, 614426.0001) | rel=r_associated | relid=0 | w=35
  925. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the thiazide-sensitive na-cl cotransporter (slc12a3, 600968.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thiazide-sensitive na-cl cotransporter (slc12a3, 600968.0001) | rel=r_associated | relid=0 | w=35
  926. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the threonyl-trna synthetase 2 gene (tars2, 612805.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the threonyl-trna synthetase 2 gene (tars2, 612805.0001) | rel=r_associated | relid=0 | w=35
  927. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the transforming growth factor, beta receptor ii, 70-80kd gene (tgfbr2, 190182.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transforming growth factor, beta receptor ii, 70-80kd gene (tgfbr2, 190182.0008) | rel=r_associated | relid=0 | w=35
  928. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the transient receptor potential cation channel, subfamily a, member 1 gene (trpa1, 604775.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transient receptor potential cation channel, subfamily a, member 1 gene (trpa1, 604775.0001) | rel=r_associated | relid=0 | w=35
  929. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the transient receptor potential cation channel, subfamily m, member 6 gene (trpm6, 607009.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transient receptor potential cation channel, subfamily m, member 6 gene (trpm6, 607009.0001) | rel=r_associated | relid=0 | w=35
  930. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the translational activator of mitochondrially encoded cytochrome c oxidase subunit 1 gene (taco1, 612958.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the translational activator of mitochondrially encoded cytochrome c oxidase subunit 1 gene (taco1, 612958.0001) | rel=r_associated | relid=0 | w=35
  931. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the transmembrane channel-like protein 1 gene (tmc1, 606706.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane channel-like protein 1 gene (tmc1, 606706.0001) | rel=r_associated | relid=0 | w=35
  932. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the transmembrane protein 138 gene (tmem138, 614459.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 138 gene (tmem138, 614459.0001) | rel=r_associated | relid=0 | w=35
  933. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the transmembrane protein 142a gene (tmem142a, 610277.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 142a gene (tmem142a, 610277.0001) | rel=r_associated | relid=0 | w=35
  934. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the transmembrane protein 231 gene (tmem231, 614949.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 231 gene (tmem231, 614949.0003) | rel=r_associated | relid=0 | w=35
  935. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the transmembrane protein 5 gene (tmem5, 605862.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 5 gene (tmem5, 605862.0001) | rel=r_associated | relid=0 | w=35
  936. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0018) | rel=r_associated | relid=0 | w=35
  937. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the trio- and f-actin-binding protein (triobp, 609761.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the trio- and f-actin-binding protein (triobp, 609761.0001) | rel=r_associated | relid=0 | w=35
  938. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the tripeptidyl peptidase 1 gene (tpp1, 607998.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tripeptidyl peptidase 1 gene (tpp1, 607998.0004) | rel=r_associated | relid=0 | w=35
  939. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the tubulin-specific chaperone e gene (tcbe, 604934.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin-specific chaperone e gene (tcbe, 604934.0001) | rel=r_associated | relid=0 | w=35
  940. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the tubulin, alpha-8 gene (tuba8, 605472.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin, alpha-8 gene (tuba8, 605472.0001) | rel=r_associated | relid=0 | w=35
  941. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the type iii voltage-gated sodium channel beta subunit gene (scn3b, 608214.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the type iii voltage-gated sodium channel beta subunit gene (scn3b, 608214.0001) | rel=r_associated | relid=0 | w=35
  942. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the uromodulin gene (umod, 191845.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the uromodulin gene (umod, 191845.0001) | rel=r_associated | relid=0 | w=35
  943. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the valyl-trna synthetase 2 gene (vars2, 612802.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the valyl-trna synthetase 2 gene (vars2, 612802.0001) | rel=r_associated | relid=0 | w=35
  944. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the ventral anterior homeobox-1 gene (vax1, 604924.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ventral anterior homeobox-1 gene (vax1, 604924.0001) | rel=r_associated | relid=0 | w=35
  945. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the voltage-dependent p/q type calcium channel alpha-1a subunit gene (cacna1a, 601011.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-dependent p/q type calcium channel alpha-1a subunit gene (cacna1a, 601011.0001) | rel=r_associated | relid=0 | w=35
  946. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the voltage-gated sodium channel, type i, beta subunit gene (scn1b, 600235.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated sodium channel, type i, beta subunit gene (scn1b, 600235.0001) | rel=r_associated | relid=0 | w=35
  947. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the von hippel-lindau gene (vhl, 608537.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the von hippel-lindau gene (vhl, 608537.0001) | rel=r_associated | relid=0 | w=35
  948. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the von willebrand factor gene (vwf, 613160.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the von willebrand factor gene (vwf, 613160.0015) | rel=r_associated | relid=0 | w=35
  949. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the wd repeat-containing protein 35 gene (wdr35, 613602.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein 35 gene (wdr35, 613602.0001) | rel=r_associated | relid=0 | w=35
  950. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the wingless-type mmtv integration site family, member 10a gene (wnt10a, 606268.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wingless-type mmtv integration site family, member 10a gene (wnt10a, 606268.0001) | rel=r_associated | relid=0 | w=35
  951. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the wingless-type mmtv integration site family, member 10a gene (wnt10a, 606268.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wingless-type mmtv integration site family, member 10a gene (wnt10a, 606268.0002) | rel=r_associated | relid=0 | w=35
  952. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0005) | rel=r_associated | relid=0 | w=35
  953. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the zinc finger and btb-domain containing 20 gene (zbtb20, 606025.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger and btb-domain containing 20 gene (zbtb20, 606025.0001) | rel=r_associated | relid=0 | w=35
  954. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the zinc finger protein 592 (znf592, 613624.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger protein 592 (znf592, 613624.0001). | rel=r_associated | relid=0 | w=35
  955. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in the zinc finger protein of cerebellum 2 gene (zic2, 603073.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger protein of cerebellum 2 gene (zic2, 603073.0001) | rel=r_associated | relid=0 | w=35
  956. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutation in type ix collagen, alpha-2 polypeptide gene (col9a2, 120260.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in type ix collagen, alpha-2 polypeptide gene (col9a2, 120260.0001) | rel=r_associated | relid=0 | w=35
  957. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the aldehyde dehydrogenase 3 family, member a2 gene (aldh3a2, 270200.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the aldehyde dehydrogenase 3 family, member a2 gene (aldh3a2, 270200.0001) | rel=r_associated | relid=0 | w=35
  958. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the alpha-3 subunit of the na+/k+-atpase gene (atp1a3, 182350.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the alpha-3 subunit of the na+/k+-atpase gene (atp1a3, 182350.0001) | rel=r_associated | relid=0 | w=35
  959. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the alpha-l-fucosidase gene (fuca1, 230000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the alpha-l-fucosidase gene (fuca1, 230000.0001) | rel=r_associated | relid=0 | w=35
  960. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the aspartoacylase gene (aspa, 271900.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the aspartoacylase gene (aspa, 271900.0001) | rel=r_associated | relid=0 | w=35
  961. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the bone morphogenetic protein receptor, type 1b gene (bmpr1b, 603248.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the bone morphogenetic protein receptor, type 1b gene (bmpr1b, 603248.0003) | rel=r_associated | relid=0 | w=35
  962. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the calcium-sensing receptor gene (casr, 601199.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the calcium-sensing receptor gene (casr, 601199.0001) | rel=r_associated | relid=0 | w=35
  963. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the caspase 10 gene (casp10, 601762.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the caspase 10 gene (casp10, 601762.0001) | rel=r_associated | relid=0 | w=35
  964. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the cathepsin k gene (ctsk, 601105.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cathepsin k gene (ctsk, 601105.0001) | rel=r_associated | relid=0 | w=35
  965. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the dna polymerase gamma gene (polg, 174763.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the dna polymerase gamma gene (polg, 174763.0001) | rel=r_associated | relid=0 | w=35
  966. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the exostosin 2 gene (ext2, 133701.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the exostosin 2 gene (ext2, 133701.0001) | rel=r_associated | relid=0 | w=35
  967. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0010) | rel=r_associated | relid=0 | w=35
  968. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the flj90140 gene (flj90130, 607461.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the flj90140 gene (flj90130, 607461.0005) | rel=r_associated | relid=0 | w=35
  969. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the homolog of drosophila muscle segment homeo box 1 gene (msx1, 142983.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the homolog of drosophila muscle segment homeo box 1 gene (msx1, 142983.0003) | rel=r_associated | relid=0 | w=35
  970. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the homolog of the mouse ank gene (ankh, 605145.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the homolog of the mouse ank gene (ankh, 605145.0006) | rel=r_associated | relid=0 | w=35
  971. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the matrilin 3 gene (matn3, 602109.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the matrilin 3 gene (matn3, 602109.0005) | rel=r_associated | relid=0 | w=35
  972. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the menin gene (men1, 131100.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the menin gene (men1, 131100.0001) | rel=r_associated | relid=0 | w=35
  973. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the midline 1 gene (mid1, 300000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the midline 1 gene (mid1, 300000.0001) | rel=r_associated | relid=0 | w=35
  974. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the myelin protein zero gene (mpz, 159440.0016)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the myelin protein zero gene (mpz, 159440.0016) | rel=r_associated | relid=0 | w=35
  975. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the nf-kappa-b essential modulator gene (ikbkg, 300248.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the nf-kappa-b essential modulator gene (ikbkg, 300248.0001) | rel=r_associated | relid=0 | w=35
  976. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the paired-like homeodomain transcription factor-2 gene (pitx2, 601542.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the paired-like homeodomain transcription factor-2 gene (pitx2, 601542.0001) | rel=r_associated | relid=0 | w=35
  977. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the parafibromin gene (hrpt2, 607393.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the parafibromin gene (hrpt2, 607393.0001) | rel=r_associated | relid=0 | w=35
  978. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the parathyroid hormone receptor 1 gene (pthr1, 168468.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the parathyroid hormone receptor 1 gene (pthr1, 168468.0003) | rel=r_associated | relid=0 | w=35
  979. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the ras-associated protein rab27a gene (rab27a, 603868.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the ras-associated protein rab27a gene (rab27a, 603868.0001) | rel=r_associated | relid=0 | w=35
  980. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the seipin gene (bscl2, 606158.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the seipin gene (bscl2, 606158.0001). | rel=r_associated | relid=0 | w=35
  981. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the serine/threonine protein kinase 11 gene (stk11, 602216.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the serine/threonine protein kinase 11 gene (stk11, 602216.0001) | rel=r_associated | relid=0 | w=35
  982. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the solute carrier family 17 (sodium phosphate), member 5 gene (slc17a5, 604322.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the solute carrier family 17 (sodium phosphate), member 5 gene (slc17a5, 604322.0001) | rel=r_associated | relid=0 | w=35
  983. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by mutations in the vitamin d receptor gene (vdr, 601769.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the vitamin d receptor gene (vdr, 601769.0001) | rel=r_associated | relid=0 | w=35
  984. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by simultaneous mutation in the g protein-coupled receptor 98 gene (gpr98, 602851.0010) and the pdz domain-containing 7 gene (pdzd7, 612971.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by simultaneous mutation in the g protein-coupled receptor 98 gene (gpr98, 602851.0010) and the pdz domain-containing 7 gene (pdzd7, 612971.0002) | rel=r_associated | relid=0 | w=35
  985. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by somatic mutation in the neuroblastoma ras viral oncogene homolog gene (nras, 164790.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the neuroblastoma ras viral oncogene homolog gene (nras, 164790.0003) | rel=r_associated | relid=0 | w=35
  986. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:caused by trinucleotide repeat expansion (cgg)n in the fragile site mental retardation gene (fmr1, 309550.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by trinucleotide repeat expansion (cgg)n in the fragile site mental retardation gene (fmr1, 309550.0004) | rel=r_associated | relid=0 | w=35
  987. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:contiguous gene deletion of 12 mb encompassing 47 genes on 1p32-p31
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene deletion of 12 mb encompassing 47 genes on 1p32-p31 | rel=r_associated | relid=0 | w=35
  988. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:contiguous gene deletion syndrome caused by deletion of 300 to 500 kb between bp1 and bp2 on 15q11.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene deletion syndrome caused by deletion of 300 to 500 kb between bp1 and bp2 on 15q11.2 | rel=r_associated | relid=0 | w=35
  989. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:contiguous gene syndrome associated with duplication (4.5 - 9.2mb) of chromosome xp11.22-p11.23
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome associated with duplication (4.5 - 9.2mb) of chromosome xp11.22-p11.23 | rel=r_associated | relid=0 | w=35
  990. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:due to mutation in the retinol-binding protein 4 gene (rbp4, 180250.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:due to mutation in the retinol-binding protein 4 gene (rbp4, 180250.0001) | rel=r_associated | relid=0 | w=35
  991. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:supernumerary inv dup(22)(q11) chromosome, occasionally due to interstitial duplication of 22q11
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:supernumerary inv dup(22)(q11) chromosome, occasionally due to interstitial duplication of 22q11 | rel=r_associated | relid=0 | w=35
  992. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:susceptibility conferred by 9-snp haplotype in malic enzyme 2 (me2, 154270.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by 9-snp haplotype in malic enzyme 2 (me2, 154270.0001) | rel=r_associated | relid=0 | w=35
  993. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:susceptibility conferred by mutation in the complement component 3 gene (c3, 120700.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the complement component 3 gene (c3, 120700.0005) | rel=r_associated | relid=0 | w=35
  994. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:susceptibility conferred by mutation in the homolog of the drosophila bicaudal c gene (bicc1, 614295.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the homolog of the drosophila bicaudal c gene (bicc1, 614295.0001) | rel=r_associated | relid=0 | w=35
  995. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:susceptibility conferred by mutation in the homolog of the s. cerevisiae coq2 gene (coq2, 609825.0006).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the homolog of the s. cerevisiae coq2 gene (coq2, 609825.0006). | rel=r_associated | relid=0 | w=35
  996. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:susceptibility conferred by mutation in the major histocompatibility complex, class ii, dr beta-1 gene (hla-dr1b, 142857.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the major histocompatibility complex, class ii, dr beta-1 gene (hla-dr1b, 142857.0001) | rel=r_associated | relid=0 | w=35
  997. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 35 / 0.814 -> en:susceptibility conferred by mutation in the peripherin gene (prph, 170710.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the peripherin gene (prph, 170710.0001) | rel=r_associated | relid=0 | w=35
  998. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:cause by mutation in the homolog of the s. cerevisiae alg2 gene (alg2, 607905.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:cause by mutation in the homolog of the s. cerevisiae alg2 gene (alg2, 607905.0003) | rel=r_associated | relid=0 | w=34
  999. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by a 1.35-mb deletion of chromosome 1q21
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a 1.35-mb deletion of chromosome 1q21 | rel=r_associated | relid=0 | w=34
  1000. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by a pentanucleotide repeat expansion (attct)n in the ataxin 10 gene (atxn10, 603516.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a pentanucleotide repeat expansion (attct)n in the ataxin 10 gene (atxn10, 603516.0001). | rel=r_associated | relid=0 | w=34
  1001. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by a trinucleotide repeat expansion (ctg)n in the ataxin 8 opposite strand gene (atxn8os, 603680.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a trinucleotide repeat expansion (ctg)n in the ataxin 8 opposite strand gene (atxn8os, 603680.0001) | rel=r_associated | relid=0 | w=34
  1002. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by a trinucleotide repeat expansion (ctg)n in the dystrophia myotonica-protein kinase gene (dmpk, 605377.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a trinucleotide repeat expansion (ctg)n in the dystrophia myotonica-protein kinase gene (dmpk, 605377.0001) | rel=r_associated | relid=0 | w=34
  1003. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by a trinucleotide repeat expansion (gcg)n in the poly(a)-binding protein-2 gene (pabpn1, 602279.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a trinucleotide repeat expansion (gcg)n in the poly(a)-binding protein-2 gene (pabpn1, 602279.0001) | rel=r_associated | relid=0 | w=34
  1004. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by a trinucleotide repeat expansion cag(n) in the androgen receptor gene (ar, 313700.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a trinucleotide repeat expansion cag(n) in the androgen receptor gene (ar, 313700.0014) | rel=r_associated | relid=0 | w=34
  1005. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by by mutations in the prophet of pit1, paired-like homeodomain transcription factor gene (prop1, 601538.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by by mutations in the prophet of pit1, paired-like homeodomain transcription factor gene (prop1, 601538.0001) | rel=r_associated | relid=0 | w=34
  1006. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by deletion (1.7mb) of 1q41-q42
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion (1.7mb) of 1q41-q42 | rel=r_associated | relid=0 | w=34
  1007. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by duplication of 8q22.1-qter and deletion of 8pter-p23.1
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of 8q22.1-qter and deletion of 8pter-p23.1 | rel=r_associated | relid=0 | w=34
  1008. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by expanded cag trinucleotide repeats in the alpha-1a calcium channel subunit gene (cacna1a, 601011.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by expanded cag trinucleotide repeats in the alpha-1a calcium channel subunit gene (cacna1a, 601011.0007) | rel=r_associated | relid=0 | w=34
  1009. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by expanded cag trinucleotide repeats in the ataxin-2 gene (atx2, 601517.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by expanded cag trinucleotide repeats in the ataxin-2 gene (atx2, 601517.0001). | rel=r_associated | relid=0 | w=34
  1010. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by expanded cag trinucleotide repeats in the beta subunit of the protein phosphatase 2 gene (ppp2r2b, 604325.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by expanded cag trinucleotide repeats in the beta subunit of the protein phosphatase 2 gene (ppp2r2b, 604325.0001) | rel=r_associated | relid=0 | w=34
  1011. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by fusion of the cytochrome p450, subfamily xib, polypeptide 1 gene (cyp11b1, 610613) and the cytochrome p450, subfamily xib, polypeptide 2 gene (cyp11b2, 124080)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by fusion of the cytochrome p450, subfamily xib, polypeptide 1 gene (cyp11b1, 610613) and the cytochrome p450, subfamily xib, polypeptide 2 gene (cyp11b2, 124080) | rel=r_associated | relid=0 | w=34
  1012. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by fusion of the ret protooncogene (164761) with tif1g (605769), d10s170 (601985), ele1 (601984), and prkar1a (188830)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by fusion of the ret protooncogene (164761) with tif1g (605769), d10s170 (601985), ele1 (601984), and prkar1a (188830) | rel=r_associated | relid=0 | w=34
  1013. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in cyclin-dependent kinase inhibitor 2a (cdkn2a, 600160.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in cyclin-dependent kinase inhibitor 2a (cdkn2a, 600160.0003) | rel=r_associated | relid=0 | w=34
  1014. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in myosin, heavy chain 9, non-muscle gene (myh9, 160775.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in myosin, heavy chain 9, non-muscle gene (myh9, 160775.0001) | rel=r_associated | relid=0 | w=34
  1015. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the 152-kd centrosomal protein gene (cep152, 613529.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 152-kd centrosomal protein gene (cep152, 613529.0001) | rel=r_associated | relid=0 | w=34
  1016. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the 4-hydroxyphenylpyruvate dioxygenase gene (hpd, 609695.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 4-hydroxyphenylpyruvate dioxygenase gene (hpd, 609695.0001) | rel=r_associated | relid=0 | w=34
  1017. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the 6-@pyruvoyl-tetrahydropterin synthase gene pts, (612719.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 6-@pyruvoyl-tetrahydropterin synthase gene pts, (612719.0001) | rel=r_associated | relid=0 | w=34
  1018. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the 68-kd transforming growth factor-beta-induced gene (tgfbi, 601692.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 68-kd transforming growth factor-beta-induced gene (tgfbi, 601692.0003) | rel=r_associated | relid=0 | w=34
  1019. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the abhydrolase domain-containing protein 12 gene (abhd12, 613599.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the abhydrolase domain-containing protein 12 gene (abhd12, 613599.0001) | rel=r_associated | relid=0 | w=34
  1020. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the acetylglucosaminyltransferase-like protein gene (large, 603590.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the acetylglucosaminyltransferase-like protein gene (large, 603590.0003) | rel=r_associated | relid=0 | w=34
  1021. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the adamts-like protein 2 gene (adamtsl2, 612277.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adamts-like protein 2 gene (adamtsl2, 612277.0001) | rel=r_associated | relid=0 | w=34
  1022. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the alanine-glyoxylate aminotransferase gene (agxt, 604285.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alanine-glyoxylate aminotransferase gene (agxt, 604285.0001) | rel=r_associated | relid=0 | w=34
  1023. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the aldehyde dehydrogenase 5 family, member a1 gene (aldh5a1, 610045.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aldehyde dehydrogenase 5 family, member a1 gene (aldh5a1, 610045.0001) | rel=r_associated | relid=0 | w=34
  1024. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the alms1 gene (alms1, 606844.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alms1 gene (alms1, 606844.0001) | rel=r_associated | relid=0 | w=34
  1025. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the alpha-aminoadipic semialdehyde synthase gene (aass, 605113.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-aminoadipic semialdehyde synthase gene (aass, 605113.0001) | rel=r_associated | relid=0 | w=34
  1026. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the alpha-n-acetylgalactosaminidase gene (naga, 104170.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-n-acetylgalactosaminidase gene (naga, 104170.0002) | rel=r_associated | relid=0 | w=34
  1027. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the alpha-synuclein gene (snca, 163890.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-synuclein gene (snca, 163890.0001) | rel=r_associated | relid=0 | w=34
  1028. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the amelogenin gene (amelx, 300391.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the amelogenin gene (amelx, 300391.0001) | rel=r_associated | relid=0 | w=34
  1029. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the antithrombin iii gene (at3, 107300.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the antithrombin iii gene (at3, 107300.0001) | rel=r_associated | relid=0 | w=34
  1030. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the aprataxin gene (aptx, 606350.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aprataxin gene (aptx, 606350.0001). | rel=r_associated | relid=0 | w=34
  1031. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ataxia-telangiectasia and rad3-related gene (atr, 601215.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ataxia-telangiectasia and rad3-related gene (atr, 601215.0002) | rel=r_associated | relid=0 | w=34
  1032. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0005) | rel=r_associated | relid=0 | w=34
  1033. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the atp-binding cassette, subfamily b, member 6 gene (abcb6, 605452.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily b, member 6 gene (abcb6, 605452.0001) | rel=r_associated | relid=0 | w=34
  1034. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the atpase, ca(2+)-transporting, type 2c, member 1 gene (atp2c1, 604384.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, ca(2+)-transporting, type 2c, member 1 gene (atp2c1, 604384.0001) | rel=r_associated | relid=0 | w=34
  1035. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the atpase, class i, type 8a, member 2 gene (atp8a2, 605870.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, class i, type 8a, member 2 gene (atp8a2, 605870.0001) | rel=r_associated | relid=0 | w=34
  1036. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the atpase, cu(2+)-transporting, alpha polypeptide (atp7a, 300011.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, cu(2+)-transporting, alpha polypeptide (atp7a, 300011.0015) | rel=r_associated | relid=0 | w=34
  1037. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the autoimmune regulator gene (aire, 607358.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the autoimmune regulator gene (aire, 607358.0001) | rel=r_associated | relid=0 | w=34
  1038. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the barrier-to-autointegration factor-1 gene (banf1, 603811.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the barrier-to-autointegration factor-1 gene (banf1, 603811.0001) | rel=r_associated | relid=0 | w=34
  1039. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the beta filamin b gene (flnb, 603381.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta filamin b gene (flnb, 603381.0001) | rel=r_associated | relid=0 | w=34
  1040. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the beta-1,4-n-acetylgalactosaminyltransferase 1 gene (b4galnt1, 601873.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1,4-n-acetylgalactosaminyltransferase 1 gene (b4galnt1, 601873.0001) | rel=r_associated | relid=0 | w=34
  1041. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the beta-3 laminin gene (lamb3, 150130.001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-3 laminin gene (lamb3, 150130.001) | rel=r_associated | relid=0 | w=34
  1042. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the beta-sarcoglycan gene (sgcb, 600900.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-sarcoglycan gene (sgcb, 600900.0001) | rel=r_associated | relid=0 | w=34
  1043. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the beta-tubulin gene (tubb, 191130.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-tubulin gene (tubb, 191130.0001) | rel=r_associated | relid=0 | w=34
  1044. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the biliverdin reductase a gene (blvra, 109750.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the biliverdin reductase a gene (blvra, 109750.0001) | rel=r_associated | relid=0 | w=34
  1045. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the breast cancer type 2 gene (brca2, 600185.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the breast cancer type 2 gene (brca2, 600185.0001) | rel=r_associated | relid=0 | w=34
  1046. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the bromodomain-and wd repeat domain-containing protein 3 gene (brwd3, 300553.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bromodomain-and wd repeat domain-containing protein 3 gene (brwd3, 300553.0001) | rel=r_associated | relid=0 | w=34
  1047. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the c. elegans homolog of the ectopic p-granules autophagy protein 5 gene (epg5, 615068.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the c. elegans homolog of the ectopic p-granules autophagy protein 5 gene (epg5, 615068.0001) | rel=r_associated | relid=0 | w=34
  1048. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the c1 esterase inhibitor gene (c1nh, 106100.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the c1 esterase inhibitor gene (c1nh, 106100.0001) | rel=r_associated | relid=0 | w=34
  1049. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cadherin-1 gene (cdh1, 192090.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cadherin-1 gene (cdh1, 192090.0002) | rel=r_associated | relid=0 | w=34
  1050. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the calcium- and integrin-binding protein 2 gene (cib2, 605564.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calcium- and integrin-binding protein 2 gene (cib2, 605564.0004) | rel=r_associated | relid=0 | w=34
  1051. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the calcium/calmodulin-dependent serine protein kinase gene (cask, 300172.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calcium/calmodulin-dependent serine protein kinase gene (cask, 300172.0001) | rel=r_associated | relid=0 | w=34
  1052. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the calsequestrin 1 gene (casq1, 114250.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calsequestrin 1 gene (casq1, 114250.0001) | rel=r_associated | relid=0 | w=34
  1053. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the camp-dependent protein kinase, regulatory, type i, alpha gene (prkar1a, 188830.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the camp-dependent protein kinase, regulatory, type i, alpha gene (prkar1a, 188830.0001) | rel=r_associated | relid=0 | w=34
  1054. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the casein kinase 1, delta, gene (csnk1d, 600864.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the casein kinase 1, delta, gene (csnk1d, 600864.0001) | rel=r_associated | relid=0 | w=34
  1055. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the caspase recruitment domain-containing protein 11 gene (card11, 607210.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the caspase recruitment domain-containing protein 11 gene (card11, 607210.0003) | rel=r_associated | relid=0 | w=34
  1056. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cathepsin c gene (ctsc, 602365.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cathepsin c gene (ctsc, 602365.0012) | rel=r_associated | relid=0 | w=34
  1057. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the caveolin-3 gene (cav3, 601253.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the caveolin-3 gene (cav3, 601253.0001) | rel=r_associated | relid=0 | w=34
  1058. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the chloride intracellular channel-5 gene (clic5, 607293.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chloride intracellular channel-5 gene (clic5, 607293.0001) | rel=r_associated | relid=0 | w=34
  1059. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0001) | rel=r_associated | relid=0 | w=34
  1060. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the chondroitin sulfate proteoglycan-2 gene (cspg2, 118661.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chondroitin sulfate proteoglycan-2 gene (cspg2, 118661.0001) | rel=r_associated | relid=0 | w=34
  1061. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the chordin-like-1 gene (chrdl1, 300350.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chordin-like-1 gene (chrdl1, 300350.0001) | rel=r_associated | relid=0 | w=34
  1062. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the chromosome 2 open reading frame 64 gene (c2orf64, 613920.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 2 open reading frame 64 gene (c2orf64, 613920.0001) | rel=r_associated | relid=0 | w=34
  1063. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cln5 gene (cln5, 608102.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cln5 gene (cln5, 608102.0001) | rel=r_associated | relid=0 | w=34
  1064. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the coiled-coil and c2 domains-containing protein 2a gene (cc2d2a, 612013.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil and c2 domains-containing protein 2a gene (cc2d2a, 612013.0006) | rel=r_associated | relid=0 | w=34
  1065. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the coiled-coil domain-containing protein 103 (ccdc103, 614677.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil domain-containing protein 103 (ccdc103, 614677.0001) | rel=r_associated | relid=0 | w=34
  1066. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0024)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0024) | rel=r_associated | relid=0 | w=34
  1067. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0005) | rel=r_associated | relid=0 | w=34
  1068. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0029)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0029) | rel=r_associated | relid=0 | w=34
  1069. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the collagen v, alpha-1 polypeptide gene (col5a1, 120215.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen v, alpha-1 polypeptide gene (col5a1, 120215.0002) | rel=r_associated | relid=0 | w=34
  1070. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the collagen vi, alpha-1 polypeptide gene (col6a1, 120220.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen vi, alpha-1 polypeptide gene (col6a1, 120220.0007) | rel=r_associated | relid=0 | w=34
  1071. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0007) | rel=r_associated | relid=0 | w=34
  1072. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0009) | rel=r_associated | relid=0 | w=34
  1073. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the collagen, type xxvii, alpha-1 gene (col27a1, 608461.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type xxvii, alpha-1 gene (col27a1, 608461.0001) | rel=r_associated | relid=0 | w=34
  1074. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the complement component 4a gene (c4a, 120810.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement component 4a gene (c4a, 120810.0001) | rel=r_associated | relid=0 | w=34
  1075. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the creatine transporter gene (slc6a8, 300036.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the creatine transporter gene (slc6a8, 300036.0001) | rel=r_associated | relid=0 | w=34
  1076. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cullin 3 gene (cul3, 603136.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cullin 3 gene (cul3, 603136.0001) | rel=r_associated | relid=0 | w=34
  1077. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cyclin-dependent kinase inhibitor 1c gene (cdkn1c, 600856.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclin-dependent kinase inhibitor 1c gene (cdkn1c, 600856.0007) | rel=r_associated | relid=0 | w=34
  1078. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cytochrome c oxidase, subunit iv, isoform 2 gene (cox4i2, 607976.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase, subunit iv, isoform 2 gene (cox4i2, 607976.0001) | rel=r_associated | relid=0 | w=34
  1079. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cytochrome c1 gene (cyc1, 123980.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c1 gene (cyc1, 123980.0001) | rel=r_associated | relid=0 | w=34
  1080. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cytochrome p450 subfamily xib, polypeptide 2 gene (cyp11b2, 124080.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450 subfamily xib, polypeptide 2 gene (cyp11b2, 124080.0002) | rel=r_associated | relid=0 | w=34
  1081. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cytokine-like factor 1 gene (crlf1, 604237.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytokine-like factor 1 gene (crlf1, 604237.0001) | rel=r_associated | relid=0 | w=34
  1082. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the cytoskeleton-associated protein 2-like gene (ckap2l, 616174.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytoskeleton-associated protein 2-like gene (ckap2l, 616174.0001) | rel=r_associated | relid=0 | w=34
  1083. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ddhd domain-containing protein 1 gene (ddhd1, 614603.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ddhd domain-containing protein 1 gene (ddhd1, 614603.0001) | rel=r_associated | relid=0 | w=34
  1084. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the dead/h box-11 gene (ddx11, 601150.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dead/h box-11 gene (ddx11, 601150.0001) | rel=r_associated | relid=0 | w=34
  1085. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the delta-aminolevulinate dehydratase gene (alad, 125270.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the delta-aminolevulinate dehydratase gene (alad, 125270.0001) | rel=r_associated | relid=0 | w=34
  1086. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the delta-aminolevulinate synthase 2 gene (alas2, 301300.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the delta-aminolevulinate synthase 2 gene (alas2, 301300.0015) | rel=r_associated | relid=0 | w=34
  1087. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the diacylglycerol o-acyltransferase 1 gene (dgat1, 604900.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the diacylglycerol o-acyltransferase 1 gene (dgat1, 604900.0001) | rel=r_associated | relid=0 | w=34
  1088. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the dihydropyrimidine dehydrogenase gene (dpyd, 612779.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dihydropyrimidine dehydrogenase gene (dpyd, 612779.0001). | rel=r_associated | relid=0 | w=34
  1089. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the dj1 gene (602533.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dj1 gene (602533.0001) | rel=r_associated | relid=0 | w=34
  1090. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the dolichyl-diphosphooligosaccharide-protein glycosyltransferase gene (ddost, 602202.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dolichyl-diphosphooligosaccharide-protein glycosyltransferase gene (ddost, 602202.0001) | rel=r_associated | relid=0 | w=34
  1091. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the downstream of tyrosine kinase 7 gene (dok7, 610285.0009).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the downstream of tyrosine kinase 7 gene (dok7, 610285.0009). | rel=r_associated | relid=0 | w=34
  1092. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the dual-specificity tyrosine phosphorylation-regulated kinase 1b gene (dyrk1b, 604556.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dual-specificity tyrosine phosphorylation-regulated kinase 1b gene (dyrk1b, 604556.0001) | rel=r_associated | relid=0 | w=34
  1093. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the dynein, axonemal, intermediate chain 1 gene (dnai1, 604366.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynein, axonemal, intermediate chain 1 gene (dnai1, 604366.0001). | rel=r_associated | relid=0 | w=34
  1094. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the dynein, axonemal, light chain 4 gene (dnal4, 610565.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynein, axonemal, light chain 4 gene (dnal4, 610565.0001) | rel=r_associated | relid=0 | w=34
  1095. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the dysferlin gene (dysf, 603009.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dysferlin gene (dysf, 603009.0002) | rel=r_associated | relid=0 | w=34
  1096. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the dystonin gene (dst, 113810.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dystonin gene (dst, 113810.0001) | rel=r_associated | relid=0 | w=34
  1097. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the elongation factor tu gtp-binding domain-containing 2 gene (eftud2, 603892.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the elongation factor tu gtp-binding domain-containing 2 gene (eftud2, 603892.0001) | rel=r_associated | relid=0 | w=34
  1098. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the endothelin-converting enzyme-like 1 gene (ecel1, 605896.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endothelin-converting enzyme-like 1 gene (ecel1, 605896.0001) | rel=r_associated | relid=0 | w=34
  1099. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ephrin b1 gene (efnb1, 300035.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ephrin b1 gene (efnb1, 300035.0001) | rel=r_associated | relid=0 | w=34
  1100. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the erythrocytic protein 4.2 gene (epb42, 177070.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the erythrocytic protein 4.2 gene (epb42, 177070.0001) | rel=r_associated | relid=0 | w=34
  1101. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the feline leukemia virus subgroup c receptor 1 gene (flvcr1, 609144.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the feline leukemia virus subgroup c receptor 1 gene (flvcr1, 609144.0001) | rel=r_associated | relid=0 | w=34
  1102. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ferritin light chain gene (ftl, 134790.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ferritin light chain gene (ftl, 134790.0018) | rel=r_associated | relid=0 | w=34
  1103. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the fibroblast growth factor receptor 1 gene (fgfr1, 136350.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor 1 gene (fgfr1, 136350.0011) | rel=r_associated | relid=0 | w=34
  1104. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0002) | rel=r_associated | relid=0 | w=34
  1105. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the fibronectin 1 gene (fn1, 135600.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibronectin 1 gene (fn1, 135600.0001) | rel=r_associated | relid=0 | w=34
  1106. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the fibulin 5 gene (fbln5, 604580.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibulin 5 gene (fbln5, 604580.0001) | rel=r_associated | relid=0 | w=34
  1107. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the fms-like tyrosine kinase-4 gene (flt4, 136352.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fms-like tyrosine kinase-4 gene (flt4, 136352.0001) | rel=r_associated | relid=0 | w=34
  1108. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the forkhead box p1 gene (foxp1, 605515.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead box p1 gene (foxp1, 605515.0001) | rel=r_associated | relid=0 | w=34
  1109. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the forkhead, drosophila, homolog-like 7 gene (foxc1, 601090.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead, drosophila, homolog-like 7 gene (foxc1, 601090.0001) | rel=r_associated | relid=0 | w=34
  1110. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the frizzled 4 gene (fzd4, 604579.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the frizzled 4 gene (fzd4, 604579.0001) | rel=r_associated | relid=0 | w=34
  1111. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the galactokinase 1 gene (galk1, 604313.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the galactokinase 1 gene (galk1, 604313.0001) | rel=r_associated | relid=0 | w=34
  1112. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the gamma-2 laminin gene (lamc2, 150292.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma-2 laminin gene (lamc2, 150292.0006) | rel=r_associated | relid=0 | w=34
  1113. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the gap junction protein, beta-2, 26kd gene (gjb2, 121011.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gap junction protein, beta-2, 26kd gene (gjb2, 121011.0012) | rel=r_associated | relid=0 | w=34
  1114. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the gap junction protein, gamma-2 gene (gjc2, 608803.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gap junction protein, gamma-2 gene (gjc2, 608803.0008) | rel=r_associated | relid=0 | w=34
  1115. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the gdp-mannose pyrophosphorylase a gene (gmppa, 615495.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gdp-mannose pyrophosphorylase a gene (gmppa, 615495.0001) | rel=r_associated | relid=0 | w=34
  1116. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the gli-kruppel family member gli3 gene (gli3, 165240.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gli-kruppel family member gli3 gene (gli3, 165240.0001) | rel=r_associated | relid=0 | w=34
  1117. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the glucose-6-phosphatase, catalytic subunit 3 gene (g6pc3, 611045.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glucose-6-phosphatase, catalytic subunit 3 gene (g6pc3, 611045.0001) | rel=r_associated | relid=0 | w=34
  1118. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the glutamine:fructose-6-phosphate aminotransferase 1 gene (gfpt1, 138292.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutamine:fructose-6-phosphate aminotransferase 1 gene (gfpt1, 138292.0001) | rel=r_associated | relid=0 | w=34
  1119. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the glutaryl-coa dehydrogenase gene (gcdh, 608801.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutaryl-coa dehydrogenase gene (gcdh, 608801.0001) | rel=r_associated | relid=0 | w=34
  1120. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the glycogenin-1 gene (gyg1, 603942.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycogenin-1 gene (gyg1, 603942.0003) | rel=r_associated | relid=0 | w=34
  1121. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the gnas complex locus gene (gnas, 139320.0031)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gnas complex locus gene (gnas, 139320.0031) | rel=r_associated | relid=0 | w=34
  1122. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the golgi snap receptor complex member 2 gene (gosr2, 604027.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the golgi snap receptor complex member 2 gene (gosr2, 604027.0001) | rel=r_associated | relid=0 | w=34
  1123. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the goosecoid homeobox gene (gsc, 138890.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the goosecoid homeobox gene (gsc, 138890.0001) | rel=r_associated | relid=0 | w=34
  1124. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the guanine nucleotide-binding protein, alpha-activating activity polypeptide, olfactory type gene (gnal, 139312.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the guanine nucleotide-binding protein, alpha-activating activity polypeptide, olfactory type gene (gnal, 139312.0001) | rel=r_associated | relid=0 | w=34
  1125. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the guanylate cyclase 2c gene (gucy2c, 601330.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the guanylate cyclase 2c gene (gucy2c, 601330.0002) | rel=r_associated | relid=0 | w=34
  1126. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the h19 gene (h19, 103290.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the h19 gene (h19, 103290.0002) | rel=r_associated | relid=0 | w=34
  1127. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the heat-shock 22-kd protein 8 gene (hspb8, 608014.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heat-shock 22-kd protein 8 gene (hspb8, 608014.0001) | rel=r_associated | relid=0 | w=34
  1128. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the heat-shock transcription factor 4 (hsf4, 602438.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heat-shock transcription factor 4 (hsf4, 602438.0001) | rel=r_associated | relid=0 | w=34
  1129. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the hexose-6-phosphate dehydrogenase gene (h6pd, 138090.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hexose-6-phosphate dehydrogenase gene (h6pd, 138090.0001) | rel=r_associated | relid=0 | w=34
  1130. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of mouse peripherin 2 (prph2, 179605.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of mouse peripherin 2 (prph2, 179605.0009) | rel=r_associated | relid=0 | w=34
  1131. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of mouse peripherin 2 gene
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of mouse peripherin 2 gene | rel=r_associated | relid=0 | w=34
  1132. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport-43 gene (itf43, 614068.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport-43 gene (itf43, 614068.0001) | rel=r_associated | relid=0 | w=34
  1133. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the drosophila diaphanous, 3, gene (diaph3, 614567.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila diaphanous, 3, gene (diaph3, 614567.0001). | rel=r_associated | relid=0 | w=34
  1134. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the drosophila sine oculis homeobox gene (six3, 603714.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila sine oculis homeobox gene (six3, 603714.0001). | rel=r_associated | relid=0 | w=34
  1135. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the e. coli bola, 3 gene (bola3, 613183.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the e. coli bola, 3 gene (bola3, 613183.0001) | rel=r_associated | relid=0 | w=34
  1136. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the mouse peripherin 2 gene (prph2, 179605.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse peripherin 2 gene (prph2, 179605.0001) | rel=r_associated | relid=0 | w=34
  1137. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the s. cerevisiae alg11 gene (alg11, 613666.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae alg11 gene (alg11, 613666.0001) | rel=r_associated | relid=0 | w=34
  1138. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the s. cerevisiae bms1 ribosome assembly protein gene (bms1, 611448.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae bms1 ribosome assembly protein gene (bms1, 611448.0001) | rel=r_associated | relid=0 | w=34
  1139. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the s. cerevisiae mediator of rna polymerase ii transcription, subunit 12 (med12, 300188.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae mediator of rna polymerase ii transcription, subunit 12 (med12, 300188.0003) | rel=r_associated | relid=0 | w=34
  1140. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the s. cerevisiae pet100 gene (pet100, 614770.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae pet100 gene (pet100, 614770.0001). | rel=r_associated | relid=0 | w=34
  1141. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the s. cerevisiae precursor rna-processing factor 31 gene (prpf31, 606419.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae precursor rna-processing factor 31 gene (prpf31, 606419.0001) | rel=r_associated | relid=0 | w=34
  1142. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of the s. cerevisiae vacuolar protein sorting 53 gene (vps53, 615850.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae vacuolar protein sorting 53 gene (vps53, 615850.0001) | rel=r_associated | relid=0 | w=34
  1143. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the homolog of yeast dna replication helicase-2 gene (dna2, 601810.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of yeast dna replication helicase-2 gene (dna2, 601810.0004) | rel=r_associated | relid=0 | w=34
  1144. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the human homolog of the mouse noggin gene (nog, 602991.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the human homolog of the mouse noggin gene (nog, 602991.0012) | rel=r_associated | relid=0 | w=34
  1145. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the immunoglobulin mu gene (ighm, 147020.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the immunoglobulin mu gene (ighm, 147020.0001) | rel=r_associated | relid=0 | w=34
  1146. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the indian hedgehog gene (ihh, 600726.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the indian hedgehog gene (ihh, 600726.0005) | rel=r_associated | relid=0 | w=34
  1147. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the inducible costimulator gene (icos, 605448.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inducible costimulator gene (icos, 605448.0001) | rel=r_associated | relid=0 | w=34
  1148. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the inositol polyphosphate-5-phosphatase, 72-kd gene (inpp5e, 613037.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inositol polyphosphate-5-phosphatase, 72-kd gene (inpp5e, 613037.0001). | rel=r_associated | relid=0 | w=34
  1149. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the insulin gene (ins, 176730.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the insulin gene (ins, 176730.0001) | rel=r_associated | relid=0 | w=34
  1150. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the integrin-alpha-6 gene (itga6, 147556.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the integrin-alpha-6 gene (itga6, 147556.0001) | rel=r_associated | relid=0 | w=34
  1151. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the integrin, alpha-2b gene (itga2b, 607759.0017)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the integrin, alpha-2b gene (itga2b, 607759.0017) | rel=r_associated | relid=0 | w=34
  1152. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ionotropic n-methyl-d-aspartate glutamate receptor subunit 2a gene (grin2a, 138253.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ionotropic n-methyl-d-aspartate glutamate receptor subunit 2a gene (grin2a, 138253.0001) | rel=r_associated | relid=0 | w=34
  1153. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the kcnq1-overlapping transcript 1 gene (kcnq1ot1, 604115.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kcnq1-overlapping transcript 1 gene (kcnq1ot1, 604115.0001) | rel=r_associated | relid=0 | w=34
  1154. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the keratin 10 gene (krt10, 148080.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 10 gene (krt10, 148080.0001) | rel=r_associated | relid=0 | w=34
  1155. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the keratin-14 gene (krt14, 148066.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin-14 gene (krt14, 148066.0015) | rel=r_associated | relid=0 | w=34
  1156. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the keratin-5 gene (krt5, 148040.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin-5 gene (krt5, 148040.0009) | rel=r_associated | relid=0 | w=34
  1157. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the keratin-6c gene (krt6c, 612315.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin-6c gene (krt6c, 612315.0001) | rel=r_associated | relid=0 | w=34
  1158. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the kinesin heavy chain member 2a (kif2a, 602591.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin heavy chain member 2a (kif2a, 602591.0001) | rel=r_associated | relid=0 | w=34
  1159. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the l-3-hydroxyacyl-coa dehydrogenase gene (had, 601609.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the l-3-hydroxyacyl-coa dehydrogenase gene (had, 601609.0001). | rel=r_associated | relid=0 | w=34
  1160. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the l-3-hydroxyacyl-coa dehydrogenase gene (hadh, 601609.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the l-3-hydroxyacyl-coa dehydrogenase gene (hadh, 601609.0003) | rel=r_associated | relid=0 | w=34
  1161. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the l-arginine:glycine amidinotransferase gene (gatm, 602360.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the l-arginine:glycine amidinotransferase gene (gatm, 602360.0001) | rel=r_associated | relid=0 | w=34
  1162. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the lamin a/c gene (lmna, 150330.0022)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin a/c gene (lmna, 150330.0022) | rel=r_associated | relid=0 | w=34
  1163. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the laminin, gamma-3 gene (lamc3, 604349.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the laminin, gamma-3 gene (lamc3, 604349.0001) | rel=r_associated | relid=0 | w=34
  1164. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the latent transforming growth factor-beta-binding protein 3 gene (ltbp3, 602090.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the latent transforming growth factor-beta-binding protein 3 gene (ltbp3, 602090.0001) | rel=r_associated | relid=0 | w=34
  1165. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the lem domain-containing-3 gene (lemd3, 607844.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lem domain-containing-3 gene (lemd3, 607844.0001) | rel=r_associated | relid=0 | w=34
  1166. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the leucine-rich repeat kinase 2 gene (lrrk2, 609007.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucine-rich repeat kinase 2 gene (lrrk2, 609007.0001) | rel=r_associated | relid=0 | w=34
  1167. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the leucine-rich repeat-containing protein 6 gene (lrrc6, 614930.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucine-rich repeat-containing protein 6 gene (lrrc6, 614930.0001) | rel=r_associated | relid=0 | w=34
  1168. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the leucyl-trna synthetase 2 gene (lars2, 604544.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucyl-trna synthetase 2 gene (lars2, 604544.0001) | rel=r_associated | relid=0 | w=34
  1169. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the lipase n gene (lipn, 613924.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lipase n gene (lipn, 613924.0001) | rel=r_associated | relid=0 | w=34
  1170. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the lipin 1 gene (lpin1, 605518.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lipin 1 gene (lpin1, 605518.0001) | rel=r_associated | relid=0 | w=34
  1171. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the lipopolysaccharide-induced tumor necrosis factor-alpha factor gene (litaf, 603795.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lipopolysaccharide-induced tumor necrosis factor-alpha factor gene (litaf, 603795.0001) | rel=r_associated | relid=0 | w=34
  1172. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the lipopolysaccharide-responsive, beige-like anchor protein (lrba, 606453.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lipopolysaccharide-responsive, beige-like anchor protein (lrba, 606453.0001) | rel=r_associated | relid=0 | w=34
  1173. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the long-chain base subunit 1 of the serine palmitoyltransferase gene (sptlc1, 605712.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the long-chain base subunit 1 of the serine palmitoyltransferase gene (sptlc1, 605712.0001) | rel=r_associated | relid=0 | w=34
  1174. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the low density lipoprotein receptor-related protein-6 gene (lrp6, 603507.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the low density lipoprotein receptor-related protein-6 gene (lrp6, 603507.0001) | rel=r_associated | relid=0 | w=34
  1175. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the lysine (k)-specific demethylase-6a gene (kdm6a, 300128.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lysine (k)-specific demethylase-6a gene (kdm6a, 300128.0001) | rel=r_associated | relid=0 | w=34
  1176. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the lysosomal trafficking regulator gene (chs1, 606897.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lysosomal trafficking regulator gene (chs1, 606897.0001) | rel=r_associated | relid=0 | w=34
  1177. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the m-phase specific plk1 interacting protein (mplkip, 609188.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the m-phase specific plk1 interacting protein (mplkip, 609188.0001) | rel=r_associated | relid=0 | w=34
  1178. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0002) | rel=r_associated | relid=0 | w=34
  1179. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the microtubule-associated tau protein gene (mapt, 157140.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the microtubule-associated tau protein gene (mapt, 157140.0001) | rel=r_associated | relid=0 | w=34
  1180. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the mitochondrial complex i, subunit nd6 gene (mtnd6, 516006.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial complex i, subunit nd6 gene (mtnd6, 516006.0002) | rel=r_associated | relid=0 | w=34
  1181. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the mitochondrial complex i, subunit nd6 gene (mtnd6, 516006.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial complex i, subunit nd6 gene (mtnd6, 516006.0005) | rel=r_associated | relid=0 | w=34
  1182. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the mitochondrial genome maintenance exonuclease 1 gene (mgme1, 615076.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial genome maintenance exonuclease 1 gene (mgme1, 615076.0001) | rel=r_associated | relid=0 | w=34
  1183. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the mitochondrial nad kinase 2 gene (nadk2, 615787.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial nad kinase 2 gene (nadk2, 615787.0001) | rel=r_associated | relid=0 | w=34
  1184. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the mitochondrial transfer rna lysine gene (mttk, 590060.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial transfer rna lysine gene (mttk, 590060.0002) | rel=r_associated | relid=0 | w=34
  1185. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the mitochondrial trna (lysine) gene (mttk, 590060.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial trna (lysine) gene (mttk, 590060.0001) | rel=r_associated | relid=0 | w=34
  1186. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the mitogen-activated protein kinase kinase 1 gene (map2k1, 176872.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitogen-activated protein kinase kinase 1 gene (map2k1, 176872.0001) | rel=r_associated | relid=0 | w=34
  1187. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the mlc1 gene (mlc1, 605908.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mlc1 gene (mlc1, 605908.0001) | rel=r_associated | relid=0 | w=34
  1188. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the mmachc gene (mmachc gene 609831.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mmachc gene (mmachc gene 609831.0001) | rel=r_associated | relid=0 | w=34
  1189. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the multiple pdz domain protein gene (mpdz, 603785.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the multiple pdz domain protein gene (mpdz, 603785.0001) | rel=r_associated | relid=0 | w=34
  1190. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the muscle-specific phosphorylase kinase subunit a1 gene (phka1, 311870.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the muscle-specific phosphorylase kinase subunit a1 gene (phka1, 311870.0001) | rel=r_associated | relid=0 | w=34
  1191. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the myocilin gene (myoc, 601652.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myocilin gene (myoc, 601652.0001) | rel=r_associated | relid=0 | w=34
  1192. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the myosin 5a gene (myo5a, 160777.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin 5a gene (myo5a, 160777.0004) | rel=r_associated | relid=0 | w=34
  1193. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the myosin viia gene (myo7a, 276903.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin viia gene (myo7a, 276903.0011) | rel=r_associated | relid=0 | w=34
  1194. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the myosin, heavy chain 14, nonmuscle gene (myh14, 608568.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin, heavy chain 14, nonmuscle gene (myh14, 608568.0001) | rel=r_associated | relid=0 | w=34
  1195. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 4 gene (ndufs4, 602694.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 4 gene (ndufs4, 602694.0004) | rel=r_associated | relid=0 | w=34
  1196. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 beta subcomplex 9 gene (ndufb9, 601445.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 beta subcomplex 9 gene (ndufb9, 601445.0001) | rel=r_associated | relid=0 | w=34
  1197. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the nephrin gene (nphs1, 602716.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nephrin gene (nphs1, 602716.0001) | rel=r_associated | relid=0 | w=34
  1198. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the nephrocystin 4 gene (nphp4, 607215.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nephrocystin 4 gene (nphp4, 607215.0001) | rel=r_associated | relid=0 | w=34
  1199. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the nephrocystin gene (nphp1, 607100.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nephrocystin gene (nphp1, 607100.0005) | rel=r_associated | relid=0 | w=34
  1200. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the nerve growth factor-beta gene (ngfb, 162030.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nerve growth factor-beta gene (ngfb, 162030.0001) | rel=r_associated | relid=0 | w=34
  1201. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the neurobeachin-like 2 gene (nbeal2, 614169.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neurobeachin-like 2 gene (nbeal2, 614169.0001). | rel=r_associated | relid=0 | w=34
  1202. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the neutrophil cytosolic factor-2 gene, p67-phox (ncf2, 608515.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neutrophil cytosolic factor-2 gene, p67-phox (ncf2, 608515.0001) | rel=r_associated | relid=0 | w=34
  1203. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the nicotinamide nucleotide transhydrogenase gene (nnt, 607878.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nicotinamide nucleotide transhydrogenase gene (nnt, 607878.0001) | rel=r_associated | relid=0 | w=34
  1204. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0004) | rel=r_associated | relid=0 | w=34
  1205. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0021)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0021) | rel=r_associated | relid=0 | w=34
  1206. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the nuclear receptor subfamily 5, group a, member 1 gene (nr5a1, 184757.0016)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear receptor subfamily 5, group a, member 1 gene (nr5a1, 184757.0016) | rel=r_associated | relid=0 | w=34
  1207. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the opa1 gene (opa1, 605290.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the opa1 gene (opa1, 605290.0011) | rel=r_associated | relid=0 | w=34
  1208. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the paired box gene 6 gene (pax6, 607108.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the paired box gene 6 gene (pax6, 607108.0001) | rel=r_associated | relid=0 | w=34
  1209. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the paired box homeotic gene 2 (pax2, 167409.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the paired box homeotic gene 2 (pax2, 167409.0001) | rel=r_associated | relid=0 | w=34
  1210. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the paired-like homeobox 2b gene (phox2b, 603851.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the paired-like homeobox 2b gene (phox2b, 603851.0001) | rel=r_associated | relid=0 | w=34
  1211. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the paired-like homeodomain transcription factor-3 gene (pitx3, 602669.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the paired-like homeodomain transcription factor-3 gene (pitx3, 602669.0001) | rel=r_associated | relid=0 | w=34
  1212. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the pantothenate kinase-2 gene (pank2, 607157.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pantothenate kinase-2 gene (pank2, 607157.0011) | rel=r_associated | relid=0 | w=34
  1213. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the periaxin gene (prx, 605725.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the periaxin gene (prx, 605725.0001) | rel=r_associated | relid=0 | w=34
  1214. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the peroxisome biogenesis factor-14 gene (pex14, 601791.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor-14 gene (pex14, 601791.0001) | rel=r_associated | relid=0 | w=34
  1215. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the peroxisome biogenesis factor-2 gene (pex2, 170993.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor-2 gene (pex2, 170993.0002) | rel=r_associated | relid=0 | w=34
  1216. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the phenylalanine hydroxylase gene (pah, 261600.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phenylalanine hydroxylase gene (pah, 261600.0001) | rel=r_associated | relid=0 | w=34
  1217. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory, 1 gene (pik3r1, 171833.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory, 1 gene (pik3r1, 171833.0002) | rel=r_associated | relid=0 | w=34
  1218. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the phosphodiesterase 8b gene (pde8b, 603390.0002).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphodiesterase 8b gene (pde8b, 603390.0002). | rel=r_associated | relid=0 | w=34
  1219. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the phosphoglucomutase-3 gene (pgm3, 172100.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoglucomutase-3 gene (pgm3, 172100.0001) | rel=r_associated | relid=0 | w=34
  1220. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0009) | rel=r_associated | relid=0 | w=34
  1221. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the phospholipase c, beta-1 gene (plcb1, 607120.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phospholipase c, beta-1 gene (plcb1, 607120.0001) | rel=r_associated | relid=0 | w=34
  1222. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the plasminogen gene (plg, 173350.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the plasminogen gene (plg, 173350.0001) | rel=r_associated | relid=0 | w=34
  1223. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the poliovirus receptor-like 1 gene (pvrl1, 600644.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the poliovirus receptor-like 1 gene (pvrl1, 600644.0001) | rel=r_associated | relid=0 | w=34
  1224. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the polynucleotide kinase 3-prime phosphatase gene (pnkp, 605610.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polynucleotide kinase 3-prime phosphatase gene (pnkp, 605610.0001) | rel=r_associated | relid=0 | w=34
  1225. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the potassium voltage-gated channel, isk-related family, member 2 gene (kcne2, 603796.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, isk-related family, member 2 gene (kcne2, 603796.0001) | rel=r_associated | relid=0 | w=34
  1226. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the potassium voltage-gated channel, isk-related subfamily, member 1 gene (kcne1, 176261.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, isk-related subfamily, member 1 gene (kcne1, 176261.0003) | rel=r_associated | relid=0 | w=34
  1227. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the prenyl diphosphate synthase, subunit 2 gene (pdss2, 610564.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prenyl diphosphate synthase, subunit 2 gene (pdss2, 610564.0001) | rel=r_associated | relid=0 | w=34
  1228. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the prolactin receptor gene (prlr, 176761.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prolactin receptor gene (prlr, 176761.0001) | rel=r_associated | relid=0 | w=34
  1229. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the propionyl coenzyme a carboxylase, alpha polypeptide gene (pcca, 232000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the propionyl coenzyme a carboxylase, alpha polypeptide gene (pcca, 232000.0001) | rel=r_associated | relid=0 | w=34
  1230. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the prosaposin gene (psap, 176801.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prosaposin gene (psap, 176801.0001) | rel=r_associated | relid=0 | w=34
  1231. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein kinase c, delta gene (prkcd, 176977.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein kinase c, delta gene (prkcd, 176977.0001) | rel=r_associated | relid=0 | w=34
  1232. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein kinase, amp-activated, noncatalytic, gamma-2 gene (prkag2, 602743.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein kinase, amp-activated, noncatalytic, gamma-2 gene (prkag2, 602743.0007) | rel=r_associated | relid=0 | w=34
  1233. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase 1 gene (pomgnt1, 606822.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase 1 gene (pomgnt1, 606822.0013) | rel=r_associated | relid=0 | w=34
  1234. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase gene (pomgnt1, 606822.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase gene (pomgnt1, 606822.0014) | rel=r_associated | relid=0 | w=34
  1235. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein o-mannosyltransferase 2 gene (pomt2, 607439.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein o-mannosyltransferase 2 gene (pomt2, 607439.0004) | rel=r_associated | relid=0 | w=34
  1236. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein o-mannosyltransferase 2 gene (pomt2, 607439.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein o-mannosyltransferase 2 gene (pomt2, 607439.0010) | rel=r_associated | relid=0 | w=34
  1237. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0001) | rel=r_associated | relid=0 | w=34
  1238. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0006) | rel=r_associated | relid=0 | w=34
  1239. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein tyrosine phosphatase, receptor type, c polypeptide gene (ptprc, 151460.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein tyrosine phosphatase, receptor type, c polypeptide gene (ptprc, 151460.0002) | rel=r_associated | relid=0 | w=34
  1240. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein-o-mannose kinase gene (pomk, 615247.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein-o-mannose kinase gene (pomk, 615247.0001) | rel=r_associated | relid=0 | w=34
  1241. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein-o-mannose kinase gene (pomk, 615247.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein-o-mannose kinase gene (pomk, 615247.0003) | rel=r_associated | relid=0 | w=34
  1242. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the protein-tyrosine phosphatase, nonreceptor-type, 11 (ptpn11, 176876.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein-tyrosine phosphatase, nonreceptor-type, 11 (ptpn11, 176876.0005) | rel=r_associated | relid=0 | w=34
  1243. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the proteolipid protein 1 gene (plp1, 300401.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the proteolipid protein 1 gene (plp1, 300401.0001) | rel=r_associated | relid=0 | w=34
  1244. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the psmc3-interacting protein gene (psmc3ip, 608665.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the psmc3-interacting protein gene (psmc3ip, 608665.0001) | rel=r_associated | relid=0 | w=34
  1245. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the purine nucleoside phosphorylase gene (pnp, 164050.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the purine nucleoside phosphorylase gene (pnp, 164050.0001) | rel=r_associated | relid=0 | w=34
  1246. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the pyrin domain-containing-1 of the nlr family gene (nlrp1, 606626.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pyrin domain-containing-1 of the nlr family gene (nlrp1, 606626.0002) | rel=r_associated | relid=0 | w=34
  1247. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the radixin gene (rdx, 179410.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the radixin gene (rdx, 179410.0001) | rel=r_associated | relid=0 | w=34
  1248. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the receptor-interacting serine-threonine kinase-4 gene (ripk4, 605706.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the receptor-interacting serine-threonine kinase-4 gene (ripk4, 605706.0001) | rel=r_associated | relid=0 | w=34
  1249. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the retinoblastoma-binding protein-8 gene (rbbp8, 604124.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the retinoblastoma-binding protein-8 gene (rbbp8, 604124.0002) | rel=r_associated | relid=0 | w=34
  1250. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the retinoschisin gene (rs1, 300839.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the retinoschisin gene (rs1, 300839.0001) | rel=r_associated | relid=0 | w=34
  1251. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the rho guanine-nucleotide exchange factor-10 gene (arhgef10, 608136.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rho guanine-nucleotide exchange factor-10 gene (arhgef10, 608136.0001) | rel=r_associated | relid=0 | w=34
  1252. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ribonuclease h2, subunit b gene (rnaseh2b, 610326.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribonuclease h2, subunit b gene (rnaseh2b, 610326.0001) | rel=r_associated | relid=0 | w=34
  1253. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ribose 5-phosphate isomerase a gene (rpia, 180430.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribose 5-phosphate isomerase a gene (rpia, 180430.0001) | rel=r_associated | relid=0 | w=34
  1254. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ribosomal protein s19 gene (rps19, 603474.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribosomal protein s19 gene (rps19, 603474.0001) | rel=r_associated | relid=0 | w=34
  1255. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the rna polymerase i and transcript release factor gene (ptrf, 603198.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rna polymerase i and transcript release factor gene (ptrf, 603198.0001) | rel=r_associated | relid=0 | w=34
  1256. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the runt-related transcription factor 2 gene (runx2, 600211.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the runt-related transcription factor 2 gene (runx2, 600211.0001) | rel=r_associated | relid=0 | w=34
  1257. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ryanodine receptor-1 gene (ryr1, 180901.0025)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ryanodine receptor-1 gene (ryr1, 180901.0025) | rel=r_associated | relid=0 | w=34
  1258. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ryanodine receptor-2 gene (ryr2, 180902.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ryanodine receptor-2 gene (ryr2, 180902.0001) | rel=r_associated | relid=0 | w=34
  1259. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the sepiapterin reductase gene (spr, 182125.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sepiapterin reductase gene (spr, 182125.0001) | rel=r_associated | relid=0 | w=34
  1260. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the serine protease inhibitor, kazal type, 5 gene (spink5, 605010.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the serine protease inhibitor, kazal type, 5 gene (spink5, 605010.0001) | rel=r_associated | relid=0 | w=34
  1261. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the serpin peptidase inhibitor, clade e, member 1 gene (serpine1, 173360.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the serpin peptidase inhibitor, clade e, member 1 gene (serpine1, 173360.0001) | rel=r_associated | relid=0 | w=34
  1262. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the serpin peptidase inhibitor, clade h, member 1 (serpinh1, 600943.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the serpin peptidase inhibitor, clade h, member 1 (serpinh1, 600943.0002) | rel=r_associated | relid=0 | w=34
  1263. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the small integral membrane protein 1 gene (smim1, 615242.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the small integral membrane protein 1 gene (smim1, 615242.0001) | rel=r_associated | relid=0 | w=34
  1264. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the sodium channel, voltage-gated, type ix, alpha subunit gene (scn9a, 603415.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sodium channel, voltage-gated, type ix, alpha subunit gene (scn9a, 603415.0018) | rel=r_associated | relid=0 | w=34
  1265. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 10 gene (slc2a10, 606145.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 10 gene (slc2a10, 606145.0001) | rel=r_associated | relid=0 | w=34
  1266. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 gene (slc24a5, 609802.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 gene (slc24a5, 609802.0001) | rel=r_associated | relid=0 | w=34
  1267. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the solute carrier family 25 (mitochondrial citrate transporter), member 1 gene (slc25a1, 190315.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (mitochondrial citrate transporter), member 1 gene (slc25a1, 190315.0001) | rel=r_associated | relid=0 | w=34
  1268. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 222600.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 222600.0005) | rel=r_associated | relid=0 | w=34
  1269. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the solute carrier family 30 (zinc transporter), member 10 gene (slc30a10, 611146.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 30 (zinc transporter), member 10 gene (slc30a10, 611146.0001) | rel=r_associated | relid=0 | w=34
  1270. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the solute carrier family 35, member d1 gene (slc25d1, 610804.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 35, member d1 gene (slc25d1, 610804.0001) | rel=r_associated | relid=0 | w=34
  1271. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the solute carrier family 39 (zinc transporter), member 13 gene (slc39a13, 608735.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 39 (zinc transporter), member 13 gene (slc39a13, 608735.0001) | rel=r_associated | relid=0 | w=34
  1272. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the solute carrier family 9, isoform a3, regulatory factor 1 gene (slc9a3r1, 604990.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 9, isoform a3, regulatory factor 1 gene (slc9a3r1, 604990.0001) | rel=r_associated | relid=0 | w=34
  1273. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the spatacsin gene (spg11, 610844.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the spatacsin gene (spg11, 610844.0001) | rel=r_associated | relid=0 | w=34
  1274. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the spectrin beta-1 gene (sptb, 182870.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the spectrin beta-1 gene (sptb, 182870.0010) | rel=r_associated | relid=0 | w=34
  1275. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the sperm-associated antigen 1 gene (spag1, 603395.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sperm-associated antigen 1 gene (spag1, 603395.0001) | rel=r_associated | relid=0 | w=34
  1276. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the splicing factor 3b, subunit 4 gene (sf3b4, 605593.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the splicing factor 3b, subunit 4 gene (sf3b4, 605593.0001) | rel=r_associated | relid=0 | w=34
  1277. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the sry-box 17 gene (sox17, 610928.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sry-box 17 gene (sox17, 610928.0001) | rel=r_associated | relid=0 | w=34
  1278. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the steroid 5-alpha-reductase 3 gene (srd5a3, 611715.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the steroid 5-alpha-reductase 3 gene (srd5a3, 611715.0001) | rel=r_associated | relid=0 | w=34
  1279. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the steroid 5-alpha-reductase 3 gene (srd5a3, 611715.0006).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the steroid 5-alpha-reductase 3 gene (srd5a3, 611715.0006). | rel=r_associated | relid=0 | w=34
  1280. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the succinate dehydrogenase complex assembly factor 1 gene (sdhaf1, 612848.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the succinate dehydrogenase complex assembly factor 1 gene (sdhaf1, 612848.0001) | rel=r_associated | relid=0 | w=34
  1281. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the tectonic family, member 3 gene (tctn3, 613847.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tectonic family, member 3 gene (tctn3, 613847.0001) | rel=r_associated | relid=0 | w=34
  1282. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the telomerase rna component gene (terc, 602322.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the telomerase rna component gene (terc, 602322.0004) | rel=r_associated | relid=0 | w=34
  1283. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the traf3-interacting protein-2 gene (traf3ip2, 607043.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the traf3-interacting protein-2 gene (traf3ip2, 607043.0002) | rel=r_associated | relid=0 | w=34
  1284. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the transmembrane protease, serine 6 gene (tmprss6, 609862.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protease, serine 6 gene (tmprss6, 609862.0001) | rel=r_associated | relid=0 | w=34
  1285. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the transmembrane protein 165 gene (tmem165, 614726.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 165 gene (tmem165, 614726.0001) | rel=r_associated | relid=0 | w=34
  1286. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the transmembrane protein 216 gene (tmem216, 613277.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 216 gene (tmem216, 613277.0001) | rel=r_associated | relid=0 | w=34
  1287. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the transporter, atp-binding cassette, major histocompatibility complex, 2 gene (tap2, 170261.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transporter, atp-binding cassette, major histocompatibility complex, 2 gene (tap2, 170261.0004) | rel=r_associated | relid=0 | w=34
  1288. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the tripartite motif-containing protein 32 gene (trim32, 602290.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tripartite motif-containing protein 32 gene (trim32, 602290.0002) | rel=r_associated | relid=0 | w=34
  1289. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the trk-fused gene (tfg, 602498.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the trk-fused gene (tfg, 602498.0002) | rel=r_associated | relid=0 | w=34
  1290. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the tropomyosin 3 gene (tpm3, 191030.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tropomyosin 3 gene (tpm3, 191030.0005) | rel=r_associated | relid=0 | w=34
  1291. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the troponin i, fast-twitch skeletal muscle isoform, gene (tnni2, 191043.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the troponin i, fast-twitch skeletal muscle isoform, gene (tnni2, 191043.0001) | rel=r_associated | relid=0 | w=34
  1292. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the tubby-like protein 1 gene (tulp1, 602280.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubby-like protein 1 gene (tulp1, 602280.0004) | rel=r_associated | relid=0 | w=34
  1293. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the tubulin, gamma-1 gene (tubg1, 191135.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin, gamma-1 gene (tubg1, 191135.0001) | rel=r_associated | relid=0 | w=34
  1294. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the twinkle gene (c10orf2, 606075.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the twinkle gene (c10orf2, 606075.0001) | rel=r_associated | relid=0 | w=34
  1295. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the type iv collagen alpha-2 gene (col4a2, 120090.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the type iv collagen alpha-2 gene (col4a2, 120090.0001) | rel=r_associated | relid=0 | w=34
  1296. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the type ix, voltage-gated sodium channel, alpha subunit gene (scn9a, 603415.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the type ix, voltage-gated sodium channel, alpha subunit gene (scn9a, 603415.0008) | rel=r_associated | relid=0 | w=34
  1297. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the tyrosinase-related protein 1 gene (tyrp1, 115501.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tyrosinase-related protein 1 gene (tyrp1, 115501.0001) | rel=r_associated | relid=0 | w=34
  1298. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the ubiquinol-cytochrome c reductase complex assembly factor 3 gene (uqcc3, 616097.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquinol-cytochrome c reductase complex assembly factor 3 gene (uqcc3, 616097.0001) | rel=r_associated | relid=0 | w=34
  1299. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the uroporphyrinogen iii cosynthase gene (uros, 606938.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the uroporphyrinogen iii cosynthase gene (uros, 606938.0001) | rel=r_associated | relid=0 | w=34
  1300. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the v-akt murine thymoma viral oncogene homolog 3 gene (akt3, 611223.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-akt murine thymoma viral oncogene homolog 3 gene (akt3, 611223.0001) | rel=r_associated | relid=0 | w=34
  1301. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the v-maf musculoaponeurotic fibrosarcoma oncogene family, protein b gene (mafb, 608968.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-maf musculoaponeurotic fibrosarcoma oncogene family, protein b gene (mafb, 608968.0001) | rel=r_associated | relid=0 | w=34
  1302. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the voltage-gated potassium channel, subfamily h, member 1 gene (kcnh1, 603305.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated potassium channel, subfamily h, member 1 gene (kcnh1, 603305.0001) | rel=r_associated | relid=0 | w=34
  1303. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the vps33b-interacting protein, apical-basolateral polarity regulator gene (vipar, 613401.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the vps33b-interacting protein, apical-basolateral polarity regulator gene (vipar, 613401.0001) | rel=r_associated | relid=0 | w=34
  1304. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the wingless-type mmtv integration site family, member 7a gene (wnt7a, 601570.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wingless-type mmtv integration site family, member 7a gene (wnt7a, 601570.0002) | rel=r_associated | relid=0 | w=34
  1305. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the wnk lysine deficient protein kinase 1 gene (wnk1, 605232.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wnk lysine deficient protein kinase 1 gene (wnk1, 605232.0001) | rel=r_associated | relid=0 | w=34
  1306. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0001) | rel=r_associated | relid=0 | w=34
  1307. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the zinc finger mynd domain-containing protein 10 (zmynd10, 607070.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger mynd domain-containing protein 10 (zmynd10, 607070.0001) | rel=r_associated | relid=0 | w=34
  1308. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the zinc finger mynd domain-containing protein 11 gene (zmynd11, 608668.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger mynd domain-containing protein 11 gene (zmynd11, 608668.0001) | rel=r_associated | relid=0 | w=34
  1309. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the zinc finger protein 469 gene (znf469, 612078.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger protein 469 gene (znf469, 612078.0001) | rel=r_associated | relid=0 | w=34
  1310. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the zinc finger protein 644 gene (znf644, 614159.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger protein 644 gene (znf644, 614159.0001) | rel=r_associated | relid=0 | w=34
  1311. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the zinc finger swim domain-containing protein 6 (zswim6, 615951.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger swim domain-containing protein 6 (zswim6, 615951.0001) | rel=r_associated | relid=0 | w=34
  1312. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the zinc finger- and btb domain-containing protein 16 gene (zbtb16, 176797.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger- and btb domain-containing protein 16 gene (zbtb16, 176797.0001) | rel=r_associated | relid=0 | w=34
  1313. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in the zinc finger- and btb domain-containing protein 24 gene (zbtb24, 614064.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger- and btb domain-containing protein 24 gene (zbtb24, 614064.0001) | rel=r_associated | relid=0 | w=34
  1314. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutation in zinc finger mynd-containing protein-15 gene (zmynd15, 614312.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in zinc finger mynd-containing protein-15 gene (zmynd15, 614312.0001) | rel=r_associated | relid=0 | w=34
  1315. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in homolog 3 of the drosophila 'roundabout' gene (robo3, 608630.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in homolog 3 of the drosophila 'roundabout' gene (robo3, 608630.0001) | rel=r_associated | relid=0 | w=34
  1316. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in lecithin:cholesterol acyltransferase gene (lcat, 606967.0005).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in lecithin:cholesterol acyltransferase gene (lcat, 606967.0005). | rel=r_associated | relid=0 | w=34
  1317. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in merlin (nf2, 101000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in merlin (nf2, 101000.0001) | rel=r_associated | relid=0 | w=34
  1318. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the 1-acylglycerol-3-phosphate o-acyltransferase 2 gene (agpat2, 603100.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the 1-acylglycerol-3-phosphate o-acyltransferase 2 gene (agpat2, 603100.0001). | rel=r_associated | relid=0 | w=34
  1319. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0003) | rel=r_associated | relid=0 | w=34
  1320. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the cysteine-rich protein with egf-like domain 1 gene (creld1, 607170.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cysteine-rich protein with egf-like domain 1 gene (creld1, 607170.0001) | rel=r_associated | relid=0 | w=34
  1321. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the delta-1-pyrroline-5-carboxylate dehydrogenase gene (p5cdh, 606811.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the delta-1-pyrroline-5-carboxylate dehydrogenase gene (p5cdh, 606811.0001) | rel=r_associated | relid=0 | w=34
  1322. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the glutamate dehydrogenase gene (glud1, 138130.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the glutamate dehydrogenase gene (glud1, 138130.0001) | rel=r_associated | relid=0 | w=34
  1323. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the hamartin gene (tsc1, 605284.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the hamartin gene (tsc1, 605284.0007) | rel=r_associated | relid=0 | w=34
  1324. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the holocarbyoxylase synthetase gene (hlcs, 253270.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the holocarbyoxylase synthetase gene (hlcs, 253270.0001) | rel=r_associated | relid=0 | w=34
  1325. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the keratin 6b gene (krt6b, 148042.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the keratin 6b gene (krt6b, 148042.0001) | rel=r_associated | relid=0 | w=34
  1326. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the ocrl1 gene (ocrl1, 300535.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the ocrl1 gene (ocrl1, 300535.0001) | rel=r_associated | relid=0 | w=34
  1327. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the parkin gene (park2, 602544.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the parkin gene (park2, 602544.0001) | rel=r_associated | relid=0 | w=34
  1328. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the swi/snf related, matrix associated, actin dependent regulator of chromatin, subfamily a-like gene (smarcal1, 606622.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the swi/snf related, matrix associated, actin dependent regulator of chromatin, subfamily a-like gene (smarcal1, 606622.0001) | rel=r_associated | relid=0 | w=34
  1329. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the titin immunoglobulin domain protein gene (ttid, 604103.0002).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the titin immunoglobulin domain protein gene (ttid, 604103.0002). | rel=r_associated | relid=0 | w=34
  1330. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the udp-galaltose-4-epimerase gene, 'mild' form (gale, 606953.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the udp-galaltose-4-epimerase gene, 'mild' form (gale, 606953.0001). | rel=r_associated | relid=0 | w=34
  1331. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by mutations in the zinc finger transcription factor trps1 gene (trps1, 604386.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the zinc finger transcription factor trps1 gene (trps1, 604386.0007) | rel=r_associated | relid=0 | w=34
  1332. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by postzygotic somatic mosaic mutation in the phosphatidylinositol 3-kinase, catalytic, alpha polypeptide gene (pik3ca, 171834.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by postzygotic somatic mosaic mutation in the phosphatidylinositol 3-kinase, catalytic, alpha polypeptide gene (pik3ca, 171834.0001) | rel=r_associated | relid=0 | w=34
  1333. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:caused by somatic mutation in the guanine nucleotide-binding protein, alpha-stimulating activity polypeptide 1 gene (gnas1, 139320.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the guanine nucleotide-binding protein, alpha-stimulating activity polypeptide 1 gene (gnas1, 139320.0008) | rel=r_associated | relid=0 | w=34
  1334. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:chromosome 15q26-qter deletion syndrome
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:chromosome 15q26-qter deletion syndrome | rel=r_associated | relid=0 | w=34
  1335. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:contiguous gene syndrome involving mutation of genes on 7q11.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome involving mutation of genes on 7q11.2 | rel=r_associated | relid=0 | w=34
  1336. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:susceptibility conferred by mutation in the lysyl oxidase-like 1 gene (loxl1, 153456.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the lysyl oxidase-like 1 gene (loxl1, 153456.0001) | rel=r_associated | relid=0 | w=34
  1337. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:susceptibility conferred by mutation in the melanocortin 2 receptor accessory protein 2 gene (mrap2, 615410.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the melanocortin 2 receptor accessory protein 2 gene (mrap2, 615410.0001) | rel=r_associated | relid=0 | w=34
  1338. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:susceptibility conferred by mutation in the platelet thromboxane a2 receptor gene (tbxa2r, 188070.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the platelet thromboxane a2 receptor gene (tbxa2r, 188070.0001) | rel=r_associated | relid=0 | w=34
  1339. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:susceptibility conferred by mutation in the protection of telomeres 1 gene (pot1, 606478.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the protection of telomeres 1 gene (pot1, 606478.0001) | rel=r_associated | relid=0 | w=34
  1340. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:susceptibility conferred by mutation in the transmembrane 4 l6 family, member 20 gene (tm4sf20, 615404.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the transmembrane 4 l6 family, member 20 gene (tm4sf20, 615404.0001) | rel=r_associated | relid=0 | w=34
  1341. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 34 / 0.791 -> en:susceptibility conferred by somatic mutation in the homolog of the myeloproliferative leukemia virus gene (mpl, 159530.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by somatic mutation in the homolog of the myeloproliferative leukemia virus gene (mpl, 159530.0011) | rel=r_associated | relid=0 | w=34
  1342. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:a contiguous gene syndrome caused by deletion of chromosome 16q22 including the cbfb gene (121360)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome caused by deletion of chromosome 16q22 including the cbfb gene (121360) | rel=r_associated | relid=0 | w=32
  1343. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:a contiguous gene syndrome caused by deletion of the stereocilin gene (strc, 606440) and the sperm-associated cation channel-2 gene (catsper2, 607249) gene
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome caused by deletion of the stereocilin gene (strc, 606440) and the sperm-associated cation channel-2 gene (catsper2, 607249) gene | rel=r_associated | relid=0 | w=32
  1344. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:associated with mutation in the neuroligin-4 gene (nlgn4, 300427.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:associated with mutation in the neuroligin-4 gene (nlgn4, 300427.0001) | rel=r_associated | relid=0 | w=32
  1345. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by 750kb to 2.7mb deletion of chromosome 19q13.11
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by 750kb to 2.7mb deletion of chromosome 19q13.11 | rel=r_associated | relid=0 | w=32
  1346. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by a trinucleotide repeat expansion (cag)n in the tata box-binding protein gene (tbp, 600075.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a trinucleotide repeat expansion (cag)n in the tata box-binding protein gene (tbp, 600075.0001) | rel=r_associated | relid=0 | w=32
  1347. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by deletion of 539.77kb (grch37 chr8 77226464-77766239) on chromosome 8q21.11
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion of 539.77kb (grch37 chr8 77226464-77766239) on chromosome 8q21.11 | rel=r_associated | relid=0 | w=32
  1348. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by duplication of 59kb on chromosome 2q35
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of 59kb on chromosome 2q35 | rel=r_associated | relid=0 | w=32
  1349. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by duplication of at least 325kb on 10q24
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of at least 325kb on 10q24 | rel=r_associated | relid=0 | w=32
  1350. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by fusion of rad51b (602948) and hmgic (600698) genes
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by fusion of rad51b (602948) and hmgic (600698) genes | rel=r_associated | relid=0 | w=32
  1351. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by germline mutation in the armadillo repeat-containing protein 5 gene (armc5, 615549.0001) coupled with somatic mutation of the other armc5 allele in the adrenal tumors
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by germline mutation in the armadillo repeat-containing protein 5 gene (armc5, 615549.0001) coupled with somatic mutation of the other armc5 allele in the adrenal tumors | rel=r_associated | relid=0 | w=32
  1352. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in leprecan-like-1 gene (leprel1, 610341.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in leprecan-like-1 gene (leprel1, 610341.0001) | rel=r_associated | relid=0 | w=32
  1353. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the acetylglucosaminyltransferase-like protein (large, 603590.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the acetylglucosaminyltransferase-like protein (large, 603590.0001) | rel=r_associated | relid=0 | w=32
  1354. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the acid beta-glucocerebrosidase gene (gba, 606643.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the acid beta-glucocerebrosidase gene (gba, 606643.0001) | rel=r_associated | relid=0 | w=32
  1355. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the activin a receptor, type i gene (acvr1, 102576.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the activin a receptor, type i gene (acvr1, 102576.0001) | rel=r_associated | relid=0 | w=32
  1356. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the activin receptor-like kinase gene (alk1, 601284.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the activin receptor-like kinase gene (alk1, 601284.0001) | rel=r_associated | relid=0 | w=32
  1357. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the acylglycerol kinase gene (agk, 610345.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the acylglycerol kinase gene (agk, 610345.0010) | rel=r_associated | relid=0 | w=32
  1358. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the adaptor-related protein complex 1, sigma-1 subunit gene (ap1s1, 603531.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adaptor-related protein complex 1, sigma-1 subunit gene (ap1s1, 603531.0001) | rel=r_associated | relid=0 | w=32
  1359. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the adenine phosphoribosyltransferase gene (aprt, 102600.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenine phosphoribosyltransferase gene (aprt, 102600.0001) | rel=r_associated | relid=0 | w=32
  1360. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the adenosine monophosphate deaminase 2 gene (ampd2, 102771.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenosine monophosphate deaminase 2 gene (ampd2, 102771.0002) | rel=r_associated | relid=0 | w=32
  1361. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the aggrecan gene (acan, 155760.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aggrecan gene (acan, 155760.0003) | rel=r_associated | relid=0 | w=32
  1362. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the aladin gene (aaas, 605378.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aladin gene (aaas, 605378.0001) | rel=r_associated | relid=0 | w=32
  1363. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the alanyl-trna synthetase gene (aars, 601065.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alanyl-trna synthetase gene (aars, 601065.0001) | rel=r_associated | relid=0 | w=32
  1364. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the alpha subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0015).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0015). | rel=r_associated | relid=0 | w=32
  1365. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the alpha-1 actinin gene (actn1, 102565.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1 actinin gene (actn1, 102565.0001) | rel=r_associated | relid=0 | w=32
  1366. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0012) | rel=r_associated | relid=0 | w=32
  1367. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the alsin gene (als2, 606352.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alsin gene (als2, 606352.0002) | rel=r_associated | relid=0 | w=32
  1368. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the aminoacyl-trna synthetase complex-interacting multifunctional protein 1 gene (aimp1, 603605.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aminoacyl-trna synthetase complex-interacting multifunctional protein 1 gene (aimp1, 603605.0001) | rel=r_associated | relid=0 | w=32
  1369. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the ankyrin 1 gene (ank1, 182900.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ankyrin 1 gene (ank1, 182900.0001) | rel=r_associated | relid=0 | w=32
  1370. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the argininosuccinate synthetase gene (ass, 603470.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the argininosuccinate synthetase gene (ass, 603470.0001) | rel=r_associated | relid=0 | w=32
  1371. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the arginyl-trna synthetase 1 gene (rars, 107820.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the arginyl-trna synthetase 1 gene (rars, 107820.0001) | rel=r_associated | relid=0 | w=32
  1372. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the aspartyl-trna synthetase gene (dars, 603084.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aspartyl-trna synthetase gene (dars, 603084.0001) | rel=r_associated | relid=0 | w=32
  1373. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the atp synthase f1 complex assembly factor-2 gene (atpaf2, 608918.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp synthase f1 complex assembly factor-2 gene (atpaf2, 608918.0001) | rel=r_associated | relid=0 | w=32
  1374. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the atp-binding cassette, subfamily c, member 9 gene (abcc9, 601439.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily c, member 9 gene (abcc9, 601439.0003) | rel=r_associated | relid=0 | w=32
  1375. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the atpase, cu++ transporting, alpha polypeptide gene (atp7a, 300011.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, cu++ transporting, alpha polypeptide gene (atp7a, 300011.0002) | rel=r_associated | relid=0 | w=32
  1376. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the atr-x gene (atrx, 300032.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atr-x gene (atrx, 300032.0001) | rel=r_associated | relid=0 | w=32
  1377. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the aurora kinase c gene (aurkc, 603495.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aurora kinase c gene (aurkc, 603495.0001) | rel=r_associated | relid=0 | w=32
  1378. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the basic helix-loop-helix domain-containing protein class b, 3 gene (bhlhb3, 606200.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the basic helix-loop-helix domain-containing protein class b, 3 gene (bhlhb3, 606200.0001) | rel=r_associated | relid=0 | w=32
  1379. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the bestrophin 1 gene (best1, 607854.0020)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bestrophin 1 gene (best1, 607854.0020) | rel=r_associated | relid=0 | w=32
  1380. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the beta-1-galactosidase gene (glb, 230500.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1-galactosidase gene (glb, 230500.0003) | rel=r_associated | relid=0 | w=32
  1381. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the beta-1,4-galactosyltransferase gene (b4galt1, 137060.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1,4-galactosyltransferase gene (b4galt1, 137060.0001). | rel=r_associated | relid=0 | w=32
  1382. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the beta-ureidopropionase gene (upb1, 606673.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-ureidopropionase gene (upb1, 606673.0001) | rel=r_associated | relid=0 | w=32
  1383. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the bone morphogenetic receptor, type ii gene (bmpr2, 600799.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bone morphogenetic receptor, type ii gene (bmpr2, 600799.0001) | rel=r_associated | relid=0 | w=32
  1384. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the branched chain keto acid dehydrogenase e1, alpha polypeptide gene (bckdha, 608348.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the branched chain keto acid dehydrogenase e1, alpha polypeptide gene (bckdha, 608348.0001) | rel=r_associated | relid=0 | w=32
  1385. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the brca1-associated atm activator 1 gene (brat1, 614506.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the brca1-associated atm activator 1 gene (brat1, 614506.0001) | rel=r_associated | relid=0 | w=32
  1386. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the brca1-associated c-terminal helicase 1 gene (brip1, 605882.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the brca1-associated c-terminal helicase 1 gene (brip1, 605882.0001) | rel=r_associated | relid=0 | w=32
  1387. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the brca2 gene (brca2, 600185.0027)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the brca2 gene (brca2, 600185.0027) | rel=r_associated | relid=0 | w=32
  1388. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the bridging integrator 1 gene (bin1, 601248.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bridging integrator 1 gene (bin1, 601248.0001) | rel=r_associated | relid=0 | w=32
  1389. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the c8orf38 gene (c8orf38, 612392.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the c8orf38 gene (c8orf38, 612392.0001) | rel=r_associated | relid=0 | w=32
  1390. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the calmodulin-2 gene (calm2, 114182.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calmodulin-2 gene (calm2, 114182.0001) | rel=r_associated | relid=0 | w=32
  1391. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the calpain 3 gene (capn3, 114240.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calpain 3 gene (capn3, 114240.0001) | rel=r_associated | relid=0 | w=32
  1392. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the carbonic anhydrase xii gene (ca12, 603263.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carbonic anhydrase xii gene (ca12, 603263.0001) | rel=r_associated | relid=0 | w=32
  1393. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the caspase recruitment domain containing 9 (card9, 607212.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the caspase recruitment domain containing 9 (card9, 607212.0001) | rel=r_associated | relid=0 | w=32
  1394. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cat eye syndrome chromosome region, candidate 1 gene (cecr1, 607575.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cat eye syndrome chromosome region, candidate 1 gene (cecr1, 607575.0010) | rel=r_associated | relid=0 | w=32
  1395. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cathepsin d gene (ctsd, 116840.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cathepsin d gene (ctsd, 116840.0001). | rel=r_associated | relid=0 | w=32
  1396. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cholinergic receptor, nicotinic, gamma polypeptide gene (chrng, 100730.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, gamma polypeptide gene (chrng, 100730.0001) | rel=r_associated | relid=0 | w=32
  1397. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the chromosome 10 open reading frame 2 gene (c10orf2, 606075.0016)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 10 open reading frame 2 gene (c10orf2, 606075.0016) | rel=r_associated | relid=0 | w=32
  1398. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the chromosome 19 open reading frame 12 gene (c19orf12, 614297.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 19 open reading frame 12 gene (c19orf12, 614297.0001) | rel=r_associated | relid=0 | w=32
  1399. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cln6 gene (606725.0011).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cln6 gene (606725.0011). | rel=r_associated | relid=0 | w=32
  1400. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the coiled-coil domain-containing protein 114 gene (ccdc114, 615038.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil domain-containing protein 114 gene (ccdc114, 615038.0001) | rel=r_associated | relid=0 | w=32
  1401. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the coiled-coil-helix-coiled-coil-helix domain-containing protein 10 gene (chchd10, 615903.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil-helix-coiled-coil-helix domain-containing protein 10 gene (chchd10, 615903.0003) | rel=r_associated | relid=0 | w=32
  1402. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the collagen and calcium-binding egf domain-containing protein 1 gene (ccbe1, 612753.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen and calcium-binding egf domain-containing protein 1 gene (ccbe1, 612753.0001) | rel=r_associated | relid=0 | w=32
  1403. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0003) | rel=r_associated | relid=0 | w=32
  1404. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0039)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0039) | rel=r_associated | relid=0 | w=32
  1405. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the collagen v, alpha-2 polypeptide gene (col5a2, 120190.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen v, alpha-2 polypeptide gene (col5a2, 120190.0001) | rel=r_associated | relid=0 | w=32
  1406. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the collagen vi, alpha-3 polypeptide gene (col6a3, 120250.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen vi, alpha-3 polypeptide gene (col6a3, 120250.0001) | rel=r_associated | relid=0 | w=32
  1407. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0002) | rel=r_associated | relid=0 | w=32
  1408. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the collagen, type iv, alpha-4 gene (col4a4, 120131.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type iv, alpha-4 gene (col4a4, 120131.0001) | rel=r_associated | relid=0 | w=32
  1409. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the collectin 11 gene (612502.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collectin 11 gene (612502.0001) | rel=r_associated | relid=0 | w=32
  1410. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the complement component 1, q subcomponent, a chain gene (c1qa, 120550.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement component 1, q subcomponent, a chain gene (c1qa, 120550.0001) | rel=r_associated | relid=0 | w=32
  1411. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the complement component 2 gene (c2, 613927.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement component 2 gene (c2, 613927.0001) | rel=r_associated | relid=0 | w=32
  1412. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the complement factor h gene (cfh, 134370.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement factor h gene (cfh, 134370.0002) | rel=r_associated | relid=0 | w=32
  1413. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the component of oligomeric golgi complex 4 gene (cog4, 606976.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the component of oligomeric golgi complex 4 gene (cog4, 606976.0001) | rel=r_associated | relid=0 | w=32
  1414. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the connexin 43 gene (gja1, 121014.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the connexin 43 gene (gja1, 121014.0003) | rel=r_associated | relid=0 | w=32
  1415. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cyclic nucleotide-gated channel, beta-3 gene (cngb3, 605080.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclic nucleotide-gated channel, beta-3 gene (cngb3, 605080.0001) | rel=r_associated | relid=0 | w=32
  1416. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cyclin m2 gene (cnnm2, 607803.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclin m2 gene (cnnm2, 607803.0001) | rel=r_associated | relid=0 | w=32
  1417. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cyclin-dependent kinase-like 5 gene (cdkl5, 300203.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclin-dependent kinase-like 5 gene (cdkl5, 300203.0001) | rel=r_associated | relid=0 | w=32
  1418. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cytochrome p450, family 2, subfamily u, polypeptide 1 gene (cyp2u1, 610670.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450, family 2, subfamily u, polypeptide 1 gene (cyp2u1, 610670.0001) | rel=r_associated | relid=0 | w=32
  1419. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cytochrome p450, family 4, subfamily f, polypeptide 22 gene (cyp4f22, 611495.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450, family 4, subfamily f, polypeptide 22 gene (cyp4f22, 611495.0001) | rel=r_associated | relid=0 | w=32
  1420. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cytochrome p450, subfamily xib, polypeptide 1 gene (cyp11b1, 610613.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450, subfamily xib, polypeptide 1 gene (cyp11b1, 610613.0001) | rel=r_associated | relid=0 | w=32
  1421. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the cytochrome p450, subfamily xxvic, polypeptide 1 gene (cyp26c1, 608428.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450, subfamily xxvic, polypeptide 1 gene (cyp26c1, 608428.0001) | rel=r_associated | relid=0 | w=32
  1422. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the decorin gene (dcn, 125255.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the decorin gene (dcn, 125255.0001) | rel=r_associated | relid=0 | w=32
  1423. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the deformed epidermal autoregulatory factor 1 homolog gene (deaf1, 602635.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the deformed epidermal autoregulatory factor 1 homolog gene (deaf1, 602635.0001) | rel=r_associated | relid=0 | w=32
  1424. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the desmocollin 3 gene (dsc3, 600271.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the desmocollin 3 gene (dsc3, 600271.0001) | rel=r_associated | relid=0 | w=32
  1425. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the desmoglein 2 gene (dsg2, 125671.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the desmoglein 2 gene (dsg2, 125671.0001) | rel=r_associated | relid=0 | w=32
  1426. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the desmoplakin gene (dsp, 125647.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the desmoplakin gene (dsp, 125647.0008) | rel=r_associated | relid=0 | w=32
  1427. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the direct iap-binding protein with low pi (diablo, 605219.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the direct iap-binding protein with low pi (diablo, 605219.0001) | rel=r_associated | relid=0 | w=32
  1428. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the doublecortin domain-containing protein 2 gene (dcdc2, 605755.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the doublecortin domain-containing protein 2 gene (dcdc2, 605755.0001) | rel=r_associated | relid=0 | w=32
  1429. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the drosophila homolog of the mothers against decapentaplegic, 4 gene (smad4, 600993.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the drosophila homolog of the mothers against decapentaplegic, 4 gene (smad4, 600993.0015) | rel=r_associated | relid=0 | w=32
  1430. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the dual oxidase maturation factor 2 gene (duoxa2, 612772.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dual oxidase maturation factor 2 gene (duoxa2, 612772.0001) | rel=r_associated | relid=0 | w=32
  1431. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the e homolog of the drosophila nk2 transcription factor (nkx2e, 600584.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the e homolog of the drosophila nk2 transcription factor (nkx2e, 600584.0004) | rel=r_associated | relid=0 | w=32
  1432. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the ectodysplasin anhidrotic receptor gene (edar, 604095.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ectodysplasin anhidrotic receptor gene (edar, 604095.0001) | rel=r_associated | relid=0 | w=32
  1433. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the ectodysplasin anhidrotic receptor gene (edar, 604095.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ectodysplasin anhidrotic receptor gene (edar, 604095.0005) | rel=r_associated | relid=0 | w=32
  1434. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the elongation of very long chain fatty acids-like 5 gene (elovl5, 611805.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the elongation of very long chain fatty acids-like 5 gene (elovl5, 611805.0001) | rel=r_associated | relid=0 | w=32
  1435. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the endoplasmic reticulum lipid raft-associated protein 2 gene (erlin2, 611605.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endoplasmic reticulum lipid raft-associated protein 2 gene (erlin2, 611605.0001) | rel=r_associated | relid=0 | w=32
  1436. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the ercc6-like 2 gene (ercc6l2, 615667.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ercc6-like 2 gene (ercc6l2, 615667.0001) | rel=r_associated | relid=0 | w=32
  1437. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the fibroblast growth factor 5 gene (fgf5, 165190.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor 5 gene (fgf5, 165190.0001) | rel=r_associated | relid=0 | w=32
  1438. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the fibroblast growth factor receptor 1 gene (fgfr1, 136350.0030)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor 1 gene (fgfr1, 136350.0030) | rel=r_associated | relid=0 | w=32
  1439. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0014) | rel=r_associated | relid=0 | w=32
  1440. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0015) | rel=r_associated | relid=0 | w=32
  1441. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the folliculin gene (flcn, 607273.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the folliculin gene (flcn, 607273.0009) | rel=r_associated | relid=0 | w=32
  1442. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0016)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0016) | rel=r_associated | relid=0 | w=32
  1443. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the gamma-aminobutyric acid receptor, alpha-1 gene (137160.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma-aminobutyric acid receptor, alpha-1 gene (137160.0003) | rel=r_associated | relid=0 | w=32
  1444. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the gap junction protein, alpha-1 gene (gja1, 121014.0021)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gap junction protein, alpha-1 gene (gja1, 121014.0021) | rel=r_associated | relid=0 | w=32
  1445. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the gata-binding protein 1 gene (gata1, 305371.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein 1 gene (gata1, 305371.0008) | rel=r_associated | relid=0 | w=32
  1446. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the gata-binding protein-2 gene (gata2, 137295.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein-2 gene (gata2, 137295.0009) | rel=r_associated | relid=0 | w=32
  1447. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the gata-binding protein-3 gene (gata3, 131320.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein-3 gene (gata3, 131320.0001) | rel=r_associated | relid=0 | w=32
  1448. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the glutamate decarboxylase 1 gene (gad1, 605363.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutamate decarboxylase 1 gene (gad1, 605363.0001) | rel=r_associated | relid=0 | w=32
  1449. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the glycerate kinase gene (glyctk, 610516.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycerate kinase gene (glyctk, 610516.0001) | rel=r_associated | relid=0 | w=32
  1450. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the glycerol kinase gene (gk, 300474)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycerol kinase gene (gk, 300474) | rel=r_associated | relid=0 | w=32
  1451. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the glycine dehydrogenase gene (gldc, 238300.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycine dehydrogenase gene (gldc, 238300.0001) | rel=r_associated | relid=0 | w=32
  1452. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the granulin precursor gene (grn, 138945.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the granulin precursor gene (grn, 138945.0015) | rel=r_associated | relid=0 | w=32
  1453. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the growth/differentiation factor-5 gene (gdf5, 601146.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the growth/differentiation factor-5 gene (gdf5, 601146.0013) | rel=r_associated | relid=0 | w=32
  1454. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the hereditary hemochromatosis gene (hfe, 613609.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hereditary hemochromatosis gene (hfe, 613609.0001) | rel=r_associated | relid=0 | w=32
  1455. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the heterogeneous nuclear ribonucleoprotein d-like protein gene (hnrnpdl, 607137.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heterogeneous nuclear ribonucleoprotein d-like protein gene (hnrnpdl, 607137.0001) | rel=r_associated | relid=0 | w=32
  1456. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homeobox a13 gene (hoxa13, 142959.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeobox a13 gene (hoxa13, 142959.0001) | rel=r_associated | relid=0 | w=32
  1457. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homogentisate 1,2-dioxygenase gene (hgd, 607474.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homogentisate 1,2-dioxygenase gene (hgd, 607474.0001) | rel=r_associated | relid=0 | w=32
  1458. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog a of s. cerevisiae trna methyltransferase 10 gene (trmt10a, 616013.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog a of s. cerevisiae trna methyltransferase 10 gene (trmt10a, 616013.0001) | rel=r_associated | relid=0 | w=32
  1459. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of chlamydomonas dynein regulatory complex, subunit 1 gene (drc1, 615288.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of chlamydomonas dynein regulatory complex, subunit 1 gene (drc1, 615288.0001) | rel=r_associated | relid=0 | w=32
  1460. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of drosophila peroxidasin gene (pxdn, 605158.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of drosophila peroxidasin gene (pxdn, 605158.0001) | rel=r_associated | relid=0 | w=32
  1461. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of s. cerevisiae rad51 gene (rad51, 179617.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of s. cerevisiae rad51 gene (rad51, 179617.0003) | rel=r_associated | relid=0 | w=32
  1462. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of the drosophila crumbs 2 gene (crb2, 609720.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila crumbs 2 gene (crb2, 609720.0001) | rel=r_associated | relid=0 | w=32
  1463. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of the drosophila lines 1 gene (lins1, 610350.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila lines 1 gene (lins1, 610350.0001) | rel=r_associated | relid=0 | w=32
  1464. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of the drosophila notch 2 gene (notch2, 600275.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila notch 2 gene (notch2, 600275.0003) | rel=r_associated | relid=0 | w=32
  1465. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of the drosophila orthodenticle 2 gene (otx2, 600038.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila orthodenticle 2 gene (otx2, 600038.0006) | rel=r_associated | relid=0 | w=32
  1466. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of the drosophila period 2 gene (per2, 603426.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila period 2 gene (per2, 603426.0001) | rel=r_associated | relid=0 | w=32
  1467. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of the rat nexilin gene (nexn, 613121.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the rat nexilin gene (nexn, 613121.0004) | rel=r_associated | relid=0 | w=32
  1468. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of the s. cerevisiae coq9 gene (coq9, 612837.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae coq9 gene (coq9, 612837.0001) | rel=r_associated | relid=0 | w=32
  1469. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of the s. cerevisiae, cytochrome c oxidase 20 gene (cox20, 614698.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae, cytochrome c oxidase 20 gene (cox20, 614698.0001) | rel=r_associated | relid=0 | w=32
  1470. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of the yeast dna replication helicase 2 gene (dna2, 601810.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the yeast dna replication helicase 2 gene (dna2, 601810.0001) | rel=r_associated | relid=0 | w=32
  1471. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the homolog of the yeast vacuolar protein sorting 13 gene (vps13b, 607817.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the yeast vacuolar protein sorting 13 gene (vps13b, 607817.0001) | rel=r_associated | relid=0 | w=32
  1472. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the hormone-sensitive lipase gene (lipe, 151750.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hormone-sensitive lipase gene (lipe, 151750.0001) | rel=r_associated | relid=0 | w=32
  1473. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the hps5 gene (hps5, 607521)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hps5 gene (hps5, 607521) | rel=r_associated | relid=0 | w=32
  1474. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the htra serine peptidase 1 gene (htra1, 602194.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the htra serine peptidase 1 gene (htra1, 602194.0002) | rel=r_associated | relid=0 | w=32
  1475. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the human homolog a of the s. cerevisiae sec23 gene (sec23a, 610511.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the human homolog a of the s. cerevisiae sec23 gene (sec23a, 610511.0001) | rel=r_associated | relid=0 | w=32
  1476. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the hyls1 gene (hyls1, 610693.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hyls1 gene (hyls1, 610693.0001) | rel=r_associated | relid=0 | w=32
  1477. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the il2-inducible t-cell kinase gene (itk, 186973.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the il2-inducible t-cell kinase gene (itk, 186973.0001) | rel=r_associated | relid=0 | w=32
  1478. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the immediate-early response 3-interacting protein 1 (ier3ip1, 609382.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the immediate-early response 3-interacting protein 1 (ier3ip1, 609382.0001) | rel=r_associated | relid=0 | w=32
  1479. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the immunoglobulin kappa constant region gene (igkc, 147200.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the immunoglobulin kappa constant region gene (igkc, 147200.0004) | rel=r_associated | relid=0 | w=32
  1480. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the immunoglobulin-like domain-containing receptor 1 gene (ildr1, 609739.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the immunoglobulin-like domain-containing receptor 1 gene (ildr1, 609739.0001). | rel=r_associated | relid=0 | w=32
  1481. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the insulin receptor gene (insr, 147670.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the insulin receptor gene (insr, 147670.0002) | rel=r_associated | relid=0 | w=32
  1482. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0001) | rel=r_associated | relid=0 | w=32
  1483. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the interleukin 21 receptor gene (il21r, 605383.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interleukin 21 receptor gene (il21r, 605383.0002) | rel=r_associated | relid=0 | w=32
  1484. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the interleukin-1 receptor antagonist gene (il1rn, 147679.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interleukin-1 receptor antagonist gene (il1rn, 147679.0002) | rel=r_associated | relid=0 | w=32
  1485. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the iodotyrosine deiodinase gene (iyd, 612025.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the iodotyrosine deiodinase gene (iyd, 612025.0001) | rel=r_associated | relid=0 | w=32
  1486. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the isoleucyl-trna synthetase 2 gene (iars2, 612801.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the isoleucyl-trna synthetase 2 gene (iars2, 612801.0001) | rel=r_associated | relid=0 | w=32
  1487. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the kelch-like 3 gene (klhl3, 605775.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kelch-like 3 gene (klhl3, 605775.0001) | rel=r_associated | relid=0 | w=32
  1488. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the keratin 1 gene (krt1, 139350.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 1 gene (krt1, 139350.0005) | rel=r_associated | relid=0 | w=32
  1489. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the keratin 1 gene (krt1, 139350.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 1 gene (krt1, 139350.0014) | rel=r_associated | relid=0 | w=32
  1490. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the keratin 14 gene (krt14, 148066.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 14 gene (krt14, 148066.0001) | rel=r_associated | relid=0 | w=32
  1491. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the keratin 81 gene (krt81, 602153.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 81 gene (krt81, 602153.0001) | rel=r_associated | relid=0 | w=32
  1492. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the keratin 83 gene (krt83, 602765.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 83 gene (krt83, 602765.0001) | rel=r_associated | relid=0 | w=32
  1493. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the keratin 86 gene (krt86, 601928.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 86 gene (krt86, 601928.0001). | rel=r_associated | relid=0 | w=32
  1494. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the kiaa0415 gene (kiaa0415, 613653.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kiaa0415 gene (kiaa0415, 613653.0001) | rel=r_associated | relid=0 | w=32
  1495. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the kinesin family member 11 gene (kif11, 148760.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 11 gene (kif11, 148760.0001) | rel=r_associated | relid=0 | w=32
  1496. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the l-2-hydroxyglutarate dehydrogenase gene (l2hgdh, 609584.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the l-2-hydroxyglutarate dehydrogenase gene (l2hgdh, 609584.0001) | rel=r_associated | relid=0 | w=32
  1497. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the l1 cell adhesion molecule gene (l1cam, 308840.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the l1 cell adhesion molecule gene (l1cam, 308840.0004) | rel=r_associated | relid=0 | w=32
  1498. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the laforin gene (epm2a, 607566.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the laforin gene (epm2a, 607566.0001) | rel=r_associated | relid=0 | w=32
  1499. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the lamin b receptor (lbr, 600024.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin b receptor (lbr, 600024.0003) | rel=r_associated | relid=0 | w=32
  1500. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the lecithin retinol acyltransferase gene (lrat, 604863.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lecithin retinol acyltransferase gene (lrat, 604863.0001) | rel=r_associated | relid=0 | w=32
  1501. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the leucine zipper-like transcriptional regulator 1 gene (lztr1, 600574.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucine zipper-like transcriptional regulator 1 gene (lztr1, 600574.0001) | rel=r_associated | relid=0 | w=32
  1502. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the member-5 subfamily-j inwardly rectifying potassium channel gene (kcnj5, 600734.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the member-5 subfamily-j inwardly rectifying potassium channel gene (kcnj5, 600734.0001) | rel=r_associated | relid=0 | w=32
  1503. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the microtubule-associated protein tau gene (mapt, 157140.0019)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the microtubule-associated protein tau gene (mapt, 157140.0019) | rel=r_associated | relid=0 | w=32
  1504. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the microtubule-associated serine/threonine kinase-like gene (mastl, 608221.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the microtubule-associated serine/threonine kinase-like gene (mastl, 608221.0001) | rel=r_associated | relid=0 | w=32
  1505. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the minichromosome maintenance deficient domain containing-1 gene (mcmdc1, 610098.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the minichromosome maintenance deficient domain containing-1 gene (mcmdc1, 610098.0001) | rel=r_associated | relid=0 | w=32
  1506. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the mitochondrial transfer rna cysteine gene (mttc, 590020.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial transfer rna cysteine gene (mttc, 590020.0001) | rel=r_associated | relid=0 | w=32
  1507. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the mitochondrial transfer rna histidine gene (mtth, 590040.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial transfer rna histidine gene (mtth, 590040.0003) | rel=r_associated | relid=0 | w=32
  1508. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the mkks gene (mkks, 604896.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mkks gene (mkks, 604896.0001) | rel=r_associated | relid=0 | w=32
  1509. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the mks1 gene (mks1, 609883.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mks1 gene (mks1, 609883.0001) | rel=r_associated | relid=0 | w=32
  1510. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the molybdenum cofactor synthesis gene 1 (mocs1, 603707.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the molybdenum cofactor synthesis gene 1 (mocs1, 603707.0001) | rel=r_associated | relid=0 | w=32
  1511. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the muscle phosphofructokinase gene (pfkm, 610681.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the muscle phosphofructokinase gene (pfkm, 610681.0001) | rel=r_associated | relid=0 | w=32
  1512. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the myosin ie gene (myo1e, 601479.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin ie gene (myo1e, 601479.0001) | rel=r_associated | relid=0 | w=32
  1513. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0001) | rel=r_associated | relid=0 | w=32
  1514. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0022)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0022) | rel=r_associated | relid=0 | w=32
  1515. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the myosin, heavy polypeptide-8 gene (myh8, 160741.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin, heavy polypeptide-8 gene (myh8, 160741.0001) | rel=r_associated | relid=0 | w=32
  1516. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0001) | rel=r_associated | relid=0 | w=32
  1517. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the myozenin 2 gene (myoz2, 605602.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myozenin 2 gene (myoz2, 605602.0001) | rel=r_associated | relid=0 | w=32
  1518. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the n-acetylglutamate synthase gene (nags, 608300.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the n-acetylglutamate synthase gene (nags, 608300.0001) | rel=r_associated | relid=0 | w=32
  1519. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) 1 alpha subcomplex, 2 gene (ndufa2, 602137.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) 1 alpha subcomplex, 2 gene (ndufa2, 602137.0001) | rel=r_associated | relid=0 | w=32
  1520. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 3 gene (ndufv3, 603846.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 3 gene (ndufv3, 603846.0001) | rel=r_associated | relid=0 | w=32
  1521. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the nata catalytic subunit n-alpha-acetyltransferase-10 gene (naa10, 300013.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nata catalytic subunit n-alpha-acetyltransferase-10 gene (naa10, 300013.0001) | rel=r_associated | relid=0 | w=32
  1522. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the neuraminidase 1 gene (neu1, 608272.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neuraminidase 1 gene (neu1, 608272.0001) | rel=r_associated | relid=0 | w=32
  1523. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the neurexin 1 gene (nrxn1, 600565.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neurexin 1 gene (nrxn1, 600565.0001) | rel=r_associated | relid=0 | w=32
  1524. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the npc1 gene (npc1, 607623.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the npc1 gene (npc1, 607623.0001) | rel=r_associated | relid=0 | w=32
  1525. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the nuclear receptor subfamily 2, group f, member 1 gene (nr2f1, 132890.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear receptor subfamily 2, group f, member 1 gene (nr2f1, 132890.0001) | rel=r_associated | relid=0 | w=32
  1526. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the nuclear receptor subfamily 3, group c, member 2 gene (nr3c2, 600983.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear receptor subfamily 3, group c, member 2 gene (nr3c2, 600983.0001) | rel=r_associated | relid=0 | w=32
  1527. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the nucleolar protein family a, member 2 gene (nola2, 606470.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nucleolar protein family a, member 2 gene (nola2, 606470.0001) | rel=r_associated | relid=0 | w=32
  1528. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the oligophrenin 1 gene (ophn1, 300127.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the oligophrenin 1 gene (ophn1, 300127.0001) | rel=r_associated | relid=0 | w=32
  1529. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the opa3 gene (opa3, 606580.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the opa3 gene (opa3, 606580.0001) | rel=r_associated | relid=0 | w=32
  1530. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the orai calcium release-activated calcium modulator 1 gene (orai1, 610277.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the orai calcium release-activated calcium modulator 1 gene (orai1, 610277.0002) | rel=r_associated | relid=0 | w=32
  1531. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the ornithine aminotransferase gene (oat, 258870.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ornithine aminotransferase gene (oat, 258870.0001) | rel=r_associated | relid=0 | w=32
  1532. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the perlecan gene (hspg2, 142461.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the perlecan gene (hspg2, 142461.0001) | rel=r_associated | relid=0 | w=32
  1533. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the peroxisome biogenesis factor-1 gene (pex1, 602136.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor-1 gene (pex1, 602136.0001) | rel=r_associated | relid=0 | w=32
  1534. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0004) | rel=r_associated | relid=0 | w=32
  1535. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 1 gene (pik3r1, 171833.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 1 gene (pik3r1, 171833.0007) | rel=r_associated | relid=0 | w=32
  1536. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the phosphatidylserine synthase 1 gene (ptdss1, 612792.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylserine synthase 1 gene (ptdss1, 612792.0001) | rel=r_associated | relid=0 | w=32
  1537. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the platelet-derived growth factor receptor alpha gene (pdgfra, 173490.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the platelet-derived growth factor receptor alpha gene (pdgfra, 173490.0001) | rel=r_associated | relid=0 | w=32
  1538. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the platelet-derived growth factor receptor, beta polypeptide gene (pdgfrb, 173410.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the platelet-derived growth factor receptor, beta polypeptide gene (pdgfrb, 173410.0001) | rel=r_associated | relid=0 | w=32
  1539. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the plectin gene (plec1, 601282.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the plectin gene (plec1, 601282.0001) | rel=r_associated | relid=0 | w=32
  1540. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the polyhomeotic-like 1 gene (phc1, 602978.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polyhomeotic-like 1 gene (phc1, 602978.0001) | rel=r_associated | relid=0 | w=32
  1541. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the polymerase (dna-directed), delta 1, catalytic subunit gene (pold1, 174761.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polymerase (dna-directed), delta 1, catalytic subunit gene (pold1, 174761.0001) | rel=r_associated | relid=0 | w=32
  1542. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the potassium channel tetramerisation domain containing 7 gene (kctd7, 611725.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium channel tetramerisation domain containing 7 gene (kctd7, 611725.0001) | rel=r_associated | relid=0 | w=32
  1543. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the potassium voltage-gated channel, shal-related subfamily, member 3 gene (kcnd3, 605411.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, shal-related subfamily, member 3 gene (kcnd3, 605411.0001) | rel=r_associated | relid=0 | w=32
  1544. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the prenyl diphosphate synthase, subunit 1 gene (pdss1, 607429.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prenyl diphosphate synthase, subunit 1 gene (pdss1, 607429.0001) | rel=r_associated | relid=0 | w=32
  1545. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the presenilin-1 gene (psen1, 104311.0034)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the presenilin-1 gene (psen1, 104311.0034) | rel=r_associated | relid=0 | w=32
  1546. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the prion protein gene (prnp, 176640.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prion protein gene (prnp, 176640.0002) | rel=r_associated | relid=0 | w=32
  1547. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the prokineticin-2 gene (prok2, 607002.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prokineticin-2 gene (prok2, 607002.0001) | rel=r_associated | relid=0 | w=32
  1548. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the prominin 1 gene (prom1, 604365.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prominin 1 gene (prom1, 604365.0003) | rel=r_associated | relid=0 | w=32
  1549. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the prosaposin gene (psap, 176801.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prosaposin gene (psap, 176801.0005) | rel=r_associated | relid=0 | w=32
  1550. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the prosaposin gene (psap, 176801.0009).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prosaposin gene (psap, 176801.0009). | rel=r_associated | relid=0 | w=32
  1551. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the proteasome subunit, beta-type, 8 gene (psmb8, 177046.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the proteasome subunit, beta-type, 8 gene (psmb8, 177046.0001) | rel=r_associated | relid=0 | w=32
  1552. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the r-spondin family, member 4 gene (rspo4, 610573.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the r-spondin family, member 4 gene (rspo4, 610573.0001) | rel=r_associated | relid=0 | w=32
  1553. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the receptor expression-enhancing protein-1 gene (reep1, 609139.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the receptor expression-enhancing protein-1 gene (reep1, 609139.0001) | rel=r_associated | relid=0 | w=32
  1554. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the recombination signal-binding protein for immunoglobulin kappa j region gene (rbpj, 147183.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the recombination signal-binding protein for immunoglobulin kappa j region gene (rbpj, 147183.0001) | rel=r_associated | relid=0 | w=32
  1555. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the recombination-activating gene 1 (rag1, 179615.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the recombination-activating gene 1 (rag1, 179615.0018) | rel=r_associated | relid=0 | w=32
  1556. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the ret protooncogene (ret, 164761.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ret protooncogene (ret, 164761.0013) | rel=r_associated | relid=0 | w=32
  1557. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the retinal rod photoreceptor cgmp phosphodiesterase, beta subunit gene (pde6b, 180072.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the retinal rod photoreceptor cgmp phosphodiesterase, beta subunit gene (pde6b, 180072.0001) | rel=r_associated | relid=0 | w=32
  1558. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the retinoblastoma-binding protein 8 gene (rbbp8, 604124.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the retinoblastoma-binding protein 8 gene (rbbp8, 604124.0003) | rel=r_associated | relid=0 | w=32
  1559. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the retinol dehydrogenase 12 gene (rdh12, 608830.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the retinol dehydrogenase 12 gene (rdh12, 608830.0001) | rel=r_associated | relid=0 | w=32
  1560. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the rho guanine nucleotide exchange factor-6 gene (300267.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rho guanine nucleotide exchange factor-6 gene (300267.0001) | rel=r_associated | relid=0 | w=32
  1561. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the rhodopsin gene (rho, 180380.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rhodopsin gene (rho, 180380.0001) | rel=r_associated | relid=0 | w=32
  1562. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the ribosomal protein s6 kinase, 90kd, polypeptide 3 gene (rps6ka3, 300075.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribosomal protein s6 kinase, 90kd, polypeptide 3 gene (rps6ka3, 300075.0001) | rel=r_associated | relid=0 | w=32
  1563. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the rna-binding motif protein 8a gene (rbm8a, 605313.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rna-binding motif protein 8a gene (rbm8a, 605313.0001) | rel=r_associated | relid=0 | w=32
  1564. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the sacsin gene (sacs, 604490.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sacsin gene (sacs, 604490.0001) | rel=r_associated | relid=0 | w=32
  1565. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the scavenger receptor class b, member 2 gene (scarb2, 602257.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the scavenger receptor class b, member 2 gene (scarb2, 602257.0001) | rel=r_associated | relid=0 | w=32
  1566. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the seipin gene (bscl2, 606158.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the seipin gene (bscl2, 606158.0013) | rel=r_associated | relid=0 | w=32
  1567. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the seipin gene (bscl2, 606158.0017)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the seipin gene (bscl2, 606158.0017) | rel=r_associated | relid=0 | w=32
  1568. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the set-binding protein-1 gene (setbp1, 611060.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the set-binding protein-1 gene (setbp1, 611060.0001) | rel=r_associated | relid=0 | w=32
  1569. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the short chain acyl-coa dehydrogenase gene (acads, 606885.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the short chain acyl-coa dehydrogenase gene (acads, 606885.0001) | rel=r_associated | relid=0 | w=32
  1570. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the slow-type myosin-binding protein-c gene (mybpc1, 160794.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the slow-type myosin-binding protein-c gene (mybpc1, 160794.0003) | rel=r_associated | relid=0 | w=32
  1571. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0001) | rel=r_associated | relid=0 | w=32
  1572. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the solute carrier family 12 (sodium/potassium/chloride transporters), member 1 gene (slc12a1, 600839.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 12 (sodium/potassium/chloride transporters), member 1 gene (slc12a1, 600839.0001) | rel=r_associated | relid=0 | w=32
  1573. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0018) | rel=r_associated | relid=0 | w=32
  1574. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the solute carrier family 25, member 19 gene (mitochondrial thiamine pyrophosphate carrier) (slc25a19, 606521.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25, member 19 gene (mitochondrial thiamine pyrophosphate carrier) (slc25a19, 606521.0001) | rel=r_associated | relid=0 | w=32
  1575. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 606718.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 606718.0002) | rel=r_associated | relid=0 | w=32
  1576. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the solute carrier family 34 (sodium/phosphate cotransporter), member 1 gene (slc34a1, 182309.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 34 (sodium/phosphate cotransporter), member 1 gene (slc34a1, 182309.0001) | rel=r_associated | relid=0 | w=32
  1577. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the solute carrier family 34, member 3 gene (609826.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 34, member 3 gene (609826.0001) | rel=r_associated | relid=0 | w=32
  1578. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the solute carrier family 38 (amino acid transporter), member 8 gene (slc38a8, 615585.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 38 (amino acid transporter), member 8 gene (slc38a8, 615585.0001) | rel=r_associated | relid=0 | w=32
  1579. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the speg complex locus gene (speg, 615950.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the speg complex locus gene (speg, 615950.0001) | rel=r_associated | relid=0 | w=32
  1580. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the succinate dehydrogenase complex, subunit a, flavoprotein gene (sdha, 600857.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the succinate dehydrogenase complex, subunit a, flavoprotein gene (sdha, 600857.0001) | rel=r_associated | relid=0 | w=32
  1581. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the succinate-coa ligase adp-forming beta-subunit gene (sucla2, 603921.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the succinate-coa ligase adp-forming beta-subunit gene (sucla2, 603921.0001) | rel=r_associated | relid=0 | w=32
  1582. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the taf4b rna polymerase ii, tata box-binding protein-associated factor, 105kd gene (taf4b, 601689.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the taf4b rna polymerase ii, tata box-binding protein-associated factor, 105kd gene (taf4b, 601689.0001) | rel=r_associated | relid=0 | w=32
  1583. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0001) | rel=r_associated | relid=0 | w=32
  1584. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0007) | rel=r_associated | relid=0 | w=32
  1585. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0012) | rel=r_associated | relid=0 | w=32
  1586. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the tectonic family member 3 gene (tctn3, 613847.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tectonic family member 3 gene (tctn3, 613847.0006) | rel=r_associated | relid=0 | w=32
  1587. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the tectonin beta-propeller repeat-containing protein 2 gene (tecpr2, 615000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tectonin beta-propeller repeat-containing protein 2 gene (tecpr2, 615000.0001) | rel=r_associated | relid=0 | w=32
  1588. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the tenascin xb gene (tnxb, 600985.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tenascin xb gene (tnxb, 600985.0006) | rel=r_associated | relid=0 | w=32
  1589. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the testis-specific protein-like 1 gene (tspyl1, 604714.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the testis-specific protein-like 1 gene (tspyl1, 604714.0001) | rel=r_associated | relid=0 | w=32
  1590. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the titin gene (ttn, 188840.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the titin gene (ttn, 188840.0012) | rel=r_associated | relid=0 | w=32
  1591. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the trafficking protein particle complex, subunit 9 gene (trappc9, 611966.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the trafficking protein particle complex, subunit 9 gene (trappc9, 611966.0001) | rel=r_associated | relid=0 | w=32
  1592. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the transforming growth factor, beta receptor i, 53kd gene (tgfbr1, 190181.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transforming growth factor, beta receptor i, 53kd gene (tgfbr1, 190181.0001) | rel=r_associated | relid=0 | w=32
  1593. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the transforming growth factor, beta-induced, 68kd gene (tgfbi, 601692.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transforming growth factor, beta-induced, 68kd gene (tgfbi, 601692.0005) | rel=r_associated | relid=0 | w=32
  1594. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the transmembrane and coiled-coil domains protein 1 gene (tmco1, 614123.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane and coiled-coil domains protein 1 gene (tmco1, 614123.0001) | rel=r_associated | relid=0 | w=32
  1595. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0013) | rel=r_associated | relid=0 | w=32
  1596. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the transmembrane protein-43 gene (tmem43, 612048.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein-43 gene (tmem43, 612048.0001) | rel=r_associated | relid=0 | w=32
  1597. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the tuberin gene (tsc2, 191092.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tuberin gene (tsc2, 191092.0001) | rel=r_associated | relid=0 | w=32
  1598. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the type iv voltage-gated sodium channel beta subunit gene (scn4b, 608256.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the type iv voltage-gated sodium channel beta subunit gene (scn4b, 608256.0001) | rel=r_associated | relid=0 | w=32
  1599. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the tyrosyl-trna synthetase gene (yars, 603623.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tyrosyl-trna synthetase gene (yars, 603623.0001) | rel=r_associated | relid=0 | w=32
  1600. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the upf3, b, yeast homolog gene (upf3b, 300298.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the upf3, b, yeast homolog gene (upf3b, 300298.0001) | rel=r_associated | relid=0 | w=32
  1601. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the uracil-dna glycosylase gene (ung, 191525.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the uracil-dna glycosylase gene (ung, 191525.0001) | rel=r_associated | relid=0 | w=32
  1602. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the v-akt murine thymoma viral oncogene homolog-2 gene (akt2, 164731.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-akt murine thymoma viral oncogene homolog-2 gene (akt2, 164731.0002) | rel=r_associated | relid=0 | w=32
  1603. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 4 gene (erbb4, 600543.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 4 gene (erbb4, 600543.0001) | rel=r_associated | relid=0 | w=32
  1604. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog (maf, 177075.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog (maf, 177075.0001) | rel=r_associated | relid=0 | w=32
  1605. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the vacuolar protein sorting 13a gene (vps13a, 605978.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the vacuolar protein sorting 13a gene (vps13a, 605978.0001) | rel=r_associated | relid=0 | w=32
  1606. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the very long-chain acyl-coa dehydrogenase gene (acavld, 609575.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the very long-chain acyl-coa dehydrogenase gene (acavld, 609575.0001) | rel=r_associated | relid=0 | w=32
  1607. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the vesicle-associated membrane protein 1 gene (vamp1, 185880.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the vesicle-associated membrane protein 1 gene (vamp1, 185880.0001) | rel=r_associated | relid=0 | w=32
  1608. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the voltage-gated potassium channel, shab-related subfamily, member 1 gene (kcnb1, 600397.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated potassium channel, shab-related subfamily, member 1 gene (kcnb1, 600397.0001) | rel=r_associated | relid=0 | w=32
  1609. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the voltage-gated potassium channel, shaw-related subfamily, member 1 gene (kcnc1, 176258.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated potassium channel, shaw-related subfamily, member 1 gene (kcnc1, 176258.0001) | rel=r_associated | relid=0 | w=32
  1610. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the voltage-gated sodium channel type i, alpha polypeptide gene (scn1a, 182389.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated sodium channel type i, alpha polypeptide gene (scn1a, 182389.0001) | rel=r_associated | relid=0 | w=32
  1611. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the von willebrand factor gene (vwf, 613160.0028)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the von willebrand factor gene (vwf, 613160.0028) | rel=r_associated | relid=0 | w=32
  1612. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the wd repeat-containing protein 73 gene (wdr73, 616144.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein 73 gene (wdr73, 616144.0001) | rel=r_associated | relid=0 | w=32
  1613. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the wd repeat-containing protein 81 gene (wdr81, 614218.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein 81 gene (wdr81, 614218.0001) | rel=r_associated | relid=0 | w=32
  1614. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0004) | rel=r_associated | relid=0 | w=32
  1615. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the wfs1 gene (606201)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wfs1 gene (606201) | rel=r_associated | relid=0 | w=32
  1616. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the wilms tumor 1 gene (wt1, 607102.0003).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wilms tumor 1 gene (wt1, 607102.0003). | rel=r_associated | relid=0 | w=32
  1617. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the ww domain-containing oxidoreductase gene (wwox, 605131.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ww domain-containing oxidoreductase gene (wwox, 605131.0002) | rel=r_associated | relid=0 | w=32
  1618. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0002).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0002). | rel=r_associated | relid=0 | w=32
  1619. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the zinc finger fyve-domain containing protein-27 gene (zfyve27, 610243.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger fyve-domain containing protein-27 gene (zfyve27, 610243.0001) | rel=r_associated | relid=0 | w=32
  1620. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutation in the zinc finger protein 41 gene (znf41, 314995.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger protein 41 gene (znf41, 314995.0001) | rel=r_associated | relid=0 | w=32
  1621. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the acid lysosomal sphingomyelin phosphodiesterase-1 gene (smpd1, 607608.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the acid lysosomal sphingomyelin phosphodiesterase-1 gene (smpd1, 607608.0002) | rel=r_associated | relid=0 | w=32
  1622. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the atp-binding cassette, subfamily b, member 7 gene (abcb7, 300135.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the atp-binding cassette, subfamily b, member 7 gene (abcb7, 300135.0001). | rel=r_associated | relid=0 | w=32
  1623. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the bcl6 corepressor gene (bcor, 300485.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the bcl6 corepressor gene (bcor, 300485.0001) | rel=r_associated | relid=0 | w=32
  1624. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the canalicular multispecific organic anion transporter gene (abcc2, 601107.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the canalicular multispecific organic anion transporter gene (abcc2, 601107.0001) | rel=r_associated | relid=0 | w=32
  1625. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the cartilage-derived morphogenetic protein-1 gene (cdmp1, 601146.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cartilage-derived morphogenetic protein-1 gene (cdmp1, 601146.0005) | rel=r_associated | relid=0 | w=32
  1626. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the cystic fibrosis transmembrane conductance regulator gene (cftr, 602421.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cystic fibrosis transmembrane conductance regulator gene (cftr, 602421.0005) | rel=r_associated | relid=0 | w=32
  1627. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the dentin sialophosphoprotein gene (dspp, 125485.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the dentin sialophosphoprotein gene (dspp, 125485.0004) | rel=r_associated | relid=0 | w=32
  1628. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the gap junction protein, beta-6 gene (gjb6, 604418.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the gap junction protein, beta-6 gene (gjb6, 604418.0002) | rel=r_associated | relid=0 | w=32
  1629. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the mitofusin 2 gene (mfn2, 608507.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the mitofusin 2 gene (mfn2, 608507.0009) | rel=r_associated | relid=0 | w=32
  1630. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0010) | rel=r_associated | relid=0 | w=32
  1631. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the n-acetyl-alpha-d-glucosaminidase gene (naglu, 609701.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the n-acetyl-alpha-d-glucosaminidase gene (naglu, 609701.0001) | rel=r_associated | relid=0 | w=32
  1632. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the pkhd1 gene (606702.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the pkhd1 gene (606702.0001). | rel=r_associated | relid=0 | w=32
  1633. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the platelet glycoprotein iiia gene (itgb3, 173470.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the platelet glycoprotein iiia gene (itgb3, 173470.0001) | rel=r_associated | relid=0 | w=32
  1634. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the plectin 1 gene (plec1, 601282.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the plectin 1 gene (plec1, 601282.0005) | rel=r_associated | relid=0 | w=32
  1635. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the protein tyrosine kinase-binding protein gene (tyrobp, 604142.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the protein tyrosine kinase-binding protein gene (tyrobp, 604142.0001) | rel=r_associated | relid=0 | w=32
  1636. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the recombinase activating gene 2 (rag2, 179616.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the recombinase activating gene 2 (rag2, 179616.0001) | rel=r_associated | relid=0 | w=32
  1637. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the ryanodine receptor 1 gene (ryr1, 180901.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the ryanodine receptor 1 gene (ryr1, 180901.0003) | rel=r_associated | relid=0 | w=32
  1638. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the ryanodine receptor gene (ryr1, 180901.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the ryanodine receptor gene (ryr1, 180901.0001) | rel=r_associated | relid=0 | w=32
  1639. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the sry-box 9 gene (sox9, 114290.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the sry-box 9 gene (sox9, 114290.0001) | rel=r_associated | relid=0 | w=32
  1640. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the tumor protein 63 gene (tp63, 603273.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the tumor protein 63 gene (tp63, 603273.0012) | rel=r_associated | relid=0 | w=32
  1641. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in the xylosylprotein 4-beta-galactosyltransferase, polypeptide 7 gene (b4galt7, 604327.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the xylosylprotein 4-beta-galactosyltransferase, polypeptide 7 gene (b4galt7, 604327.0001) | rel=r_associated | relid=0 | w=32
  1642. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by mutations in treacle gene (tcof1, 154500.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in treacle gene (tcof1, 154500.0001) | rel=r_associated | relid=0 | w=32
  1643. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by somatic mutation in the gnas gene (gnas1, 139320.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the gnas gene (gnas1, 139320.0009) | rel=r_associated | relid=0 | w=32
  1644. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by somatic mutation in the phosphatidylinositol glycan, class a gene (piga, 311770.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the phosphatidylinositol glycan, class a gene (piga, 311770.0001) | rel=r_associated | relid=0 | w=32
  1645. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by somatic mutation in the v-akt murine thymoma viral oncogene homolog 1 gene (akt1, 164730.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the v-akt murine thymoma viral oncogene homolog 1 gene (akt1, 164730.0001) | rel=r_associated | relid=0 | w=32
  1646. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:caused by translocation disrupting the fibulin-1 gene (fbln1, 135820)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by translocation disrupting the fibulin-1 gene (fbln1, 135820) | rel=r_associated | relid=0 | w=32
  1647. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:contiguous gene syndrome caused by 4.3-mb triplication of chromosome 4q32.1-q32.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by 4.3-mb triplication of chromosome 4q32.1-q32.2 | rel=r_associated | relid=0 | w=32
  1648. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:hcs is a contiguous gene syndrome caused by 23.8-75.5kb deletion containing the slc3a1 (104614) and prepl (609557) genes
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:hcs is a contiguous gene syndrome caused by 23.8-75.5kb deletion containing the slc3a1 (104614) and prepl (609557) genes | rel=r_associated | relid=0 | w=32
  1649. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:molecular basis
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:molecular basis | rel=r_associated | relid=0 | w=32
  1650. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:mutation in the axis inhibitor 2 gene (axin2, 604025.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:mutation in the axis inhibitor 2 gene (axin2, 604025.0003) | rel=r_associated | relid=0 | w=32
  1651. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:resistance conferred by mutation in the potassium large conductance calcium-activated channel, subfamily m, beta member 1 gene (kcnmb1, 603951.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:resistance conferred by mutation in the potassium large conductance calcium-activated channel, subfamily m, beta member 1 gene (kcnmb1, 603951.0001) | rel=r_associated | relid=0 | w=32
  1652. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:susceptibility associated with variants in the frizzled-related protein gene (frzb, 605083.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility associated with variants in the frizzled-related protein gene (frzb, 605083.0001) | rel=r_associated | relid=0 | w=32
  1653. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:susceptibility conferred by mutation in the complement factor b gene (cfb, 138470.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the complement factor b gene (cfb, 138470.0005) | rel=r_associated | relid=0 | w=32
  1654. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:susceptibility conferred by mutation in the dopamine receptor d3 gene (drd3, 126451.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the dopamine receptor d3 gene (drd3, 126451.0001) | rel=r_associated | relid=0 | w=32
  1655. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:susceptibility conferred by mutation in the paired box gene 4 (pax4, 167413.0022 )
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the paired box gene 4 (pax4, 167413.0022 ) | rel=r_associated | relid=0 | w=32
  1656. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:susceptibility conferred by somatic mutation in the calreticulin gene (calr, 109091.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by somatic mutation in the calreticulin gene (calr, 109091.0001) | rel=r_associated | relid=0 | w=32
  1657. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 32 / 0.744 -> en:susceptibility conferred by somatic mutation in the sh2b adaptor protein 3 (sh2b3, 605093.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by somatic mutation in the sh2b adaptor protein 3 (sh2b3, 605093.0001) | rel=r_associated | relid=0 | w=32
  1658. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:(prph2, 179605.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:(prph2, 179605.0008) | rel=r_associated | relid=0 | w=31
  1659. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:a contiguous gene deletion syndrome caused by heterozygous deletion (582-738 kb) of 8q13 including the sulf1 (610012) and slco5a1 (613543) genes
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene deletion syndrome caused by heterozygous deletion (582-738 kb) of 8q13 including the sulf1 (610012) and slco5a1 (613543) genes | rel=r_associated | relid=0 | w=31
  1660. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:cause by mutation in the xylosyltransferase-1 gene (xylt1, 608124.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:cause by mutation in the xylosyltransferase-1 gene (xylt1, 608124.0002) | rel=r_associated | relid=0 | w=31
  1661. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by a 1.37mb deletion on 4q21 encompassing 5 genes
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a 1.37mb deletion on 4q21 encompassing 5 genes | rel=r_associated | relid=0 | w=31
  1662. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by a trinucleotide repeat expansion (cag)n in the ataxin 8 gene (atxn8, 613289.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a trinucleotide repeat expansion (cag)n in the ataxin 8 gene (atxn8, 613289.0001) | rel=r_associated | relid=0 | w=31
  1663. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by deletion of 3.7mb on chromosome 6q13-q14
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion of 3.7mb on chromosome 6q13-q14 | rel=r_associated | relid=0 | w=31
  1664. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by deletion of at least 600kb in 10q26.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion of at least 600kb in 10q26.2 | rel=r_associated | relid=0 | w=31
  1665. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by deletion of mtdna
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion of mtdna | rel=r_associated | relid=0 | w=31
  1666. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in aldo-keto reductase family 1, member c2 gene (akr1c2, 600450.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in aldo-keto reductase family 1, member c2 gene (akr1c2, 600450.0001) | rel=r_associated | relid=0 | w=31
  1667. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in alkaline phosphatase gene (alpl, 171760.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in alkaline phosphatase gene (alpl, 171760.0003) | rel=r_associated | relid=0 | w=31
  1668. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in cartilage oligomeric matrix protein (comp, 600310.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in cartilage oligomeric matrix protein (comp, 600310.0005) | rel=r_associated | relid=0 | w=31
  1669. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the 15-alpha-hydroxyprostaglandin dehydrogenase gene (hpgd, 601688.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 15-alpha-hydroxyprostaglandin dehydrogenase gene (hpgd, 601688.0001). | rel=r_associated | relid=0 | w=31
  1670. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the 290-kd centrosomal protein gene (cep290, 610142.0004).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 290-kd centrosomal protein gene (cep290, 610142.0004). | rel=r_associated | relid=0 | w=31
  1671. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the 300-kd e1a-binding protein gene (ep300, 602700.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 300-kd e1a-binding protein gene (ep300, 602700.0003) | rel=r_associated | relid=0 | w=31
  1672. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the 45-kd receptor-associated protein of the synapse (rapsyn, 601592.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 45-kd receptor-associated protein of the synapse (rapsyn, 601592.0001) | rel=r_associated | relid=0 | w=31
  1673. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the 65-kd yes-associated protein-1 gene (yap1, 606608.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 65-kd yes-associated protein-1 gene (yap1, 606608.0001) | rel=r_associated | relid=0 | w=31
  1674. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the acid beta-glucosidase gene (gba, 606463.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the acid beta-glucosidase gene (gba, 606463.0004) | rel=r_associated | relid=0 | w=31
  1675. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the actin-binding protein anillin gene (anln, 616027.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the actin-binding protein anillin gene (anln, 616027.0001) | rel=r_associated | relid=0 | w=31
  1676. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the activity-dependent neuroprotector homeobox gene (adnp, 611386.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the activity-dependent neuroprotector homeobox gene (adnp, 611386.0001) | rel=r_associated | relid=0 | w=31
  1677. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the adamts-like 4 gene (adamtsl4, 610113.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adamts-like 4 gene (adamtsl4, 610113.0001) | rel=r_associated | relid=0 | w=31
  1678. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the adamts-like 4 gene (adamtsl4, 610113.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adamts-like 4 gene (adamtsl4, 610113.0003) | rel=r_associated | relid=0 | w=31
  1679. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the adenosine monophosphate deaminase 1 gene (ampd1, 102770.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenosine monophosphate deaminase 1 gene (ampd1, 102770.0001) | rel=r_associated | relid=0 | w=31
  1680. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the adp ribosylation factor-like 2-binding protein gene (arl2bp, 615407.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adp ribosylation factor-like 2-binding protein gene (arl2bp, 615407.0001) | rel=r_associated | relid=0 | w=31
  1681. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the aggrecan-1 gene (agc1, 155760.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aggrecan-1 gene (agc1, 155760.0001) | rel=r_associated | relid=0 | w=31
  1682. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the alkylglycerone-phosphate synthase gene (agps, 603051.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alkylglycerone-phosphate synthase gene (agps, 603051.0001) | rel=r_associated | relid=0 | w=31
  1683. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the alpha subunit of the hydroxyacyl-coa dehydrogenase/3-ketoacyl-coa thiolase/enoyl-coa hydratase (hadha, 600890.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha subunit of the hydroxyacyl-coa dehydrogenase/3-ketoacyl-coa thiolase/enoyl-coa hydratase (hadha, 600890.0003) | rel=r_associated | relid=0 | w=31
  1684. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the alpha-1 gap junction protein gene (gja1, 121014.0016)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1 gap junction protein gene (gja1, 121014.0016) | rel=r_associated | relid=0 | w=31
  1685. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the alpha-1s subunit of l-type voltage-dependent calcium channel gene (cacna1s, 114208.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1s subunit of l-type voltage-dependent calcium channel gene (cacna1s, 114208.0001). | rel=r_associated | relid=0 | w=31
  1686. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the alpha-2 subunit of collagen type ix gene (col9a2, 120260.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-2 subunit of collagen type ix gene (col9a2, 120260.0006) | rel=r_associated | relid=0 | w=31
  1687. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the alpha-b crystallin gene (cryab, 123590.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-b crystallin gene (cryab, 123590.0006) | rel=r_associated | relid=0 | w=31
  1688. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the alpha-dystrobrevin gene (dtna, 601239.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-dystrobrevin gene (dtna, 601239.0001) | rel=r_associated | relid=0 | w=31
  1689. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the alpha-mannosidase gene (man2b1, 609458.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-mannosidase gene (man2b1, 609458.0001) | rel=r_associated | relid=0 | w=31
  1690. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the alsin gene (als2, 606352.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alsin gene (als2, 606352.0001) | rel=r_associated | relid=0 | w=31
  1691. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene (agl, 610860.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene (agl, 610860.0001) | rel=r_associated | relid=0 | w=31
  1692. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the amyloid precursor protein gene (app, 104760.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the amyloid precursor protein gene (app, 104760.0001) | rel=r_associated | relid=0 | w=31
  1693. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the angiotensin ii receptor type 1 gene (agtr1, 106165.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the angiotensin ii receptor type 1 gene (agtr1, 106165.0003) | rel=r_associated | relid=0 | w=31
  1694. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the angiotensinogen gene (agt, 106150.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the angiotensinogen gene (agt, 106150.0003) | rel=r_associated | relid=0 | w=31
  1695. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ankyrin 3 gene (ank3, 600465.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ankyrin 3 gene (ank3, 600465.0001) | rel=r_associated | relid=0 | w=31
  1696. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the atp-binding cassette, subfamily a, member 12 gene (abca12, 607800.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily a, member 12 gene (abca12, 607800.0006) | rel=r_associated | relid=0 | w=31
  1697. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the atp-binding cassette, subfamily c, member 9 gene (abcc9, 601439.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily c, member 9 gene (abcc9, 601439.0004) | rel=r_associated | relid=0 | w=31
  1698. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the atp-binding cassette, subfamily g, member 8 gene (abcg8, 605460.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily g, member 8 gene (abcg8, 605460.0001) | rel=r_associated | relid=0 | w=31
  1699. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the atpase family gene 3-like 2 gene (afg3l2, 604581.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase family gene 3-like 2 gene (afg3l2, 604581.0001) | rel=r_associated | relid=0 | w=31
  1700. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0006) | rel=r_associated | relid=0 | w=31
  1701. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the au-specific rna-binding protein gene (auh, 600529.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the au-specific rna-binding protein gene (auh, 600529.0001) | rel=r_associated | relid=0 | w=31
  1702. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the barttin gene (bsnd, 606412.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the barttin gene (bsnd, 606412.0001) | rel=r_associated | relid=0 | w=31
  1703. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the bbs protein complex-interacting protein 1 gene (bbip1, 613605.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bbs protein complex-interacting protein 1 gene (bbip1, 613605.0001) | rel=r_associated | relid=0 | w=31
  1704. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the beta retinoic acid receptor (rarb, 180220.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta retinoic acid receptor (rarb, 180220.0001) | rel=r_associated | relid=0 | w=31
  1705. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the beta-3 laminin gene (lamb3, 150310.0017)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-3 laminin gene (lamb3, 150310.0017) | rel=r_associated | relid=0 | w=31
  1706. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the beta-a2 crystallin gene (cryba2, 600836.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-a2 crystallin gene (cryba2, 600836.0001) | rel=r_associated | relid=0 | w=31
  1707. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the beta-b3 crystallin gene (crybb3, 123630.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-b3 crystallin gene (crybb3, 123630.0001) | rel=r_associated | relid=0 | w=31
  1708. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the beta-synuclein gene (sncb, 602569.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-synuclein gene (sncb, 602569.0001) | rel=r_associated | relid=0 | w=31
  1709. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the brain-derived neurotrophic factor gene (bdnf, 113505.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the brain-derived neurotrophic factor gene (bdnf, 113505.0001) | rel=r_associated | relid=0 | w=31
  1710. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the branched chain keto acid dehydrogenase e1, beta polypeptide gene (bckdhb, 248611.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the branched chain keto acid dehydrogenase e1, beta polypeptide gene (bckdhb, 248611.0001) | rel=r_associated | relid=0 | w=31
  1711. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the btb/poz domain-containing protein 12 (btbd12, 613278.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the btb/poz domain-containing protein 12 (btbd12, 613278.0001) | rel=r_associated | relid=0 | w=31
  1712. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the c2 calcium-dependent domain-containing protein 3 gene (c2cd3, 615944.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the c2 calcium-dependent domain-containing protein 3 gene (c2cd3, 615944.0001) | rel=r_associated | relid=0 | w=31
  1713. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the calcium-sensing receptor gene (casr, 601199.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calcium-sensing receptor gene (casr, 601199.0004) | rel=r_associated | relid=0 | w=31
  1714. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the calreticulin-3 gene (calr3, 611414.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calreticulin-3 gene (calr3, 611414.0001) | rel=r_associated | relid=0 | w=31
  1715. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the carbonic anhydrase viii gene (ca8, 114815.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carbonic anhydrase viii gene (ca8, 114815.0001) | rel=r_associated | relid=0 | w=31
  1716. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the catalytic subunit of the dolichyl-phosphate mannosyltransferase 1 gene (dpm1, 603503.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the catalytic subunit of the dolichyl-phosphate mannosyltransferase 1 gene (dpm1, 603503.0001) | rel=r_associated | relid=0 | w=31
  1717. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the cd3 antigen, epsilon subunit gene (cd3e, 186830.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd3 antigen, epsilon subunit gene (cd3e, 186830.0001) | rel=r_associated | relid=0 | w=31
  1718. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the centromeric protein j gene (cenpj, 609279.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the centromeric protein j gene (cenpj, 609279.0001) | rel=r_associated | relid=0 | w=31
  1719. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the cereblon gene (crbn, 609262.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cereblon gene (crbn, 609262.0001) | rel=r_associated | relid=0 | w=31
  1720. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0007) | rel=r_associated | relid=0 | w=31
  1721. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the choline acetyltransferase gene (chat, 118490.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the choline acetyltransferase gene (chat, 118490.0001) | rel=r_associated | relid=0 | w=31
  1722. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the chromosome 8 open reading frame 37 gene (c8orf37, 614477.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 8 open reading frame 37 gene (c8orf37, 614477.0001) | rel=r_associated | relid=0 | w=31
  1723. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the coagulation factor xii gene (f12, 610619.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coagulation factor xii gene (f12, 610619.0006) | rel=r_associated | relid=0 | w=31
  1724. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the coiled-coil domain-containing protein 65 (ccdc65, 611088.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil domain-containing protein 65 (ccdc65, 611088.0001) | rel=r_associated | relid=0 | w=31
  1725. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0005) | rel=r_associated | relid=0 | w=31
  1726. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0001) | rel=r_associated | relid=0 | w=31
  1727. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0005) | rel=r_associated | relid=0 | w=31
  1728. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the collagen vi, alpha-2 polypeptide gene (col6a2, 120240.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen vi, alpha-2 polypeptide gene (col6a2, 120240.0002) | rel=r_associated | relid=0 | w=31
  1729. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the collagen x, alpha-1 polypeptide gene (col10a1, 120110.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen x, alpha-1 polypeptide gene (col10a1, 120110.0001) | rel=r_associated | relid=0 | w=31
  1730. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the collagen, type iv, alpha-5 gene (col4a5, 303630.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type iv, alpha-5 gene (col4a5, 303630.0001) | rel=r_associated | relid=0 | w=31
  1731. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the collagenic tail of endplate acetylcholinesterase gene (colq, 603033.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagenic tail of endplate acetylcholinesterase gene (colq, 603033.0001) | rel=r_associated | relid=0 | w=31
  1732. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the complement factor i gene (cfi, 217030.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement factor i gene (cfi, 217030.0001) | rel=r_associated | relid=0 | w=31
  1733. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the complex i, subunit nd6 gene (mtnd6, 516006.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complex i, subunit nd6 gene (mtnd6, 516006.0001) | rel=r_associated | relid=0 | w=31
  1734. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the corneodesmosin gene (cdsn, 602593.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the corneodesmosin gene (cdsn, 602593.0003) | rel=r_associated | relid=0 | w=31
  1735. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the creb-binding protein gene (crebbp, 600140.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the creb-binding protein gene (crebbp, 600140.0001). | rel=r_associated | relid=0 | w=31
  1736. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the cytochrome b of complex iii gene (mtcyb, 516020.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome b of complex iii gene (mtcyb, 516020.0001) | rel=r_associated | relid=0 | w=31
  1737. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the cytochrome c oxidase subunit i gene (mtco1, 516030.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase subunit i gene (mtco1, 516030.0004) | rel=r_associated | relid=0 | w=31
  1738. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the cytochrome c oxidase subunit x gene (cox10, 602125.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase subunit x gene (cox10, 602125.0001) | rel=r_associated | relid=0 | w=31
  1739. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the delta-4-3-oxosteroid 5-beta-reductase gene (akr1d1, 604741.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the delta-4-3-oxosteroid 5-beta-reductase gene (akr1d1, 604741.0001) | rel=r_associated | relid=0 | w=31
  1740. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0005) | rel=r_associated | relid=0 | w=31
  1741. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the desmocollin 2 gene (dsc2, 125645.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the desmocollin 2 gene (dsc2, 125645.0001) | rel=r_associated | relid=0 | w=31
  1742. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the dihydrolipoamide acetyltransferase gene (dlat, 608770.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dihydrolipoamide acetyltransferase gene (dlat, 608770.0001) | rel=r_associated | relid=0 | w=31
  1743. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the dna-activated protein kinase, catalytic subunit gene (prkdc, 600899.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna-activated protein kinase, catalytic subunit gene (prkdc, 600899.0001) | rel=r_associated | relid=0 | w=31
  1744. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the dopa decarboxylase gene (ddc, 107930.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dopa decarboxylase gene (ddc, 107930.0001) | rel=r_associated | relid=0 | w=31
  1745. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the early growth response-2 gene (egr2, 129010.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the early growth response-2 gene (egr2, 129010.0002) | rel=r_associated | relid=0 | w=31
  1746. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ectodysplasin a gene (eda, 300451.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ectodysplasin a gene (eda, 300451.0014) | rel=r_associated | relid=0 | w=31
  1747. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ectonucleotide pyrophosphatase/phosphodiesterase-1 gene (enpp1, 173335.0020)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ectonucleotide pyrophosphatase/phosphodiesterase-1 gene (enpp1, 173335.0020) | rel=r_associated | relid=0 | w=31
  1748. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the egf-containing fibulin-like extracellular matrix protein-2 gene (efemp2, 604633.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the egf-containing fibulin-like extracellular matrix protein-2 gene (efemp2, 604633.0001) | rel=r_associated | relid=0 | w=31
  1749. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the emopamil-binding protein gene (ebp, 300205.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the emopamil-binding protein gene (ebp, 300205.0001) | rel=r_associated | relid=0 | w=31
  1750. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the erythropoeitin receptor gene (epor, 133171.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the erythropoeitin receptor gene (epor, 133171.0001) | rel=r_associated | relid=0 | w=31
  1751. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the evc gene (evc, 604831.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the evc gene (evc, 604831.0006) | rel=r_associated | relid=0 | w=31
  1752. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the excision-repair cross-complementing group 1 gene (ercc1, 126380.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the excision-repair cross-complementing group 1 gene (ercc1, 126380.0001) | rel=r_associated | relid=0 | w=31
  1753. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the excision-repair cross-complementing group 4 gene (ercc4, 133520.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the excision-repair cross-complementing group 4 gene (ercc4, 133520.0004) | rel=r_associated | relid=0 | w=31
  1754. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0040)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0040) | rel=r_associated | relid=0 | w=31
  1755. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the fibroblast growth factor 17 gene (fgf17, 603725.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor 17 gene (fgf17, 603725.0001) | rel=r_associated | relid=0 | w=31
  1756. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0029)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0029) | rel=r_associated | relid=0 | w=31
  1757. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0001) | rel=r_associated | relid=0 | w=31
  1758. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0005) | rel=r_associated | relid=0 | w=31
  1759. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the fmr1 gene (fmr1, 309550.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fmr1 gene (fmr1, 309550.0001) | rel=r_associated | relid=0 | w=31
  1760. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the forkhead box e3 gene (foxe3, 601094.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead box e3 gene (foxe3, 601094.0002) | rel=r_associated | relid=0 | w=31
  1761. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the forkhead box p3 gene (foxp3, 300292.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead box p3 gene (foxp3, 300292.0001) | rel=r_associated | relid=0 | w=31
  1762. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the fras1 gene (fras1, 607830.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fras1 gene (fras1, 607830.0001) | rel=r_associated | relid=0 | w=31
  1763. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0004) | rel=r_associated | relid=0 | w=31
  1764. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the fused in sarcoma gene (fus, 137070.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fused in sarcoma gene (fus, 137070.0007) | rel=r_associated | relid=0 | w=31
  1765. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the gaip c-terminus-interacting protein 3 (gipc3, 608792.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gaip c-terminus-interacting protein 3 (gipc3, 608792.0001) | rel=r_associated | relid=0 | w=31
  1766. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the gamma-1 actin gene (actg1, 102560.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma-1 actin gene (actg1, 102560.0001) | rel=r_associated | relid=0 | w=31
  1767. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606598.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606598.0002) | rel=r_associated | relid=0 | w=31
  1768. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the gene encoding interleukin 10 receptor, beta (il10rb, 123889.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding interleukin 10 receptor, beta (il10rb, 123889.0002) | rel=r_associated | relid=0 | w=31
  1769. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the gene encoding the beaded filament structural protein 2 (bfsp2, 603212.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding the beaded filament structural protein 2 (bfsp2, 603212.0001) | rel=r_associated | relid=0 | w=31
  1770. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the gli-kruppel family member 2 gene (gli2, 165230.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gli-kruppel family member 2 gene (gli2, 165230.0001) | rel=r_associated | relid=0 | w=31
  1771. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the glucokinase gene (gck, 138079.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glucokinase gene (gck, 138079.0011) | rel=r_associated | relid=0 | w=31
  1772. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the glutamate receptor, ionotropic, ampa, 3 gene (gria3, 305915.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutamate receptor, ionotropic, ampa, 3 gene (gria3, 305915.0001) | rel=r_associated | relid=0 | w=31
  1773. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the glutamate-ammonia ligase gene (glul, 138290.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutamate-ammonia ligase gene (glul, 138290.0001) | rel=r_associated | relid=0 | w=31
  1774. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the glutaredoxin 5 gene (glrx5, 609588.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutaredoxin 5 gene (glrx5, 609588.0001) | rel=r_associated | relid=0 | w=31
  1775. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the glycoprotein ib, platelet, alpha polypeptide gene (gp1ba, 606672.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycoprotein ib, platelet, alpha polypeptide gene (gp1ba, 606672.0006) | rel=r_associated | relid=0 | w=31
  1776. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the glycosyltransferase-like domain-containing protein 2 gene (gtdc2, 614828.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycosyltransferase-like domain-containing protein 2 gene (gtdc2, 614828.0001) | rel=r_associated | relid=0 | w=31
  1777. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the glycyl trna synthetase gene (gars, 600287.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycyl trna synthetase gene (gars, 600287.0002) | rel=r_associated | relid=0 | w=31
  1778. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the granulocyte colony-stimulating factor-3 receptor gene (csf3r, 138971.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the granulocyte colony-stimulating factor-3 receptor gene (csf3r, 138971.0001) | rel=r_associated | relid=0 | w=31
  1779. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the growth/differentiation factor-5 gene (gdf5, 601146.0020)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the growth/differentiation factor-5 gene (gdf5, 601146.0020) | rel=r_associated | relid=0 | w=31
  1780. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the guanidinoacetate methyltransferase gene (gamt, 601240.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the guanidinoacetate methyltransferase gene (gamt, 601240.0001) | rel=r_associated | relid=0 | w=31
  1781. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the guanine nucleotide-binding protein, beta-4 gene (gnb4, 610863.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the guanine nucleotide-binding protein, beta-4 gene (gnb4, 610863.0001) | rel=r_associated | relid=0 | w=31
  1782. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the hcls1-associated protein x1 (hax1, 605998.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hcls1-associated protein x1 (hax1, 605998.0001). | rel=r_associated | relid=0 | w=31
  1783. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the heat-shock 27-kd protein (hspb1, 602195.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heat-shock 27-kd protein (hspb1, 602195.0001) | rel=r_associated | relid=0 | w=31
  1784. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the histone deacetylase 8 gene (hdac8, 300269.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the histone deacetylase 8 gene (hdac8, 300269.0001) | rel=r_associated | relid=0 | w=31
  1785. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog 2 of drosophila enhancer of zeste (ezh2, 601573.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog 2 of drosophila enhancer of zeste (ezh2, 601573.0001) | rel=r_associated | relid=0 | w=31
  1786. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of c. elegans unc119 gene (unc119, 604011.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of c. elegans unc119 gene (unc119, 604011.0002) | rel=r_associated | relid=0 | w=31
  1787. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of drosophila mindbomb-1 gene (mib1, 608677.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of drosophila mindbomb-1 gene (mib1, 608677.0001) | rel=r_associated | relid=0 | w=31
  1788. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of mouse newborn ovary homeobox gene (nobox, 610934.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of mouse newborn ovary homeobox gene (nobox, 610934.0001) | rel=r_associated | relid=0 | w=31
  1789. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 122 gene (ift122, 606045.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 122 gene (ift122, 606045.0001). | rel=r_associated | relid=0 | w=31
  1790. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of the drosophila atonal 7 gene (atoh7, 609875.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila atonal 7 gene (atoh7, 609875.0001) | rel=r_associated | relid=0 | w=31
  1791. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of the drosophila jagunal 1 gene (jagn1, 616012.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila jagunal 1 gene (jagn1, 616012.0001) | rel=r_associated | relid=0 | w=31
  1792. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of the drosophila muscle segment homeo box (msx1, 142983.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila muscle segment homeo box (msx1, 142983.0004) | rel=r_associated | relid=0 | w=31
  1793. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of the e. coli muts 2 gene (msh2, 120435.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the e. coli muts 2 gene (msh2, 120435.0006) | rel=r_associated | relid=0 | w=31
  1794. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of the mouse mpv17 gene (mpv17, 136960.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse mpv17 gene (mpv17, 136960.0001) | rel=r_associated | relid=0 | w=31
  1795. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of the s. cerevisiae alg13 gene (alg13, 300776.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae alg13 gene (alg13, 300776.0001) | rel=r_associated | relid=0 | w=31
  1796. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of the s. cerevisiae coq6 gene (coq6, 614647.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae coq6 gene (coq6, 614647.0001) | rel=r_associated | relid=0 | w=31
  1797. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of the s. cerevisiae nfu1 iron-sulfur cluster scaffold gene (nfu1, 608100.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae nfu1 iron-sulfur cluster scaffold gene (nfu1, 608100.0001) | rel=r_associated | relid=0 | w=31
  1798. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the homolog of the yeast cleavage and polyadenylation factor i subunit 1 gene (clp1, 608757.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the yeast cleavage and polyadenylation factor i subunit 1 gene (clp1, 608757.0001) | rel=r_associated | relid=0 | w=31
  1799. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the hps1 gene (hps1, 203300)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hps1 gene (hps1, 203300) | rel=r_associated | relid=0 | w=31
  1800. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the hps3 gene (hps3, 606118)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hps3 gene (hps3, 606118) | rel=r_associated | relid=0 | w=31
  1801. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the iduronate-2-sulfatase gene (ids, 309900.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the iduronate-2-sulfatase gene (ids, 309900.0001) | rel=r_associated | relid=0 | w=31
  1802. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the immunoglobulin mu binding protein 2 gene (ighmbp2, 600502.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the immunoglobulin mu binding protein 2 gene (ighmbp2, 600502.0001) | rel=r_associated | relid=0 | w=31
  1803. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the inhibitor of kappa light polypeptide gene enhancer in b cells, kinase of, beta gene (ikbkb, 603258.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inhibitor of kappa light polypeptide gene enhancer in b cells, kinase of, beta gene (ikbkb, 603258.0001) | rel=r_associated | relid=0 | w=31
  1804. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the interleukin-17 receptor d gene (il17rd, 606807.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interleukin-17 receptor d gene (il17rd, 606807.0001) | rel=r_associated | relid=0 | w=31
  1805. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the intestinal cell kinase gene (ick, 612325.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the intestinal cell kinase gene (ick, 612325.0001) | rel=r_associated | relid=0 | w=31
  1806. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ionotrophic glutamate receptor, n-methyl-d-aspartate, subunit 2b gene (grin2b, 138252.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ionotrophic glutamate receptor, n-methyl-d-aspartate, subunit 2b gene (grin2b, 138252.0010) | rel=r_associated | relid=0 | w=31
  1807. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the kaptin gene (kptn, 615620.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kaptin gene (kptn, 615620.0001) | rel=r_associated | relid=0 | w=31
  1808. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the kelch repeat and btb/poz domains-containing protein 13 gene (kbtbd13, 613727.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kelch repeat and btb/poz domains-containing protein 13 gene (kbtbd13, 613727.0001). | rel=r_associated | relid=0 | w=31
  1809. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the keratin 1 gene (krt1, 139350.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 1 gene (krt1, 139350.0004) | rel=r_associated | relid=0 | w=31
  1810. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the keratin 14 gene (krt14, 148066.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 14 gene (krt14, 148066.0002) | rel=r_associated | relid=0 | w=31
  1811. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the keratin 9 gene (krt9, 607606.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 9 gene (krt9, 607606.0001) | rel=r_associated | relid=0 | w=31
  1812. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the keratin-14 gene (krt14, 148066.0004).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin-14 gene (krt14, 148066.0004). | rel=r_associated | relid=0 | w=31
  1813. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the keratin-14 gene (krt14, 148066.0016)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin-14 gene (krt14, 148066.0016) | rel=r_associated | relid=0 | w=31
  1814. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ketohexokinase gene (khk, 614058.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ketohexokinase gene (khk, 614058.0001) | rel=r_associated | relid=0 | w=31
  1815. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the kinesin family member 14 gene (kif14, 611279.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 14 gene (kif14, 611279.0001) | rel=r_associated | relid=0 | w=31
  1816. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the kinesin family member 1a gene (kif1a, 601255.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 1a gene (kif1a, 601255.0001) | rel=r_associated | relid=0 | w=31
  1817. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the kinesin family member 7 gene (kif7, 611254.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 7 gene (kif7, 611254.0001) | rel=r_associated | relid=0 | w=31
  1818. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the kiss1 receptor gene (kiss1r, 604161.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kiss1 receptor gene (kiss1r, 604161.0001) | rel=r_associated | relid=0 | w=31
  1819. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the l1 cell adhesion molecule gene (l1cam, 308840.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the l1 cell adhesion molecule gene (l1cam, 308840.0001) | rel=r_associated | relid=0 | w=31
  1820. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the lamin a/c gene (lmna, 150330.0047)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin a/c gene (lmna, 150330.0047) | rel=r_associated | relid=0 | w=31
  1821. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the lamin b receptor gene (lbr, 600024.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin b receptor gene (lbr, 600024.0007) | rel=r_associated | relid=0 | w=31
  1822. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the laminin alpha-3 gene (lama3, 600805.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the laminin alpha-3 gene (lama3, 600805.0001) | rel=r_associated | relid=0 | w=31
  1823. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the laminin, alpha-1 gene (lama1, 150320.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the laminin, alpha-1 gene (lama1, 150320.0001) | rel=r_associated | relid=0 | w=31
  1824. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the latent transforming growth factor beta binding protein 2 gene (ltbp2, 602091.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the latent transforming growth factor beta binding protein 2 gene (ltbp2, 602091.0005) | rel=r_associated | relid=0 | w=31
  1825. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the leiomodin 3 (lmod3, 616112.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leiomodin 3 (lmod3, 616112.0001) | rel=r_associated | relid=0 | w=31
  1826. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the leucine-rich ppr motif-containing protein gene (lrpprc, 607544.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucine-rich ppr motif-containing protein gene (lrpprc, 607544.0001) | rel=r_associated | relid=0 | w=31
  1827. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the lipoic acid synthase gene (lias, 607031.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lipoic acid synthase gene (lias, 607031.0001) | rel=r_associated | relid=0 | w=31
  1828. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0001) | rel=r_associated | relid=0 | w=31
  1829. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the low-density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the low-density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0013) | rel=r_associated | relid=0 | w=31
  1830. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the mads box transcription enhancer factor 2, polypeptide a gene (mef2a, 600660.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mads box transcription enhancer factor 2, polypeptide a gene (mef2a, 600660.0001) | rel=r_associated | relid=0 | w=31
  1831. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the mannosyl-oligosaccharide glucosidase gene (mogs, 601336.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mannosyl-oligosaccharide glucosidase gene (mogs, 601336.0001) | rel=r_associated | relid=0 | w=31
  1832. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0009) | rel=r_associated | relid=0 | w=31
  1833. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the mhc class ii transactivator gene (mhc2ta, 600005.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mhc class ii transactivator gene (mhc2ta, 600005.0001) | rel=r_associated | relid=0 | w=31
  1834. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the micro rna 2861 gene (mir2861, 613405.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the micro rna 2861 gene (mir2861, 613405.0001) | rel=r_associated | relid=0 | w=31
  1835. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the microfibrillar-associated protein-5 gene (mfap5, 601103.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the microfibrillar-associated protein-5 gene (mfap5, 601103.0001) | rel=r_associated | relid=0 | w=31
  1836. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the microphthalmia-associated transcription factor gene (mitf, 156845.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the microphthalmia-associated transcription factor gene (mitf, 156845.0001) | rel=r_associated | relid=0 | w=31
  1837. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the mitochondrial complex i, subunit nd1 gene (mtnd1, 516000.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial complex i, subunit nd1 gene (mtnd1, 516000.0012) | rel=r_associated | relid=0 | w=31
  1838. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the mitochondrial rna-processing endoribonuclease (rmrp, 157660.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial rna-processing endoribonuclease (rmrp, 157660.0018) | rel=r_associated | relid=0 | w=31
  1839. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the mitochondrial transfer rna serine 1 gene (mtts1, 590080.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial transfer rna serine 1 gene (mtts1, 590080.0001) | rel=r_associated | relid=0 | w=31
  1840. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the mitochondrial trna-leucine 1 gene (mttl1, 590050.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial trna-leucine 1 gene (mttl1, 590050.0001) | rel=r_associated | relid=0 | w=31
  1841. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the mitogen-activated kinase kinase kinase 1 gene (map3k1, 600982.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitogen-activated kinase kinase kinase 1 gene (map3k1, 600982.0001) | rel=r_associated | relid=0 | w=31
  1842. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the monoamine oxidase a gene (maoa, 309850.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the monoamine oxidase a gene (maoa, 309850.0001) | rel=r_associated | relid=0 | w=31
  1843. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the muscarinic cholinergic receptor-3 gene (chrm3, 118494.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the muscarinic cholinergic receptor-3 gene (chrm3, 118494.0001) | rel=r_associated | relid=0 | w=31
  1844. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the myelin-oligodendrocyte glycoprotein (mog, 159465.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myelin-oligodendrocyte glycoprotein (mog, 159465.0001) | rel=r_associated | relid=0 | w=31
  1845. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the myeloproliferative leukemia virus oncogene (mpl, 159530.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myeloproliferative leukemia virus oncogene (mpl, 159530.0009) | rel=r_associated | relid=0 | w=31
  1846. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0006) | rel=r_associated | relid=0 | w=31
  1847. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the myotubularin gene (mtm1, 300415.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myotubularin gene (mtm1, 300415.0001). | rel=r_associated | relid=0 | w=31
  1848. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the n-acylsphingosine amidohydrolase 1 gene (asah1, 613468.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the n-acylsphingosine amidohydrolase 1 gene (asah1, 613468.0001) | rel=r_associated | relid=0 | w=31
  1849. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the n-glycanase 1 gene (ngly1, 610661.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the n-glycanase 1 gene (ngly1, 610661.0001) | rel=r_associated | relid=0 | w=31
  1850. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) flavoprotein 1 gene (ndufv1, 161015.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) flavoprotein 1 gene (ndufv1, 161015.0001) | rel=r_associated | relid=0 | w=31
  1851. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the nadh dehydrogenase, subunit 3 gene (mtnd3, 516002.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase, subunit 3 gene (mtnd3, 516002.0003) | rel=r_associated | relid=0 | w=31
  1852. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex, assembly factor 1 gene (ndufaf1, 606934.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex, assembly factor 1 gene (ndufaf1, 606934.0001) | rel=r_associated | relid=0 | w=31
  1853. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex, assembly factor 3 gene (ndufaf3, 612911.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex, assembly factor 3 gene (ndufaf3, 612911.0001) | rel=r_associated | relid=0 | w=31
  1854. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the nephrocystin 4 gene (nphp4, 607215.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nephrocystin 4 gene (nphp4, 607215.0006) | rel=r_associated | relid=0 | w=31
  1855. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the nipa-like domain-containing 4 gene (nipal4, 609383.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nipa-like domain-containing 4 gene (nipal4, 609383.0001) | rel=r_associated | relid=0 | w=31
  1856. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the nuclear receptor binding set domain protein 1 gene (nsd1, 606681.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear receptor binding set domain protein 1 gene (nsd1, 606681.0001) | rel=r_associated | relid=0 | w=31
  1857. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the nucleotide-binding oligomerization domain protein 2 gene (nod2, 605956.0004).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nucleotide-binding oligomerization domain protein 2 gene (nod2, 605956.0004). | rel=r_associated | relid=0 | w=31
  1858. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the otogelin-like protein gene (otogl, 614925.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the otogelin-like protein gene (otogl, 614925.0001) | rel=r_associated | relid=0 | w=31
  1859. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the pancreas/duodenum homeobox protein 1 gene (pdx1, 600733.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pancreas/duodenum homeobox protein 1 gene (pdx1, 600733.0001) | rel=r_associated | relid=0 | w=31
  1860. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the patatin-like phospholipase domain-containing protein 2 gene (pnpla2, 609059.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the patatin-like phospholipase domain-containing protein 2 gene (pnpla2, 609059.0001) | rel=r_associated | relid=0 | w=31
  1861. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the patatin-like phospholipase domain-containing protein 6 (pnpla6, 603197.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the patatin-like phospholipase domain-containing protein 6 (pnpla6, 603197.0004) | rel=r_associated | relid=0 | w=31
  1862. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the peptidyl-prolyl isomerase b gene (ppib, 123841.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peptidyl-prolyl isomerase b gene (ppib, 123841.0001) | rel=r_associated | relid=0 | w=31
  1863. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the peroxisome biogenesis factor-26 gene (pex26, 608666.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor-26 gene (pex26, 608666.0002) | rel=r_associated | relid=0 | w=31
  1864. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the plasma cholesteryl ester transfer protein gene (cetp, 118470.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the plasma cholesteryl ester transfer protein gene (cetp, 118470.0001) | rel=r_associated | relid=0 | w=31
  1865. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the platelet glycoprotein ib, alpha polypeptide, gene (gp1ba, 606672.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the platelet glycoprotein ib, alpha polypeptide, gene (gp1ba, 606672.0001) | rel=r_associated | relid=0 | w=31
  1866. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the podocin gene (nphs2, 604766.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the podocin gene (nphs2, 604766.0001) | rel=r_associated | relid=0 | w=31
  1867. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the polo-like kinase 4 gene (plk4, 605031.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polo-like kinase 4 gene (plk4, 605031.0001) | rel=r_associated | relid=0 | w=31
  1868. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the polycystin 2 gene (pkd2, 173910.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polycystin 2 gene (pkd2, 173910.0001) | rel=r_associated | relid=0 | w=31
  1869. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the polymerase i, rna, subunit c gene (polr1c, 610060.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polymerase i, rna, subunit c gene (polr1c, 610060.0001) | rel=r_associated | relid=0 | w=31
  1870. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the potassium channel tetramerization domain-containing 1 (kctd1, 613420.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium channel tetramerization domain-containing 1 (kctd1, 613420.0001) | rel=r_associated | relid=0 | w=31
  1871. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 10 gene (kcnj10, 602208.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 10 gene (kcnj10, 602208.0001) | rel=r_associated | relid=0 | w=31
  1872. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the potassium channel, subfamily t, member 1 gene (kcnt1, 608167.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium channel, subfamily t, member 1 gene (kcnt1, 608167.0005) | rel=r_associated | relid=0 | w=31
  1873. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 1 gene (kcnj1, 600359.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 1 gene (kcnj1, 600359.0001) | rel=r_associated | relid=0 | w=31
  1874. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the potassium voltage-gated channel, isk-related subfamily, member 1 gene (kcne1, 176261.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, isk-related subfamily, member 1 gene (kcne1, 176261.0001) | rel=r_associated | relid=0 | w=31
  1875. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the presenilin-1 gene (psen1, 104311.0023)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the presenilin-1 gene (psen1, 104311.0023) | rel=r_associated | relid=0 | w=31
  1876. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the protein s gene (psa, 176880.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein s gene (psa, 176880.0002) | rel=r_associated | relid=0 | w=31
  1877. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the purine-rich element-binding protein a gene (pura, 600473.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the purine-rich element-binding protein a gene (pura, 600473.0001) | rel=r_associated | relid=0 | w=31
  1878. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the putative protein o-mannosyltransferase 2 gene (pomt2, 607439.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the putative protein o-mannosyltransferase 2 gene (pomt2, 607439.0001) | rel=r_associated | relid=0 | w=31
  1879. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the pyridoxamine 5-prime-phosphate oxidase gene (pnpo, 603287.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pyridoxamine 5-prime-phosphate oxidase gene (pnpo, 603287.0001) | rel=r_associated | relid=0 | w=31
  1880. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the rab escort protein 1 gene (chm, 300390.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rab escort protein 1 gene (chm, 300390.0001) | rel=r_associated | relid=0 | w=31
  1881. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the rab6-interacting golgin gene (gorab, 607893.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rab6-interacting golgin gene (gorab, 607893.0001) | rel=r_associated | relid=0 | w=31
  1882. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ras-associated protein rab33b gene (rab33b, 605950.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ras-associated protein rab33b gene (rab33b, 605950.0001) | rel=r_associated | relid=0 | w=31
  1883. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ras-associated protein rab39b (300774.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ras-associated protein rab39b (300774.0001) | rel=r_associated | relid=0 | w=31
  1884. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ras-associated protein-28 gene (rab28, 612994.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ras-associated protein-28 gene (rab28, 612994.0001) | rel=r_associated | relid=0 | w=31
  1885. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the recombinase activating gene 1 (rag1, 179615.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the recombinase activating gene 1 (rag1, 179615.0005) | rel=r_associated | relid=0 | w=31
  1886. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the rho gdp-dissociation inhibitor alpha gene (arhgdia, 601925.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rho gdp-dissociation inhibitor alpha gene (arhgdia, 601925.0001) | rel=r_associated | relid=0 | w=31
  1887. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ring finger protein 125 gene (rnf125, 610432.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ring finger protein 125 gene (rnf125, 610432.0001) | rel=r_associated | relid=0 | w=31
  1888. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the rpgrip1-like gene (rpgrip1l, 610937.0005).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rpgrip1-like gene (rpgrip1l, 610937.0005). | rel=r_associated | relid=0 | w=31
  1889. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the s. cerevisiae homolog of the trna splicing endonuclease 2 gene (tsen2, 608753.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the s. cerevisiae homolog of the trna splicing endonuclease 2 gene (tsen2, 608753.0001) | rel=r_associated | relid=0 | w=31
  1890. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the scavenger receptor class f, member 2 gene (scarf2, 613619.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the scavenger receptor class f, member 2 gene (scarf2, 613619.0001) | rel=r_associated | relid=0 | w=31
  1891. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the serologically defined colon cancer antigen 8 gene (sdccag8, 613524.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the serologically defined colon cancer antigen 8 gene (sdccag8, 613524.0004) | rel=r_associated | relid=0 | w=31
  1892. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the sh3 domain and tetratricopeptide repeat domain 2 gene (sh3tc2, 608206.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sh3 domain and tetratricopeptide repeat domain 2 gene (sh3tc2, 608206.0005) | rel=r_associated | relid=0 | w=31
  1893. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the signal sequence receptor, delta gene (ssr4, 300090.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the signal sequence receptor, delta gene (ssr4, 300090.0001) | rel=r_associated | relid=0 | w=31
  1894. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the skeletal muscle alpha-1 actin gene (acta1, 102610.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the skeletal muscle alpha-1 actin gene (acta1, 102610.0011) | rel=r_associated | relid=0 | w=31
  1895. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the skeletal muscle chloride channel-1 gene (clcn1, 118425.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the skeletal muscle chloride channel-1 gene (clcn1, 118425.0001) | rel=r_associated | relid=0 | w=31
  1896. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the skeletal muscle receptor tyrosine kinase gene (musk, 601296.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the skeletal muscle receptor tyrosine kinase gene (musk, 601296.0001). | rel=r_associated | relid=0 | w=31
  1897. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the solute carrier family 16 (monocarboxylic acid transporter), member 1 (slc16a1, 600682.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 16 (monocarboxylic acid transporter), member 1 (slc16a1, 600682.0005) | rel=r_associated | relid=0 | w=31
  1898. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the solute carrier family 16, member 1 gene (slc16a1, 600682.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 16, member 1 gene (slc16a1, 600682.0003) | rel=r_associated | relid=0 | w=31
  1899. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the solute carrier family 19 (thiamine transporter), member 2 gene (slc19a2, 603941.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 19 (thiamine transporter), member 2 gene (slc19a2, 603941.0001) | rel=r_associated | relid=0 | w=31
  1900. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the solute carrier family 33 (acetyl-coa transporter), member 1 gene (slc33a1, 603690.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 33 (acetyl-coa transporter), member 1 gene (slc33a1, 603690.0001). | rel=r_associated | relid=0 | w=31
  1901. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the solute carrier family 5 (choline transporter), member 7 gene (slc5a7, 608761.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 5 (choline transporter), member 7 gene (slc5a7, 608761.0001) | rel=r_associated | relid=0 | w=31
  1902. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the solute carrier family 6 (dopamine neurotransmitter transporter), member 3 gene (slc6a3, 126455.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 6 (dopamine neurotransmitter transporter), member 3 gene (slc6a3, 126455.0002) | rel=r_associated | relid=0 | w=31
  1903. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene (slc7a7, 603593.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene (slc7a7, 603593.0001) | rel=r_associated | relid=0 | w=31
  1904. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the steroid sulfatase gene (sts, 300747.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the steroid sulfatase gene (sts, 300747.0001) | rel=r_associated | relid=0 | w=31
  1905. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the stromalin-3 gene (stag3, 608489.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the stromalin-3 gene (stag3, 608489.0001) | rel=r_associated | relid=0 | w=31
  1906. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the succinate dehydrogenase complex assembly factor-2 gene (sdhaf2, 613019.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the succinate dehydrogenase complex assembly factor-2 gene (sdhaf2, 613019.0001) | rel=r_associated | relid=0 | w=31
  1907. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the superkiller viralicidic activity 2-like, s. cerevisiae homolog gene (skiv2l, 600478.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the superkiller viralicidic activity 2-like, s. cerevisiae homolog gene (skiv2l, 600478.0001) | rel=r_associated | relid=0 | w=31
  1908. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the synaptotagmin 14 gene (syt14, 610949.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the synaptotagmin 14 gene (syt14, 610949.0001) | rel=r_associated | relid=0 | w=31
  1909. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the syntaxin-binding protein 1 gene (stxbp1, 602926.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the syntaxin-binding protein 1 gene (stxbp1, 602926.0001) | rel=r_associated | relid=0 | w=31
  1910. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the t-box 3 gene (tbx3, 601621.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the t-box 3 gene (tbx3, 601621.0001) | rel=r_associated | relid=0 | w=31
  1911. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the tau tubulin kinase 2 gene (ttbk2, 611695.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tau tubulin kinase 2 gene (ttbk2, 611695.0001) | rel=r_associated | relid=0 | w=31
  1912. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the tetratricopeptide repeat domain 19 gene (ttc19, 613814.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tetratricopeptide repeat domain 19 gene (ttc19, 613814.0001) | rel=r_associated | relid=0 | w=31
  1913. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the thyroid-stimulating hormone receptor gene (tshr, 603372.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thyroid-stimulating hormone receptor gene (tshr, 603372.0004) | rel=r_associated | relid=0 | w=31
  1914. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the thyroid-stimulating hormone receptor gene (tshr, 603372.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thyroid-stimulating hormone receptor gene (tshr, 603372.0005) | rel=r_associated | relid=0 | w=31
  1915. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the transcription factor ap2-alpha gene (tfap2a, 107580.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transcription factor ap2-alpha gene (tfap2a, 107580.0001) | rel=r_associated | relid=0 | w=31
  1916. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the transcription factor sp7 gene gene (sp7, 606633.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transcription factor sp7 gene gene (sp7, 606633.0001) | rel=r_associated | relid=0 | w=31
  1917. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the transglutaminase 6 gene (tgm6, 613900.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transglutaminase 6 gene (tgm6, 613900.0001) | rel=r_associated | relid=0 | w=31
  1918. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 3 gene (trpv3, 607066.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 3 gene (trpv3, 607066.0001) | rel=r_associated | relid=0 | w=31
  1919. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the transmembrane protein 15 gene (tmem15, 610746.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 15 gene (tmem15, 610746.0001) | rel=r_associated | relid=0 | w=31
  1920. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the triosephosphate isomerase-1 gene (tpi1, 190450.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the triosephosphate isomerase-1 gene (tpi1, 190450.0001) | rel=r_associated | relid=0 | w=31
  1921. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the tripartite motif-containing protein 2 gene (trim2, 614141.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tripartite motif-containing protein 2 gene (trim2, 614141.0001) | rel=r_associated | relid=0 | w=31
  1922. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the tumor necrosis factor receptor superfamily, member 13b gene (tnfrsf13b, 604907.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tumor necrosis factor receptor superfamily, member 13b gene (tnfrsf13b, 604907.0001) | rel=r_associated | relid=0 | w=31
  1923. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the tyrosine hydroxylase gene (th, 191290.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tyrosine hydroxylase gene (th, 191290.0001). | rel=r_associated | relid=0 | w=31
  1924. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ubiquilin 2 gene (ubqln2, 300264.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquilin 2 gene (ubqln2, 300264.0001) | rel=r_associated | relid=0 | w=31
  1925. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the ubiquinol-cytochrome c reductase-protein complex iii subunit vii gene (uqcrq, 612080.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquinol-cytochrome c reductase-protein complex iii subunit vii gene (uqcrq, 612080.0001) | rel=r_associated | relid=0 | w=31
  1926. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the uridine diphosphate glycosyltransferase 1 gene (ugt1, 191740.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the uridine diphosphate glycosyltransferase 1 gene (ugt1, 191740.0005) | rel=r_associated | relid=0 | w=31
  1927. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the v-ha-ras harvey rat sarcoma viral oncogene homolog gene (hras, 190020.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-ha-ras harvey rat sarcoma viral oncogene homolog gene (hras, 190020.0001) | rel=r_associated | relid=0 | w=31
  1928. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog gene (kit, 164920.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog gene (kit, 164920.0011) | rel=r_associated | relid=0 | w=31
  1929. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the vaccinia-related kinase 1 gene (vrk1, 602168.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the vaccinia-related kinase 1 gene (vrk1, 602168.0001) | rel=r_associated | relid=0 | w=31
  1930. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the vesicle-associated membrane protein-associated protein b gene (vapb, 605704.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the vesicle-associated membrane protein-associated protein b gene (vapb, 605704.0001) | rel=r_associated | relid=0 | w=31
  1931. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the voltage-gated sodium channel, type ix, alpha subunit gene (scn9a, 603415.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated sodium channel, type ix, alpha subunit gene (scn9a, 603415.0005) | rel=r_associated | relid=0 | w=31
  1932. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the voltage-gated sodium channel, type viii, alpha subunit gene (scn8a, 600702.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated sodium channel, type viii, alpha subunit gene (scn8a, 600702.0001) | rel=r_associated | relid=0 | w=31
  1933. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the von willebrand-cleaving protease gene (adamts13, 604134.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the von willebrand-cleaving protease gene (adamts13, 604134.0001) | rel=r_associated | relid=0 | w=31
  1934. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the wd repeat-containing planar cell polarity effector gene (wdpcp, 613580.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing planar cell polarity effector gene (wdpcp, 613580.0001) | rel=r_associated | relid=0 | w=31
  1935. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the wd repeat-containing protein 11 gene (wdr11, 606417.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein 11 gene (wdr11, 606417.0001) | rel=r_associated | relid=0 | w=31
  1936. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the zinc finger e box-binding homeobox 2 gene (zeb2, 605802.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger e box-binding homeobox 2 gene (zeb2, 605802.0001) | rel=r_associated | relid=0 | w=31
  1937. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutation in the zinc finger protein-141 gene (znf141, 194648.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger protein-141 gene (znf141, 194648.0001) | rel=r_associated | relid=0 | w=31
  1938. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in myeloproliferative leukemia virus oncogene (mpl, 159530.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in myeloproliferative leukemia virus oncogene (mpl, 159530.0001) | rel=r_associated | relid=0 | w=31
  1939. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the 17-beta-hydroxysteroid dehydrogenase iv gene (hsd17b4, 601860.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the 17-beta-hydroxysteroid dehydrogenase iv gene (hsd17b4, 601860.0001) | rel=r_associated | relid=0 | w=31
  1940. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the 25-hydroxyvitamin d3-1-alpha-hydroxylase gene (cyp27b1, 609506.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the 25-hydroxyvitamin d3-1-alpha-hydroxylase gene (cyp27b1, 609506.0001). | rel=r_associated | relid=0 | w=31
  1941. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the ataxin 7 gene (sca7, 607640.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the ataxin 7 gene (sca7, 607640.0001) | rel=r_associated | relid=0 | w=31
  1942. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0002) | rel=r_associated | relid=0 | w=31
  1943. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the cystic fibrosis transmembrane conductance regulator gene (cftr, 602421.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cystic fibrosis transmembrane conductance regulator gene (cftr, 602421.0001) | rel=r_associated | relid=0 | w=31
  1944. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the deafness/dystonia-1 gene (timm8a, 300356.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the deafness/dystonia-1 gene (timm8a, 300356.0001). | rel=r_associated | relid=0 | w=31
  1945. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the filamin c gene (flnc, 102565.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the filamin c gene (flnc, 102565.0001) | rel=r_associated | relid=0 | w=31
  1946. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0001) | rel=r_associated | relid=0 | w=31
  1947. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the heparan sulfate sulfatase gene (sgsh, 605270.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the heparan sulfate sulfatase gene (sgsh, 605270.0001) | rel=r_associated | relid=0 | w=31
  1948. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the kindlin 1 gene (kind1, 607900.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the kindlin 1 gene (kind1, 607900.0001) | rel=r_associated | relid=0 | w=31
  1949. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the mitochondrial atp synthase 6 gene (mtatp6, 516060.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the mitochondrial atp synthase 6 gene (mtatp6, 516060.0001) | rel=r_associated | relid=0 | w=31
  1950. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the parathyoid hormone receptor 1 gene (pthr1, 168468.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the parathyoid hormone receptor 1 gene (pthr1, 168468.0001) | rel=r_associated | relid=0 | w=31
  1951. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the peroxisomal acyl-coa oxidase gene (acox1, 609751.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the peroxisomal acyl-coa oxidase gene (acox1, 609751.0001) | rel=r_associated | relid=0 | w=31
  1952. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the peroxisomal biogenesis factor-7 gene (pex7, 601757.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the peroxisomal biogenesis factor-7 gene (pex7, 601757.0001) | rel=r_associated | relid=0 | w=31
  1953. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the procollagen i n-proteinase gene (adamts2, 604539.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the procollagen i n-proteinase gene (adamts2, 604539.0001) | rel=r_associated | relid=0 | w=31
  1954. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the recombinase activating gene 1 (rag1, 179615.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the recombinase activating gene 1 (rag1, 179615.0001) | rel=r_associated | relid=0 | w=31
  1955. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the solute carrier family 17 (sodium phosphate), member 5 gene (slc17a5, 604322.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the solute carrier family 17 (sodium phosphate), member 5 gene (slc17a5, 604322.0002) | rel=r_associated | relid=0 | w=31
  1956. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the succinate dehydrogenase complex subunit d gene (sdhd, 602690.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the succinate dehydrogenase complex subunit d gene (sdhd, 602690.0001) | rel=r_associated | relid=0 | w=31
  1957. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the t-box 4 gene (tbx4, 601719.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the t-box 4 gene (tbx4, 601719.0001) | rel=r_associated | relid=0 | w=31
  1958. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the t-box 5 gene (tbx5, 601620.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the t-box 5 gene (tbx5, 601620.0001) | rel=r_associated | relid=0 | w=31
  1959. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0018).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0018). | rel=r_associated | relid=0 | w=31
  1960. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by mutations in the wnt1-inducible signalling pathways protein 3 (wisp3, 603400.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the wnt1-inducible signalling pathways protein 3 (wisp3, 603400.0001) | rel=r_associated | relid=0 | w=31
  1961. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by simultaneous heterozygous mutation in both the never in mitosis gene a-related kinase 1 gene (nek1, 604588.0003) and the dynein, cytoplasmic-2, heavy chain-1 gene (dyn2ch1, 603297.0016)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by simultaneous heterozygous mutation in both the never in mitosis gene a-related kinase 1 gene (nek1, 604588.0003) and the dynein, cytoplasmic-2, heavy chain-1 gene (dyn2ch1, 603297.0016) | rel=r_associated | relid=0 | w=31
  1962. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:caused by trinucleotide repeat expansion (cag)n in the ataxin-3 gene (mjd, 607047.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by trinucleotide repeat expansion (cag)n in the ataxin-3 gene (mjd, 607047.0001) | rel=r_associated | relid=0 | w=31
  1963. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:contiguous duplication of 2.2mb on chromosome 17q23.1-q23.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous duplication of 2.2mb on chromosome 17q23.1-q23.2 | rel=r_associated | relid=0 | w=31
  1964. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:contiguous gene syndrome caused by duplication (269kb) on 9q21.11 including the tight junction protein 2 (tjp2, 607709) gene and the family with sequence similarity 189, member a2 (fam189a2, 607710) gene
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by duplication (269kb) on 9q21.11 including the tight junction protein 2 (tjp2, 607709) gene and the family with sequence similarity 189, member a2 (fam189a2, 607710) gene | rel=r_associated | relid=0 | w=31
  1965. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:contiguous gene syndrome caused by mosaicism for tetrasomy of chromosome 12p
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by mosaicism for tetrasomy of chromosome 12p | rel=r_associated | relid=0 | w=31
  1966. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:linked to locus at 17q12-q21.
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:linked to locus at 17q12-q21. | rel=r_associated | relid=0 | w=31
  1967. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:susceptibility conferred by mutation in the adaptor-related protein complex 1, sigma-3 subunit gene (ap1s3, 615781.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the adaptor-related protein complex 1, sigma-3 subunit gene (ap1s3, 615781.0001) | rel=r_associated | relid=0 | w=31
  1968. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:susceptibility conferred by mutation in the breast cancer 2 gene (brca2, 600185.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the breast cancer 2 gene (brca2, 600185.0001) | rel=r_associated | relid=0 | w=31
  1969. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:susceptibility conferred by mutation in the dynactin 1 gene (dctn1, 601143.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the dynactin 1 gene (dctn1, 601143.0002) | rel=r_associated | relid=0 | w=31
  1970. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:susceptibility conferred by mutation in the homolog of the s. pombe checkpoint kinase 2 gene (chek2, 604373.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the homolog of the s. pombe checkpoint kinase 2 gene (chek2, 604373.0007) | rel=r_associated | relid=0 | w=31
  1971. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:susceptibility conferred by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0013) | rel=r_associated | relid=0 | w=31
  1972. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:susceptibility conferred by mutation in the lamin b2 gene (lmnb2, 150341.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the lamin b2 gene (lmnb2, 150341.0001) | rel=r_associated | relid=0 | w=31
  1973. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:susceptibility conferred by mutation in the neuroligin-3 gene (nlgn3, 300336.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the neuroligin-3 gene (nlgn3, 300336.0001) | rel=r_associated | relid=0 | w=31
  1974. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 31 / 0.721 -> en:susceptibility conferred by mutations in the matrilin-3 gene (matn3, 602109.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutations in the matrilin-3 gene (matn3, 602109.0003) | rel=r_associated | relid=0 | w=31
  1975. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:a contiguous gene syndrome caused by deletion of 2.2 to 10.6mb of terminal 1p36
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome caused by deletion of 2.2 to 10.6mb of terminal 1p36 | rel=r_associated | relid=0 | w=30
  1976. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:a contiguous gene syndrome caused by deletion of the alpha-1 hemoglobin (141800) and alpha-2 hemoglobin (141850) genes
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome caused by deletion of the alpha-1 hemoglobin (141800) and alpha-2 hemoglobin (141850) genes | rel=r_associated | relid=0 | w=30
  1977. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by a 1.75 mb deletion at 15q24
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a 1.75 mb deletion at 15q24 | rel=r_associated | relid=0 | w=30
  1978. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by a 2.5- to 3.8-kb insertion containing pentanucleotide expansion repeats including (tggaa)n within an intron of the brain-expressed, associated with nedd4 gene (bean, 612051.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a 2.5- to 3.8-kb insertion containing pentanucleotide expansion repeats including (tggaa)n within an intron of the brain-expressed, associated with nedd4 gene (bean, 612051.0001) | rel=r_associated | relid=0 | w=30
  1979. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by a deletion of 11q23
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a deletion of 11q23 | rel=r_associated | relid=0 | w=30
  1980. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by a trinucleotide repeat expansion cag(n) in the junctophilin-3 gene (jph3, 605268.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a trinucleotide repeat expansion cag(n) in the junctophilin-3 gene (jph3, 605268.0001) | rel=r_associated | relid=0 | w=30
  1981. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by an expanded hexanucleotide repeat (ggggcc)n in the chromosome 9 open reading frame 72 gene (c9orf72, 614260.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by an expanded hexanucleotide repeat (ggggcc)n in the chromosome 9 open reading frame 72 gene (c9orf72, 614260.0001) | rel=r_associated | relid=0 | w=30
  1982. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by chromosomal mosaicism
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by chromosomal mosaicism | rel=r_associated | relid=0 | w=30
  1983. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by complex genomic rearrangement resulting in misexpression of the paired-like homeodomain transcription factor-1 gene (pitx1, 602149)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by complex genomic rearrangement resulting in misexpression of the paired-like homeodomain transcription factor-1 gene (pitx1, 602149) | rel=r_associated | relid=0 | w=30
  1984. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by contiguous gene deletion of imprinted region of 11p15.5
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by contiguous gene deletion of imprinted region of 11p15.5 | rel=r_associated | relid=0 | w=30
  1985. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by deletion (4.06 mb) of chromosome 14q22.1-q22.3
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion (4.06 mb) of chromosome 14q22.1-q22.3 | rel=r_associated | relid=0 | w=30
  1986. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by deletion of 1.0-2.5mb on chromosome 17q12
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion of 1.0-2.5mb on chromosome 17q12 | rel=r_associated | relid=0 | w=30
  1987. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by disruption of the calmodulin-binding transcription activator 1 gene (camta1, 611501.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by disruption of the calmodulin-binding transcription activator 1 gene (camta1, 611501.0001) | rel=r_associated | relid=0 | w=30
  1988. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by duplication of 294 kb to 2.7 mb including the prkaca gene on chromosome 19p13
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of 294 kb to 2.7 mb including the prkaca gene on chromosome 19p13 | rel=r_associated | relid=0 | w=30
  1989. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by microduplication of 3q29.
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by microduplication of 3q29. | rel=r_associated | relid=0 | w=30
  1990. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0005) and the gap junction protein, beta-6 gene (gjb6, 604418.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0005) and the gap junction protein, beta-6 gene (gjb6, 604418.0004) | rel=r_associated | relid=0 | w=30
  1991. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the 135-kd centrosomal protein gene (cep135, 611423.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 135-kd centrosomal protein gene (cep135, 611423.0001) | rel=r_associated | relid=0 | w=30
  1992. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the 155-kd nucleoporin gene (nup155, 606694.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 155-kd nucleoporin gene (nup155, 606694.0001) | rel=r_associated | relid=0 | w=30
  1993. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the 164-kd centrosomal protein gene (cep164, 614848.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 164-kd centrosomal protein gene (cep164, 614848.0001) | rel=r_associated | relid=0 | w=30
  1994. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the 3-prime repair exonuclease 1 gene (trex1, 606609.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 3-prime repair exonuclease 1 gene (trex1, 606609.0001) | rel=r_associated | relid=0 | w=30
  1995. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the 3-prime repair exonuclease 1 gene (trex1, 606609.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 3-prime repair exonuclease 1 gene (trex1, 606609.0008) | rel=r_associated | relid=0 | w=30
  1996. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the 83-kd centrosomal protein gene (cep83, 615847.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 83-kd centrosomal protein gene (cep83, 615847.0001) | rel=r_associated | relid=0 | w=30
  1997. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the acid phosphatase 5, tartrate resistant gene (acp5, 171640.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the acid phosphatase 5, tartrate resistant gene (acp5, 171640.0001) | rel=r_associated | relid=0 | w=30
  1998. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the aldolase a, fructose-bisphosphatase gene (aldoa, 103850.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aldolase a, fructose-bisphosphatase gene (aldoa, 103850.0001) | rel=r_associated | relid=0 | w=30
  1999. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the alpha subunit of the nonvoltage-gated sodium channel 1 gene (scnn1a, 600228.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha subunit of the nonvoltage-gated sodium channel 1 gene (scnn1a, 600228.0001) | rel=r_associated | relid=0 | w=30
  2000. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the alpha subunit of the type v voltage-gated sodium channel gene (scn5a, 600163.0034)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha subunit of the type v voltage-gated sodium channel gene (scn5a, 600163.0034) | rel=r_associated | relid=0 | w=30
  2001. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the angiopoietin-like 4 gene (angptl4, 605910.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the angiopoietin-like 4 gene (angptl4, 605910.0001) | rel=r_associated | relid=0 | w=30
  2002. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the apolipoprotein b gene (apob, 107730.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the apolipoprotein b gene (apob, 107730.0001) | rel=r_associated | relid=0 | w=30
  2003. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the armadillo repeat-containing protein 4 gene (armc4, 615408.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the armadillo repeat-containing protein 4 gene (armc4, 615408.0001) | rel=r_associated | relid=0 | w=30
  2004. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the atp-binding cassette, subfamily a, member 3 gene (abca3, 601615.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily a, member 3 gene (abca3, 601615.0001) | rel=r_associated | relid=0 | w=30
  2005. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the atp-binding cassette, subfamily b, member 11 gene (abcb11, 603201.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily b, member 11 gene (abcb11, 603201.0002) | rel=r_associated | relid=0 | w=30
  2006. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0016)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0016) | rel=r_associated | relid=0 | w=30
  2007. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the atpase type 13a2 gene (atp13a2, 610513.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase type 13a2 gene (atp13a2, 610513.0001) | rel=r_associated | relid=0 | w=30
  2008. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the atpase, ca++ dependent, slow-twitch, cardiac muscle-2 gene (atp2a2, 108740.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, ca++ dependent, slow-twitch, cardiac muscle-2 gene (atp2a2, 108740.0001) | rel=r_associated | relid=0 | w=30
  2009. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the atpase, cu++ transporting, beta polypeptide gene (atp7b, 277900.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, cu++ transporting, beta polypeptide gene (atp7b, 277900.0001) | rel=r_associated | relid=0 | w=30
  2010. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the atpase, h+ transporting, lysosomal, v0 subunit a2 gene (atp6v0a2, 611716.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, h+ transporting, lysosomal, v0 subunit a2 gene (atp6v0a2, 611716.0003) | rel=r_associated | relid=0 | w=30
  2011. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the b-cell adhesion molecule gene (bcam, 612773.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the b-cell adhesion molecule gene (bcam, 612773.0001) | rel=r_associated | relid=0 | w=30
  2012. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the bbs1 gene (bbs1, 209901.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bbs1 gene (bbs1, 209901.0001) | rel=r_associated | relid=0 | w=30
  2013. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0008) | rel=r_associated | relid=0 | w=30
  2014. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the beta-2 transforming growth factor gene (tgfb2, 190220.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-2 transforming growth factor gene (tgfb2, 190220.0001) | rel=r_associated | relid=0 | w=30
  2015. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the beta-3 gap junction protein gene (gjb3, 603324.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-3 gap junction protein gene (gjb3, 603324.0001) | rel=r_associated | relid=0 | w=30
  2016. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the beta-galactosidase gene (glb1, 611458.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-galactosidase gene (glb1, 611458.0009) | rel=r_associated | relid=0 | w=30
  2017. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the beta-mannosidase gene (manba, 609489.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-mannosidase gene (manba, 609489.0001) | rel=r_associated | relid=0 | w=30
  2018. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the blk nonreceptor tyrosine kinase gene (blk, 191305.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the blk nonreceptor tyrosine kinase gene (blk, 191305.0001) | rel=r_associated | relid=0 | w=30
  2019. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the brca1-associated protein 1 (bap1, 603089.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the brca1-associated protein 1 (bap1, 603089.0001) | rel=r_associated | relid=0 | w=30
  2020. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cadherin 3 gene (cdh3, 114021.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cadherin 3 gene (cdh3, 114021.0003) | rel=r_associated | relid=0 | w=30
  2021. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the calcium channel, voltage-dependent, p/q type, alpha 1a subunit gene (cacna1a, 601011.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calcium channel, voltage-dependent, p/q type, alpha 1a subunit gene (cacna1a, 601011.0005) | rel=r_associated | relid=0 | w=30
  2022. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the calsequestrin-2 gene (casq2, 114251.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calsequestrin-2 gene (casq2, 114251.0002) | rel=r_associated | relid=0 | w=30
  2023. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the camp-dependent protein kinase, catalytic, gamma gene (prkacg, 176893.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the camp-dependent protein kinase, catalytic, gamma gene (prkacg, 176893.0001) | rel=r_associated | relid=0 | w=30
  2024. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the carbohydrate sulfotransferase 8 gene (chst8, 610190.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carbohydrate sulfotransferase 8 gene (chst8, 610190.0001) | rel=r_associated | relid=0 | w=30
  2025. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the carbohydrate synthase 1 gene (chsy1, 608123.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carbohydrate synthase 1 gene (chsy1, 608123.0001) | rel=r_associated | relid=0 | w=30
  2026. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the carcinoembryonic antigen-related cell adhesion molecule-16 gene (ceacam16, 614591.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carcinoembryonic antigen-related cell adhesion molecule-16 gene (ceacam16, 614591.0001) | rel=r_associated | relid=0 | w=30
  2027. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cardiac myosin-binding protein-c gene (mybpc3, 600958.0024)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cardiac myosin-binding protein-c gene (mybpc3, 600958.0024) | rel=r_associated | relid=0 | w=30
  2028. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cardiac troponin i gene (tnni3, 191044.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cardiac troponin i gene (tnni3, 191044.0001) | rel=r_associated | relid=0 | w=30
  2029. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cartilage-associated protein gene (crtap, 605497.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cartilage-associated protein gene (crtap, 605497.0001) | rel=r_associated | relid=0 | w=30
  2030. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cbp/p300-interacting transactivator, with glu/asp-rich c-terminal domain, 2 gene (cited2, 602937.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cbp/p300-interacting transactivator, with glu/asp-rich c-terminal domain, 2 gene (cited2, 602937.0001) | rel=r_associated | relid=0 | w=30
  2031. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cd36 antigen gene (cd36, 173510.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd36 antigen gene (cd36, 173510.0001) | rel=r_associated | relid=0 | w=30
  2032. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cd96 gene (cd96, 606037.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd96 gene (cd96, 606037.0001) | rel=r_associated | relid=0 | w=30
  2033. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the centromeric protein j gene (cenpj, 609279.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the centromeric protein j gene (cenpj, 609279.0004) | rel=r_associated | relid=0 | w=30
  2034. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0001) | rel=r_associated | relid=0 | w=30
  2035. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the chmp family, member 1a gene (chmp1a, 164010.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chmp family, member 1a gene (chmp1a, 164010.0001) | rel=r_associated | relid=0 | w=30
  2036. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0001) | rel=r_associated | relid=0 | w=30
  2037. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the chromatin licensing and dna replication factor 1 gene (cdt1, 605525.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromatin licensing and dna replication factor 1 gene (cdt1, 605525.0001) | rel=r_associated | relid=0 | w=30
  2038. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the chromosome 10 open reading frame 11 gene (c10orf11, 614537.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 10 open reading frame 11 gene (c10orf11, 614537.0001) | rel=r_associated | relid=0 | w=30
  2039. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cln2 gene (cln2, 607998.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cln2 gene (cln2, 607998.0001) | rel=r_associated | relid=0 | w=30
  2040. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cln8 gene (cln8, 607837.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cln8 gene (cln8, 607837.0001) | rel=r_associated | relid=0 | w=30
  2041. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the coiled-coil-helix-coiled-coil-helix domain-containing protein 10 gene (chchd10, 615903.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil-helix-coiled-coil-helix domain-containing protein 10 gene (chchd10, 615903.0004) | rel=r_associated | relid=0 | w=30
  2042. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0002) | rel=r_associated | relid=0 | w=30
  2043. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0003) | rel=r_associated | relid=0 | w=30
  2044. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0018) | rel=r_associated | relid=0 | w=30
  2045. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the collagen iv, alpha-1 polypeptide gene (col4a1, 120130.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen iv, alpha-1 polypeptide gene (col4a1, 120130.0003) | rel=r_associated | relid=0 | w=30
  2046. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0001) | rel=r_associated | relid=0 | w=30
  2047. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0009).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0009). | rel=r_associated | relid=0 | w=30
  2048. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the collagen vi, alpha-2 gene (col6a2, 120240.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen vi, alpha-2 gene (col6a2, 120240.0011) | rel=r_associated | relid=0 | w=30
  2049. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the collagen xviii, alpha-1 polypeptide gene (col18a1, 120328.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen xviii, alpha-1 polypeptide gene (col18a1, 120328.0001) | rel=r_associated | relid=0 | w=30
  2050. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the collagen, type iv, alpha-6 gene (col4a6, 303631.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type iv, alpha-6 gene (col4a6, 303631.0002) | rel=r_associated | relid=0 | w=30
  2051. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the complex i, subunit nd5 gene (mtnd5, 516005.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complex i, subunit nd5 gene (mtnd5, 516005.0001) | rel=r_associated | relid=0 | w=30
  2052. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the component of oligomeric golgi complex 6 gene (cog6, 606977.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the component of oligomeric golgi complex 6 gene (cog6, 606977.0001) | rel=r_associated | relid=0 | w=30
  2053. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the contactin 1 gene (cntn1, 600016.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the contactin 1 gene (cntn1, 600016.0001) | rel=r_associated | relid=0 | w=30
  2054. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the coronin 1a gene (coro1a, 605000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coronin 1a gene (coro1a, 605000.0001) | rel=r_associated | relid=0 | w=30
  2055. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cytochrome b5a gene (cyb5a, 613218.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome b5a gene (cyb5a, 613218.0001) | rel=r_associated | relid=0 | w=30
  2056. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cytochrome p450, family 7, subfamily b, polypeptide 1 gene (cyp7b1, 603711.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450, family 7, subfamily b, polypeptide 1 gene (cyp7b1, 603711.0001) | rel=r_associated | relid=0 | w=30
  2057. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the cytotoxic t lymphocyte-associated 4 gene (ctla4, 123890.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytotoxic t lymphocyte-associated 4 gene (ctla4, 123890.0003) | rel=r_associated | relid=0 | w=30
  2058. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the dehydrogenase e1 and transketolase domains-containing protein 1 (dhtkd1, 614984.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dehydrogenase e1 and transketolase domains-containing protein 1 (dhtkd1, 614984.0004) | rel=r_associated | relid=0 | w=30
  2059. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the desmoglein 4 gene (dsg4, 607892.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the desmoglein 4 gene (dsg4, 607892.0001) | rel=r_associated | relid=0 | w=30
  2060. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the dis3 mitotic control, s. cerevisiae, homolog-like 2 gene (dis3l2, 614184.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dis3 mitotic control, s. cerevisiae, homolog-like 2 gene (dis3l2, 614184.0001) | rel=r_associated | relid=0 | w=30
  2061. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the discoidin domain receptor family, member 2 gene (ddr2, 191311.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the discoidin domain receptor family, member 2 gene (ddr2, 191311.0001) | rel=r_associated | relid=0 | w=30
  2062. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the disintegrin and metalloproteinase domain 17 gene (adam17, 603639.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the disintegrin and metalloproteinase domain 17 gene (adam17, 603639.0001) | rel=r_associated | relid=0 | w=30
  2063. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the distal-less homeobox-5 gene (dlx5, 600028.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the distal-less homeobox-5 gene (dlx5, 600028.0001) | rel=r_associated | relid=0 | w=30
  2064. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the dmx-like 2 gene (dmxl2, 612186.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dmx-like 2 gene (dmxl2, 612186.0001) | rel=r_associated | relid=0 | w=30
  2065. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 2 gene (dnajb2, 604139.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 2 gene (dnajb2, 604139.0001) | rel=r_associated | relid=0 | w=30
  2066. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the downstream of tyrosine kinase 7 gene (dok7, 610285.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the downstream of tyrosine kinase 7 gene (dok7, 610285.0001) | rel=r_associated | relid=0 | w=30
  2067. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0004).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0004). | rel=r_associated | relid=0 | w=30
  2068. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the dynein, axonemal, light chain 1 gene (dnal1, 610062.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynein, axonemal, light chain 1 gene (dnal1, 610062.0001) | rel=r_associated | relid=0 | w=30
  2069. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the dynein, cytoplasmic 1, heavy chain 1 gene (dync1h1, 600112.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynein, cytoplasmic 1, heavy chain 1 gene (dync1h1, 600112.0002) | rel=r_associated | relid=0 | w=30
  2070. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the dystrophin gene (dmd, 300377.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dystrophin gene (dmd, 300377.0002) | rel=r_associated | relid=0 | w=30
  2071. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the dystrophin-associated glycoprotein 1 gene (dag1, 128239.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dystrophin-associated glycoprotein 1 gene (dag1, 128239.0001) | rel=r_associated | relid=0 | w=30
  2072. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the early growth response-2 gene (egr2, 129010.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the early growth response-2 gene (egr2, 129010.0001) | rel=r_associated | relid=0 | w=30
  2073. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the endothelin 3 (edn3, 131242.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endothelin 3 (edn3, 131242.0003) | rel=r_associated | relid=0 | w=30
  2074. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the endothelin 3 gene (edn3, 131242.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endothelin 3 gene (edn3, 131242.0004) | rel=r_associated | relid=0 | w=30
  2075. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the epsilon-sarcoglycan gene (sgce, 604149.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the epsilon-sarcoglycan gene (sgce, 604149.0001) | rel=r_associated | relid=0 | w=30
  2076. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the eukaryotic translation elongation factor-2 gene (eef2, 130610.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation elongation factor-2 gene (eef2, 130610.0001) | rel=r_associated | relid=0 | w=30
  2077. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 4 gene (eif2b4, 606687.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 4 gene (eif2b4, 606687.0001) | rel=r_associated | relid=0 | w=30
  2078. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the evc gene (evc, 604831.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the evc gene (evc, 604831.0001) | rel=r_associated | relid=0 | w=30
  2079. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the eyes absent-1 gene (eya1, 601653.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eyes absent-1 gene (eya1, 601653.0001) | rel=r_associated | relid=0 | w=30
  2080. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the f-box and leucine-rich repeat protein 4 gene (fbxl4, 605654.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the f-box and leucine-rich repeat protein 4 gene (fbxl4, 605654.0001) | rel=r_associated | relid=0 | w=30
  2081. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the faciogenital dysplasia gene (fgd1, 300546.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the faciogenital dysplasia gene (fgd1, 300546.0001) | rel=r_associated | relid=0 | w=30
  2082. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the feline leukemia virus subgroup c receptor 2 gene (flvcr2, 610865.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the feline leukemia virus subgroup c receptor 2 gene (flvcr2, 610865.0001) | rel=r_associated | relid=0 | w=30
  2083. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0055)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0055) | rel=r_associated | relid=0 | w=30
  2084. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0010) | rel=r_associated | relid=0 | w=30
  2085. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0012) | rel=r_associated | relid=0 | w=30
  2086. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the fk506-binding protein 10 gene (fkbp10, 607093.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fk506-binding protein 10 gene (fkbp10, 607093.0002) | rel=r_associated | relid=0 | w=30
  2087. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the forkhead box g1 gene (foxg1, 164874.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead box g1 gene (foxg1, 164874.0001) | rel=r_associated | relid=0 | w=30
  2088. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0006).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0006). | rel=r_associated | relid=0 | w=30
  2089. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the fukutin gene (fktn, 607440.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fukutin gene (fktn, 607440.0009) | rel=r_associated | relid=0 | w=30
  2090. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the gamma-c-crystallin (crygc, 123680.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma-c-crystallin (crygc, 123680.0001) | rel=r_associated | relid=0 | w=30
  2091. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the gap junction, alpha-3, 46kd protein gene (gja3, 121015.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gap junction, alpha-3, 46kd protein gene (gja3, 121015.0001) | rel=r_associated | relid=0 | w=30
  2092. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0005) | rel=r_associated | relid=0 | w=30
  2093. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the gene encoding alpha-b crystallin (cryab, 123590.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding alpha-b crystallin (cryab, 123590.0002) | rel=r_associated | relid=0 | w=30
  2094. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the gene encoding homolog of drosophila nanos-1 (nanos1, 608226.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding homolog of drosophila nanos-1 (nanos1, 608226.0001) | rel=r_associated | relid=0 | w=30
  2095. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the glycine cleavage system h protein gene (gcsh, 238330.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycine cleavage system h protein gene (gcsh, 238330.0001) | rel=r_associated | relid=0 | w=30
  2096. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the glycogen branching enzyme gene (gbe1, 607839.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycogen branching enzyme gene (gbe1, 607839.0002) | rel=r_associated | relid=0 | w=30
  2097. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the gonadotropic-releasing hormone 1 gene (gnrh1, 152760.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gonadotropic-releasing hormone 1 gene (gnrh1, 152760.0001) | rel=r_associated | relid=0 | w=30
  2098. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the growth/differentiation factor 5 gene (gd5, 601146.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the growth/differentiation factor 5 gene (gd5, 601146.0005) | rel=r_associated | relid=0 | w=30
  2099. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the heat repeat-containing protein-2 gene (heatr2, 614864.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heat repeat-containing protein-2 gene (heatr2, 614864.0001) | rel=r_associated | relid=0 | w=30
  2100. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the hepatic growth factor gene (hgf, 142409.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hepatic growth factor gene (hgf, 142409.0001) | rel=r_associated | relid=0 | w=30
  2101. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the hepatic lipase gene (lipc, 151670.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hepatic lipase gene (lipc, 151670.0001) | rel=r_associated | relid=0 | w=30
  2102. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the hepatocyte cell adhesion molecule gene (hepacam, 611642.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hepatocyte cell adhesion molecule gene (hepacam, 611642.0001) | rel=r_associated | relid=0 | w=30
  2103. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the hepatocyte cell adhesion molecule gene (hepacam, 611642.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hepatocyte cell adhesion molecule gene (hepacam, 611642.0006) | rel=r_associated | relid=0 | w=30
  2104. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the hexokinase-1 gene (hk1, 142600.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hexokinase-1 gene (hk1, 142600.0003) | rel=r_associated | relid=0 | w=30
  2105. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the histidine triad nucleotide-binding protein 1 gene (hint1, 601314.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the histidine triad nucleotide-binding protein 1 gene (hint1, 601314.0001) | rel=r_associated | relid=0 | w=30
  2106. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the histidyl-trna synthetase 2 gene (hars2, 600783.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the histidyl-trna synthetase 2 gene (hars2, 600783.0001) | rel=r_associated | relid=0 | w=30
  2107. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homeo box gene expressed in es cells (hesx1, 601802.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeo box gene expressed in es cells (hesx1, 601802.0001) | rel=r_associated | relid=0 | w=30
  2108. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homeobox d13 gene (hoxd13, 142989.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeobox d13 gene (hoxd13, 142989.0001) | rel=r_associated | relid=0 | w=30
  2109. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homeobox-hb9 gene (hlxb9, 142994.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeobox-hb9 gene (hlxb9, 142994.0001) | rel=r_associated | relid=0 | w=30
  2110. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of drosophila odz-3 gene (odz3, 610083.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of drosophila odz-3 gene (odz3, 610083.0001) | rel=r_associated | relid=0 | w=30
  2111. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of drosophila sprouty-4 gene (spry4, 607984.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of drosophila sprouty-4 gene (spry4, 607984.0001) | rel=r_associated | relid=0 | w=30
  2112. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of s. cerevisiae atp-dependent dna helicase hfm1 gene (hfm1, 615684.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of s. cerevisiae atp-dependent dna helicase hfm1 gene (hfm1, 615684.0001) | rel=r_associated | relid=0 | w=30
  2113. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of s. cerevisiae fig4 gene (fig4, 609390.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of s. cerevisiae fig4 gene (fig4, 609390.0009) | rel=r_associated | relid=0 | w=30
  2114. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of the drosophila dicer 1 gene (dicer1, 606241.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila dicer 1 gene (dicer1, 606241.0001) | rel=r_associated | relid=0 | w=30
  2115. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of the drosophila mothers against decapentaplegic 9 gene (smad9, 603295.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila mothers against decapentaplegic 9 gene (smad9, 603295.0001) | rel=r_associated | relid=0 | w=30
  2116. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of the drosophila sine oculis-binding protein gene (sobp, 613667.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila sine oculis-binding protein gene (sobp, 613667.0001) | rel=r_associated | relid=0 | w=30
  2117. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of the drosophila snail 2 gene (snai2, 602150.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila snail 2 gene (snai2, 602150.0001) | rel=r_associated | relid=0 | w=30
  2118. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of the e. coli atp-dependent protease clpap, proteolytic subunit gene (clpp, 601119.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the e. coli atp-dependent protease clpap, proteolytic subunit gene (clpp, 601119.0001) | rel=r_associated | relid=0 | w=30
  2119. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of the e. coli mutl 1 gene (mlh1, 120436.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the e. coli mutl 1 gene (mlh1, 120436.0003) | rel=r_associated | relid=0 | w=30
  2120. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of the e. coli muts 2 gene (msh2, 609309.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the e. coli muts 2 gene (msh2, 609309.0014) | rel=r_associated | relid=0 | w=30
  2121. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of the mouse t brachyury gene (t, 601397.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse t brachyury gene (t, 601397.0002) | rel=r_associated | relid=0 | w=30
  2122. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of the s. cerevisiae alg3 gene (alg3, 608750.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae alg3 gene (alg3, 608750.0001) | rel=r_associated | relid=0 | w=30
  2123. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the homolog of the s. cerevisiae fig4 gene (fig4, 609390.0016)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae fig4 gene (fig4, 609390.0016) | rel=r_associated | relid=0 | w=30
  2124. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the host cell factor c1 gene (hcfc1, 300019.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the host cell factor c1 gene (hcfc1, 300019.0001) | rel=r_associated | relid=0 | w=30
  2125. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the human homolog of the drosophila 'patched' gene 1 (ptch1, 601309.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the human homolog of the drosophila 'patched' gene 1 (ptch1, 601309.0001) | rel=r_associated | relid=0 | w=30
  2126. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the immunoglobulin mu-binding protein 2 gene (ighmbp2, 600502.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the immunoglobulin mu-binding protein 2 gene (ighmbp2, 600502.0010) | rel=r_associated | relid=0 | w=30
  2127. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the inositol polyphosphate phosphatase-like 1 gene (inppl1, 600829.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inositol polyphosphate phosphatase-like 1 gene (inppl1, 600829.0001) | rel=r_associated | relid=0 | w=30
  2128. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the insulin-like growth factor-binding protein-7 gene (igfbp7, 602867.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the insulin-like growth factor-binding protein-7 gene (igfbp7, 602867.0001) | rel=r_associated | relid=0 | w=30
  2129. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the integrin alpha-7 gene (itga7, 600536.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the integrin alpha-7 gene (itga7, 600536.0001) | rel=r_associated | relid=0 | w=30
  2130. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the interferon-induced transmembrane protein 5 gene (ifitm5, 614757.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interferon-induced transmembrane protein 5 gene (ifitm5, 614757.0001) | rel=r_associated | relid=0 | w=30
  2131. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the interleukin 11 receptor alpha gene (il11ra, 600939.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interleukin 11 receptor alpha gene (il11ra, 600939.0001) | rel=r_associated | relid=0 | w=30
  2132. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the interleukin 21 gene (il21, 605384.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interleukin 21 gene (il21, 605384.0001) | rel=r_associated | relid=0 | w=30
  2133. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the interleukin receptor gamma chain gene (il2rg, 308380.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interleukin receptor gamma chain gene (il2rg, 308380.0001) | rel=r_associated | relid=0 | w=30
  2134. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the intestinal zinc-specific transporter gene (slc39a4, 607059.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the intestinal zinc-specific transporter gene (slc39a4, 607059.0001) | rel=r_associated | relid=0 | w=30
  2135. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the inversin gene (invs, 243305.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inversin gene (invs, 243305.0001) | rel=r_associated | relid=0 | w=30
  2136. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the isoprenoid synthase domain-containing protein gene (ispd, 614631.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the isoprenoid synthase domain-containing protein gene (ispd, 614631.0001) | rel=r_associated | relid=0 | w=30
  2137. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the isovaleryl co-a dehydrogenase gene (ivd, 607036.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the isovaleryl co-a dehydrogenase gene (ivd, 607036.0001) | rel=r_associated | relid=0 | w=30
  2138. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the junctophilin-2 gene (jph2, 605267.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the junctophilin-2 gene (jph2, 605267.0001) | rel=r_associated | relid=0 | w=30
  2139. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the keratin 16 gene (krt16, 148068.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 16 gene (krt16, 148068.0002) | rel=r_associated | relid=0 | w=30
  2140. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the keratin 85 gene (krt85, 602767.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 85 gene (krt85, 602767.0001) | rel=r_associated | relid=0 | w=30
  2141. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the kinesin family member 1a gene (kif1a, 601255.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 1a gene (kif1a, 601255.0002) | rel=r_associated | relid=0 | w=30
  2142. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the kinesin family member 1c gene (kif1c, 603060.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 1c gene (kif1c, 603060.0001) | rel=r_associated | relid=0 | w=30
  2143. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the kinesin family member 4a gene (kif4a, 300521.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin family member 4a gene (kif4a, 300521.0001) | rel=r_associated | relid=0 | w=30
  2144. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the kiss1 metastasis suppressor gene (kiss1, 603286.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kiss1 metastasis suppressor gene (kiss1, 603286.0001) | rel=r_associated | relid=0 | w=30
  2145. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the lactate dehydrogenase a gene (ldha, 150000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lactate dehydrogenase a gene (ldha, 150000.0001) | rel=r_associated | relid=0 | w=30
  2146. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the low density lipoprotein receptor-related protein-5 gene (lrp5, 603506.0020)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the low density lipoprotein receptor-related protein-5 gene (lrp5, 603506.0020) | rel=r_associated | relid=0 | w=30
  2147. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the lyr motif-containing protein 4 gene (lyrm4, 613311.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lyr motif-containing protein 4 gene (lyrm4, 613311.0001) | rel=r_associated | relid=0 | w=30
  2148. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the magnesium-dependent protein phosphatase 2c gene (ppm2c, 605993.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the magnesium-dependent protein phosphatase 2c gene (ppm2c, 605993.0001). | rel=r_associated | relid=0 | w=30
  2149. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the matrin-3 gene (matr3, 164017.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the matrin-3 gene (matr3, 164017.0001) | rel=r_associated | relid=0 | w=30
  2150. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the matrix gla protein gene (mgp, 154870.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the matrix gla protein gene (mgp, 154870.0001) | rel=r_associated | relid=0 | w=30
  2151. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the member-5 subfamily-j inwardly rectifying potassium channel gene (kcnj5, 600734.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the member-5 subfamily-j inwardly rectifying potassium channel gene (kcnj5, 600734.0002) | rel=r_associated | relid=0 | w=30
  2152. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0006) | rel=r_associated | relid=0 | w=30
  2153. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the mitochondrial ribosomal protein s22 gene (mrps22, 605810.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial ribosomal protein s22 gene (mrps22, 605810.0001) | rel=r_associated | relid=0 | w=30
  2154. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the mitochondrial transfer rna serine 2 gene (mtts2, 590085.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial transfer rna serine 2 gene (mtts2, 590085.0002) | rel=r_associated | relid=0 | w=30
  2155. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the mitochondrial transfer rna-leucine gene (mttl1, 590050.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial transfer rna-leucine gene (mttl1, 590050.0001) | rel=r_associated | relid=0 | w=30
  2156. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the mothers against decapentaplegic, drosophila, homolog of, 6 gene (smad6, 602931.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mothers against decapentaplegic, drosophila, homolog of, 6 gene (smad6, 602931.0001) | rel=r_associated | relid=0 | w=30
  2157. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the myelin protein zero gene (mpz, 159440.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0018) | rel=r_associated | relid=0 | w=30
  2158. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the myosin heavy chain 11 gene (myh11, 160745.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin heavy chain 11 gene (myh11, 160745.0001) | rel=r_associated | relid=0 | w=30
  2159. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the myosin heavy chain 3 gene (myh3, 160720.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin heavy chain 3 gene (myh3, 160720.0005) | rel=r_associated | relid=0 | w=30
  2160. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, alpha/beta subunits gene (gnptab, 607840.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, alpha/beta subunits gene (gnptab, 607840.0001) | rel=r_associated | relid=0 | w=30
  2161. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex 10 gene (ndufa10, 603835.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex 10 gene (ndufa10, 603835.0001) | rel=r_associated | relid=0 | w=30
  2162. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the nephrocystin 3 gene (nphp3, 608002.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nephrocystin 3 gene (nphp3, 608002.0004) | rel=r_associated | relid=0 | w=30
  2163. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the neutrophil cytosolic factor 4 gene (ncf4, 601488.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neutrophil cytosolic factor 4 gene (ncf4, 601488.0001) | rel=r_associated | relid=0 | w=30
  2164. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the nlr family, caspase recruitment domain-containing 4 gene (nlrc4, 606831.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nlr family, caspase recruitment domain-containing 4 gene (nlrc4, 606831.0003) | rel=r_associated | relid=0 | w=30
  2165. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the nol1/nop2/sun domain family, member 2 gene nsun2 (610916.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nol1/nop2/sun domain family, member 2 gene nsun2 (610916.0001) | rel=r_associated | relid=0 | w=30
  2166. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the nonerythrocytic beta-spectrin 2 gene (sptbn2, 604985.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nonerythrocytic beta-spectrin 2 gene (sptbn2, 604985.0004) | rel=r_associated | relid=0 | w=30
  2167. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the nuclear-encoded mitochondrial dna polymerase-gamma gene (polg, 174763.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear-encoded mitochondrial dna polymerase-gamma gene (polg, 174763.0008) | rel=r_associated | relid=0 | w=30
  2168. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the nyctalopin gene (nyx, 300278.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nyctalopin gene (nyx, 300278.0001) | rel=r_associated | relid=0 | w=30
  2169. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the o-phosphoserine trna-selenocysteine trna synthase gene (sepsecs, 613009.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the o-phosphoserine trna-selenocysteine trna synthase gene (sepsecs, 613009.0001) | rel=r_associated | relid=0 | w=30
  2170. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ofd1 protein gene (ofd1, 300170.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ofd1 protein gene (ofd1, 300170.0001) | rel=r_associated | relid=0 | w=30
  2171. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the otogelin gene (otog, 064487.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the otogelin gene (otog, 064487.0001) | rel=r_associated | relid=0 | w=30
  2172. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the palladin gene (pldn, 604310.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the palladin gene (pldn, 604310.0001) | rel=r_associated | relid=0 | w=30
  2173. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the patatin-like phospholipase domain-containing protein 6 (pnpla6, 603197.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the patatin-like phospholipase domain-containing protein 6 (pnpla6, 603197.0001) | rel=r_associated | relid=0 | w=30
  2174. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the peroxisome biogenesis factor-2 gene (pex2, 170993.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor-2 gene (pex2, 170993.0001) | rel=r_associated | relid=0 | w=30
  2175. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the peroxisome biogenesis factor-3 gene (pex3, 603164.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor-3 gene (pex3, 603164.0001) | rel=r_associated | relid=0 | w=30
  2176. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the phosphatidylinositol 3-kinase, catalytic subunit delta gene (pik3cd, 602839.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol 3-kinase, catalytic subunit delta gene (pik3cd, 602839.0001) | rel=r_associated | relid=0 | w=30
  2177. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the phosphatidylinositol glycan, class n gene (pign, 606097.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol glycan, class n gene (pign, 606097.0001) | rel=r_associated | relid=0 | w=30
  2178. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the phospholipase c, beta-4 gene (plcb4, 600810.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phospholipase c, beta-4 gene (plcb4, 600810.0001) | rel=r_associated | relid=0 | w=30
  2179. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the plakoglobin gene (jup, 173325.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the plakoglobin gene (jup, 173325.0001) | rel=r_associated | relid=0 | w=30
  2180. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the platelet glycoprotein vi gene (gp6, 605546.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the platelet glycoprotein vi gene (gp6, 605546.0001) | rel=r_associated | relid=0 | w=30
  2181. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 5 gene (plekhg5, 611101.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 5 gene (plekhg5, 611101.0001) | rel=r_associated | relid=0 | w=30
  2182. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the post-gpi attachment to proteins 3 gene (pgap3, 611801.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the post-gpi attachment to proteins 3 gene (pgap3, 611801.0001) | rel=r_associated | relid=0 | w=30
  2183. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 13 gene (kcnj13, 603208.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 13 gene (kcnj13, 603208.0002) | rel=r_associated | relid=0 | w=30
  2184. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the potassium voltage-gated channel, subfamily h, member 2 gene or human ether-a-go-go related gene (kcnh2, 152427.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, subfamily h, member 2 gene or human ether-a-go-go related gene (kcnh2, 152427.0001) | rel=r_associated | relid=0 | w=30
  2185. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the presenilin-1 gene (psen1, 104311.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the presenilin-1 gene (psen1, 104311.0001) | rel=r_associated | relid=0 | w=30
  2186. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the presenilin-1 gene (psen1, 104311.0027)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the presenilin-1 gene (psen1, 104311.0027) | rel=r_associated | relid=0 | w=30
  2187. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the prickle-like 1 gene (prickle1, 608500.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prickle-like 1 gene (prickle1, 608500.0001) | rel=r_associated | relid=0 | w=30
  2188. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the prickle-like 2 gene (prickle2, 608501.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prickle-like 2 gene (prickle2, 608501.0001) | rel=r_associated | relid=0 | w=30
  2189. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the prion protein gene (prnp, 176640.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prion protein gene (prnp, 176640.0010) | rel=r_associated | relid=0 | w=30
  2190. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the proliferating cell nuclear antigen gene (pcna, 176740.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the proliferating cell nuclear antigen gene (pcna, 176740.0001) | rel=r_associated | relid=0 | w=30
  2191. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the proline dehydrogenase gene (prodh, 606810.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the proline dehydrogenase gene (prodh, 606810.0001) | rel=r_associated | relid=0 | w=30
  2192. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the proline-rich transmembrane protein 2 gene (prrt2, 614386.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the proline-rich transmembrane protein 2 gene (prrt2, 614386.0001). | rel=r_associated | relid=0 | w=30
  2193. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the protease inhibitor 1 gene (pi, 107400.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protease inhibitor 1 gene (pi, 107400.0001) | rel=r_associated | relid=0 | w=30
  2194. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the proteasome maturation protein gene (pomp, 613386.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the proteasome maturation protein gene (pomp, 613386.0001) | rel=r_associated | relid=0 | w=30
  2195. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the protein kinase c, gamma polypeptide gene (prkcg, 176980.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein kinase c, gamma polypeptide gene (prkcg, 176980.0001) | rel=r_associated | relid=0 | w=30
  2196. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the protocadherin 15 gene (pcdh15, 605514.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protocadherin 15 gene (pcdh15, 605514.0001) | rel=r_associated | relid=0 | w=30
  2197. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the protocadherin-15 gene (pcdh15, 605514.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protocadherin-15 gene (pcdh15, 605514.0006) | rel=r_associated | relid=0 | w=30
  2198. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the pulmonary-associated surfactant protein b gene (sftpb, 178640.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pulmonary-associated surfactant protein b gene (sftpb, 178640.0001) | rel=r_associated | relid=0 | w=30
  2199. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the purinergic receptor p2y, g protein-coupled, 12 gene (p2ry12, 600515.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the purinergic receptor p2y, g protein-coupled, 12 gene (p2ry12, 600515.0001) | rel=r_associated | relid=0 | w=30
  2200. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the r-type arachidonate 12-lipoxygenase gene (alox12b, 603741.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the r-type arachidonate 12-lipoxygenase gene (alox12b, 603741.0001) | rel=r_associated | relid=0 | w=30
  2201. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ranbp-type and c3hc4-type zinc finger-containing 1 gene (rbck1, 610924.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ranbp-type and c3hc4-type zinc finger-containing 1 gene (rbck1, 610924.0001) | rel=r_associated | relid=0 | w=30
  2202. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ras and rab interactor 2 gene (rin2, 610222.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ras and rab interactor 2 gene (rin2, 610222.0001) | rel=r_associated | relid=0 | w=30
  2203. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ras-associated protein rab23 gene (rab23, 606144.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ras-associated protein rab23 gene (rab23, 606144.0001) | rel=r_associated | relid=0 | w=30
  2204. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ras-associated protein rab7 (602298.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ras-associated protein rab7 (602298.0001) | rel=r_associated | relid=0 | w=30
  2205. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the regulatory factor x, ankyrin repeat-containing gene (rfxank, 603200.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the regulatory factor x, ankyrin repeat-containing gene (rfxank, 603200.0001) | rel=r_associated | relid=0 | w=30
  2206. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the retinol-binding protein-3 gene (rbp3, 180920.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the retinol-binding protein-3 gene (rbp3, 180920.0001) | rel=r_associated | relid=0 | w=30
  2207. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the rho gtpase-activating protein 31 gene (arhgap31, 610911.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rho gtpase-activating protein 31 gene (arhgap31, 610911.0001) | rel=r_associated | relid=0 | w=30
  2208. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ribosomal protein l15 gene (rpl15, 604174.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribosomal protein l15 gene (rpl15, 604174.0001) | rel=r_associated | relid=0 | w=30
  2209. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ring finger protein 168 gene (rnf168, 612688.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ring finger protein 168 gene (rnf168, 612688.0001) | rel=r_associated | relid=0 | w=30
  2210. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the rna polymerase iii, subunit a gene (polr3a, 614258.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rna polymerase iii, subunit a gene (polr3a, 614258.0001) | rel=r_associated | relid=0 | w=30
  2211. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the s-antigen gene (sag, 181031.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the s-antigen gene (sag, 181031.0001) | rel=r_associated | relid=0 | w=30
  2212. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the sal-like 2 gene (sall2, 602219.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sal-like 2 gene (sall2, 602219.0001) | rel=r_associated | relid=0 | w=30
  2213. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the sal-like 4 gene (sall4, 607323.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sal-like 4 gene (sall4, 607323.0001) | rel=r_associated | relid=0 | w=30
  2214. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the sal-like 4 gene (sall4, 607343.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sal-like 4 gene (sall4, 607343.0013) | rel=r_associated | relid=0 | w=30
  2215. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the serine protease inhibitor, kunitz-type, 2 gene (spint2, 605124.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the serine protease inhibitor, kunitz-type, 2 gene (spint2, 605124.0001) | rel=r_associated | relid=0 | w=30
  2216. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the seryl-trna synthetase 2 gene (sars2, 612804.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the seryl-trna synthetase 2 gene (sars2, 612804.0001) | rel=r_associated | relid=0 | w=30
  2217. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the signal transducer and activator of transcription 1 gene (stat1, 600555.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the signal transducer and activator of transcription 1 gene (stat1, 600555.0008) | rel=r_associated | relid=0 | w=30
  2218. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the signal transducer and activator of transcription 3 gene (stat3, 102582.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the signal transducer and activator of transcription 3 gene (stat3, 102582.0008) | rel=r_associated | relid=0 | w=30
  2219. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the skeletal muscle chloride channel-1 gene (clcn1, 118425.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the skeletal muscle chloride channel-1 gene (clcn1, 118425.0002) | rel=r_associated | relid=0 | w=30
  2220. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the snf2-related cbp activatory protein gene (srcap, 611421.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the snf2-related cbp activatory protein gene (srcap, 611421.0001) | rel=r_associated | relid=0 | w=30
  2221. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the sodium channel, voltage-gated, type v, alpha subunit gene (scn5a, 600163.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sodium channel, voltage-gated, type v, alpha subunit gene (scn5a, 600163.0004) | rel=r_associated | relid=0 | w=30
  2222. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the solute carrier family 20 (phosphate transporter), member 2 gene (slc20a, 158378.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 20 (phosphate transporter), member 2 gene (slc20a, 158378.0001) | rel=r_associated | relid=0 | w=30
  2223. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene (slc24a4, 609840.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene (slc24a4, 609840.0002) | rel=r_associated | relid=0 | w=30
  2224. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the solute carrier family 33 (acetyl-coa transporter), member 1 gene (slc33a1, 603690.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 33 (acetyl-coa transporter), member 1 gene (slc33a1, 603690.0002) | rel=r_associated | relid=0 | w=30
  2225. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the solute carrier family 35, member c1 gene (slc35c1, 605881.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 35, member c1 gene (slc35c1, 605881.0001) | rel=r_associated | relid=0 | w=30
  2226. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the solute carrier family 52 (riboflavin transporter), member 2 gene (slc52a2, 607882.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 52 (riboflavin transporter), member 2 gene (slc52a2, 607882.0001) | rel=r_associated | relid=0 | w=30
  2227. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene (slc7a9, 604144.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene (slc7a9, 604144.0001) | rel=r_associated | relid=0 | w=30
  2228. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the solute carrier family 7, member 14 gene (slc7a14, 615720.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 7, member 14 gene (slc7a14, 615720.0001) | rel=r_associated | relid=0 | w=30
  2229. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the special at-rich sequence-binding protein 2 gene (satb2, 608148.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the special at-rich sequence-binding protein 2 gene (satb2, 608148.0001) | rel=r_associated | relid=0 | w=30
  2230. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the spectrin repeat-containing nuclear envelope protein 4 gene (syne4, 615535.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the spectrin repeat-containing nuclear envelope protein 4 gene (syne4, 615535.0001) | rel=r_associated | relid=0 | w=30
  2231. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the spectrin, alpha, erythrocytic-1 gene (spta1, 182860.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the spectrin, alpha, erythrocytic-1 gene (spta1, 182860.0001) | rel=r_associated | relid=0 | w=30
  2232. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the sprt-like n-terminal domain-protein gene (splrtn, 616086.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sprt-like n-terminal domain-protein gene (splrtn, 616086.0001) | rel=r_associated | relid=0 | w=30
  2233. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the sterile alpha motif domain-containing protein-9 gene (samd9, 610456.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sterile alpha motif domain-containing protein-9 gene (samd9, 610456.0001). | rel=r_associated | relid=0 | w=30
  2234. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the subunit 1 phosphatase of the c-terminal domain of rna polymerase ii subunit a gene (ctdp1, 604927.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the subunit 1 phosphatase of the c-terminal domain of rna polymerase ii subunit a gene (ctdp1, 604927.0001) | rel=r_associated | relid=0 | w=30
  2235. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the succinate dehydrogenase complex, subunit a, flavoprotein gene (sdha, 614165.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the succinate dehydrogenase complex, subunit a, flavoprotein gene (sdha, 614165.0005) | rel=r_associated | relid=0 | w=30
  2236. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0003) | rel=r_associated | relid=0 | w=30
  2237. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0004) | rel=r_associated | relid=0 | w=30
  2238. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0014) | rel=r_associated | relid=0 | w=30
  2239. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the telomerase rna component gene (terc, 602322.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the telomerase rna component gene (terc, 602322.0001) | rel=r_associated | relid=0 | w=30
  2240. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tenascin c gene (tnc, 187380.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tenascin c gene (tnc, 187380.0001) | rel=r_associated | relid=0 | w=30
  2241. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tetraspanin-12 gene (tspan12, 613138.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tetraspanin-12 gene (tspan12, 613138.0001) | rel=r_associated | relid=0 | w=30
  2242. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tetratricopeptide repeat domain 37 gene (ttc37, 614589.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tetratricopeptide repeat domain 37 gene (ttc37, 614589.0001) | rel=r_associated | relid=0 | w=30
  2243. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the thiopurine s-methyltransferase gene (tpmt, 187680.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thiopurine s-methyltransferase gene (tpmt, 187680.0001) | rel=r_associated | relid=0 | w=30
  2244. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the thioredoxin-like 4a gene (txnl4a, 611595.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thioredoxin-like 4a gene (txnl4a, 611595.0001) | rel=r_associated | relid=0 | w=30
  2245. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tight junction protein 2 gene (tjp2, 607709.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tight junction protein 2 gene (tjp2, 607709.0002) | rel=r_associated | relid=0 | w=30
  2246. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the transglutaminase 1 gene (tgm1, 190195.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transglutaminase 1 gene (tgm1, 190195.0001) | rel=r_associated | relid=0 | w=30
  2247. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the transthyretin gene (ttr, 176300.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transthyretin gene (ttr, 176300.0001) | rel=r_associated | relid=0 | w=30
  2248. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the trf1-interacting nuclear factor 2 gene (tinf2, 604319.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the trf1-interacting nuclear factor 2 gene (tinf2, 604319.0001) | rel=r_associated | relid=0 | w=30
  2249. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tripartite motif-containing 37 gene (trim37, 605073.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tripartite motif-containing 37 gene (trim37, 605073.0001) | rel=r_associated | relid=0 | w=30
  2250. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tropomyosin 2 gene (tpm2, 190990.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tropomyosin 2 gene (tpm2, 190990.0002) | rel=r_associated | relid=0 | w=30
  2251. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tubulin beta-1 gene (tubb1, 612901.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin beta-1 gene (tubb1, 612901.0001). | rel=r_associated | relid=0 | w=30
  2252. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tumor necrosis factor receptor superfamily, member 11a gene (tnfrsf11a, 603499.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tumor necrosis factor receptor superfamily, member 11a gene (tnfrsf11a, 603499.0001) | rel=r_associated | relid=0 | w=30
  2253. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tyrosinase gene (tyr, 606933.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tyrosinase gene (tyr, 606933.0001) | rel=r_associated | relid=0 | w=30
  2254. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the tyrosyl-trna synthetase 2 gene (yars2, 610957.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tyrosyl-trna synthetase 2 gene (yars2, 610957.0001) | rel=r_associated | relid=0 | w=30
  2255. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ubiquinol-cytochrome c reductase complex assembly factor 2 gene (uqcc2, 614461.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquinol-cytochrome c reductase complex assembly factor 2 gene (uqcc2, 614461.0001) | rel=r_associated | relid=0 | w=30
  2256. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ubiquitin carboxyl-terminal esterase l1 gene (uchl1, 191342.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquitin carboxyl-terminal esterase l1 gene (uchl1, 191342.0003) | rel=r_associated | relid=0 | w=30
  2257. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ubiquitin-conjugating enzyme e2a gene (ube2a, 312180.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquitin-conjugating enzyme e2a gene (ube2a, 312180.0001) | rel=r_associated | relid=0 | w=30
  2258. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ubiquitin-protein ligase e3 component n-recognin 1 gene (ubr1, 605981.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquitin-protein ligase e3 component n-recognin 1 gene (ubr1, 605981.0001) | rel=r_associated | relid=0 | w=30
  2259. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the ubiquitin-protein ligase e3b gene (ube3b, 608047.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquitin-protein ligase e3b gene (ube3b, 608047.0001) | rel=r_associated | relid=0 | w=30
  2260. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the valosin-containing protein gene (vcp, 601023.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the valosin-containing protein gene (vcp, 601023.0001) | rel=r_associated | relid=0 | w=30
  2261. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the vascular endothelial growth factor c gene (vegfc, 601528.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the vascular endothelial growth factor c gene (vegfc, 601528.0001) | rel=r_associated | relid=0 | w=30
  2262. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the very low density lipoprotein receptor (vldlr, 192977.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the very low density lipoprotein receptor (vldlr, 192977.0001) | rel=r_associated | relid=0 | w=30
  2263. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the voltage-gated potassium channel, shaw-related subfamily, member 3 gene (kcnc3, 176264.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated potassium channel, shaw-related subfamily, member 3 gene (kcnc3, 176264.0001) | rel=r_associated | relid=0 | w=30
  2264. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the voltage-gated sodium channel, type xi, alpha subunit gene (scn11a, 604385.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated sodium channel, type xi, alpha subunit gene (scn11a, 604385.0002) | rel=r_associated | relid=0 | w=30
  2265. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the zinc finger c4h2 domain-containing protein gene (zc4h2, 300897.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger c4h2 domain-containing protein gene (zc4h2, 300897.0001) | rel=r_associated | relid=0 | w=30
  2266. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the zinc finger fyve domain-containing protein 26 (zfyve26, 612012.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger fyve domain-containing protein 26 (zfyve26, 612012.0001). | rel=r_associated | relid=0 | w=30
  2267. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the zinc metalloproteinase ste24 gene (zmpste24, 606480.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc metalloproteinase ste24 gene (zmpste24, 606480.0001) | rel=r_associated | relid=0 | w=30
  2268. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in the zona pellucida glycoprotein-1 gene (zp1, 195000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zona pellucida glycoprotein-1 gene (zp1, 195000.0001) | rel=r_associated | relid=0 | w=30
  2269. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutation in tumor protein p53 (tp53, 191170.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in tumor protein p53 (tp53, 191170.0001) | rel=r_associated | relid=0 | w=30
  2270. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0001) | rel=r_associated | relid=0 | w=30
  2271. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the cd40 gene (tnfrsf5, 109535.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cd40 gene (tnfrsf5, 109535.0001). | rel=r_associated | relid=0 | w=30
  2272. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the cystathionase gene (cth, 607657.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cystathionase gene (cth, 607657.0001) | rel=r_associated | relid=0 | w=30
  2273. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the cystatin c gene (cst3, 604312.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cystatin c gene (cst3, 604312.0001) | rel=r_associated | relid=0 | w=30
  2274. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the interleukin-2 receptor, gamma chain, gene (il2rg, 308380.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the interleukin-2 receptor, gamma chain, gene (il2rg, 308380.0008) | rel=r_associated | relid=0 | w=30
  2275. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the leukemia inhibitory factor receptor gene (lifr, 151443.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the leukemia inhibitory factor receptor gene (lifr, 151443.0001) | rel=r_associated | relid=0 | w=30
  2276. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the lim homeo box transcription factor 1, beta gene (lmx1b, 602575.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the lim homeo box transcription factor 1, beta gene (lmx1b, 602575.0001) | rel=r_associated | relid=0 | w=30
  2277. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the nhs gene (nhs, 300457.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the nhs gene (nhs, 300457.0001) | rel=r_associated | relid=0 | w=30
  2278. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the nlr family, pyrin-domain containing 12 gene (nlrp12, 609648.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the nlr family, pyrin-domain containing 12 gene (nlrp12, 609648.0001) | rel=r_associated | relid=0 | w=30
  2279. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the pyrin gene (mefv, 608107.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the pyrin gene (mefv, 608107.0001) | rel=r_associated | relid=0 | w=30
  2280. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the req-like dna helicase type 4 gene (reql4, 603780.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the req-like dna helicase type 4 gene (reql4, 603780.0001) | rel=r_associated | relid=0 | w=30
  2281. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the tumor protein p63 gene (tp63, 603273.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the tumor protein p63 gene (tp63, 603273.0009) | rel=r_associated | relid=0 | w=30
  2282. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the vitamin d 25-hydroxylase gene (cyp2r1, 608713.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the vitamin d 25-hydroxylase gene (cyp2r1, 608713.0001) | rel=r_associated | relid=0 | w=30
  2283. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by mutations in the zinc finger transcription factor trps1 (trps1, 604386.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the zinc finger transcription factor trps1 (trps1, 604386.0001) | rel=r_associated | relid=0 | w=30
  2284. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by partial duplication of mtdna
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by partial duplication of mtdna | rel=r_associated | relid=0 | w=30
  2285. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by tandem duplication of the urinary plasminogen activator gene (plau, 191840.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by tandem duplication of the urinary plasminogen activator gene (plau, 191840.0002) | rel=r_associated | relid=0 | w=30
  2286. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:caused by trinucleotide repeat expansion (cag)n in the drpla gene (drpla, 607462.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by trinucleotide repeat expansion (cag)n in the drpla gene (drpla, 607462.0001) | rel=r_associated | relid=0 | w=30
  2287. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:contiguous gene syndrome caused by deletion (minimum 1.3mb) of chromosome 6pter-p24
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by deletion (minimum 1.3mb) of chromosome 6pter-p24 | rel=r_associated | relid=0 | w=30
  2288. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:contiguous gene syndrome caused by deletion of 3.2mb deletion on 8q22.1
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by deletion of 3.2mb deletion on 8q22.1 | rel=r_associated | relid=0 | w=30
  2289. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:contiguous gene syndrome caused by deletion of chromosome xq21 including at least the rab escort protein 1 gene (chm, 300390) and the pou domain, class 3, transcription factor 4 gene (pou3f4, 300039)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by deletion of chromosome xq21 including at least the rab escort protein 1 gene (chm, 300390) and the pou domain, class 3, transcription factor 4 gene (pou3f4, 300039) | rel=r_associated | relid=0 | w=30
  2290. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:contiguous gene syndrome caused by deletion on chromosome 22q11.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by deletion on chromosome 22q11.2 | rel=r_associated | relid=0 | w=30
  2291. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:remainder of cases secondary to maternal disomy
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:remainder of cases secondary to maternal disomy | rel=r_associated | relid=0 | w=30
  2292. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:susceptibility conferred by duplication of the homolog of the mouse t brachyury gene (t, 601397)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by duplication of the homolog of the mouse t brachyury gene (t, 601397) | rel=r_associated | relid=0 | w=30
  2293. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:susceptibility conferred by mutation in the complement factor h gene (chf, 134370.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the complement factor h gene (chf, 134370.0001) | rel=r_associated | relid=0 | w=30
  2294. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 30 / 0.698 -> en:susceptibility conferred by mutation in the soluble adenylyl cyclase gene (sac, 605205.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the soluble adenylyl cyclase gene (sac, 605205.0001) | rel=r_associated | relid=0 | w=30
  2295. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:a contiguous gene deletion syndrome involving deletion of 1.4mb on chromosome 17q11.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene deletion syndrome involving deletion of 1.4mb on chromosome 17q11.2 | rel=r_associated | relid=0 | w=29
  2296. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:a mutation in the homeobox d13 gene (hoxd13, 142989.0012) has been identified in 1 patient.
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a mutation in the homeobox d13 gene (hoxd13, 142989.0012) has been identified in 1 patient. | rel=r_associated | relid=0 | w=29
  2297. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:associated with mutation in the beta-1 catenin gene (ctnnb1, 116806.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:associated with mutation in the beta-1 catenin gene (ctnnb1, 116806.0013) | rel=r_associated | relid=0 | w=29
  2298. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:associated with mutation in the neuroligin-3 gene (nlgn3, 300336.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:associated with mutation in the neuroligin-3 gene (nlgn3, 300336.0001) | rel=r_associated | relid=0 | w=29
  2299. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by a 5.1-mb duplication of chromosome xq27.3-q28
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a 5.1-mb duplication of chromosome xq27.3-q28 | rel=r_associated | relid=0 | w=29
  2300. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by deletion of multiple genes in the mitochondrial dna
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion of multiple genes in the mitochondrial dna | rel=r_associated | relid=0 | w=29
  2301. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by duplication of 72 kb of 5q23.2 including at a minimum the lamin b1 gene (lmnb1, 150340.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of 72 kb of 5q23.2 including at a minimum the lamin b1 gene (lmnb1, 150340.0001) | rel=r_associated | relid=0 | w=29
  2302. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in both the opsin 1, long-wave-sensitive (red cone pigment) gene (opn1lw, 300822.0001) and opsin 1, medium-wave-sensitive (green cone pigment) gene (opn1mw, 300821.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in both the opsin 1, long-wave-sensitive (red cone pigment) gene (opn1lw, 300822.0001) and opsin 1, medium-wave-sensitive (green cone pigment) gene (opn1mw, 300821.0002) | rel=r_associated | relid=0 | w=29
  2303. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in glycoprotein 1b, platelet, alpha polypeptide (gp1ba, 606672.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in glycoprotein 1b, platelet, alpha polypeptide (gp1ba, 606672.0003) | rel=r_associated | relid=0 | w=29
  2304. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the 11-beta-hydroxysteroid dehydrogenase, type ii gene (hsd11b2, 614232.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 11-beta-hydroxysteroid dehydrogenase, type ii gene (hsd11b2, 614232.0001) | rel=r_associated | relid=0 | w=29
  2305. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the 24-dehydrocholesterol reductase gene (dhcr24, 606418.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 24-dehydrocholesterol reductase gene (dhcr24, 606418.0001) | rel=r_associated | relid=0 | w=29
  2306. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the 43-kd receptor-association protein of the synapse, gene (rapsn, 601592.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 43-kd receptor-association protein of the synapse, gene (rapsn, 601592.0013) | rel=r_associated | relid=0 | w=29
  2307. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the a disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 17 gene (adamts17, 607511.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the a disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 17 gene (adamts17, 607511.0001) | rel=r_associated | relid=0 | w=29
  2308. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the aarf domain-containing kinase 3 gene (adck3, 606980.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aarf domain-containing kinase 3 gene (adck3, 606980.0001) | rel=r_associated | relid=0 | w=29
  2309. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the abnormal spindle-like, microcephaly-associated gene (aspm, 605481.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the abnormal spindle-like, microcephaly-associated gene (aspm, 605481.0001) | rel=r_associated | relid=0 | w=29
  2310. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the adaptor-related protein complex 3, beta-1 subunit gene (ap3b1, 603401.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adaptor-related protein complex 3, beta-1 subunit gene (ap3b1, 603401.0001) | rel=r_associated | relid=0 | w=29
  2311. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the aicar formyltransferase/imp cyclohydrolase gene (atic, 601731.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aicar formyltransferase/imp cyclohydrolase gene (atic, 601731.0001) | rel=r_associated | relid=0 | w=29
  2312. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the alpha subunit of succinate-coenzyme a ligase (suclg1, 611224.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha subunit of succinate-coenzyme a ligase (suclg1, 611224.0001) | rel=r_associated | relid=0 | w=29
  2313. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the alpha-1 subunit of the glycine receptor gene (glra1, 138491.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1 subunit of the glycine receptor gene (glra1, 138491.0001) | rel=r_associated | relid=0 | w=29
  2314. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the alpha-b crystallin gene (cryab, 123590.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-b crystallin gene (cryab, 123590.0005) | rel=r_associated | relid=0 | w=29
  2315. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the alpha-methylacyl-coa racemase gene (amacr, 604489.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-methylacyl-coa racemase gene (amacr, 604489.0001) | rel=r_associated | relid=0 | w=29
  2316. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the amyloid beta (a4) precursor protein gene (app, 104760.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the amyloid beta (a4) precursor protein gene (app, 104760.0002) | rel=r_associated | relid=0 | w=29
  2317. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the anoctamin 5 gene (ano5, 608662.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the anoctamin 5 gene (ano5, 608662.0004) | rel=r_associated | relid=0 | w=29
  2318. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the apolipoprotein c-ii gene (apoc2, 608083.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the apolipoprotein c-ii gene (apoc2, 608083.0002) | rel=r_associated | relid=0 | w=29
  2319. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the aristaless-like 4, mouse, homolog of, gene (alx4, 605420.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aristaless-like 4, mouse, homolog of, gene (alx4, 605420.0008) | rel=r_associated | relid=0 | w=29
  2320. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the arylhydrocarbon-interacting receptor protein-like 1 gene (aipl1, 604392.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the arylhydrocarbon-interacting receptor protein-like 1 gene (aipl1, 604392.0001) | rel=r_associated | relid=0 | w=29
  2321. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the arylsulfatase a gene (arsa, 607574.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the arylsulfatase a gene (arsa, 607574.0003) | rel=r_associated | relid=0 | w=29
  2322. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the asparaginyl-trna synthetase 2 gene (nars2, 612803.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the asparaginyl-trna synthetase 2 gene (nars2, 612803.0001) | rel=r_associated | relid=0 | w=29
  2323. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the at-hook dna-binding motif-containing protein 1 gene (ahdc1, 615790.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the at-hook dna-binding motif-containing protein 1 gene (ahdc1, 615790.0001) | rel=r_associated | relid=0 | w=29
  2324. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the ataxia-telangiectasia and rad3-related gene (atr, 601215.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ataxia-telangiectasia and rad3-related gene (atr, 601215.0001) | rel=r_associated | relid=0 | w=29
  2325. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atlastin gene (spg3a, 606439.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atlastin gene (spg3a, 606439.0001) | rel=r_associated | relid=0 | w=29
  2326. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atp synthase 6 gene (mtatp6, 516060.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp synthase 6 gene (mtatp6, 516060.0001) | rel=r_associated | relid=0 | w=29
  2327. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atp synthase, h+ transporting, mitochondrial f1 complex, alpha subunit 1 gene (atp5a1, 164360.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp synthase, h+ transporting, mitochondrial f1 complex, alpha subunit 1 gene (atp5a1, 164360.0002) | rel=r_associated | relid=0 | w=29
  2328. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0002) | rel=r_associated | relid=0 | w=29
  2329. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0001) | rel=r_associated | relid=0 | w=29
  2330. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0001) | rel=r_associated | relid=0 | w=29
  2331. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atp-binding cassette, subfamily d, member 4 gene (abcd4, 603214.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily d, member 4 gene (abcd4, 603214.0001) | rel=r_associated | relid=0 | w=29
  2332. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atpase family gene 3-like 2 gene (afg3l2, 604581.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase family gene 3-like 2 gene (afg3l2, 604581.0010) | rel=r_associated | relid=0 | w=29
  2333. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0001) | rel=r_associated | relid=0 | w=29
  2334. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atpase, h+ transporting, lysosomal, accessory protein-2 gene (atp6ap2, 300556.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, h+ transporting, lysosomal, accessory protein-2 gene (atp6ap2, 300556.0001) | rel=r_associated | relid=0 | w=29
  2335. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the atpase, na+/k+ transporting, alpha-3 polypeptide (atp1a3, 182350.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, na+/k+ transporting, alpha-3 polypeptide (atp1a3, 182350.0014) | rel=r_associated | relid=0 | w=29
  2336. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the bbs4 gene (bbs4, 600374.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bbs4 gene (bbs4, 600374.0001) | rel=r_associated | relid=0 | w=29
  2337. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the bcl2-associated athanogene 3 gene (bag3, 603883.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bcl2-associated athanogene 3 gene (bag3, 603883.0001) | rel=r_associated | relid=0 | w=29
  2338. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the beta cardiac myosin heavy chain gene (myh7, 160760.0028)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta cardiac myosin heavy chain gene (myh7, 160760.0028) | rel=r_associated | relid=0 | w=29
  2339. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the beta-1 catenin gene (ctnnb1, 116806.0017)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1 catenin gene (ctnnb1, 116806.0017) | rel=r_associated | relid=0 | w=29
  2340. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the beta-1-galactosidase gene (glb1, 230500.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1-galactosidase gene (glb1, 230500.0004) | rel=r_associated | relid=0 | w=29
  2341. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the beta-2-microglobulin gene (b2m, 109700.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-2-microglobulin gene (b2m, 109700.0001) | rel=r_associated | relid=0 | w=29
  2342. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the bone morphogenetic protein 2 gene (bmp2, 112261.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bone morphogenetic protein 2 gene (bmp2, 112261.0001) | rel=r_associated | relid=0 | w=29
  2343. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cadherin 23 gene (cdh23, 605516.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cadherin 23 gene (cdh23, 605516.0005) | rel=r_associated | relid=0 | w=29
  2344. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the calcium- and integrin-binding protein 2 gene (cib2, 605564.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calcium- and integrin-binding protein 2 gene (cib2, 605564.0001) | rel=r_associated | relid=0 | w=29
  2345. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the camp-dependent regulatory subunit 1 of protein kinase a gene (prkar1a, 188830.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the camp-dependent regulatory subunit 1 of protein kinase a gene (prkar1a, 188830.0015) | rel=r_associated | relid=0 | w=29
  2346. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the camp-specific phosphodiesterase 4d gene (pde4d, 600129.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the camp-specific phosphodiesterase 4d gene (pde4d, 600129.0001) | rel=r_associated | relid=0 | w=29
  2347. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cardiac troponin i gene (tnni3, 191044.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cardiac troponin i gene (tnni3, 191044.0009) | rel=r_associated | relid=0 | w=29
  2348. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the carnitine palmitoyltransferase ia gene (cpt1a, 600528.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carnitine palmitoyltransferase ia gene (cpt1a, 600528.0001) | rel=r_associated | relid=0 | w=29
  2349. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cd79a antigen gene (cd79a, 112205.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd79a antigen gene (cd79a, 112205.0001) | rel=r_associated | relid=0 | w=29
  2350. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cd81 antigen gene (cd81, 186845.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd81 antigen gene (cd81, 186845.0001) | rel=r_associated | relid=0 | w=29
  2351. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the chloride channel-2 gene (clcn2, 600570.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chloride channel-2 gene (clcn2, 600570.0001) | rel=r_associated | relid=0 | w=29
  2352. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the chromodomain helicase dna-binding protein 7 gene (chd7, 608892.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromodomain helicase dna-binding protein 7 gene (chd7, 608892.0001) | rel=r_associated | relid=0 | w=29
  2353. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the chromosome 12 open reading frame 65 gene (c12orf65, 613541.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 12 open reading frame 65 gene (c12orf65, 613541.0001) | rel=r_associated | relid=0 | w=29
  2354. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the chromosome 15 open reading frame 41 gene (c15orf41, 615626.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 15 open reading frame 41 gene (c15orf41, 615626.0001) | rel=r_associated | relid=0 | w=29
  2355. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the chromosome 21 open reading frame 59 gene (c21orf59, 615494.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 21 open reading frame 59 gene (c21orf59, 615494.0001) | rel=r_associated | relid=0 | w=29
  2356. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the coagulation factor v gene (f5, 612309.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coagulation factor v gene (f5, 612309.0001) | rel=r_associated | relid=0 | w=29
  2357. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cofilin 2 gene (cfl2, 601443.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cofilin 2 gene (cfl2, 601443.0001) | rel=r_associated | relid=0 | w=29
  2358. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the coiled-coil domain-containing protein 111 gene (ccdc111, 615421.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil domain-containing protein 111 gene (ccdc111, 615421.0001) | rel=r_associated | relid=0 | w=29
  2359. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0017)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0017) | rel=r_associated | relid=0 | w=29
  2360. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the collagen iii, alpha-1 polypeptide gene (col3a1, 120180.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen iii, alpha-1 polypeptide gene (col3a1, 120180.0001) | rel=r_associated | relid=0 | w=29
  2361. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the collagen iv, alpha-1 polypeptide gene (col4a1, 120130.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen iv, alpha-1 polypeptide gene (col4a1, 120130.0007) | rel=r_associated | relid=0 | w=29
  2362. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0002).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0002). | rel=r_associated | relid=0 | w=29
  2363. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the collagen vi, alpha-1 polypeptide gene (col6a1, 120220.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen vi, alpha-1 polypeptide gene (col6a1, 120220.0001) | rel=r_associated | relid=0 | w=29
  2364. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the collagen vi, alpha-3 polypeptide gene (col6a3, 120250.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen vi, alpha-3 polypeptide gene (col6a3, 120250.0002) | rel=r_associated | relid=0 | w=29
  2365. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0002) | rel=r_associated | relid=0 | w=29
  2366. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0012) | rel=r_associated | relid=0 | w=29
  2367. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the collagen, type iv, alpha-1 gene (col4a1, 120130.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type iv, alpha-1 gene (col4a1, 120130.0001) | rel=r_associated | relid=0 | w=29
  2368. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a4, 120131.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a4, 120131.0003) | rel=r_associated | relid=0 | w=29
  2369. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the complex i, subunit nd1 gene (mtnd1, 516000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complex i, subunit nd1 gene (mtnd1, 516000.0001) | rel=r_associated | relid=0 | w=29
  2370. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the controller of the opn1lw and opn1mw genes (300824)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the controller of the opn1lw and opn1mw genes (300824) | rel=r_associated | relid=0 | w=29
  2371. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cullin 4b gene (cul4b, 300304.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cullin 4b gene (cul4b, 300304.0001) | rel=r_associated | relid=0 | w=29
  2372. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cyclin-dependent kinase inhibitor 1c gene (cdkn1c, 600856.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclin-dependent kinase inhibitor 1c gene (cdkn1c, 600856.0001) | rel=r_associated | relid=0 | w=29
  2373. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cystatin b gene (cstb, 601145.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cystatin b gene (cstb, 601145.0001) | rel=r_associated | relid=0 | w=29
  2374. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cytochrome b5 reductase 3 gene (cyb5r3, 613213.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome b5 reductase 3 gene (cyb5r3, 613213.0001) | rel=r_associated | relid=0 | w=29
  2375. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cytochrome c oxidase subunit vib, polypeptide 1 gene (cox6b1, 124089.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase subunit vib, polypeptide 1 gene (cox6b1, 124089.0001) | rel=r_associated | relid=0 | w=29
  2376. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cytochrome c oxidase, subunit viib gene (cox7b, 300885.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase, subunit viib gene (cox7b, 300885.0001) | rel=r_associated | relid=0 | w=29
  2377. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cytochrome p450 oxidoreductase gene (por, 124015.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450 oxidoreductase gene (por, 124015.0001) | rel=r_associated | relid=0 | w=29
  2378. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the cytochrome p450, subfamily xib, polypeptide 2 gene (cyp11b2, 124080.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450, subfamily xib, polypeptide 2 gene (cyp11b2, 124080.0001) | rel=r_associated | relid=0 | w=29
  2379. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the dead box polypeptide 59 gene (ddx59, 615464.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dead box polypeptide 59 gene (ddx59, 615464.0001) | rel=r_associated | relid=0 | w=29
  2380. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the dep domain-containing protein 5 gene (depdc, 614191.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dep domain-containing protein 5 gene (depdc, 614191.0001) | rel=r_associated | relid=0 | w=29
  2381. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the dihydroorotate dehydrogenase gene (dhodh, 126064.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dihydroorotate dehydrogenase gene (dhodh, 126064.0001) | rel=r_associated | relid=0 | w=29
  2382. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 5 gene (dnajc5, 611203.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 5 gene (dnajc5, 611203.0001) | rel=r_associated | relid=0 | w=29
  2383. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the dystrobrevin-binding protein 1 gene (dtnbp1, 607145.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dystrobrevin-binding protein 1 gene (dtnbp1, 607145.0001) | rel=r_associated | relid=0 | w=29
  2384. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the elastin gene (eln, 130160.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the elastin gene (eln, 130160.0008) | rel=r_associated | relid=0 | w=29
  2385. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the elongation of very long chain fatty acids-like 4 gene (elovl4, 605512.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the elongation of very long chain fatty acids-like 4 gene (elovl4, 605512.0007) | rel=r_associated | relid=0 | w=29
  2386. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the enamelin gene (enam, 606585.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the enamelin gene (enam, 606585.0001) | rel=r_associated | relid=0 | w=29
  2387. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the ethe1 gene (ethe1, 608451.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ethe1 gene (ethe1, 608451.0001) | rel=r_associated | relid=0 | w=29
  2388. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the ets2 repressor factor gene (erf, 611888.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ets2 repressor factor gene (erf, 611888.0001) | rel=r_associated | relid=0 | w=29
  2389. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 3 gene (eif2b3, 606273.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 3 gene (eif2b3, 606273.0001) | rel=r_associated | relid=0 | w=29
  2390. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the excision-repair cross-complementing group 8 gene (ercc8, 609412.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the excision-repair cross-complementing group 8 gene (ercc8, 609412.0006) | rel=r_associated | relid=0 | w=29
  2391. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the extracellular matrix protein 1 gene (ecm1, 602201.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the extracellular matrix protein 1 gene (ecm1, 602201.0001) | rel=r_associated | relid=0 | w=29
  2392. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the f-box only protein 7 gene (fbxo7, 605648.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the f-box only protein 7 gene (fbxo7, 605648.0001) | rel=r_associated | relid=0 | w=29
  2393. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the fad-dependent oxidoreductase domain-containing protein 1 gene (foxred1, 613622.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fad-dependent oxidoreductase domain-containing protein 1 gene (foxred1, 613622.0001) | rel=r_associated | relid=0 | w=29
  2394. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the family with sequence similarity 20, member c gene (fam20c, 611061.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the family with sequence similarity 20, member c gene (fam20c, 611061.0001) | rel=r_associated | relid=0 | w=29
  2395. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the fermitin family (drosophila) homolog 3 gene (fermt3, 607901.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fermitin family (drosophila) homolog 3 gene (fermt3, 607901.0001) | rel=r_associated | relid=0 | w=29
  2396. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0050)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0050) | rel=r_associated | relid=0 | w=29
  2397. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the fibroblast growth factor 20 gene (fgf20, 605558.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor 20 gene (fgf20, 605558.0002) | rel=r_associated | relid=0 | w=29
  2398. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the filamin b gene (flnb, 603381.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the filamin b gene (flnb, 603381.0006) | rel=r_associated | relid=0 | w=29
  2399. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the forkhead box f1 gene (foxf1, 601089.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead box f1 gene (foxf1, 601089.0001) | rel=r_associated | relid=0 | w=29
  2400. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the formin 2 gene (fmn2, 606373.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the formin 2 gene (fmn2, 606373.0001) | rel=r_associated | relid=0 | w=29
  2401. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0004).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0004). | rel=r_associated | relid=0 | w=29
  2402. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the fras1-related extracellular matrix protein 2 gene (frem2, 608945.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fras1-related extracellular matrix protein 2 gene (frem2, 608945.0001) | rel=r_associated | relid=0 | w=29
  2403. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the fras1-related extracellular matrix protein-1 gene (frem1, 608944.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fras1-related extracellular matrix protein-1 gene (frem1, 608944.0008) | rel=r_associated | relid=0 | w=29
  2404. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the fructose-1,6-bisphosphatase gene (fbp1, 611570.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fructose-1,6-bisphosphatase gene (fbp1, 611570.0001) | rel=r_associated | relid=0 | w=29
  2405. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the g-protein, alpha-stimulating 1 gene (gnas1, 139320.0035)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the g-protein, alpha-stimulating 1 gene (gnas1, 139320.0035) | rel=r_associated | relid=0 | w=29
  2406. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the gamma-aminobutyric acid (gaba) a receptor, gamma-2 gene (gabrg2, 137164.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma-aminobutyric acid (gaba) a receptor, gamma-2 gene (gabrg2, 137164.0003) | rel=r_associated | relid=0 | w=29
  2407. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the gap junction protein, beta-2, 26kd gene (gjb2, 121011.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gap junction protein, beta-2, 26kd gene (gjb2, 121011.0015) | rel=r_associated | relid=0 | w=29
  2408. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0006) | rel=r_associated | relid=0 | w=29
  2409. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the gdp-mannose pyrophosphorylase b gene (gmppb, 615320.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gdp-mannose pyrophosphorylase b gene (gmppb, 615320.0001) | rel=r_associated | relid=0 | w=29
  2410. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the gene encoding desmoglein-1 (dsg1, 125670.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding desmoglein-1 (dsg1, 125670.0001) | rel=r_associated | relid=0 | w=29
  2411. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the gene encoding growth/differentiation factor-g (gdf6, 601147.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding growth/differentiation factor-g (gdf6, 601147.0001) | rel=r_associated | relid=0 | w=29
  2412. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the glucokinase gene (gck, 138079.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glucokinase gene (gck, 138079.0009) | rel=r_associated | relid=0 | w=29
  2413. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the glyceronephosphate o-acyltransferase gene (gnpat, 602744.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glyceronephosphate o-acyltransferase gene (gnpat, 602744.0001) | rel=r_associated | relid=0 | w=29
  2414. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the glycyl trna synthetase gene (gars, 600287.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycyl trna synthetase gene (gars, 600287.0001) | rel=r_associated | relid=0 | w=29
  2415. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the growth/differentiation factor 6 gene (gdf6, 601147.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the growth/differentiation factor 6 gene (gdf6, 601147.0001) | rel=r_associated | relid=0 | w=29
  2416. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the hamartin gene (tsc1, 605284.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hamartin gene (tsc1, 605284.0001) | rel=r_associated | relid=0 | w=29
  2417. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the heat-shock 60-kd protein 1 gene (hspd1, 118190.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heat-shock 60-kd protein 1 gene (hspd1, 118190.0002) | rel=r_associated | relid=0 | w=29
  2418. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the heat-shock 60kd protein 1 gene (hspd1, 118190.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heat-shock 60kd protein 1 gene (hspd1, 118190.0001) | rel=r_associated | relid=0 | w=29
  2419. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the hemoglobin gamma b gene (hbg2, 142250.0026)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hemoglobin gamma b gene (hbg2, 142250.0026) | rel=r_associated | relid=0 | w=29
  2420. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the hepatocyte nuclear factor 4-alpha gene (hnf4a, 600281.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hepatocyte nuclear factor 4-alpha gene (hnf4a, 600281.0008) | rel=r_associated | relid=0 | w=29
  2421. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the histone deacetylase 4 gene (hdac4, 605314.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the histone deacetylase 4 gene (hdac4, 605314.0001) | rel=r_associated | relid=0 | w=29
  2422. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the homeobox d13 gene (hoxd13, 142989.0008).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeobox d13 gene (hoxd13, 142989.0008). | rel=r_associated | relid=0 | w=29
  2423. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the homolog of chlamydomonas intraflagellar transport 172 gene (ift172, 607386.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of chlamydomonas intraflagellar transport 172 gene (ift172, 607386.0001) | rel=r_associated | relid=0 | w=29
  2424. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the homolog of s. cerevisiae mediator of rna polymerase ii transcription, subunit 12 gene (med12, 300188.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of s. cerevisiae mediator of rna polymerase ii transcription, subunit 12 gene (med12, 300188.0001) | rel=r_associated | relid=0 | w=29
  2425. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the homolog of the a. nidulans nude 1 gene (nde1, 609449.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the a. nidulans nude 1 gene (nde1, 609449.0001) | rel=r_associated | relid=0 | w=29
  2426. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the homolog of the chlamydomonas radial spoke head 1 gene (rsph1, 609314.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the chlamydomonas radial spoke head 1 gene (rsph1, 609314.0001) | rel=r_associated | relid=0 | w=29
  2427. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the homolog of the drosophila notch, 3, gene (notch3, 600276.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila notch, 3, gene (notch3, 600276.0012) | rel=r_associated | relid=0 | w=29
  2428. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the homolog of the drosophila rogdi gene (rogdi, 614574.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila rogdi gene (rogdi, 614574.0001) | rel=r_associated | relid=0 | w=29
  2429. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the homolog of the e. coli elac 2 gene (elac2, 605367.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the e. coli elac 2 gene (elac2, 605367.0006) | rel=r_associated | relid=0 | w=29
  2430. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the homolog of the s. cerevisiae precursor mrna-processing factor-6 gene (prpf6, 613979.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae precursor mrna-processing factor-6 gene (prpf6, 613979.0001) | rel=r_associated | relid=0 | w=29
  2431. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the homolog of the s. cerevisiae rad51a gene (rad51a, 179617.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae rad51a gene (rad51a, 179617.0001) | rel=r_associated | relid=0 | w=29
  2432. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the human homolog of the mouse progressive ankylosis gene (ankh, 605145.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the human homolog of the mouse progressive ankylosis gene (ankh, 605145.0001) | rel=r_associated | relid=0 | w=29
  2433. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the hypoxanthine phosphoribosyltransferase gene (hprt1, 308000.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hypoxanthine phosphoribosyltransferase gene (hprt1, 308000.0004) | rel=r_associated | relid=0 | w=29
  2434. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the inhibitor of kappa light polypeptide gene enhancer in b cells, kinase complex-associated protein gene (ikbkap, 603722.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inhibitor of kappa light polypeptide gene enhancer in b cells, kinase complex-associated protein gene (ikbkap, 603722.0001) | rel=r_associated | relid=0 | w=29
  2435. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the inositol 1,4,5-triphosphate receptor 1 gene (itpr1, 147265.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inositol 1,4,5-triphosphate receptor 1 gene (itpr1, 147265.0003) | rel=r_associated | relid=0 | w=29
  2436. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the insulin-like growth factor-1 gene (igf1, 147440.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the insulin-like growth factor-1 gene (igf1, 147440.0001) | rel=r_associated | relid=0 | w=29
  2437. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the integrin, alpha-2b gene (itga2b, 607759.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the integrin, alpha-2b gene (itga2b, 607759.0002) | rel=r_associated | relid=0 | w=29
  2438. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the interleukin 7 receptor gene (il7r, 146661.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interleukin 7 receptor gene (il7r, 146661.0001) | rel=r_associated | relid=0 | w=29
  2439. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the interphotoreceptor matrix proteoglycan 2 gene (impg2, 607056.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interphotoreceptor matrix proteoglycan 2 gene (impg2, 607056.0001) | rel=r_associated | relid=0 | w=29
  2440. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the inverted formin 2 gene (inf2, 610982.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inverted formin 2 gene (inf2, 610982.0006) | rel=r_associated | relid=0 | w=29
  2441. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the keratin 5 gene (krt5, 148040.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 5 gene (krt5, 148040.0003) | rel=r_associated | relid=0 | w=29
  2442. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the kiaa1279 gene (kiaa1279, 609367.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kiaa1279 gene (kiaa1279, 609367.0001) | rel=r_associated | relid=0 | w=29
  2443. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the klotho gene (kl, 604824.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the klotho gene (kl, 604824.0002) | rel=r_associated | relid=0 | w=29
  2444. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the krupple-like factor 1 gene (klf1, 600599.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the krupple-like factor 1 gene (klf1, 600599.0006) | rel=r_associated | relid=0 | w=29
  2445. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the lamin a/c gene (lmna, 150330.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin a/c gene (lmna, 150330.0003) | rel=r_associated | relid=0 | w=29
  2446. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the lamin a/c gene (lmna, 150330.0021)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin a/c gene (lmna, 150330.0021) | rel=r_associated | relid=0 | w=29
  2447. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the laminin beta-2 gene (lamb2, 150325.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the laminin beta-2 gene (lamb2, 150325.0001) | rel=r_associated | relid=0 | w=29
  2448. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the leucine- and proline-enriched proteoglycan 1 gene (lepre1, 610339.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucine- and proline-enriched proteoglycan 1 gene (lepre1, 610339.0001) | rel=r_associated | relid=0 | w=29
  2449. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the leucine-rich repeats- and immunoglobulin-like domains-containing protein 2 gene (lrig2, 608869.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucine-rich repeats- and immunoglobulin-like domains-containing protein 2 gene (lrig2, 608869.0001) | rel=r_associated | relid=0 | w=29
  2450. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the light polypeptide neurofilament protein gene (nefl, 162280.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the light polypeptide neurofilament protein gene (nefl, 162280.0001) | rel=r_associated | relid=0 | w=29
  2451. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the lim domain binding 3 gene (ldb3, 605906.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lim domain binding 3 gene (ldb3, 605906.0005) | rel=r_associated | relid=0 | w=29
  2452. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0009) | rel=r_associated | relid=0 | w=29
  2453. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the lyr motif-containing protein 7 gene (lyrm7, 615831.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lyr motif-containing protein 7 gene (lyrm7, 615831.0001) | rel=r_associated | relid=0 | w=29
  2454. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the mastermind-like domain containing 1 gene (mamld1, 300120.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mastermind-like domain containing 1 gene (mamld1, 300120.0001) | rel=r_associated | relid=0 | w=29
  2455. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the melanocortin-2 receptor gene (mc2r, 607397.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the melanocortin-2 receptor gene (mc2r, 607397.0001) | rel=r_associated | relid=0 | w=29
  2456. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0001) | rel=r_associated | relid=0 | w=29
  2457. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0008) | rel=r_associated | relid=0 | w=29
  2458. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the mer tyrosine kinase protooncogene (mertk, 604705.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mer tyrosine kinase protooncogene (mertk, 604705.0001) | rel=r_associated | relid=0 | w=29
  2459. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the methionine synthase reductase gene (mtrr, 602568.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methionine synthase reductase gene (mtrr, 602568.0001) | rel=r_associated | relid=0 | w=29
  2460. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the methyl-cpg-binding protein-2 gene (mecp2, 300005.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methyl-cpg-binding protein-2 gene (mecp2, 300005.0001) | rel=r_associated | relid=0 | w=29
  2461. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the methyltransferase-like 23 gene (mettl23, 615262.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methyltransferase-like 23 gene (mettl23, 615262.0001) | rel=r_associated | relid=0 | w=29
  2462. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the microphthalmia-associated transcription factor gene (mitf, 156845.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the microphthalmia-associated transcription factor gene (mitf, 156845.0006) | rel=r_associated | relid=0 | w=29
  2463. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the mitochondrial complex i, subunit nd3 gene (mtnd3, 516002.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial complex i, subunit nd3 gene (mtnd3, 516002.0004) | rel=r_associated | relid=0 | w=29
  2464. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the mitochondrial complex i, subunit nd5 gene (mtnd5, 516005.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial complex i, subunit nd5 gene (mtnd5, 516005.0004) | rel=r_associated | relid=0 | w=29
  2465. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the mitochondrial glutamic acid transfer rna gene (mtte, 590025.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial glutamic acid transfer rna gene (mtte, 590025.0002) | rel=r_associated | relid=0 | w=29
  2466. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the mitochondrial ribosomal protein l3 gene (mrpl3, 607118.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial ribosomal protein l3 gene (mrpl3, 607118.0001) | rel=r_associated | relid=0 | w=29
  2467. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the mitochondrial transfer rna glutamine gene (mttq, 590030.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial transfer rna glutamine gene (mttq, 590030.0003) | rel=r_associated | relid=0 | w=29
  2468. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the mitochondrial transfer rna leucine 1 gene (mttl1, 590050.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial transfer rna leucine 1 gene (mttl1, 590050.0001) | rel=r_associated | relid=0 | w=29
  2469. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the mitogen-activated protein kinase kinase 1 gene (map2k2, 601263.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitogen-activated protein kinase kinase 1 gene (map2k2, 601263.0001) | rel=r_associated | relid=0 | w=29
  2470. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the multiple epidermal growth factor-like domains 10 gene (megf10, 612453.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the multiple epidermal growth factor-like domains 10 gene (megf10, 612453.0001) | rel=r_associated | relid=0 | w=29
  2471. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the myc-induced mitochondrial protein gene (mmtn, 609653.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myc-induced mitochondrial protein gene (mmtn, 609653.0001) | rel=r_associated | relid=0 | w=29
  2472. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the myelin protein zero gene (mpz, 159440.0017)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0017) | rel=r_associated | relid=0 | w=29
  2473. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the myelin protein zero gene (mpz, 159440.0021)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0021) | rel=r_associated | relid=0 | w=29
  2474. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the myogenic factor 6 gene (myf6, 159991.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myogenic factor 6 gene (myf6, 159991.0001) | rel=r_associated | relid=0 | w=29
  2475. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the myosin light chain kinase gene (mylk, 600922.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin light chain kinase gene (mylk, 600922.0001) | rel=r_associated | relid=0 | w=29
  2476. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the myosin, heavy chain 9, nonmuscle gene (myh9, 160775.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin, heavy chain 9, nonmuscle gene (myh9, 160775.0008) | rel=r_associated | relid=0 | w=29
  2477. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the myotilin gene (ttid, 604103.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myotilin gene (ttid, 604103.0006) | rel=r_associated | relid=0 | w=29
  2478. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the n-myc downstream regulated gene-1 (ndrg1, 605262.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the n-myc downstream regulated gene-1 (ndrg1, 605262.0001) | rel=r_associated | relid=0 | w=29
  2479. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the nad(p)h steroid dehydrogenase-like protein (nsdhl, 300275.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nad(p)h steroid dehydrogenase-like protein (nsdhl, 300275.0007) | rel=r_associated | relid=0 | w=29
  2480. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) flavoprotein 2 gene (ndufv2, 600532.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) flavoprotein 2 gene (ndufv2, 600532.0001) | rel=r_associated | relid=0 | w=29
  2481. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the nadh dehydrogenase, subunit 2 gene (mtnd2, 516001.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase, subunit 2 gene (mtnd2, 516001.0006) | rel=r_associated | relid=0 | w=29
  2482. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex 11 gene (ndufa11, 612638.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex 11 gene (ndufa11, 612638.0001) | rel=r_associated | relid=0 | w=29
  2483. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 10 gene (ndufa10, 603835.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 10 gene (ndufa10, 603835.0001) | rel=r_associated | relid=0 | w=29
  2484. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 2 gene (ndufa2, 602137.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 2 gene (ndufa2, 602137.0001) | rel=r_associated | relid=0 | w=29
  2485. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the natriuretic peptide precursor a gene (nppa, 108780.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the natriuretic peptide precursor a gene (nppa, 108780.0001) | rel=r_associated | relid=0 | w=29
  2486. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the natriuretic peptide precursor-a gene (nppa, 108780.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the natriuretic peptide precursor-a gene (nppa, 108780.0003) | rel=r_associated | relid=0 | w=29
  2487. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the neuroblastoma-amplified sequence gene (nbas, 608025.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neuroblastoma-amplified sequence gene (nbas, 608025.0001) | rel=r_associated | relid=0 | w=29
  2488. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the neurofibromin gene (nf1, 162200.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neurofibromin gene (nf1, 162200.0001) | rel=r_associated | relid=0 | w=29
  2489. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0001) | rel=r_associated | relid=0 | w=29
  2490. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the nuclear factor kappa-beta, subunit 2 gene (nfkb2, 164012.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear factor kappa-beta, subunit 2 gene (nfkb2, 164012.0001) | rel=r_associated | relid=0 | w=29
  2491. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the nuclear receptor subfamily 0, group b, member 1 gene (nr0b1, 300473.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear receptor subfamily 0, group b, member 1 gene (nr0b1, 300473.0001) | rel=r_associated | relid=0 | w=29
  2492. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the nuclear-encoded mitochondrial thymidine kinase gene (tk2, 188250.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nuclear-encoded mitochondrial thymidine kinase gene (tk2, 188250.0001) | rel=r_associated | relid=0 | w=29
  2493. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the parathyroid hormone-responsive b1 gene (pthb1, 607968.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the parathyroid hormone-responsive b1 gene (pthb1, 607968.0001) | rel=r_associated | relid=0 | w=29
  2494. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the periaxin gene (prx, 605725.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the periaxin gene (prx, 605725.0005) | rel=r_associated | relid=0 | w=29
  2495. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0010) | rel=r_associated | relid=0 | w=29
  2496. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 5 gene (pik3r5, 611317.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 5 gene (pik3r5, 611317.0001) | rel=r_associated | relid=0 | w=29
  2497. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the phosphatidylinositol-3-phosphate 5-kinase, type iii gene (pip5k3, 609414.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol-3-phosphate 5-kinase, type iii gene (pip5k3, 609414.0001) | rel=r_associated | relid=0 | w=29
  2498. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the phosphodiesterase 6d, cgmp-specific, rod, delta gene (pde6d, 602676.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphodiesterase 6d, cgmp-specific, rod, delta gene (pde6d, 602676.0001) | rel=r_associated | relid=0 | w=29
  2499. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0002) | rel=r_associated | relid=0 | w=29
  2500. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the platelet-derived growth factor receptor, beta, gene (pdgfrb, 173410.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the platelet-derived growth factor receptor, beta, gene (pdgfrb, 173410.0003) | rel=r_associated | relid=0 | w=29
  2501. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 5 gene (plekhg5, 611101.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 5 gene (plekhg5, 611101.0002) | rel=r_associated | relid=0 | w=29
  2502. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the plectin 1 gene (plec1, 601282.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the plectin 1 gene (plec1, 601282.0006) | rel=r_associated | relid=0 | w=29
  2503. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the presynaptic glycine transporter-2 gene (slc6a5, 604159.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the presynaptic glycine transporter-2 gene (slc6a5, 604159.0001) | rel=r_associated | relid=0 | w=29
  2504. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the prominin-1 gene (prom1, 604365.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prominin-1 gene (prom1, 604365.0013) | rel=r_associated | relid=0 | w=29
  2505. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the proprotein convertase 1 gene (pc1, 162150.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the proprotein convertase 1 gene (pc1, 162150.0001) | rel=r_associated | relid=0 | w=29
  2506. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0005) | rel=r_associated | relid=0 | w=29
  2507. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the protein s gene (pros1, 176880.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein s gene (pros1, 176880.0010) | rel=r_associated | relid=0 | w=29
  2508. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the protein-tyrosine phosphatase, nonreceptor-type, 14 gene (ptpn14, 603155.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein-tyrosine phosphatase, nonreceptor-type, 14 gene (ptpn14, 603155.0001) | rel=r_associated | relid=0 | w=29
  2509. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the proteolipid protein 1 gene (plp1, 300401.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the proteolipid protein 1 gene (plp1, 300401.0012) | rel=r_associated | relid=0 | w=29
  2510. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the quinoid dihydropteridine reductase gene (qdpr, 612676.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the quinoid dihydropteridine reductase gene (qdpr, 612676.0001) | rel=r_associated | relid=0 | w=29
  2511. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the ran-binding protein 2 gene (ranbp2, 601181.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ran-binding protein 2 gene (ranbp2, 601181.0001) | rel=r_associated | relid=0 | w=29
  2512. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the receptor expression-enhancing protein 1 gene (reep1, 609139.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the receptor expression-enhancing protein 1 gene (reep1, 609139.0006) | rel=r_associated | relid=0 | w=29
  2513. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the recombinase activating gene 2 (rag2, 179616.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the recombinase activating gene 2 (rag2, 179616.0003) | rel=r_associated | relid=0 | w=29
  2514. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the regulatory factor x, 5 gene (rfx5, 601863.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the regulatory factor x, 5 gene (rfx5, 601863.0001) | rel=r_associated | relid=0 | w=29
  2515. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the renin gene (ren, 179820.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the renin gene (ren, 179820.0002) | rel=r_associated | relid=0 | w=29
  2516. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the renin gene (ren, 179820.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the renin gene (ren, 179820.0004) | rel=r_associated | relid=0 | w=29
  2517. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the ribonuclease t2 gene (rnaset2, 612944.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribonuclease t2 gene (rnaset2, 612944.0001). | rel=r_associated | relid=0 | w=29
  2518. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the ribonucleotide reductase, m2 b gene (rrm2b, 604712.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribonucleotide reductase, m2 b gene (rrm2b, 604712.0006) | rel=r_associated | relid=0 | w=29
  2519. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the ring finger protein 170 gene (rnf170, 614649.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ring finger protein 170 gene (rnf170, 614649.0001) | rel=r_associated | relid=0 | w=29
  2520. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the s. cerevisiae homolog of the required for meiotic nuclear division 1 gene (rmnd1, 614917.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the s. cerevisiae homolog of the required for meiotic nuclear division 1 gene (rmnd1, 614917.0001) | rel=r_associated | relid=0 | w=29
  2521. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the secreted modular calcium-binding protein 2 gene (smoc2, 607223.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the secreted modular calcium-binding protein 2 gene (smoc2, 607223.0001) | rel=r_associated | relid=0 | w=29
  2522. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the selenoprotein n, 1 gene (sepn1, 606210.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the selenoprotein n, 1 gene (sepn1, 606210.0008) | rel=r_associated | relid=0 | w=29
  2523. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the short stature homeo box gene (shox, 312865.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the short stature homeo box gene (shox, 312865.0002) | rel=r_associated | relid=0 | w=29
  2524. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the short/branched-chain acyl-coa dehydrogenase gene (acadsb, 600301.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the short/branched-chain acyl-coa dehydrogenase gene (acadsb, 600301.0001) | rel=r_associated | relid=0 | w=29
  2525. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the sodium channel, voltage-gated, type v, alpha subunit gene (scn5a, 600163.0033)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sodium channel, voltage-gated, type v, alpha subunit gene (scn5a, 600163.0033) | rel=r_associated | relid=0 | w=29
  2526. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the solute carrier 22 (urate transporter), member 12 gene (slc22a12, 607096.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier 22 (urate transporter), member 12 gene (slc22a12, 607096.0001) | rel=r_associated | relid=0 | w=29
  2527. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the solute carrier family 22, member 1-like gene (slc22a1l, 602631.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 22, member 1-like gene (slc22a1l, 602631.0001) | rel=r_associated | relid=0 | w=29
  2528. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, citrin), member 13 gene (slc25a13, 603859.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, citrin), member 13 gene (slc25a13, 603859.0001) | rel=r_associated | relid=0 | w=29
  2529. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the solute carrier family 29 (nucleoside transporter), member 3 gene (slc29a3, 612373.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 29 (nucleoside transporter), member 3 gene (slc29a3, 612373.0001) | rel=r_associated | relid=0 | w=29
  2530. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the solute carrier family 34 (sodium/phosphate cotransporter), member 2 gene (slc34a2, 604217.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 34 (sodium/phosphate cotransporter), member 2 gene (slc34a2, 604217.0001) | rel=r_associated | relid=0 | w=29
  2531. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the solute carrier family 35 (udp-galactose transporter), member 2 gene (slc35a2, 314375.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 35 (udp-galactose transporter), member 2 gene (slc35a2, 314375.0001) | rel=r_associated | relid=0 | w=29
  2532. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the solute carrier family 35 (udp-n-acetylglucosamine transporter), member 3 gene (slc35a3, 605632.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 35 (udp-n-acetylglucosamine transporter), member 3 gene (slc35a3, 605632.0001) | rel=r_associated | relid=0 | w=29
  2533. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the solute carrier organic anion transporter family, member 2a1 gene (slco2a1, 601460.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier organic anion transporter family, member 2a1 gene (slco2a1, 601460.0001) | rel=r_associated | relid=0 | w=29
  2534. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the sorting nexin 10 gene (snx10, 614780.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sorting nexin 10 gene (snx10, 614780.0001) | rel=r_associated | relid=0 | w=29
  2535. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the spartin gene (spg20, 607111.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the spartin gene (spg20, 607111.0001) | rel=r_associated | relid=0 | w=29
  2536. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the sperm antigen with calponin homology and coiled-coil domains 1-like gene (specc1l, 614140.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sperm antigen with calponin homology and coiled-coil domains 1-like gene (specc1l, 614140.0001) | rel=r_associated | relid=0 | w=29
  2537. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the sry (sex determining region y)-box 2 gene (sox2, 184427.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sry (sex determining region y)-box 2 gene (sox2, 184427.0001) | rel=r_associated | relid=0 | w=29
  2538. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the sry-box-10 gene (sox10, 602229.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sry-box-10 gene (sox10, 602229.0006) | rel=r_associated | relid=0 | w=29
  2539. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605921.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605921.0008) | rel=r_associated | relid=0 | w=29
  2540. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the sulfite oxidase gene (suox, 606887.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sulfite oxidase gene (suox, 606887.0001) | rel=r_associated | relid=0 | w=29
  2541. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the superoxide dismutase-1 gene (sod-1, 147450.0001) susceptibility conferred by mutation in the angiogenin gene (ang, 105850.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the superoxide dismutase-1 gene (sod-1, 147450.0001) susceptibility conferred by mutation in the angiogenin gene (ang, 105850.0001) | rel=r_associated | relid=0 | w=29
  2542. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the suppression of tumorigenicity 14 gene (st14, 606797.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the suppression of tumorigenicity 14 gene (st14, 606797.0001) | rel=r_associated | relid=0 | w=29
  2543. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the surfactant pulmonary-associated protein c gene (sftpc, 178620.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the surfactant pulmonary-associated protein c gene (sftpc, 178620.0001) | rel=r_associated | relid=0 | w=29
  2544. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the swi/snf related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene (smarca2, 600014.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the swi/snf related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene (smarca2, 600014.0001) | rel=r_associated | relid=0 | w=29
  2545. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the synaptotagmin-2 gene (syt2, 600104.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the synaptotagmin-2 gene (syt2, 600104.0001) | rel=r_associated | relid=0 | w=29
  2546. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the syntaxin 16 gene (stx16, 603666.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the syntaxin 16 gene (stx16, 603666.0001) | rel=r_associated | relid=0 | w=29
  2547. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the t-cell immune regulator 1 gene (tcirg1, 604592.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the t-cell immune regulator 1 gene (tcirg1, 604592.0001) | rel=r_associated | relid=0 | w=29
  2548. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the taf2 ran polymerase ii, tata box-binding protein-associated factor, 150kd gene (taf2, 604912.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the taf2 ran polymerase ii, tata box-binding protein-associated factor, 150kd gene (taf2, 604912.0001) | rel=r_associated | relid=0 | w=29
  2549. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the transcobalamin ii gene (tcn2, 613441.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transcobalamin ii gene (tcn2, 613441.0001) | rel=r_associated | relid=0 | w=29
  2550. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the transforming growth factor, beta-3 gene (tgfb3, 190230.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transforming growth factor, beta-3 gene (tgfb3, 190230.0001) | rel=r_associated | relid=0 | w=29
  2551. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0008) | rel=r_associated | relid=0 | w=29
  2552. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the trf1-interacting nuclear factor 2 gene (tinf2, 604319.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the trf1-interacting nuclear factor 2 gene (tinf2, 604319.0002) | rel=r_associated | relid=0 | w=29
  2553. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the tropomyosin-3 gene (tpm3, 191030.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tropomyosin-3 gene (tpm3, 191030.0001) | rel=r_associated | relid=0 | w=29
  2554. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the troponin t1 gene (tnnt1, 191041.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the troponin t1 gene (tnnt1, 191041.0001) | rel=r_associated | relid=0 | w=29
  2555. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the tubulin beta-3 gene (tubb3, 602661.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin beta-3 gene (tubb3, 602661.0001) | rel=r_associated | relid=0 | w=29
  2556. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the tumor necrosis factor receptor superfamily, member 7 gene (tnfrsf7, 186711.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tumor necrosis factor receptor superfamily, member 7 gene (tnfrsf7, 186711.0001) | rel=r_associated | relid=0 | w=29
  2557. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the tumor protein p63 gene (tp63, 603273.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tumor protein p63 gene (tp63, 603273.0007) | rel=r_associated | relid=0 | w=29
  2558. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the type v collagen, alpha-1 gene (col5a1, 120215.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the type v collagen, alpha-1 gene (col5a1, 120215.0005) | rel=r_associated | relid=0 | w=29
  2559. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the ubiquitin protein ligase e3a gene (ube3a, 601623.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquitin protein ligase e3a gene (ube3a, 601623.0001) | rel=r_associated | relid=0 | w=29
  2560. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the uroporphyrinogen decarboxylase gene (urod, 176100.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the uroporphyrinogen decarboxylase gene (urod, 176100.0001) | rel=r_associated | relid=0 | w=29
  2561. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the v-ha-ras harvey rat sarcoma viral oncogene homolog gene (hras, 190020.0017)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-ha-ras harvey rat sarcoma viral oncogene homolog gene (hras, 190020.0017) | rel=r_associated | relid=0 | w=29
  2562. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the v-ki-ras2 kirsten rat sarcoma 2 viral oncogene homolog gene (kras, 190070.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-ki-ras2 kirsten rat sarcoma 2 viral oncogene homolog gene (kras, 190070.0009) | rel=r_associated | relid=0 | w=29
  2563. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the voltage-gated potassium channel, kqt-like subfamily, member 2 gene (kcnq2, 602235.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated potassium channel, kqt-like subfamily, member 2 gene (kcnq2, 602235.0007) | rel=r_associated | relid=0 | w=29
  2564. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the voltage-gated sodium channel 9 alpha-subunit gene (scn9a, 603415.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated sodium channel 9 alpha-subunit gene (scn9a, 603415.0001) | rel=r_associated | relid=0 | w=29
  2565. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0001) | rel=r_associated | relid=0 | w=29
  2566. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the wd-repeat containing protein 34 gene (wdr34, 613363.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd-repeat containing protein 34 gene (wdr34, 613363.0001) | rel=r_associated | relid=0 | w=29
  2567. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the wingless-type mmtv integration site family, member 7a gene (wnt7a, 601570.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wingless-type mmtv integration site family, member 7a gene (wnt7a, 601570.0001) | rel=r_associated | relid=0 | w=29
  2568. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the ww domain-containing oxidoreductase gene (wwox, 605131.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ww domain-containing oxidoreductase gene (wwox, 605131.0004) | rel=r_associated | relid=0 | w=29
  2569. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0015) | rel=r_associated | relid=0 | w=29
  2570. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the x-prolyl aminopeptidase 3 gene (xpnpep3, 613553.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the x-prolyl aminopeptidase 3 gene (xpnpep3, 613553.0001) | rel=r_associated | relid=0 | w=29
  2571. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the xpc gene (xpc, 613208.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the xpc gene (xpc, 613208.0001) | rel=r_associated | relid=0 | w=29
  2572. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutation in the zinc finger protein 335 gene (znf335, 610827.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger protein 335 gene (znf335, 610827.0001) | rel=r_associated | relid=0 | w=29
  2573. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the acid lysosomal sphingomyelin phosphodiesterase-1 gene (smpd1, 607608.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the acid lysosomal sphingomyelin phosphodiesterase-1 gene (smpd1, 607608.0001) | rel=r_associated | relid=0 | w=29
  2574. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the alpha subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the alpha subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0001) | rel=r_associated | relid=0 | w=29
  2575. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the beta-1 transforming growth factor gene (tgfb1, 190180.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the beta-1 transforming growth factor gene (tgfb1, 190180.0001) | rel=r_associated | relid=0 | w=29
  2576. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the cyclin-dependent kinase inhibitor 2a gene (cdkn2a, 600160.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cyclin-dependent kinase inhibitor 2a gene (cdkn2a, 600160.0001) | rel=r_associated | relid=0 | w=29
  2577. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the cystinosis gene (ctns, 219800.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cystinosis gene (ctns, 219800.0008) | rel=r_associated | relid=0 | w=29
  2578. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the cytochrome p450, subfamily xxviia, polypeptide 1 gene (cyp27a1, 213700.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cytochrome p450, subfamily xxviia, polypeptide 1 gene (cyp27a1, 213700.0001) | rel=r_associated | relid=0 | w=29
  2579. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the exostosin 1 gene (ext1, 133700.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the exostosin 1 gene (ext1, 133700.0001) | rel=r_associated | relid=0 | w=29
  2580. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0001) | rel=r_associated | relid=0 | w=29
  2581. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the gli-kruppel family member 3 gene (gli3, 165240.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the gli-kruppel family member 3 gene (gli3, 165240.0002) | rel=r_associated | relid=0 | w=29
  2582. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the glial fibrillary acidic protein gene (gfap, 137780.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the glial fibrillary acidic protein gene (gfap, 137780.0001) | rel=r_associated | relid=0 | w=29
  2583. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the glycine n-methyltransferase gene (gnmt, 606628.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the glycine n-methyltransferase gene (gnmt, 606628.0001) | rel=r_associated | relid=0 | w=29
  2584. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0003) | rel=r_associated | relid=0 | w=29
  2585. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the heat-shock 22-kd protein 8 gene (hspb8, 608014.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the heat-shock 22-kd protein 8 gene (hspb8, 608014.0003) | rel=r_associated | relid=0 | w=29
  2586. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the homolog of the drosophila notch 3 gene (notch3, 600276.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the homolog of the drosophila notch 3 gene (notch3, 600276.0001). | rel=r_associated | relid=0 | w=29
  2587. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the lecithin:cholesterol acyltransferase gene (lcat, 606967.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the lecithin:cholesterol acyltransferase gene (lcat, 606967.0001). | rel=r_associated | relid=0 | w=29
  2588. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the lim/homeodomain protein lhx3 gene (lhx3, 600577.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the lim/homeodomain protein lhx3 gene (lhx3, 600577.0001) | rel=r_associated | relid=0 | w=29
  2589. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the liver phosphorylase alpha-2 subunit gene (phka2, 306000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the liver phosphorylase alpha-2 subunit gene (phka2, 306000.0001) | rel=r_associated | relid=0 | w=29
  2590. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the mannosephosphate isomerase gene (mpi, 154550.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the mannosephosphate isomerase gene (mpi, 154550.0001) | rel=r_associated | relid=0 | w=29
  2591. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the neurofibromin gene (nf1, 162200.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the neurofibromin gene (nf1, 162200.0010) | rel=r_associated | relid=0 | w=29
  2592. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the nijmegen breakage syndrome gene (nbs1, 602667.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the nijmegen breakage syndrome gene (nbs1, 602667.0001) | rel=r_associated | relid=0 | w=29
  2593. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the secreted ly6/upar-related protein 1 gene (slurp1, 606119.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the secreted ly6/upar-related protein 1 gene (slurp1, 606119.0001) | rel=r_associated | relid=0 | w=29
  2594. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the senataxin gene (setx, 608465.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the senataxin gene (setx, 608465.0001) | rel=r_associated | relid=0 | w=29
  2595. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the tropomyosin 2 gene (tpm2, 190990.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the tropomyosin 2 gene (tpm2, 190990.0001) | rel=r_associated | relid=0 | w=29
  2596. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the tumor necrosis factor ligand superfamily, member 5 gene (tnfsf5, 308230.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the tumor necrosis factor ligand superfamily, member 5 gene (tnfsf5, 308230.0001) | rel=r_associated | relid=0 | w=29
  2597. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the udp-galactose-4-epimerase gene, 'severe' form (gale, 606953.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the udp-galactose-4-epimerase gene, 'severe' form (gale, 606953.0008) | rel=r_associated | relid=0 | w=29
  2598. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0001) | rel=r_associated | relid=0 | w=29
  2599. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0021)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0021) | rel=r_associated | relid=0 | w=29
  2600. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by simultaneous homozygous mutations in both the chloride channel, kidney, a gene (clcnka, 602024.0001) and chloride channel, kidney, b gene (clcnkb, 602023.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by simultaneous homozygous mutations in both the chloride channel, kidney, a gene (clcnka, 602024.0001) and chloride channel, kidney, b gene (clcnkb, 602023.0008) | rel=r_associated | relid=0 | w=29
  2601. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene (slc24a1, 603617.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene (slc24a1, 603617.0001) | rel=r_associated | relid=0 | w=29
  2602. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by somatic mosaic mutation in the neuroblastoma ras viral (v-ras) oncogene homolog gene (nras, 164790.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mosaic mutation in the neuroblastoma ras viral (v-ras) oncogene homolog gene (nras, 164790.0002) | rel=r_associated | relid=0 | w=29
  2603. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by somatic mutation in the beta-1 catenin gene (ctnnb1, 116806.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the beta-1 catenin gene (ctnnb1, 116806.0006) | rel=r_associated | relid=0 | w=29
  2604. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:caused by somatic mutation in the janus kinase 2 gene (jak2, 147796)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the janus kinase 2 gene (jak2, 147796) | rel=r_associated | relid=0 | w=29
  2605. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:contiguous gene syndrome caused by 6-mb duplication of 15q11-q13
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by 6-mb duplication of 15q11-q13 | rel=r_associated | relid=0 | w=29
  2606. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:contiguous gene syndrome caused by deletion (2.2 mb) of chromosome 17q23.1-q23
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by deletion (2.2 mb) of chromosome 17q23.1-q23 | rel=r_associated | relid=0 | w=29
  2607. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:contiguous gene syndrome caused by deletion (580kb-22.5mb) of 3q13.31
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by deletion (580kb-22.5mb) of 3q13.31 | rel=r_associated | relid=0 | w=29
  2608. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:contiguous gene syndrome involving deletion of 2.63 mb on chromosome 5q12
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome involving deletion of 2.63 mb on chromosome 5q12 | rel=r_associated | relid=0 | w=29
  2609. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:contiguous gene syndrome involving deletions of the collagen, type iv, alpha-5 (col4a5, 303630) and collagen, type iv, alpha-6 (col4a6, 303631) genes
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome involving deletions of the collagen, type iv, alpha-5 (col4a5, 303630) and collagen, type iv, alpha-6 (col4a6, 303631) genes | rel=r_associated | relid=0 | w=29
  2610. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:due to mutation in the aspartylglucosaminidase gene (aga, 208400.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:due to mutation in the aspartylglucosaminidase gene (aga, 208400.0001) | rel=r_associated | relid=0 | w=29
  2611. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:due to mutation in the microsomal triglyceride transfer protein gene (mtp, 157147.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:due to mutation in the microsomal triglyceride transfer protein gene (mtp, 157147.0001) | rel=r_associated | relid=0 | w=29
  2612. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:linked to a locus at 7p15-p11.2.
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:linked to a locus at 7p15-p11.2. | rel=r_associated | relid=0 | w=29
  2613. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:mutation in the filamin b gene (flnb, 603381)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:mutation in the filamin b gene (flnb, 603381) | rel=r_associated | relid=0 | w=29
  2614. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:susceptibility conferred by deletion that includes the complement factor h-related 1 gene (cfhr1, 134371.0001) and complement factor h-related 3 gene (cfhr3, 605366.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by deletion that includes the complement factor h-related 1 gene (cfhr1, 134371.0001) and complement factor h-related 3 gene (cfhr3, 605366.0001) | rel=r_associated | relid=0 | w=29
  2615. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:susceptibility conferred by mutation in the homolog of the mouse aristaless-like 4 gene (alx4, 605420.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the homolog of the mouse aristaless-like 4 gene (alx4, 605420.0009) | rel=r_associated | relid=0 | w=29
  2616. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:susceptibility conferred by mutation in the kinesin family member 1b gene (kif1b, 605995.0002).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the kinesin family member 1b gene (kif1b, 605995.0002). | rel=r_associated | relid=0 | w=29
  2617. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:susceptibility conferred by mutation in the neuroligin-4 gene (nlgn4, 300427.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the neuroligin-4 gene (nlgn4, 300427.0001) | rel=r_associated | relid=0 | w=29
  2618. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:susceptibility conferred by mutation in the phosphatidylinositol glycan, class t gene (pigt, 610272.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the phosphatidylinositol glycan, class t gene (pigt, 610272.0001) | rel=r_associated | relid=0 | w=29
  2619. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:susceptibility conferred by mutation in the semaphorin 3a gene (sema3a, 603961.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the semaphorin 3a gene (sema3a, 603961.0001) | rel=r_associated | relid=0 | w=29
  2620. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:susceptibility conferred by mutations in the protein tyrosine phosphatase, receptor type, c polypeptide gene (ptprc, 151460.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutations in the protein tyrosine phosphatase, receptor type, c polypeptide gene (ptprc, 151460.0001) | rel=r_associated | relid=0 | w=29
  2621. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 29 / 0.674 -> en:susceptibility to sle caused by mutation in the tumor necrosis factor ligand superfamily, member 6 gene (tnfsf6, 134638.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility to sle caused by mutation in the tumor necrosis factor ligand superfamily, member 6 gene (tnfsf6, 134638.0001) | rel=r_associated | relid=0 | w=29
  2622. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:a contiguous gene syndrome caused by deletion (160kb to 9mb) of 22q13.3
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome caused by deletion (160kb to 9mb) of 22q13.3 | rel=r_associated | relid=0 | w=28
  2623. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by a 1.35-mb duplication of chromosome 1q21
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a 1.35-mb duplication of chromosome 1q21 | rel=r_associated | relid=0 | w=28
  2624. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by chromosome 14 paternal uniparental disomy
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by chromosome 14 paternal uniparental disomy | rel=r_associated | relid=0 | w=28
  2625. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by contiguous gene deletion on chromosome xp11.3, including the rp2 gene (312600)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by contiguous gene deletion on chromosome xp11.3, including the rp2 gene (312600) | rel=r_associated | relid=0 | w=28
  2626. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by contiguous gene duplication of imprinted region of 11p15.5
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by contiguous gene duplication of imprinted region of 11p15.5 | rel=r_associated | relid=0 | w=28
  2627. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by contraction of a d4z4 repeat array at chromosome 4q35
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by contraction of a d4z4 repeat array at chromosome 4q35 | rel=r_associated | relid=0 | w=28
  2628. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by deletion of 1.5mb on 3q29 encompassing 22 genes
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion of 1.5mb on 3q29 encompassing 22 genes | rel=r_associated | relid=0 | w=28
  2629. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by duplication of 300kb (chr12:64,803,839-65,098,981 (grch37)) on 12q14
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of 300kb (chr12:64,803,839-65,098,981 (grch37)) on 12q14 | rel=r_associated | relid=0 | w=28
  2630. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by epigenetic changes of dna hypomethylation at the h19/igf2-imprinting control region (icr1, 616186)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by epigenetic changes of dna hypomethylation at the h19/igf2-imprinting control region (icr1, 616186) | rel=r_associated | relid=0 | w=28
  2631. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by insertion of 8 extra octapeptide repeats in the prion protein gene (prnp, 176640.0020)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by insertion of 8 extra octapeptide repeats in the prion protein gene (prnp, 176640.0020) | rel=r_associated | relid=0 | w=28
  2632. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by interstitial duplication (3.7mb) of 17p11.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by interstitial duplication (3.7mb) of 17p11.2 | rel=r_associated | relid=0 | w=28
  2633. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in homolog of the c. elegans suppressor of clear gene (shoc2, 602775.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in homolog of the c. elegans suppressor of clear gene (shoc2, 602775.0001) | rel=r_associated | relid=0 | w=28
  2634. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the 3-prime repair exonuclease-1 gene (trex1, 606609.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 3-prime repair exonuclease-1 gene (trex1, 606609.0005) | rel=r_associated | relid=0 | w=28
  2635. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the 5-oxoprolinase gene (oplah, 614243.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 5-oxoprolinase gene (oplah, 614243.0001) | rel=r_associated | relid=0 | w=28
  2636. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the acylglycerol kinase gene (agk, 610345.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the acylglycerol kinase gene (agk, 610345.0001) | rel=r_associated | relid=0 | w=28
  2637. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the adaptin, beta-3a gene (adtb3a, 603401.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adaptin, beta-3a gene (adtb3a, 603401.0001) | rel=r_associated | relid=0 | w=28
  2638. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the adaptor-related protein complex 4, epsilon-1 subunit gene (ap4e1, 607244.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adaptor-related protein complex 4, epsilon-1 subunit gene (ap4e1, 607244.0001) | rel=r_associated | relid=0 | w=28
  2639. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the adaptor-related protein complex 4, sigma-1 subunit (ap4s1, 607243.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adaptor-related protein complex 4, sigma-1 subunit (ap4s1, 607243.0001) | rel=r_associated | relid=0 | w=28
  2640. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the additional sex combs-like 1 gene (asxl1, 612990.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the additional sex combs-like 1 gene (asxl1, 612990.0001) | rel=r_associated | relid=0 | w=28
  2641. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the adenylate cyclase 5 gene (adcy5, 600293.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenylate cyclase 5 gene (adcy5, 600293.0001) | rel=r_associated | relid=0 | w=28
  2642. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the adenylate cyclase-1, brain gene (adcy1, 103072.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenylate cyclase-1, brain gene (adcy1, 103072.0001) | rel=r_associated | relid=0 | w=28
  2643. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the adenylate kinase-1 gene (ak1, 103000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenylate kinase-1 gene (ak1, 103000.0001) | rel=r_associated | relid=0 | w=28
  2644. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the adenylate kinase-2 gene (ak2, 103020.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenylate kinase-2 gene (ak2, 103020.0001) | rel=r_associated | relid=0 | w=28
  2645. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the adenylosuccinate lyase gene (adsl, 608222.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenylosuccinate lyase gene (adsl, 608222.0001) | rel=r_associated | relid=0 | w=28
  2646. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the af4/fmr2 family, member 2 gene (aff2, 300806.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the af4/fmr2 family, member 2 gene (aff2, 300806.0001) | rel=r_associated | relid=0 | w=28
  2647. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the alanyl-trna synthetase 2 gene (aars2, 612035.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alanyl-trna synthetase 2 gene (aars2, 612035.0001) | rel=r_associated | relid=0 | w=28
  2648. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the alpha-1a calcium channel subunit gene (cacna1a, 601011.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1a calcium channel subunit gene (cacna1a, 601011.0002) | rel=r_associated | relid=0 | w=28
  2649. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the alpha-a-crystallin gene (cryaa, 123580.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-a-crystallin gene (cryaa, 123580.0001) | rel=r_associated | relid=0 | w=28
  2650. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the amnionless gene (amn, 605799.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the amnionless gene (amn, 605799.0001) | rel=r_associated | relid=0 | w=28
  2651. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the angiopoietin-like-3 gene (angptl3, 604774.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the angiopoietin-like-3 gene (angptl3, 604774.0001) | rel=r_associated | relid=0 | w=28
  2652. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the anoctamin 10 gene (ano10, 613726.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the anoctamin 10 gene (ano10, 613726.0001) | rel=r_associated | relid=0 | w=28
  2653. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the anoctamin 3 gene (ano3, 610110.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the anoctamin 3 gene (ano3, 610110.0001) | rel=r_associated | relid=0 | w=28
  2654. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the apolipoprotein a-i gene (apoa1, 107680.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the apolipoprotein a-i gene (apoa1, 107680.0001) | rel=r_associated | relid=0 | w=28
  2655. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the aquaporin 7 gene (aqp7, 602974.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aquaporin 7 gene (aqp7, 602974.0001) | rel=r_associated | relid=0 | w=28
  2656. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the aryl hydrocarbon receptor nuclear translocator-2 gene (arnt2, 606036.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aryl hydrocarbon receptor nuclear translocator-2 gene (arnt2, 606036.0001) | rel=r_associated | relid=0 | w=28
  2657. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the aryl hydrocarbon receptor-interacting protein gene (aip, 605555.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aryl hydrocarbon receptor-interacting protein gene (aip, 605555.0001) | rel=r_associated | relid=0 | w=28
  2658. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the arylsulfatase b gene (arsb, 611542.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the arylsulfatase b gene (arsb, 611542.0001) | rel=r_associated | relid=0 | w=28
  2659. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the asparagine synthetase gene (asns, 108370.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the asparagine synthetase gene (asns, 108370.0001) | rel=r_associated | relid=0 | w=28
  2660. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the aspartate beta-hydroxylase gene (asph, 600582.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aspartate beta-hydroxylase gene (asph, 600582.0001) | rel=r_associated | relid=0 | w=28
  2661. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the atp-binding cassette, subfamily a, member 12 gene (abca12, 607800.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily a, member 12 gene (abca12, 607800.0001) | rel=r_associated | relid=0 | w=28
  2662. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the atpase, ca++ transporting, slow-twitch, cardiac muscle-2 gene (atp2a2, 108740)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, ca++ transporting, slow-twitch, cardiac muscle-2 gene (atp2a2, 108740) | rel=r_associated | relid=0 | w=28
  2663. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the b-cell linker protein gene (blnk, 604515.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the b-cell linker protein gene (blnk, 604515.0001) | rel=r_associated | relid=0 | w=28
  2664. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the bbs12 gene (bbs12, 610683.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bbs12 gene (bbs12, 610683.0001) | rel=r_associated | relid=0 | w=28
  2665. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0002) | rel=r_associated | relid=0 | w=28
  2666. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the beta choline kinase gene (chkb, 612395.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta choline kinase gene (chkb, 612395.0001) | rel=r_associated | relid=0 | w=28
  2667. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the beta-1,3-glucuronyltransferase 3 gene (b3gat3, 606374.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1,3-glucuronyltransferase 3 gene (b3gat3, 606374.0001) | rel=r_associated | relid=0 | w=28
  2668. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the beta-3 tubulin gene (tubb3, 602661.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-3 tubulin gene (tubb3, 602661.0006) | rel=r_associated | relid=0 | w=28
  2669. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the beta-4 gap junction protein gene (gjb4, 605425.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-4 gap junction protein gene (gjb4, 605425.0001) | rel=r_associated | relid=0 | w=28
  2670. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the breast cancer type 1 gene (brca1, 113705.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the breast cancer type 1 gene (brca1, 113705.0001) | rel=r_associated | relid=0 | w=28
  2671. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the calcium-activated large conductance potassium channel subfamily m, alpha member 1 gene (kcnma1, 600150.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calcium-activated large conductance potassium channel subfamily m, alpha member 1 gene (kcnma1, 600150.0001) | rel=r_associated | relid=0 | w=28
  2672. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the calmodulin-1 gene (calm1, 114180.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the calmodulin-1 gene (calm1, 114180.0003) | rel=r_associated | relid=0 | w=28
  2673. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the camp-dependent protein kinase, regulatory, type i, alpha gene (prkar1a, 188830.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the camp-dependent protein kinase, regulatory, type i, alpha gene (prkar1a, 188830.0009) | rel=r_associated | relid=0 | w=28
  2674. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the carbamoylphosphate synthetase i gene (cps1, 608307.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carbamoylphosphate synthetase i gene (cps1, 608307.0001) | rel=r_associated | relid=0 | w=28
  2675. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cat eye syndrome chromosome region, candidate 1 gene (cecr1, 607575.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cat eye syndrome chromosome region, candidate 1 gene (cecr1, 607575.0001) | rel=r_associated | relid=0 | w=28
  2676. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cathepsin f gene (ctsf, 603539.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cathepsin f gene (ctsf, 603539.0001) | rel=r_associated | relid=0 | w=28
  2677. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cd3 antigen, delta subunit gene (cd3d, 186790.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd3 antigen, delta subunit gene (cd3d, 186790.0001) | rel=r_associated | relid=0 | w=28
  2678. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cd59 antigen gene (cd59, 107271.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd59 antigen gene (cd59, 107271.0001) | rel=r_associated | relid=0 | w=28
  2679. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cd79b antigen gene (cd79b, 147245.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd79b antigen gene (cd79b, 147245.0001) | rel=r_associated | relid=0 | w=28
  2680. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cd8 antigen, alpha polypeptide gene (cd8a, 186910.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cd8 antigen, alpha polypeptide gene (cd8a, 186910.0001) | rel=r_associated | relid=0 | w=28
  2681. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the chmp family, member 2b gene (chmp2b, 609512.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chmp family, member 2b gene (chmp2b, 609512.0003) | rel=r_associated | relid=0 | w=28
  2682. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cholinergic receptor, nicotinic, gamma polypeptide gene (chrng, 100730.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, gamma polypeptide gene (chrng, 100730.0002) | rel=r_associated | relid=0 | w=28
  2683. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the chromodomain helicase dna-binding protein 2 gene (chd2, 602119.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromodomain helicase dna-binding protein 2 gene (chd2, 602119.0001) | rel=r_associated | relid=0 | w=28
  2684. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the chromosome 12 open reading frame 57 gene (c12orf57, 615140.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 12 open reading frame 57 gene (c12orf57, 615140.0001) | rel=r_associated | relid=0 | w=28
  2685. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the class 4 pou domain transcription factor 3 gene (pou4f3, 602460.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the class 4 pou domain transcription factor 3 gene (pou4f3, 602460.0001) | rel=r_associated | relid=0 | w=28
  2686. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the claudin 16 gene (cldn16, 603959.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the claudin 16 gene (cldn16, 603959.0001) | rel=r_associated | relid=0 | w=28
  2687. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the coagulation factor ii gene (f2, 176930.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coagulation factor ii gene (f2, 176930.0009) | rel=r_associated | relid=0 | w=28
  2688. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the coiled-coil domain-containing protein 151 gene (ccdc151, 615956.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil domain-containing protein 151 gene (ccdc151, 615956.0001) | rel=r_associated | relid=0 | w=28
  2689. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the coiled-coil domain-containing protein 8 gene (ccdc8, 614145.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil domain-containing protein 8 gene (ccdc8, 614145.0001) | rel=r_associated | relid=0 | w=28
  2690. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the coiled-coil domain-containing protein 88c gene (ccdc88c, 611204.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coiled-coil domain-containing protein 88c gene (ccdc88c, 611204.0004) | rel=r_associated | relid=0 | w=28
  2691. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0004) | rel=r_associated | relid=0 | w=28
  2692. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0007) | rel=r_associated | relid=0 | w=28
  2693. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0001) | rel=r_associated | relid=0 | w=28
  2694. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0012) | rel=r_associated | relid=0 | w=28
  2695. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the collagen vi, alpha-2 polypeptide gene (col6a2, 120240.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen vi, alpha-2 polypeptide gene (col6a2, 120240.0001) | rel=r_associated | relid=0 | w=28
  2696. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0001) | rel=r_associated | relid=0 | w=28
  2697. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0001) | rel=r_associated | relid=0 | w=28
  2698. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0004) | rel=r_associated | relid=0 | w=28
  2699. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0005) | rel=r_associated | relid=0 | w=28
  2700. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the collagen xvii, alpha-1 polypeptide gene (col17a2, 113811.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen xvii, alpha-1 polypeptide gene (col17a2, 113811.0001) | rel=r_associated | relid=0 | w=28
  2701. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the complex i, subunit nd3 gene (mtnd3, 516002.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complex i, subunit nd3 gene (mtnd3, 516002.0001) | rel=r_associated | relid=0 | w=28
  2702. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the conserved telomere maintenance component 1 gene (ctc1, 613129.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the conserved telomere maintenance component 1 gene (ctc1, 613129.0001) | rel=r_associated | relid=0 | w=28
  2703. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cyclic nucleotide-gated channel, alpha-3 gene (cnga3, 600053.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyclic nucleotide-gated channel, alpha-3 gene (cnga3, 600053.0001) | rel=r_associated | relid=0 | w=28
  2704. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cyld gene (605018.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cyld gene (605018.0005) | rel=r_associated | relid=0 | w=28
  2705. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cysteine- and glycine-rich protein 3 gene (csrp3, 600824.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cysteine- and glycine-rich protein 3 gene (csrp3, 600824.0002) | rel=r_associated | relid=0 | w=28
  2706. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cytochrome c oxidase subunit 15 gene (cox15, 603646)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase subunit 15 gene (cox15, 603646) | rel=r_associated | relid=0 | w=28
  2707. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the cytochrome c oxidase subunit ii gene (mtco2, 516040.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase subunit ii gene (mtco2, 516040.0001) | rel=r_associated | relid=0 | w=28
  2708. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the d-2-hydroxyglutarate dehydrogenase gene (d2hgd, 609186.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the d-2-hydroxyglutarate dehydrogenase gene (d2hgd, 609186.0001) | rel=r_associated | relid=0 | w=28
  2709. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the ddb1- and cul4-associated factor 17 gene (dcaf17, 612515.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ddb1- and cul4-associated factor 17 gene (dcaf17, 612515.0001) | rel=r_associated | relid=0 | w=28
  2710. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the dedicator of cytokinesis-6 gene (dock6, 614194.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dedicator of cytokinesis-6 gene (dock6, 614194.0001) | rel=r_associated | relid=0 | w=28
  2711. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the deleted in colorectal carcinoma gene (dcc, 120470.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the deleted in colorectal carcinoma gene (dcc, 120470.0001) | rel=r_associated | relid=0 | w=28
  2712. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the delta-aminolevulinate synthase 2 gene (alas2, 301300.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the delta-aminolevulinate synthase 2 gene (alas2, 301300.0001) | rel=r_associated | relid=0 | w=28
  2713. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the desmoplakin gene (dsp, 125647.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the desmoplakin gene (dsp, 125647.0003) | rel=r_associated | relid=0 | w=28
  2714. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the desmoplakin gene (dsp, 125647.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the desmoplakin gene (dsp, 125647.0015) | rel=r_associated | relid=0 | w=28
  2715. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the dihydrofolate reductase gene (dhfr, 126060.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dihydrofolate reductase gene (dhfr, 126060.0001) | rel=r_associated | relid=0 | w=28
  2716. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the dna helicase, recq-like, type 4 gene (recql4, 603780.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna helicase, recq-like, type 4 gene (recql4, 603780.0012) | rel=r_associated | relid=0 | w=28
  2717. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the dna polymerase gamma-2 gene (polg2, 604983.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna polymerase gamma-2 gene (polg2, 604983.0001) | rel=r_associated | relid=0 | w=28
  2718. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the dna polymerase, epsilon gene (pole, 174762.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna polymerase, epsilon gene (pole, 174762.0001) | rel=r_associated | relid=0 | w=28
  2719. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the dolichyl-phosphate mannosyltransferase 2, regulatory subunit gene (dpm2, 603564.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dolichyl-phosphate mannosyltransferase 2, regulatory subunit gene (dpm2, 603564.0001) | rel=r_associated | relid=0 | w=28
  2720. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the dual oxidase 2 gene (duox2, 606759.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dual oxidase 2 gene (duox2, 606759.0001) | rel=r_associated | relid=0 | w=28
  2721. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the dynamin 1-like gene (dnm1l, 603850.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynamin 1-like gene (dnm1l, 603850.0001) | rel=r_associated | relid=0 | w=28
  2722. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the dynein, cytoplasmic 1, heavy chain 1 gene (dync1h1, 600112.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynein, cytoplasmic 1, heavy chain 1 gene (dync1h1, 600112.0001) | rel=r_associated | relid=0 | w=28
  2723. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the dyslexia susceptibility 1 candidate 1 gene (dyx1c1, 608706.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dyslexia susceptibility 1 candidate 1 gene (dyx1c1, 608706.0001) | rel=r_associated | relid=0 | w=28
  2724. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the e1-alpha subunit of the pyruvate dehydrogenase complex (pdha1, 300502.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the e1-alpha subunit of the pyruvate dehydrogenase complex (pdha1, 300502.0001) | rel=r_associated | relid=0 | w=28
  2725. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the ectodysplasin a gene (ed1, 300451.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ectodysplasin a gene (ed1, 300451.0001) | rel=r_associated | relid=0 | w=28
  2726. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the edar-associated death domain gene (edaradd, 606603.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the edar-associated death domain gene (edaradd, 606603.0001) | rel=r_associated | relid=0 | w=28
  2727. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the egf domain-specific o-linked n-acetylglucosamine transferase gene (eogt, 614789.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the egf domain-specific o-linked n-acetylglucosamine transferase gene (eogt, 614789.0001) | rel=r_associated | relid=0 | w=28
  2728. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the elongation of very long chain fatty acids-like 4 gene (elovl4, 605512.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the elongation of very long chain fatty acids-like 4 gene (elovl4, 605512.0005) | rel=r_associated | relid=0 | w=28
  2729. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the enamelin gene (enam, 606585.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the enamelin gene (enam, 606585.0003) | rel=r_associated | relid=0 | w=28
  2730. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the endoplasmic reticulum membrane-associated rna degradation protein gene (ermard, 615532.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endoplasmic reticulum membrane-associated rna degradation protein gene (ermard, 615532.0001) | rel=r_associated | relid=0 | w=28
  2731. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the establishment of cohesion 1 homolog 2 gene (esco2, 609353.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the establishment of cohesion 1 homolog 2 gene (esco2, 609353.0001) | rel=r_associated | relid=0 | w=28
  2732. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the euchromatic histone methyltransferase-1 gene (ehmt1, 607001.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the euchromatic histone methyltransferase-1 gene (ehmt1, 607001.0001) | rel=r_associated | relid=0 | w=28
  2733. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the eukaryotic translation initiation factor 2-alpha kinase 4 gene (eif2ak4, 609280.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation initiation factor 2-alpha kinase 4 gene (eif2ak4, 609280.0001) | rel=r_associated | relid=0 | w=28
  2734. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 2 gene (eif2b2, 606454.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 2 gene (eif2b2, 606454.0001) | rel=r_associated | relid=0 | w=28
  2735. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the excision-repair cross-complementing group 8 gene (ercc6, 609413.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the excision-repair cross-complementing group 8 gene (ercc6, 609413.0009) | rel=r_associated | relid=0 | w=28
  2736. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the exosome component 3 gene (exosc3, 606489.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the exosome component 3 gene (exosc3, 606489.0001) | rel=r_associated | relid=0 | w=28
  2737. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the eyes absent-1 gene (eya1, 601653.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eyes absent-1 gene (eya1, 601653.0003) | rel=r_associated | relid=0 | w=28
  2738. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the factor xiii alpha subunit (f13a1, 134570.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the factor xiii alpha subunit (f13a1, 134570.0001) | rel=r_associated | relid=0 | w=28
  2739. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the family with sequence similarity 83, member h gene (fam83h, 611927.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the family with sequence similarity 83, member h gene (fam83h, 611927.0001) | rel=r_associated | relid=0 | w=28
  2740. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the fatty acid 2-hydroxylase gene (fa2h, 611026.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fatty acid 2-hydroxylase gene (fa2h, 611026.0001) | rel=r_associated | relid=0 | w=28
  2741. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the fibrillin 2 gene (fbn2, 612570.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibrillin 2 gene (fbn2, 612570.0011) | rel=r_associated | relid=0 | w=28
  2742. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the fibroblast growth factor gene-14 (fgf14, 601515.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor gene-14 (fgf14, 601515.0001) | rel=r_associated | relid=0 | w=28
  2743. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0004) | rel=r_associated | relid=0 | w=28
  2744. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the filamin a gene (300017.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the filamin a gene (300017.0009) | rel=r_associated | relid=0 | w=28
  2745. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the filamin a gene (flna, 300017.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the filamin a gene (flna, 300017.0010) | rel=r_associated | relid=0 | w=28
  2746. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the forkhead box c2 gene (foxc2, 602402.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead box c2 gene (foxc2, 602402.0001) | rel=r_associated | relid=0 | w=28
  2747. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the g protein-coupled receptor 98 gene (gpr98, 602851.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the g protein-coupled receptor 98 gene (gpr98, 602851.0002) | rel=r_associated | relid=0 | w=28
  2748. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the g protein-coupled receptor-179 gene (gpr179, 614515.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the g protein-coupled receptor-179 gene (gpr179, 614515.0001) | rel=r_associated | relid=0 | w=28
  2749. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the gamma-2 phospholipase c gene (plcg2, 600220.0004).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gamma-2 phospholipase c gene (plcg2, 600220.0004). | rel=r_associated | relid=0 | w=28
  2750. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0007) | rel=r_associated | relid=0 | w=28
  2751. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0004) | rel=r_associated | relid=0 | w=28
  2752. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the gene encoding exophilin-5 (exph5, 612878.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding exophilin-5 (exph5, 612878.0001) | rel=r_associated | relid=0 | w=28
  2753. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the gene encoding member a9 of the basic helix-loop-helix family (bhlha9, 615416.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding member a9 of the basic helix-loop-helix family (bhlha9, 615416.0001) | rel=r_associated | relid=0 | w=28
  2754. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the gene encoding the mapbp-interacting protein gene (mapbpip, 610389.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gene encoding the mapbp-interacting protein gene (mapbpip, 610389.0001) | rel=r_associated | relid=0 | w=28
  2755. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the glucose-6-phosphate transporter 1 gene (g6pt1, 602671.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glucose-6-phosphate transporter 1 gene (g6pt1, 602671.0001) | rel=r_associated | relid=0 | w=28
  2756. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the glutaminyl-trna synthetase gene (qars, 603727.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutaminyl-trna synthetase gene (qars, 603727.0001) | rel=r_associated | relid=0 | w=28
  2757. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the glutamyl-trna synthetase 2 gene (ears2, 612799.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glutamyl-trna synthetase 2 gene (ears2, 612799.0001) | rel=r_associated | relid=0 | w=28
  2758. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 gene (gpihbp1, 612757.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 gene (gpihbp1, 612757.0002) | rel=r_associated | relid=0 | w=28
  2759. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the glyoxylate reductase/hydroxypyruvate reductase gene (grhpr, 604296.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glyoxylate reductase/hydroxypyruvate reductase gene (grhpr, 604296.0001) | rel=r_associated | relid=0 | w=28
  2760. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the glypican 3 gene (gpc3, 300037.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glypican 3 gene (gpc3, 300037.0001) | rel=r_associated | relid=0 | w=28
  2761. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the growth factor-independent 1b gene (gfi1b, 604383.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the growth factor-independent 1b gene (gfi1b, 604383.0001) | rel=r_associated | relid=0 | w=28
  2762. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the guanine nucleotide-binding protein, alpha-activating activity polypeptide o gene (gnao1, 139311.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the guanine nucleotide-binding protein, alpha-activating activity polypeptide o gene (gnao1, 139311.0001) | rel=r_associated | relid=0 | w=28
  2763. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the guanylate cyclase 2d, membrane, retina-specific gene (gucy2d, 600179.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the guanylate cyclase 2d, membrane, retina-specific gene (gucy2d, 600179.0001) | rel=r_associated | relid=0 | w=28
  2764. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the heat-shock 27-kd protein 1 gene (hspb1, 602195.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heat-shock 27-kd protein 1 gene (hspb1, 602195.0001) | rel=r_associated | relid=0 | w=28
  2765. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the heparan-alpha-glucosaminide n-acetyltransferase gene (hgsnat, 610453.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the heparan-alpha-glucosaminide n-acetyltransferase gene (hgsnat, 610453.0001) | rel=r_associated | relid=0 | w=28
  2766. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the histone deacetylase 6 gene (hdac6, 300272.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the histone deacetylase 6 gene (hdac6, 300272.0001) | rel=r_associated | relid=0 | w=28
  2767. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homeobox (h6 family) 1 gene (hmx1, 142992.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeobox (h6 family) 1 gene (hmx1, 142992.0001) | rel=r_associated | relid=0 | w=28
  2768. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of drosophila frizzled-6 gene (fzd6, 603409.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of drosophila frizzled-6 gene (fzd6, 603409.0001) | rel=r_associated | relid=0 | w=28
  2769. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 27 gene (ift27, 615870.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 27 gene (ift27, 615870.0001) | rel=r_associated | relid=0 | w=28
  2770. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 80 gene (ift80, 611177.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 80 gene (ift80, 611177.0001) | rel=r_associated | relid=0 | w=28
  2771. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of the drosophila achaete-scute complex, 1 gene (ascl1, 100790.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila achaete-scute complex, 1 gene (ascl1, 100790.0001) | rel=r_associated | relid=0 | w=28
  2772. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of the drosophila bicaudal d, 2 gene (bicd2, 609797.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila bicaudal d, 2 gene (bicd2, 609797.0001) | rel=r_associated | relid=0 | w=28
  2773. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of the drosophila twist 2 gene (twist2, 607556.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila twist 2 gene (twist2, 607556.0001) | rel=r_associated | relid=0 | w=28
  2774. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of the mouse peripherin 2 gene (prph2, 179605.0021)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse peripherin 2 gene (prph2, 179605.0021) | rel=r_associated | relid=0 | w=28
  2775. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of the s. cerevisiae minichromosome maintenance 4 gene (mcm4, 602638.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae minichromosome maintenance 4 gene (mcm4, 602638.0001) | rel=r_associated | relid=0 | w=28
  2776. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of the s. cerevisiae sco2 gene (sco2, 604272.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae sco2 gene (sco2, 604272.0001) | rel=r_associated | relid=0 | w=28
  2777. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of the s. cerevisiae sec23 gene b (sec23b, 610512.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae sec23 gene b (sec23b, 610512.0001) | rel=r_associated | relid=0 | w=28
  2778. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the homolog of the yeast vacuolar protein sorting 37 gene (vps37a, 609927.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the yeast vacuolar protein sorting 37 gene (vps37a, 609927.0001) | rel=r_associated | relid=0 | w=28
  2779. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the hps4 gene (hps4, 606682)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hps4 gene (hps4, 606682) | rel=r_associated | relid=0 | w=28
  2780. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the hypoxanthine phosphoribosyltransferase gene (hprt1, 308000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hypoxanthine phosphoribosyltransferase gene (hprt1, 308000.0001) | rel=r_associated | relid=0 | w=28
  2781. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the il1 receptor accessory protein-like 1 gene (il1rapl, 300206.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the il1 receptor accessory protein-like 1 gene (il1rapl, 300206.0001) | rel=r_associated | relid=0 | w=28
  2782. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the insulin gene (ins, 176730.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the insulin gene (ins, 176730.0014) | rel=r_associated | relid=0 | w=28
  2783. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the insulin receptor gene (insr, 147670.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the insulin receptor gene (insr, 147670.0012) | rel=r_associated | relid=0 | w=28
  2784. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the integrin, alpha-8 gene (itga8, 604063.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the integrin, alpha-8 gene (itga8, 604063.0001) | rel=r_associated | relid=0 | w=28
  2785. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the intrinsic factor-vitamin b12 receptor gene (cubn, 602997.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the intrinsic factor-vitamin b12 receptor gene (cubn, 602997.0001) | rel=r_associated | relid=0 | w=28
  2786. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the isoprenoid synthase domain-containing protein gene (ispd, 614641.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the isoprenoid synthase domain-containing protein gene (ispd, 614641.0014) | rel=r_associated | relid=0 | w=28
  2787. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the janus kinase 2 gene (jak2, 147796.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the janus kinase 2 gene (jak2, 147796.0001) | rel=r_associated | relid=0 | w=28
  2788. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the janus kinase 3 gene (jak3, 600173.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the janus kinase 3 gene (jak3, 600173.0001) | rel=r_associated | relid=0 | w=28
  2789. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the k(lysine) acetyltransferase 6b gene (kat6b, 605880.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the k(lysine) acetyltransferase 6b gene (kat6b, 605880.0005) | rel=r_associated | relid=0 | w=28
  2790. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the keratin 5 gene (krt5, 148040.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 5 gene (krt5, 148040.0002) | rel=r_associated | relid=0 | w=28
  2791. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the keratin 74 gene (krt74, 608248.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 74 gene (krt74, 608248.0004) | rel=r_associated | relid=0 | w=28
  2792. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the kn motif- and ankyrin repeat domain-containing protein 2 gene (kank2, 614610.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kn motif- and ankyrin repeat domain-containing protein 2 gene (kank2, 614610.0001) | rel=r_associated | relid=0 | w=28
  2793. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the latent transforming growth factor-beta binding protein 4 gene (ltbp4, 604710.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the latent transforming growth factor-beta binding protein 4 gene (ltbp4, 604710.0001) | rel=r_associated | relid=0 | w=28
  2794. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the leptin gene (lep, 164160.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leptin gene (lep, 164160.0001) | rel=r_associated | relid=0 | w=28
  2795. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the leucine zipper transcription factor-like 1 gene (lztfl1, 606568.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucine zipper transcription factor-like 1 gene (lztfl1, 606568.0001) | rel=r_associated | relid=0 | w=28
  2796. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the lysophosphatidic acid receptor 6 gene (p2ry5, 609239.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lysophosphatidic acid receptor 6 gene (p2ry5, 609239.0001) | rel=r_associated | relid=0 | w=28
  2797. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the lysosome associated membrane protein-2 gene (lamp2, 309060.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lysosome associated membrane protein-2 gene (lamp2, 309060.0001) | rel=r_associated | relid=0 | w=28
  2798. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the mage-like 2 gene (magel2, 605283.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mage-like 2 gene (magel2, 605283.0001) | rel=r_associated | relid=0 | w=28
  2799. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the makorin-3 gene (mkrn3, 603856.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the makorin-3 gene (mkrn3, 603856.0001) | rel=r_associated | relid=0 | w=28
  2800. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the malin gene (nhlrc1, 608072.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the malin gene (nhlrc1, 608072.0001) | rel=r_associated | relid=0 | w=28
  2801. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the mediator complex subunit 17 gene (med17, 603810.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mediator complex subunit 17 gene (med17, 603810.0001) | rel=r_associated | relid=0 | w=28
  2802. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the melanophilin gene (mlph, 606526.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the melanophilin gene (mlph, 606526.0001) | rel=r_associated | relid=0 | w=28
  2803. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the methionyl-trna synthetase 2 gene (mars2, 609728.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methionyl-trna synthetase 2 gene (mars2, 609728.0001) | rel=r_associated | relid=0 | w=28
  2804. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the methyl-cpg-binding protein 2 gene (mecp2, 300005.0009).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methyl-cpg-binding protein 2 gene (mecp2, 300005.0009). | rel=r_associated | relid=0 | w=28
  2805. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the methylthioadenosine phosphorylase gene (mtap, 156540.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methylthioadenosine phosphorylase gene (mtap, 156540.0001) | rel=r_associated | relid=0 | w=28
  2806. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the microcephalin gene (mcph1, 607117.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the microcephalin gene (mcph1, 607117.0001) | rel=r_associated | relid=0 | w=28
  2807. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the microtubule-associated tau protein gene (mapt, 157140.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the microtubule-associated tau protein gene (mapt, 157140.0011) | rel=r_associated | relid=0 | w=28
  2808. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the midline 2 gene (mid2, 300204.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the midline 2 gene (mid2, 300204.0001) | rel=r_associated | relid=0 | w=28
  2809. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the mitochondrial acetoacetyl-coa thiolase gene (acat1, 607809.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial acetoacetyl-coa thiolase gene (acat1, 607809.0001) | rel=r_associated | relid=0 | w=28
  2810. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the mitochondrial ribosomal protein s16 (mrps16, 609204.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial ribosomal protein s16 (mrps16, 609204.0001) | rel=r_associated | relid=0 | w=28
  2811. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the mitochondrial trna-serine 2 gene (mtts2, 590085.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial trna-serine 2 gene (mtts2, 590085.0002) | rel=r_associated | relid=0 | w=28
  2812. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the mmab gene (mmab, 607568.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mmab gene (mmab, 607568.0001) | rel=r_associated | relid=0 | w=28
  2813. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the mucosa-associated lymphoid tissue lymphoma translocation gene 1 (malt1, 604860.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mucosa-associated lymphoid tissue lymphoma translocation gene 1 (malt1, 604860.0001) | rel=r_associated | relid=0 | w=28
  2814. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the muscle glycogen phosphorylase gene (pygm, 608455.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the muscle glycogen phosphorylase gene (pygm, 608455.0001) | rel=r_associated | relid=0 | w=28
  2815. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the myelin protein zero gene (mpz, 159440.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0013) | rel=r_associated | relid=0 | w=28
  2816. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the myosin va gene (myo5a, 160777)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin va gene (myo5a, 160777) | rel=r_associated | relid=0 | w=28
  2817. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the myosin viia gene (myo7a, 276903.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin viia gene (myo7a, 276903.0007) | rel=r_associated | relid=0 | w=28
  2818. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the myosin, heavy chain 9, non-muscle gene (myh9, 160775.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin, heavy chain 9, non-muscle gene (myh9, 160775.0005) | rel=r_associated | relid=0 | w=28
  2819. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the myotilin gene (ttid, 604103.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myotilin gene (ttid, 604103.0001) | rel=r_associated | relid=0 | w=28
  2820. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the myotubularin-related protein-2 gene (mtmr2, 603557.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myotubularin-related protein-2 gene (mtmr2, 603557.0001) | rel=r_associated | relid=0 | w=28
  2821. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, alpha/beta subunits gene (gnptab, 607840.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, alpha/beta subunits gene (gnptab, 607840.0003) | rel=r_associated | relid=0 | w=28
  2822. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the n-acetylglucosamine-6-sulfatase gene (gns, 607664.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the n-acetylglucosamine-6-sulfatase gene (gns, 607664.0001) | rel=r_associated | relid=0 | w=28
  2823. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 3 gene (ndufs3, 603846.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 3 gene (ndufs3, 603846.0001) | rel=r_associated | relid=0 | w=28
  2824. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 7 gene (ndufs7, 601825.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 7 gene (ndufs7, 601825.0001) | rel=r_associated | relid=0 | w=28
  2825. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 12 gene (ndufa12, 614530.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 12 gene (ndufa12, 614530.0001) | rel=r_associated | relid=0 | w=28
  2826. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the necap endocytosis-associated protein 1 gene (necap1, 611623.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the necap endocytosis-associated protein 1 gene (necap1, 611623.0001) | rel=r_associated | relid=0 | w=28
  2827. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the neurogenin 3 gene (neurog3, 604882.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neurogenin 3 gene (neurog3, 604882.0001) | rel=r_associated | relid=0 | w=28
  2828. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the never in mitosis gene a-related kinase 8 gene (nek8, 609799.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the never in mitosis gene a-related kinase 8 gene (nek8, 609799.0002) | rel=r_associated | relid=0 | w=28
  2829. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the nicastrin gene (ncstn, 605254.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nicastrin gene (ncstn, 605254.0001) | rel=r_associated | relid=0 | w=28
  2830. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the ninein gene (nin, 608684.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ninein gene (nin, 608684.0001) | rel=r_associated | relid=0 | w=28
  2831. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the nlr family, pyrin-domain containing 3 gene (nlrp3, 606416.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nlr family, pyrin-domain containing 3 gene (nlrp3, 606416.0001) | rel=r_associated | relid=0 | w=28
  2832. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the occludin gene (ocln, 602876.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the occludin gene (ocln, 602876.0001) | rel=r_associated | relid=0 | w=28
  2833. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the opa1 gene (opa1, 605290.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the opa1 gene (opa1, 605290.0001) | rel=r_associated | relid=0 | w=28
  2834. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the opa3 gene (606580.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the opa3 gene (606580.0002) | rel=r_associated | relid=0 | w=28
  2835. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the origin recognition complex, subunit 1, gene (orc1, 601902.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the origin recognition complex, subunit 1, gene (orc1, 601902.0001) | rel=r_associated | relid=0 | w=28
  2836. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the paired box gene 2 gene (pax2, 167409.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the paired box gene 2 gene (pax2, 167409.0013) | rel=r_associated | relid=0 | w=28
  2837. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the palmitoyl-protein thioesterase 1 gene (ppt1, 600722.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the palmitoyl-protein thioesterase 1 gene (ppt1, 600722.0001). | rel=r_associated | relid=0 | w=28
  2838. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the patatin-like phospholipase domain-containing protein 1 gene (pnpla1, 612121.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the patatin-like phospholipase domain-containing protein 1 gene (pnpla1, 612121.0001) | rel=r_associated | relid=0 | w=28
  2839. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the pericentrin 2 gene (pcnt2, 605925.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pericentrin 2 gene (pcnt2, 605925.0004) | rel=r_associated | relid=0 | w=28
  2840. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the peroxisome biogenesis factor 7 gene (pex7, 601757.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor 7 gene (pex7, 601757.0007) | rel=r_associated | relid=0 | w=28
  2841. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the peroxisome biogenesis factor-6 gene (pex6, 601498.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor-6 gene (pex6, 601498.0003) | rel=r_associated | relid=0 | w=28
  2842. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the phosphatidylinositol glycan, class l gene (pigl, 605947.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol glycan, class l gene (pigl, 605947.0001). | rel=r_associated | relid=0 | w=28
  2843. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the phosphatidylinositol glycan, class w gene (pigw, 610275.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol glycan, class w gene (pigw, 610275.0001) | rel=r_associated | relid=0 | w=28
  2844. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the phosphatidylinositol polyphosphate 5-phosphatase gene (ocrl, 300535.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol polyphosphate 5-phosphatase gene (ocrl, 300535.0005) | rel=r_associated | relid=0 | w=28
  2845. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the phosphoglycerate dehydrogenase gene (phgdh, 606879.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoglycerate dehydrogenase gene (phgdh, 606879.0007) | rel=r_associated | relid=0 | w=28
  2846. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the phosphoribosylpyrophosphate synthetase i gene (prps1, 311850.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoribosylpyrophosphate synthetase i gene (prps1, 311850.0001) | rel=r_associated | relid=0 | w=28
  2847. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the phosphoserine aminotransferase 1 gene (psat1, 610936.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoserine aminotransferase 1 gene (psat1, 610936.0003) | rel=r_associated | relid=0 | w=28
  2848. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the plasma membrane ca(2+)-transporting atpase 3 gene (atp2b3, 300014.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the plasma membrane ca(2+)-transporting atpase 3 gene (atp2b3, 300014.0001) | rel=r_associated | relid=0 | w=28
  2849. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the polymerase i, rna, subunit d gene (polr1d, 613715.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polymerase i, rna, subunit d gene (polr1d, 613715.0001) | rel=r_associated | relid=0 | w=28
  2850. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the post-gpi attachment to proteins 1 gene (pgap1, 611655.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the post-gpi attachment to proteins 1 gene (pgap1, 611655.0002) | rel=r_associated | relid=0 | w=28
  2851. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 11 gene (kcnj11, 600937.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 11 gene (kcnj11, 600937.0001) | rel=r_associated | relid=0 | w=28
  2852. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 607542.0032)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 607542.0032) | rel=r_associated | relid=0 | w=28
  2853. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the pr domain-containing protein-16 gene (prdm16, 605557.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pr domain-containing protein-16 gene (prdm16, 605557.0001) | rel=r_associated | relid=0 | w=28
  2854. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the prodynorphin gene (pdyn, 131340.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the prodynorphin gene (pdyn, 131340.0001) | rel=r_associated | relid=0 | w=28
  2855. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the proline/serine/threonine phosphatase-interacting protein 1 (pstpip1, 606347.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the proline/serine/threonine phosphatase-interacting protein 1 (pstpip1, 606347.0001) | rel=r_associated | relid=0 | w=28
  2856. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the protease inhibitor 12 gene (pi12, 602445.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protease inhibitor 12 gene (pi12, 602445.0001). | rel=r_associated | relid=0 | w=28
  2857. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the protein c gene (proc, 612283.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein c gene (proc, 612283.0001) | rel=r_associated | relid=0 | w=28
  2858. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the protein kinase, amp-activated, noncatalytic, gamma-2 gene (prkag2, 602743.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein kinase, amp-activated, noncatalytic, gamma-2 gene (prkag2, 602743.0001) | rel=r_associated | relid=0 | w=28
  2859. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the protein-tyrosine phosphatase receptor-type, q gene (ptprq, 603317.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein-tyrosine phosphatase receptor-type, q gene (ptprq, 603317.0001) | rel=r_associated | relid=0 | w=28
  2860. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the protein-tyrosine phosphatase, receptor-type, o gene (ptpro, 600579.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein-tyrosine phosphatase, receptor-type, o gene (ptpro, 600579.0001) | rel=r_associated | relid=0 | w=28
  2861. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the protoporphyrinogen oxidase gene (ppox, 600923.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protoporphyrinogen oxidase gene (ppox, 600923.0001) | rel=r_associated | relid=0 | w=28
  2862. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the pten-induced putative kinase-1 gene (pink1, 608309.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pten-induced putative kinase-1 gene (pink1, 608309.0001) | rel=r_associated | relid=0 | w=28
  2863. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the ras-associated protein rab18 gene (rab18, 602207.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ras-associated protein rab18 gene (rab18, 602207.0001) | rel=r_associated | relid=0 | w=28
  2864. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the rearranged during transfection protooncogene (ret, 164761.0045)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rearranged during transfection protooncogene (ret, 164761.0045) | rel=r_associated | relid=0 | w=28
  2865. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the receptor expression-enhancing protein 2 gene (reep2, 609347.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the receptor expression-enhancing protein 2 gene (reep2, 609347.0001) | rel=r_associated | relid=0 | w=28
  2866. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the regulator of telomere elongation helicase 1 gene (rtel1, 608833.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the regulator of telomere elongation helicase 1 gene (rtel1, 608833.0001) | rel=r_associated | relid=0 | w=28
  2867. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the regulatory factor x-associated protein gene (rfxap, 601861.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the regulatory factor x-associated protein gene (rfxap, 601861.0001) | rel=r_associated | relid=0 | w=28
  2868. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the retinoic acid-induced gene 1 (rai1, 607642.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the retinoic acid-induced gene 1 (rai1, 607642.0004) | rel=r_associated | relid=0 | w=28
  2869. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the ribosomal protein l21 gene (rpl12, 603636.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribosomal protein l21 gene (rpl12, 603636.0001) | rel=r_associated | relid=0 | w=28
  2870. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the ribosomal protein sa gene (rpsa, 150370.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribosomal protein sa gene (rpsa, 150370.0001) | rel=r_associated | relid=0 | w=28
  2871. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the rna-binding motif protein 10 gene (rbm10, 300080.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rna-binding motif protein 10 gene (rbm10, 300080.0001) | rel=r_associated | relid=0 | w=28
  2872. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the rna-specific adenosine deaminase gene (adar, 146920.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rna-specific adenosine deaminase gene (adar, 146920.0007) | rel=r_associated | relid=0 | w=28
  2873. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the rotatin gene (rttn, 610436.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rotatin gene (rttn, 610436.0001) | rel=r_associated | relid=0 | w=28
  2874. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the runt-related transcription factor 1 gene (runx1, 151385.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the runt-related transcription factor 1 gene (runx1, 151385.0001) | rel=r_associated | relid=0 | w=28
  2875. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the sal-like 1 gene (sall1, 602218.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sal-like 1 gene (sall1, 602218.0001) | rel=r_associated | relid=0 | w=28
  2876. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the sbds gene (sbds, 607444.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sbds gene (sbds, 607444.0001) | rel=r_associated | relid=0 | w=28
  2877. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the set-binding protein 1 gene (setbp1, 611060.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the set-binding protein 1 gene (setbp1, 611060.0006) | rel=r_associated | relid=0 | w=28
  2878. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the sh3 and cystein-rich domains 3 gene (stac3, 615521.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sh3 and cystein-rich domains 3 gene (stac3, 615521.0001) | rel=r_associated | relid=0 | w=28
  2879. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the sh3 domain and tetratricopeptide repeat domain 2 gene (sh3tc2, 608206.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sh3 domain and tetratricopeptide repeat domain 2 gene (sh3tc2, 608206.0001) | rel=r_associated | relid=0 | w=28
  2880. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the signal transducer and activator of transcription-3 gene (stat3, 102582.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the signal transducer and activator of transcription-3 gene (stat3, 102582.0001) | rel=r_associated | relid=0 | w=28
  2881. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the solute carrier family 10 (sodium/bile acid cotransporter family), member 2 gene (slc10a2, 601295.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 10 (sodium/bile acid cotransporter family), member 2 gene (slc10a2, 601295.0001) | rel=r_associated | relid=0 | w=28
  2882. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0019)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0019) | rel=r_associated | relid=0 | w=28
  2883. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, citrin), member 13 (slc25a13, 603859.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, citrin), member 13 (slc25a13, 603859.0001) | rel=r_associated | relid=0 | w=28
  2884. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, ornithine transporter), member 15 gene (slc25a15, 603861.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, ornithine transporter), member 15 gene (slc25a15, 603861.0001) | rel=r_associated | relid=0 | w=28
  2885. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the solute carrier family 30 (zinc transporter), member 2 gene (slc30a2, 609617.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 30 (zinc transporter), member 2 gene (slc30a2, 609617.0001) | rel=r_associated | relid=0 | w=28
  2886. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the solute carrier family 34 (sodium phosphate cotransporter), member 1 gene (slc34a1, 182309.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 34 (sodium phosphate cotransporter), member 1 gene (slc34a1, 182309.0003) | rel=r_associated | relid=0 | w=28
  2887. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the son of sevenless gene (sos1, 182530.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the son of sevenless gene (sos1, 182530.0002) | rel=r_associated | relid=0 | w=28
  2888. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the sprouty-related evh1 domain-containing protein 1 gene (spred1, 609291.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sprouty-related evh1 domain-containing protein 1 gene (spred1, 609291.0001) | rel=r_associated | relid=0 | w=28
  2889. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the sry-box 18 gene (sox18, 601618.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sry-box 18 gene (sox18, 601618.0001) | rel=r_associated | relid=0 | w=28
  2890. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the stt3, subunit of the oligosaccharyltransferase complex, s. cerevisiae, homolog of, a gene (stt3a, 601134.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the stt3, subunit of the oligosaccharyltransferase complex, s. cerevisiae, homolog of, a gene (stt3a, 601134.0001) | rel=r_associated | relid=0 | w=28
  2891. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the tachykinin receptor-3 gene (tac3r, 162332.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tachykinin receptor-3 gene (tac3r, 162332.0001) | rel=r_associated | relid=0 | w=28
  2892. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the teashirt zinc finger homeobox-1 gene (tshz1, 614427.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the teashirt zinc finger homeobox-1 gene (tshz1, 614427.0001) | rel=r_associated | relid=0 | w=28
  2893. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the telomerase reverse transcriptase gene (tert, 187270.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the telomerase reverse transcriptase gene (tert, 187270.0007) | rel=r_associated | relid=0 | w=28
  2894. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the tetratricopeptide repeat domain-containing protein-7a gene (ttc7a, 609332.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tetratricopeptide repeat domain-containing protein-7a gene (ttc7a, 609332.0001) | rel=r_associated | relid=0 | w=28
  2895. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the thioredoxin domain-containing 3 gene (txndc3, 607421.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thioredoxin domain-containing 3 gene (txndc3, 607421.0001) | rel=r_associated | relid=0 | w=28
  2896. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the thromboxane a synthase-1 gene (tbxas1, 274180.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thromboxane a synthase-1 gene (tbxas1, 274180.0001) | rel=r_associated | relid=0 | w=28
  2897. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the thyroid hormone receptor interactor 11 gene (trip11, 604505.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thyroid hormone receptor interactor 11 gene (trip11, 604505.0001) | rel=r_associated | relid=0 | w=28
  2898. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the thyroid transcription factor-1 gene (titf1, 600635.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thyroid transcription factor-1 gene (titf1, 600635.0001) | rel=r_associated | relid=0 | w=28
  2899. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the transcription factor-12 gene (tcf12, 600480.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transcription factor-12 gene (tcf12, 600480.0001) | rel=r_associated | relid=0 | w=28
  2900. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the transformation gene erbb-3 (erbb3, 190151.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transformation gene erbb-3 (erbb3, 190151.0001) | rel=r_associated | relid=0 | w=28
  2901. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the transient receptor potential cation channel, subfamily m, member 4 gene (trpm4, 606936.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transient receptor potential cation channel, subfamily m, member 4 gene (trpm4, 606936.0001) | rel=r_associated | relid=0 | w=28
  2902. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0002) | rel=r_associated | relid=0 | w=28
  2903. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the transmembrane protein 70 (tmem70, 612418.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 70 (tmem70, 612418.0001) | rel=r_associated | relid=0 | w=28
  2904. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the triadin gene (trdn, 603283.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the triadin gene (trdn, 603283.0001) | rel=r_associated | relid=0 | w=28
  2905. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the tripartite motif-containing protein 32 gene (trim32, 602290.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tripartite motif-containing protein 32 gene (trim32, 602290.0001) | rel=r_associated | relid=0 | w=28
  2906. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the trna 5-methylaminomethyl-2-thiouridylate methyltransferase gene (trmu, 610230.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the trna 5-methylaminomethyl-2-thiouridylate methyltransferase gene (trmu, 610230.0002) | rel=r_associated | relid=0 | w=28
  2907. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the trna nucleotidyltransferase, cca-adding, 1 gene (trnt1, 612907.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the trna nucleotidyltransferase, cca-adding, 1 gene (trnt1, 612907.0001) | rel=r_associated | relid=0 | w=28
  2908. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the trna-specific adenosine deaminase 3 gene (adat3, 615302.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the trna-specific adenosine deaminase 3 gene (adat3, 615302.0001) | rel=r_associated | relid=0 | w=28
  2909. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the troponin t3, fast skeletal muscle gene (tnnt3, 600692.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the troponin t3, fast skeletal muscle gene (tnnt3, 600692.0001) | rel=r_associated | relid=0 | w=28
  2910. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the tubulin tyrosine ligase-like family member 5 gene (ttll5, 612268.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin tyrosine ligase-like family member 5 gene (ttll5, 612268.0001) | rel=r_associated | relid=0 | w=28
  2911. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the tumor necrosis factor receptor superfamily, member 13c gene (tnfrsf13c, 606269.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tumor necrosis factor receptor superfamily, member 13c gene (tnfrsf13c, 606269.0001) | rel=r_associated | relid=0 | w=28
  2912. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the tumor protein p53 gene (tp53, 191170.0023)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tumor protein p53 gene (tp53, 191170.0023) | rel=r_associated | relid=0 | w=28
  2913. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0005) | rel=r_associated | relid=0 | w=28
  2914. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the uridine diphosphate glycosyltransferase 1 gene (ugt1, 191740.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the uridine diphosphate glycosyltransferase 1 gene (ugt1, 191740.0001) | rel=r_associated | relid=0 | w=28
  2915. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the uv-stimulated scaffold protein a gene (uvssa, 614632.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the uv-stimulated scaffold protein a gene (uvssa, 614632.0001) | rel=r_associated | relid=0 | w=28
  2916. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the v-ki-ras2 kirsten rat sarcoma viral oncogene homolog gene (kras, 190070.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-ki-ras2 kirsten rat sarcoma viral oncogene homolog gene (kras, 190070.0005) | rel=r_associated | relid=0 | w=28
  2917. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the v-raf murine sarcoma viral oncogene homolog b1 gene (braf, 164757.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the v-raf murine sarcoma viral oncogene homolog b1 gene (braf, 164757.0012) | rel=r_associated | relid=0 | w=28
  2918. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the vhl gene (vhl, 608537.0014)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the vhl gene (vhl, 608537.0014) | rel=r_associated | relid=0 | w=28
  2919. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the wd repeat-containing protein 72 gene (wdr72, 613214.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein 72 gene (wdr72, 613214.0001) | rel=r_associated | relid=0 | w=28
  2920. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0003) | rel=r_associated | relid=0 | w=28
  2921. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the wd repeat-containing protein-35 gene (wdr35, 613602.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wd repeat-containing protein-35 gene (wdr35, 613602.0005) | rel=r_associated | relid=0 | w=28
  2922. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the wfs1 gene (wfs1, 606201.0032)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wfs1 gene (wfs1, 606201.0032) | rel=r_associated | relid=0 | w=28
  2923. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the wingless-type mmtv integration site family, member 10b gene (wnt10b, 601906.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wingless-type mmtv integration site family, member 10b gene (wnt10b, 601906.0001) | rel=r_associated | relid=0 | w=28
  2924. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the wingless-type mmtv integration site family, member 4 gene (wnt4, 603490.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wingless-type mmtv integration site family, member 4 gene (wnt4, 603490.0001) | rel=r_associated | relid=0 | w=28
  2925. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the wt1 gene (wt1, 607102.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wt1 gene (wt1, 607102.0010) | rel=r_associated | relid=0 | w=28
  2926. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the yeast homolog, b, of the vacuolar protein sorting 33 gene (vps33b, 608552.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the yeast homolog, b, of the vacuolar protein sorting 33 gene (vps33b, 608552.0001) | rel=r_associated | relid=0 | w=28
  2927. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the zeta-chain-associated protein kinase 70 gene (zap70, 176947.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zeta-chain-associated protein kinase 70 gene (zap70, 176947.0001) | rel=r_associated | relid=0 | w=28
  2928. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the zinc finger and btb domain containing 18 gene (zbtb18, 608433.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger and btb domain containing 18 gene (zbtb18, 608433.0001) | rel=r_associated | relid=0 | w=28
  2929. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in receptor tyrosine kinase-like orphan receptor 2 gene (ror2, 602337.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in receptor tyrosine kinase-like orphan receptor 2 gene (ror2, 602337.0001) | rel=r_associated | relid=0 | w=28
  2930. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0001) | rel=r_associated | relid=0 | w=28
  2931. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the desmoplakin gene (dsp, 125647.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the desmoplakin gene (dsp, 125647.0004) | rel=r_associated | relid=0 | w=28
  2932. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the distal-less homeo box-3 gene (dlx3, 600525.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the distal-less homeo box-3 gene (dlx3, 600525.0001) | rel=r_associated | relid=0 | w=28
  2933. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the flj90130 gene (flj90130, 607461.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the flj90130 gene (flj90130, 607461.0001) | rel=r_associated | relid=0 | w=28
  2934. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the homolog of the mouse noggin gene (nog, 602991.0013)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the homolog of the mouse noggin gene (nog, 602991.0013) | rel=r_associated | relid=0 | w=28
  2935. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the indian hedgehog gene (ihh, 600726.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the indian hedgehog gene (ihh, 600726.0001) | rel=r_associated | relid=0 | w=28
  2936. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the keratin 17 gene (krt17, 148069.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the keratin 17 gene (krt17, 148069.0001) | rel=r_associated | relid=0 | w=28
  2937. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the lamin b receptor gene (lbr, 600024.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the lamin b receptor gene (lbr, 600024.0001) | rel=r_associated | relid=0 | w=28
  2938. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the otoferlin gene (otof, 603681.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the otoferlin gene (otof, 603681.0001) | rel=r_associated | relid=0 | w=28
  2939. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the properdin p factor gene (pfc, 300383.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the properdin p factor gene (pfc, 300383.0001) | rel=r_associated | relid=0 | w=28
  2940. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the red cell pyruvate kinase gene (pkrl, 609712.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the red cell pyruvate kinase gene (pkrl, 609712.0001). | rel=r_associated | relid=0 | w=28
  2941. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0009) | rel=r_associated | relid=0 | w=28
  2942. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the solute carrier family 16, monocarboxylic acid transporter, member 1 gene (slc16a1, 600682.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the solute carrier family 16, monocarboxylic acid transporter, member 1 gene (slc16a1, 600682.0001). | rel=r_associated | relid=0 | w=28
  2943. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the synaptosomal-associated protein 29kd gene (snap29, 604202.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the synaptosomal-associated protein 29kd gene (snap29, 604202.0001) | rel=r_associated | relid=0 | w=28
  2944. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the transcription factor ap-2 beta gene (tfap2b, 601601.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the transcription factor ap-2 beta gene (tfap2b, 601601.0001) | rel=r_associated | relid=0 | w=28
  2945. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0001). | rel=r_associated | relid=0 | w=28
  2946. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by somatic mosaic mutation in the guanine nucleotide-binding protein q gene (gnaq, 600998.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mosaic mutation in the guanine nucleotide-binding protein q gene (gnaq, 600998.0001) | rel=r_associated | relid=0 | w=28
  2947. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by somatic mutation in the alpha-stimulatory subunit of the guanine nucleotide-binding protein gene (gnas1, 139320.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the alpha-stimulatory subunit of the guanine nucleotide-binding protein gene (gnas1, 139320.0008) | rel=r_associated | relid=0 | w=28
  2948. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:caused by somatic mutation in the neuroblastoma ras viral (v-ras) oncogene homolog gene (nras, 164790.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the neuroblastoma ras viral (v-ras) oncogene homolog gene (nras, 164790.0002) | rel=r_associated | relid=0 | w=28
  2949. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:contiguous gene syndrome caused by deletion of 7.1 to 8.7mb of 16p12.2-p11.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by deletion of 7.1 to 8.7mb of 16p12.2-p11.2 | rel=r_associated | relid=0 | w=28
  2950. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:susceptibility conferred by mutation in the alpha-2-macroglobulin gene (a2m, 103950.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the alpha-2-macroglobulin gene (a2m, 103950.0005) | rel=r_associated | relid=0 | w=28
  2951. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:susceptibility conferred by mutation in the complement factor i gene (cfi, 217030.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the complement factor i gene (cfi, 217030.0010) | rel=r_associated | relid=0 | w=28
  2952. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:susceptibility conferred by mutation in the transforming growth factor-beta receptor, type i gene (tgfbr1, 190181.0009).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the transforming growth factor-beta receptor, type i gene (tgfbr1, 190181.0009). | rel=r_associated | relid=0 | w=28
  2953. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:susceptibility conferred by mutation in the tumor protein p53 gene (tp53, 191170.0042)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the tumor protein p53 gene (tp53, 191170.0042) | rel=r_associated | relid=0 | w=28
  2954. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:susceptibility conferred by mutation in the voltage-gated calcium channel beta-4 subunit gene (cacnb4, 601949.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the voltage-gated calcium channel beta-4 subunit gene (cacnb4, 601949.0001). | rel=r_associated | relid=0 | w=28
  2955. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 28 / 0.651 -> en:susceptibility conferred by mutations in the mhc class ii transactivator gene (mhc2ta, 600005.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutations in the mhc class ii transactivator gene (mhc2ta, 600005.0007) | rel=r_associated | relid=0 | w=28
  2956. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:a contiguous gene syndrome involving deletion of the digeorge syndrome chromosome region (dgcr) involving mutations in tup-like enhancer of split 1 (tuple1, 600237) and digeorge critical region gene 2 (dgcr2, 600594)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:a contiguous gene syndrome involving deletion of the digeorge syndrome chromosome region (dgcr) involving mutations in tup-like enhancer of split 1 (tuple1, 600237) and digeorge critical region gene 2 (dgcr2, 600594) | rel=r_associated | relid=0 | w=27
  2957. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:associated with mutation in the met protooncogene (met, 164860.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:associated with mutation in the met protooncogene (met, 164860.0008) | rel=r_associated | relid=0 | w=27
  2958. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:associated with snps in the b-cell cll/lymphoma 11a gene (bcl11a, 606557.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:associated with snps in the b-cell cll/lymphoma 11a gene (bcl11a, 606557.0001) | rel=r_associated | relid=0 | w=27
  2959. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by 1-mb duplication on chromosome 2q31.1
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by 1-mb duplication on chromosome 2q31.1 | rel=r_associated | relid=0 | w=27
  2960. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by a (cctg)n repeat expansion in the zinc finger protein 9 gene (znf9, 116955.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a (cctg)n repeat expansion in the zinc finger protein 9 gene (znf9, 116955.0001) | rel=r_associated | relid=0 | w=27
  2961. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by a 260-kb duplication on chromosome 11q12.2-11q12.3.
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by a 260-kb duplication on chromosome 11q12.2-11q12.3. | rel=r_associated | relid=0 | w=27
  2962. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by an sva retrotransposon insertion in an intron of the tata-binding protein-associated factor-1 gene (taf1, 313650.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by an sva retrotransposon insertion in an intron of the tata-binding protein-associated factor-1 gene (taf1, 313650.0001) | rel=r_associated | relid=0 | w=27
  2963. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by duplication of 120-527kb on 17p13.3
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by duplication of 120-527kb on 17p13.3 | rel=r_associated | relid=0 | w=27
  2964. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by imprinting defect on chromosome 14q32
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by imprinting defect on chromosome 14q32 | rel=r_associated | relid=0 | w=27
  2965. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in alpha-galactosidase a gene (gla, 300644.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in alpha-galactosidase a gene (gla, 300644.0001) | rel=r_associated | relid=0 | w=27
  2966. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in microrna 184 gene (mir184, 613146.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in microrna 184 gene (mir184, 613146.0001) | rel=r_associated | relid=0 | w=27
  2967. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in origin recognition complex, subunit 6, gene (orc6, 607213.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in origin recognition complex, subunit 6, gene (orc6, 607213.0001) | rel=r_associated | relid=0 | w=27
  2968. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the 11-beta-hydroxysteroid dehydrogenase type 1 gene (hsd11b1, 600713.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 11-beta-hydroxysteroid dehydrogenase type 1 gene (hsd11b1, 600713.0002) | rel=r_associated | relid=0 | w=27
  2969. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the 33-kd acidic cluster protein gene (acp33, 608181.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 33-kd acidic cluster protein gene (acp33, 608181.0001) | rel=r_associated | relid=0 | w=27
  2970. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the 5-hydroxytryptamine receptor-1a gene (htr1a, 109760.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 5-hydroxytryptamine receptor-1a gene (htr1a, 109760.0001) | rel=r_associated | relid=0 | w=27
  2971. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the 72-kd signal recognition particle gene (srp72. 602122.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 72-kd signal recognition particle gene (srp72. 602122.0001) | rel=r_associated | relid=0 | w=27
  2972. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the abhydrolase domain containing-5 gene (abhd5, 604780.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the abhydrolase domain containing-5 gene (abhd5, 604780.0001) | rel=r_associated | relid=0 | w=27
  2973. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the acyl-coa dehydrogenase-9 gene (acad9, 611103.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the acyl-coa dehydrogenase-9 gene (acad9, 611103.0001) | rel=r_associated | relid=0 | w=27
  2974. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the adaptor-related protein complex 1, sigma-2 subunit gene (ap1s2, 300629.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adaptor-related protein complex 1, sigma-2 subunit gene (ap1s2, 300629.0001) | rel=r_associated | relid=0 | w=27
  2975. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the adaptor-related protein complex 4, mu-1 subunit gene (ap4m1, 602296.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adaptor-related protein complex 4, mu-1 subunit gene (ap4m1, 602296.0001) | rel=r_associated | relid=0 | w=27
  2976. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the adenosine kinase gene (adk, 102750.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adenosine kinase gene (adk, 102750.0001) | rel=r_associated | relid=0 | w=27
  2977. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the aldehyde dehydrogenase 7 family, member a1 gene (aldh7a1, 107323.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aldehyde dehydrogenase 7 family, member a1 gene (aldh7a1, 107323.0001) | rel=r_associated | relid=0 | w=27
  2978. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the alpha subunit of the voltage-gated sodium channel type i gene (scn1a, 182389.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha subunit of the voltage-gated sodium channel type i gene (scn1a, 182389.0007) | rel=r_associated | relid=0 | w=27
  2979. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the alpha subunit of the voltage-gated sodium channel type ix gene (scn9a, 603415.0019)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha subunit of the voltage-gated sodium channel type ix gene (scn9a, 603415.0019) | rel=r_associated | relid=0 | w=27
  2980. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the alpha-n-acetylgalactosaminidase gene (naga, 104170.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-n-acetylgalactosaminidase gene (naga, 104170.0001) | rel=r_associated | relid=0 | w=27
  2981. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the alpha-stimulatory subunit of the guanine nucleotide-binding protein gene (gnas1, 139320.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-stimulatory subunit of the guanine nucleotide-binding protein gene (gnas1, 139320.0011) | rel=r_associated | relid=0 | w=27
  2982. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the alpha-synuclein gene (snca, 163890.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-synuclein gene (snca, 163890.0004) | rel=r_associated | relid=0 | w=27
  2983. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the ankyrin repeat domain-containing protein 26 gene (ankrd26, 610855.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ankyrin repeat domain-containing protein 26 gene (ankrd26, 610855.0001) | rel=r_associated | relid=0 | w=27
  2984. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the annexin a5 gene (anxa5, 131230.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the annexin a5 gene (anxa5, 131230.0001) | rel=r_associated | relid=0 | w=27
  2985. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the aquaporin-2 gene (aqp2, 107777.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the aquaporin-2 gene (aqp2, 107777.0001) | rel=r_associated | relid=0 | w=27
  2986. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the arginine vasopressin receptor-2 gene (avpr2, 300538.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the arginine vasopressin receptor-2 gene (avpr2, 300538.0001) | rel=r_associated | relid=0 | w=27
  2987. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the atp synthase, h+ transporting, mitochondrial f1 complex, alpha subunit 1 (atp5a1, 164360.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp synthase, h+ transporting, mitochondrial f1 complex, alpha subunit 1 (atp5a1, 164360.0001) | rel=r_associated | relid=0 | w=27
  2988. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the atp-binding cassette, subfamily a, member 1 gene (abca1, 600046.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily a, member 1 gene (abca1, 600046.0001) | rel=r_associated | relid=0 | w=27
  2989. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the atp-binding cassette, subfamily b, member 6 gene (abcb6, 605452.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily b, member 6 gene (abcb6, 605452.0008) | rel=r_associated | relid=0 | w=27
  2990. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the atp-binding cassette, subfamily d, member 1 gene (abcd1, 300371.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atp-binding cassette, subfamily d, member 1 gene (abcd1, 300371.0001) | rel=r_associated | relid=0 | w=27
  2991. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0010) | rel=r_associated | relid=0 | w=27
  2992. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the atpase, na+k+ transporting, alpha-2 polypeptide gene (atp1a2, 182340.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the atpase, na+k+ transporting, alpha-2 polypeptide gene (atp1a2, 182340.0005) | rel=r_associated | relid=0 | w=27
  2993. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the b9 domain-containing protein 2 gene (b9d2, 611951.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the b9 domain-containing protein 2 gene (b9d2, 611951.0001) | rel=r_associated | relid=0 | w=27
  2994. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the bbs2 gene (bbs2, 606151.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bbs2 gene (bbs2, 606151.0001) | rel=r_associated | relid=0 | w=27
  2995. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the beta subunit of the nonvoltage-gated sodium channel 1 gene (scnn1b, 600760.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta subunit of the nonvoltage-gated sodium channel 1 gene (scnn1b, 600760.0003) | rel=r_associated | relid=0 | w=27
  2996. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the beta-1,3-n-acetylglucosaminyltransferase gene (b3gnt1, 605581.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the beta-1,3-n-acetylglucosaminyltransferase gene (b3gnt1, 605581.0001) | rel=r_associated | relid=0 | w=27
  2997. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the brain protein 44-like gene (brp44l, 614738.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the brain protein 44-like gene (brp44l, 614738.0001) | rel=r_associated | relid=0 | w=27
  2998. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the c-type lectin domain family 7, member a gene (clec7a, 606264.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the c-type lectin domain family 7, member a gene (clec7a, 606264.0001) | rel=r_associated | relid=0 | w=27
  2999. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cadherin-related family, member 1 gene (cdhr1, 609502.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cadherin-related family, member 1 gene (cdhr1, 609502.0001) | rel=r_associated | relid=0 | w=27
  3000. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the carbohydrate sulfotransferase 3 gene (chst3, 603799.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the carbohydrate sulfotransferase 3 gene (chst3, 603799.0001) | rel=r_associated | relid=0 | w=27
  3001. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cardiac troponin-t2 gene (tnnt2, 191045.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cardiac troponin-t2 gene (tnnt2, 191045.0001) | rel=r_associated | relid=0 | w=27
  3002. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cardiotrophin-like cytokine gene (clcf1, 607672.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cardiotrophin-like cytokine gene (clcf1, 607672.0001) | rel=r_associated | relid=0 | w=27
  3003. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the caspase recruitment domain-containing protein 11 gene (card11, 607210.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the caspase recruitment domain-containing protein 11 gene (card11, 607210.0001) | rel=r_associated | relid=0 | w=27
  3004. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the caveolin-1 gene (cav1, 601047.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the caveolin-1 gene (cav1, 601047.0002) | rel=r_associated | relid=0 | w=27
  3005. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cdk5 regulatory subunit-associated protein 2 gene (cdk5rap2, 608201.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cdk5 regulatory subunit-associated protein 2 gene (cdk5rap2, 608201.0001) | rel=r_associated | relid=0 | w=27
  3006. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0005) | rel=r_associated | relid=0 | w=27
  3007. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0005) | rel=r_associated | relid=0 | w=27
  3008. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the chromatin-modifying protein 2b (chmp2b, 609512.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromatin-modifying protein 2b (chmp2b, 609512.0001) | rel=r_associated | relid=0 | w=27
  3009. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the chromosome 12 open reading frame 65 gene (c12orf65, 613541.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 12 open reading frame 65 gene (c12orf65, 613541.0003) | rel=r_associated | relid=0 | w=27
  3010. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the chromosome 5 open reading frame 42 gene (c5orf42, 614571.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 5 open reading frame 42 gene (c5orf42, 614571.0001) | rel=r_associated | relid=0 | w=27
  3011. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the chromosome 5 open reading frame 42 gene (c5orf42, 614571.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 5 open reading frame 42 gene (c5orf42, 614571.0007) | rel=r_associated | relid=0 | w=27
  3012. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cln3 gene (cln3, 607042.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cln3 gene (cln3, 607042.0001) | rel=r_associated | relid=0 | w=27
  3013. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the coagulation factor 2 gene (f2, 176930.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the coagulation factor 2 gene (f2, 176930.0009) | rel=r_associated | relid=0 | w=27
  3014. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the codanin 1 gene (cdan1, 607465.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the codanin 1 gene (cdan1, 607465.0001) | rel=r_associated | relid=0 | w=27
  3015. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0026)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0026) | rel=r_associated | relid=0 | w=27
  3016. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the collagen, type xxv, alpha-1 gene (col25a1, 610004.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type xxv, alpha-1 gene (col25a1, 610004.0001) | rel=r_associated | relid=0 | w=27
  3017. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the colony-stimulating factor 1 receptor gene (csf1r, 164770.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the colony-stimulating factor 1 receptor gene (csf1r, 164770.0001) | rel=r_associated | relid=0 | w=27
  3018. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the complement component 1, q subcomponent, c chain gene (c1qc, 120575.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement component 1, q subcomponent, c chain gene (c1qc, 120575.0001) | rel=r_associated | relid=0 | w=27
  3019. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the complement component 3 gene (c3, 120700.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement component 3 gene (c3, 120700.0001) | rel=r_associated | relid=0 | w=27
  3020. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the complement component 5 gene (c5, 120900.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement component 5 gene (c5, 120900.0006) | rel=r_associated | relid=0 | w=27
  3021. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the complement factor h-related 5 gene (cfhr5, 608593.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complement factor h-related 5 gene (cfhr5, 608593.0001) | rel=r_associated | relid=0 | w=27
  3022. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the complex i, subunit nd2 gene (mtnd2, 516001.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complex i, subunit nd2 gene (mtnd2, 516001.0001) | rel=r_associated | relid=0 | w=27
  3023. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the complex iv, cytochrome c oxidase subunit i gene (mtco1, 516030.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the complex iv, cytochrome c oxidase subunit i gene (mtco1, 516030.0001) | rel=r_associated | relid=0 | w=27
  3024. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the component of oligomeric golgi complex 6 gene (cog6, 606977.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the component of oligomeric golgi complex 6 gene (cog6, 606977.0002) | rel=r_associated | relid=0 | w=27
  3025. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the contactin 2 gene (cntn2, 190197.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the contactin 2 gene (cntn2, 190197.0001) | rel=r_associated | relid=0 | w=27
  3026. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cryptic-protein gene (cfc1, 605194.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cryptic-protein gene (cfc1, 605194.0004) | rel=r_associated | relid=0 | w=27
  3027. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cullin 7 gene (cul7, 609577.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cullin 7 gene (cul7, 609577.0001) | rel=r_associated | relid=0 | w=27
  3028. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cwf19-like protein 1 gene (cwf19l1, 616120.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cwf19-like protein 1 gene (cwf19l1, 616120.0001) | rel=r_associated | relid=0 | w=27
  3029. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cystatin a gene (csta, 184600.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cystatin a gene (csta, 184600.0001) | rel=r_associated | relid=0 | w=27
  3030. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cytochrome c oxidase, subunit via, polypeptide 1 gene (cox6a1, 602072.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase, subunit via, polypeptide 1 gene (cox6a1, 602072.0001) | rel=r_associated | relid=0 | w=27
  3031. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the cytochrome p450, subfamily iic (mephenytoin 4'-hydroxylase) gene (cyp2c, 124020.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450, subfamily iic (mephenytoin 4'-hydroxylase) gene (cyp2c, 124020.0001) | rel=r_associated | relid=0 | w=27
  3032. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the ddb1- and cul4-associated factor 8 gene (dcaf8, 615820.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ddb1- and cul4-associated factor 8 gene (dcaf8, 615820.0001). | rel=r_associated | relid=0 | w=27
  3033. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dedicator of cytokinesis 8 gene (dock8, 611432.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dedicator of cytokinesis 8 gene (dock8, 611432.0001) | rel=r_associated | relid=0 | w=27
  3034. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dehydrodolichyl diphosphate synthase gene (dhdds, 608172.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dehydrodolichyl diphosphate synthase gene (dhdds, 608172.0001) | rel=r_associated | relid=0 | w=27
  3035. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dermatan sulfate epimerase gene (dse, 605942.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dermatan sulfate epimerase gene (dse, 605942.0001) | rel=r_associated | relid=0 | w=27
  3036. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the desmin gene (des, 125660.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the desmin gene (des, 125660.0001) | rel=r_associated | relid=0 | w=27
  3037. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the desmoglein 1 gene (dsg1, 125670.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the desmoglein 1 gene (dsg1, 125670.0008) | rel=r_associated | relid=0 | w=27
  3038. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dihydropyrimidinase gene (dpys, 613326.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dihydropyrimidinase gene (dpys, 613326.0001) | rel=r_associated | relid=0 | w=27
  3039. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dimethylglycine dehydrogenase gene (dmgdh, 605849.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dimethylglycine dehydrogenase gene (dmgdh, 605849.0001) | rel=r_associated | relid=0 | w=27
  3040. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the distal-less homeobox-5 gene (dlx5, 600028.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the distal-less homeobox-5 gene (dlx5, 600028.0002) | rel=r_associated | relid=0 | w=27
  3041. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dna polymerase-gamma gene (polg, 174763.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dna polymerase-gamma gene (polg, 174763.0006) | rel=r_associated | relid=0 | w=27
  3042. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dolichyl-phosphate n-acetylglucosamine phosphotransferase gene (dpagt1, 191350.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dolichyl-phosphate n-acetylglucosamine phosphotransferase gene (dpagt1, 191350.0002) | rel=r_associated | relid=0 | w=27
  3043. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the doublecortin gene (dcx, 300121.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the doublecortin gene (dcx, 300121.0001) | rel=r_associated | relid=0 | w=27
  3044. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dynactin 1 gene (dctn1, 601143.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynactin 1 gene (dctn1, 601143.0006) | rel=r_associated | relid=0 | w=27
  3045. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dynactin-1 gene (dctn1, 601143.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynactin-1 gene (dctn1, 601143.0001) | rel=r_associated | relid=0 | w=27
  3046. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dynein, cytoplasmic 2, heavy chain 1 gene (dync2h1, 603297.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dynein, cytoplasmic 2, heavy chain 1 gene (dync2h1, 603297.0001) | rel=r_associated | relid=0 | w=27
  3047. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the dystrophin gene (dmd, 300377.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dystrophin gene (dmd, 300377.0001) | rel=r_associated | relid=0 | w=27
  3048. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the early growth response-2 gene (egr2, 129010.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the early growth response-2 gene (egr2, 129010.0004) | rel=r_associated | relid=0 | w=27
  3049. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the ecto-5-prime nucleotidase gene (nt5e, 129190.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ecto-5-prime nucleotidase gene (nt5e, 129190.0001) | rel=r_associated | relid=0 | w=27
  3050. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the ectonucleotide pyrophosphatase/phosphodiesterase-1 gene (enpp1, 173335.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ectonucleotide pyrophosphatase/phosphodiesterase-1 gene (enpp1, 173335.0002) | rel=r_associated | relid=0 | w=27
  3051. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the elg9, c. elegans, homolog of, 1 gene (egln1, 606425.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the elg9, c. elegans, homolog of, 1 gene (egln1, 606425.0004) | rel=r_associated | relid=0 | w=27
  3052. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the emerin gene (emd, 300384.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the emerin gene (emd, 300384.0001) | rel=r_associated | relid=0 | w=27
  3053. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the enolase 3 gene (eno3, 131370.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the enolase 3 gene (eno3, 131370.0001) | rel=r_associated | relid=0 | w=27
  3054. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the epidermal growth factor gene (egfr, 131550.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the epidermal growth factor gene (egfr, 131550.0007) | rel=r_associated | relid=0 | w=27
  3055. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the epididymal secretory protein he1 gene (npc1, 601015.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the epididymal secretory protein he1 gene (npc1, 601015.0001) | rel=r_associated | relid=0 | w=27
  3056. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the eukaryotic translation initiation factor 4a, isoform 3, gene (eif4a3, 608546.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation initiation factor 4a, isoform 3, gene (eif4a3, 608546.0001) | rel=r_associated | relid=0 | w=27
  3057. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the family with sequence similarity 134, member b gene (fam134b, 613114.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the family with sequence similarity 134, member b gene (fam134b, 613114.0001) | rel=r_associated | relid=0 | w=27
  3058. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the fatty acyl coa reductase 1 gene (far1, 616107.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fatty acyl coa reductase 1 gene (far1, 616107.0001) | rel=r_associated | relid=0 | w=27
  3059. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the ferritin light-chain gene (ftl, 134790.0010)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ferritin light-chain gene (ftl, 134790.0010) | rel=r_associated | relid=0 | w=27
  3060. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0028)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0028) | rel=r_associated | relid=0 | w=27
  3061. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0008) | rel=r_associated | relid=0 | w=27
  3062. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the fibroblast growth factor-16 gene (fgf16, 300827.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor-16 gene (fgf16, 300827.0001) | rel=r_associated | relid=0 | w=27
  3063. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the filamin b gene (flnb, 603381.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the filamin b gene (flnb, 603381.0004) | rel=r_associated | relid=0 | w=27
  3064. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the fk506-binding protein 10 gene (fkbp10, 607063.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fk506-binding protein 10 gene (fkbp10, 607063.0001) | rel=r_associated | relid=0 | w=27
  3065. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the fk506-binding protein-14 gene (fkbp14, 614505.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fk506-binding protein-14 gene (fkbp14, 614505.0001) | rel=r_associated | relid=0 | w=27
  3066. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the flavoprotein subunit of succinate dehydrogenase complex gene (sdha, 600857.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the flavoprotein subunit of succinate dehydrogenase complex gene (sdha, 600857.0001) | rel=r_associated | relid=0 | w=27
  3067. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the forkhead box c1 gene (foxc1, 601090.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead box c1 gene (foxc1, 601090.0001) | rel=r_associated | relid=0 | w=27
  3068. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the forkhead box p2 gene (foxp2, 605317.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the forkhead box p2 gene (foxp2, 605317.0001) | rel=r_associated | relid=0 | w=27
  3069. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606598.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606598.0006) | rel=r_associated | relid=0 | w=27
  3070. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the gap junction protein, beta-6 gene (gjb6, 604418.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gap junction protein, beta-6 gene (gjb6, 604418.0004) | rel=r_associated | relid=0 | w=27
  3071. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the gata zinc finger domain-containing protein-1 gene (gatad1, 614518.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata zinc finger domain-containing protein-1 gene (gatad1, 614518.0001) | rel=r_associated | relid=0 | w=27
  3072. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the gata-binding protein 1 gene (gata1, 305371.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gata-binding protein 1 gene (gata1, 305371.0006) | rel=r_associated | relid=0 | w=27
  3073. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the gdp-mannose pyrophosphorylase b gene (gmppb, 615320.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gdp-mannose pyrophosphorylase b gene (gmppb, 615320.0004) | rel=r_associated | relid=0 | w=27
  3074. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the glucose-6-phosphatase, catalytic gene (g6pc, 613742.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the glucose-6-phosphatase, catalytic gene (g6pc, 613742.0001) | rel=r_associated | relid=0 | w=27
  3075. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the granulocyte-macrophage colony-stimulating factor receptor, beta (csf2rb, 138981.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the granulocyte-macrophage colony-stimulating factor receptor, beta (csf2rb, 138981.0001) | rel=r_associated | relid=0 | w=27
  3076. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the gtp cyclohydrolase i gene (gch1, 600225.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the gtp cyclohydrolase i gene (gch1, 600225.0001) | rel=r_associated | relid=0 | w=27
  3077. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the guanine nucleotide-binding protein (g-protein), alpha-inhibiting activity polypeptide-3 gene (gnai3, 139370.0001])
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the guanine nucleotide-binding protein (g-protein), alpha-inhibiting activity polypeptide-3 gene (gnai3, 139370.0001]) | rel=r_associated | relid=0 | w=27
  3078. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the hexokinase 1 gene (hk1, 142600.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hexokinase 1 gene (hk1, 142600.0001) | rel=r_associated | relid=0 | w=27
  3079. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the high-mobility group box 3 gene (hmgb3, 300193.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the high-mobility group box 3 gene (hmgb3, 300193.0001) | rel=r_associated | relid=0 | w=27
  3080. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the histone deacetylase 8 gene (hdac8, 300269.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the histone deacetylase 8 gene (hdac8, 300269.0002) | rel=r_associated | relid=0 | w=27
  3081. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the holocytochrome c synthase gene (hccs, 300056.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the holocytochrome c synthase gene (hccs, 300056.0001) | rel=r_associated | relid=0 | w=27
  3082. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the homeobox b1 gene (hoxb1, 142968.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeobox b1 gene (hoxb1, 142968.0001) | rel=r_associated | relid=0 | w=27
  3083. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the homeobox d10 gene (hoxd10, 142984.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homeobox d10 gene (hoxd10, 142984.0001) | rel=r_associated | relid=0 | w=27
  3084. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the homolog of s. cerevisiae precursor mrna-processing factor-4 gene (prpf4, 607795.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of s. cerevisiae precursor mrna-processing factor-4 gene (prpf4, 607795.0001) | rel=r_associated | relid=0 | w=27
  3085. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 140 gene (ift140, 614620.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 140 gene (ift140, 614620.0001) | rel=r_associated | relid=0 | w=27
  3086. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the homolog of the drosophila hairy/enhancer of split 7 gene (hes7, 608059.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila hairy/enhancer of split 7 gene (hes7, 608059.0001) | rel=r_associated | relid=0 | w=27
  3087. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the homolog of the e. coli muts 6 gene (msh6, 600678.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the e. coli muts 6 gene (msh6, 600678.0012) | rel=r_associated | relid=0 | w=27
  3088. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the homolog of the gle1, (s. cerevisiae) rna export mediator gene (gle1, 603371.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the gle1, (s. cerevisiae) rna export mediator gene (gle1, 603371.0001) | rel=r_associated | relid=0 | w=27
  3089. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the homolog of the mouse aristaless-like 4 gene (alx4, 605420.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse aristaless-like 4 gene (alx4, 605420.0001) | rel=r_associated | relid=0 | w=27
  3090. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the homolog of the mouse hydrocephalus-inducing gene (hydin, 610812.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the mouse hydrocephalus-inducing gene (hydin, 610812.0001) | rel=r_associated | relid=0 | w=27
  3091. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the hps6 gene (hps6, 607522)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hps6 gene (hps6, 607522) | rel=r_associated | relid=0 | w=27
  3092. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the human homolog of the s. cerevisiae sil1 gene (608005.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the human homolog of the s. cerevisiae sil1 gene (608005.0001) | rel=r_associated | relid=0 | w=27
  3093. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the hydroxymethylbilane synthase gene (hmbs, 176000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the hydroxymethylbilane synthase gene (hmbs, 176000.0001) | rel=r_associated | relid=0 | w=27
  3094. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the immunoglobulin superfamily member-3 gene (igsf3, 603491.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the immunoglobulin superfamily member-3 gene (igsf3, 603491.0001) | rel=r_associated | relid=0 | w=27
  3095. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the immunoglobulin superfamily, member 1 gene (igsf1, 300137.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the immunoglobulin superfamily, member 1 gene (igsf1, 300137.0001) | rel=r_associated | relid=0 | w=27
  3096. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the insulin-like growth factor-1 receptor gene (igf1r, 147370.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the insulin-like growth factor-1 receptor gene (igf1r, 147370.0001) | rel=r_associated | relid=0 | w=27
  3097. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the integrin-beta-4 gene (itgb4, 147557.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the integrin-beta-4 gene (itgb4, 147557.0001) | rel=r_associated | relid=0 | w=27
  3098. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0003) | rel=r_associated | relid=0 | w=27
  3099. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the interleukin 10 receptor, alpha gene (il10ra, 146933.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interleukin 10 receptor, alpha gene (il10ra, 146933.0001) | rel=r_associated | relid=0 | w=27
  3100. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the iroquois homeobox protein-5 gene (irx5, 606195.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the iroquois homeobox protein-5 gene (irx5, 606195.0001) | rel=r_associated | relid=0 | w=27
  3101. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the isg15 ubiquitin-like modifier gene (isg15, 146571.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the isg15 ubiquitin-like modifier gene (isg15, 146571.0001) | rel=r_associated | relid=0 | w=27
  3102. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the jumonji, at-rich interactive domain 1c gene gene (jarid1c, 314690.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the jumonji, at-rich interactive domain 1c gene gene (jarid1c, 314690.0001) | rel=r_associated | relid=0 | w=27
  3103. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the keratin 1 gene (krt1, 139350.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 1 gene (krt1, 139350.0001) | rel=r_associated | relid=0 | w=27
  3104. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the keratin 16 gene (krt16, 148067.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 16 gene (krt16, 148067.0001) | rel=r_associated | relid=0 | w=27
  3105. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the keratin 17 gene (krt17, 148069.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 17 gene (krt17, 148069.0004) | rel=r_associated | relid=0 | w=27
  3106. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the keratin 74 gene (krt74, 608248.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the keratin 74 gene (krt74, 608248.0001) | rel=r_associated | relid=0 | w=27
  3107. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the kiaa0226 gene (kiaa0226, 613516.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kiaa0226 gene (kiaa0226, 613516.0001) | rel=r_associated | relid=0 | w=27
  3108. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the kiaa1033 gene (kiaa1033, 615748.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kiaa1033 gene (kiaa1033, 615748.0001) | rel=r_associated | relid=0 | w=27
  3109. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the kidney chloride channel b gene (clcnkb, 602023.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kidney chloride channel b gene (clcnkb, 602023.0001) | rel=r_associated | relid=0 | w=27
  3110. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the kinesin-5a gene (kif5a, 602821.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kinesin-5a gene (kif5a, 602821.0001) | rel=r_associated | relid=0 | w=27
  3111. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the kit ligand gene (kitlg, 184745.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kit ligand gene (kitlg, 184745.0003) | rel=r_associated | relid=0 | w=27
  3112. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the la ribonucleoprotein domain family, member 7 gene (larp7, 612026.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the la ribonucleoprotein domain family, member 7 gene (larp7, 612026.0001) | rel=r_associated | relid=0 | w=27
  3113. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the lamin a/c gene (lmna, 150330.0030)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lamin a/c gene (lmna, 150330.0030) | rel=r_associated | relid=0 | w=27
  3114. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the laminin alpha-2 chain gene (lama2, 156225.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the laminin alpha-2 chain gene (lama2, 156225.0001) | rel=r_associated | relid=0 | w=27
  3115. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the leucine-rich repeat-containing protein 50 gene (lrrc50, 613190.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the leucine-rich repeat-containing protein 50 gene (lrrc50, 613190.0001) | rel=r_associated | relid=0 | w=27
  3116. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the lim domain-binding 3 gene (ldb3, 605906.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lim domain-binding 3 gene (ldb3, 605906.0001) | rel=r_associated | relid=0 | w=27
  3117. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the limbin gene (evc2, 607261.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the limbin gene (evc2, 607261.0009) | rel=r_associated | relid=0 | w=27
  3118. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the lipase h gene (liph, 607365.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lipase h gene (liph, 607365.0001) | rel=r_associated | relid=0 | w=27
  3119. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the lmbr1 domain-containing protein 1 gene (lmbrd1, 612625.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lmbr1 domain-containing protein 1 gene (lmbrd1, 612625.0001). | rel=r_associated | relid=0 | w=27
  3120. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the low density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the low density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0015) | rel=r_associated | relid=0 | w=27
  3121. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the lysyl-trna synthetase gene (lars, 601421.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the lysyl-trna synthetase gene (lars, 601421.0003) | rel=r_associated | relid=0 | w=27
  3122. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the mannosyl (alpha-1,6-)-glycoprotein beta-1,2-n-acetylglucosaminyltransferase gene (mgat2, 602616.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mannosyl (alpha-1,6-)-glycoprotein beta-1,2-n-acetylglucosaminyltransferase gene (mgat2, 602616.0001) | rel=r_associated | relid=0 | w=27
  3123. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the medium-chain acyl-coa dehydrogenase (mcad) gene (acadm, 607008.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the medium-chain acyl-coa dehydrogenase (mcad) gene (acadm, 607008.0001) | rel=r_associated | relid=0 | w=27
  3124. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the member 5 solute carrier family 39 (zinc transporter) gene (slc39a5, 608730.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the member 5 solute carrier family 39 (zinc transporter) gene (slc39a5, 608730.0001) | rel=r_associated | relid=0 | w=27
  3125. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the mesenchyme homeobox 1 gene (meox1, 600147.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mesenchyme homeobox 1 gene (meox1, 600147.0001) | rel=r_associated | relid=0 | w=27
  3126. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the metabotropic glutamate receptor 1 gene (grm1, 604473.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the metabotropic glutamate receptor 1 gene (grm1, 604473.0001) | rel=r_associated | relid=0 | w=27
  3127. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the methyl-cpg-binding domain protein 5 gene (mbd5, 611472.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methyl-cpg-binding domain protein 5 gene (mbd5, 611472.0001) | rel=r_associated | relid=0 | w=27
  3128. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the methylmalonyl-coa epimerase gene (mcee, 608419.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methylmalonyl-coa epimerase gene (mcee, 608419.0001) | rel=r_associated | relid=0 | w=27
  3129. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the methylmalonyl-coa mutase gene (mut, 251000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the methylmalonyl-coa mutase gene (mut, 251000.0001) | rel=r_associated | relid=0 | w=27
  3130. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the micro rna 17 host gene (mir17hg, 609415)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the micro rna 17 host gene (mir17hg, 609415) | rel=r_associated | relid=0 | w=27
  3131. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the mitochondrial phenylalanyl-trna synthetase 2 gene (fars2, 611592.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial phenylalanyl-trna synthetase 2 gene (fars2, 611592.0001) | rel=r_associated | relid=0 | w=27
  3132. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the mitochondrial ts translation elongation factor gene (tsfm, 604723.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial ts translation elongation factor gene (tsfm, 604723.0001) | rel=r_associated | relid=0 | w=27
  3133. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the molybdenum cofactor synthesis gene 2 (mocs2, 603708.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the molybdenum cofactor synthesis gene 2 (mocs2, 603708.0001) | rel=r_associated | relid=0 | w=27
  3134. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the myeloid/lymphoid or mixed lineage leukemia 2 gene (mll2, 602113.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myeloid/lymphoid or mixed lineage leukemia 2 gene (mll2, 602113.0001) | rel=r_associated | relid=0 | w=27
  3135. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the nadh dehydrogenase, subunit 6 gene (mtnd6, 516006.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh dehydrogenase, subunit 6 gene (mtnd6, 516006.0002) | rel=r_associated | relid=0 | w=27
  3136. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 beta subcomplex 3 gene (ndufb3, 603839.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 beta subcomplex 3 gene (ndufb3, 603839.0001) | rel=r_associated | relid=0 | w=27
  3137. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the natriuretic peptide receptor b gene (npr2, 108961.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the natriuretic peptide receptor b gene (npr2, 108961.0001) | rel=r_associated | relid=0 | w=27
  3138. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the nebulin gene (neb, 160650.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nebulin gene (neb, 160650.0001) | rel=r_associated | relid=0 | w=27
  3139. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the nephrocystin 3 gene (nphp3, 608002.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nephrocystin 3 gene (nphp3, 608002.0001) | rel=r_associated | relid=0 | w=27
  3140. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the neurofibromin gene (nf1, 162200.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neurofibromin gene (nf1, 162200.0018) | rel=r_associated | relid=0 | w=27
  3141. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the neuronal nicotinic cholinergic receptor, alpha polypeptide 2 gene (chrna2, 118502.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the neuronal nicotinic cholinergic receptor, alpha polypeptide 2 gene (chrna2, 118502.0001) | rel=r_associated | relid=0 | w=27
  3142. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the never in mitosis gene a-related kinase 1 gene (nek1, 604588.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the never in mitosis gene a-related kinase 1 gene (nek1, 604588.0001) | rel=r_associated | relid=0 | w=27
  3143. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the nipped-b-like gene (nipbl, 608667.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nipped-b-like gene (nipbl, 608667.0001) | rel=r_associated | relid=0 | w=27
  3144. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the nonselective sodium leak channel gene (nalcn, 611549.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the nonselective sodium leak channel gene (nalcn, 611549.0001) | rel=r_associated | relid=0 | w=27
  3145. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the p21-activated kinase 3 gene (pak3, 300142.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the p21-activated kinase 3 gene (pak3, 300142.0001) | rel=r_associated | relid=0 | w=27
  3146. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the paired box gene 3 (pax3, 606597.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the paired box gene 3 (pax3, 606597.0009) | rel=r_associated | relid=0 | w=27
  3147. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the pancreas transcription factor 1, alpha subunit gene (ptf1a, 607094.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pancreas transcription factor 1, alpha subunit gene (ptf1a, 607094.0001) | rel=r_associated | relid=0 | w=27
  3148. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the pantothenate kinase-2 gene (pank2, 607157.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pantothenate kinase-2 gene (pank2, 607157.0001) | rel=r_associated | relid=0 | w=27
  3149. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the parathyroid hormone receptor-1 gene (pthr1, 168468.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the parathyroid hormone receptor-1 gene (pthr1, 168468.0012) | rel=r_associated | relid=0 | w=27
  3150. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the perilipin-1 gene (plin1, 170290.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the perilipin-1 gene (plin1, 170290.0001) | rel=r_associated | relid=0 | w=27
  3151. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the peroxisome biogenesis factor-5 gene (pex5, 600414.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peroxisome biogenesis factor-5 gene (pex5, 600414.0002) | rel=r_associated | relid=0 | w=27
  3152. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the phosphate regulating endopeptidase homolog, x-linked, gene (phex, 300550.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphate regulating endopeptidase homolog, x-linked, gene (phex, 300550.0001) | rel=r_associated | relid=0 | w=27
  3153. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the phosphatidylinositol glycan, class t gene (pigt, 610272.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol glycan, class t gene (pigt, 610272.0001) | rel=r_associated | relid=0 | w=27
  3154. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the phosphoglycerate kinase 1 gene (pgk1, 311800.0002).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoglycerate kinase 1 gene (pgk1, 311800.0002). | rel=r_associated | relid=0 | w=27
  3155. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the phospholamban gene (pln, 172405.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phospholamban gene (pln, 172405.0002) | rel=r_associated | relid=0 | w=27
  3156. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0001) | rel=r_associated | relid=0 | w=27
  3157. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the phospholipase c, epsilon-1 gene (plce1, 608414.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phospholipase c, epsilon-1 gene (plce1, 608414.0001) | rel=r_associated | relid=0 | w=27
  3158. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the platelet glycoprotein ib, beta polypeptide, gene (gp1bb, 138720.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the platelet glycoprotein ib, beta polypeptide, gene (gp1bb, 138720.0001) | rel=r_associated | relid=0 | w=27
  3159. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the platelet-activating factor acetylhydrolase, isoform 1b, alpha subunit gene (pafah1b1, 601545.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the platelet-activating factor acetylhydrolase, isoform 1b, alpha subunit gene (pafah1b1, 601545.0001) | rel=r_associated | relid=0 | w=27
  3160. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the polymerase (dna-directed), delta 1, catalytic subunit gene (pold1, 174761.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polymerase (dna-directed), delta 1, catalytic subunit gene (pold1, 174761.0003) | rel=r_associated | relid=0 | w=27
  3161. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the post-gpi attachment to proteins 2 gene (pgap2, 615187.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the post-gpi attachment to proteins 2 gene (pgap2, 615187.0001) | rel=r_associated | relid=0 | w=27
  3162. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 11 gene (kcnj11, 600937.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 11 gene (kcnj11, 600937.0002) | rel=r_associated | relid=0 | w=27
  3163. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 2 gene (kcnj2, 600681.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 2 gene (kcnj2, 600681.0001) | rel=r_associated | relid=0 | w=27
  3164. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the potassium channel, subfamily t, member 1 gene (kcnt1, 608167.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium channel, subfamily t, member 1 gene (kcnt1, 608167.0001) | rel=r_associated | relid=0 | w=27
  3165. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 192500.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 192500.0001) | rel=r_associated | relid=0 | w=27
  3166. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 3 gene (kcnq3, 602232.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 3 gene (kcnq3, 602232.0001) | rel=r_associated | relid=0 | w=27
  3167. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the presenilin-2 gene (psen2, 600759.0008)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the presenilin-2 gene (psen2, 600759.0008) | rel=r_associated | relid=0 | w=27
  3168. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the protein kinase c substrate, 80-kd heavy chain gene (prkcsh, 177060.0001), or in the gene encoding the human homolog of s. cerevisiae sec63 (sec63, 608648.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the protein kinase c substrate, 80-kd heavy chain gene (prkcsh, 177060.0001), or in the gene encoding the human homolog of s. cerevisiae sec63 (sec63, 608648.0001) | rel=r_associated | relid=0 | w=27
  3169. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the pulmonary-associated surfactant protein a2 gene (sftpa2, 178642.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pulmonary-associated surfactant protein a2 gene (sftpa2, 178642.0001) | rel=r_associated | relid=0 | w=27
  3170. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the pyrin gene (mefv, 608107.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pyrin gene (mefv, 608107.0018) | rel=r_associated | relid=0 | w=27
  3171. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the pyruvate carboxylase gene (pc, 608786.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pyruvate carboxylase gene (pc, 608786.0001) | rel=r_associated | relid=0 | w=27
  3172. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the pyruvate dehydrogenase kinase, isoenzyme 3 gene (pdk3, 300906.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pyruvate dehydrogenase kinase, isoenzyme 3 gene (pdk3, 300906.0001) | rel=r_associated | relid=0 | w=27
  3173. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the ras guanyl nucleotide-releasing protein 2 gene (rasgrp2, 605577.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ras guanyl nucleotide-releasing protein 2 gene (rasgrp2, 605577.0001) | rel=r_associated | relid=0 | w=27
  3174. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the rb1 gene (rb1, 614041.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rb1 gene (rb1, 614041.0001) | rel=r_associated | relid=0 | w=27
  3175. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the receptor tyrosine kinase-like orphan receptor 2 gene (ror2, 602337.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the receptor tyrosine kinase-like orphan receptor 2 gene (ror2, 602337.0004) | rel=r_associated | relid=0 | w=27
  3176. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the retina and anterior neural fold homeobox gene (rax, 601881.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the retina and anterior neural fold homeobox gene (rax, 601881.0001) | rel=r_associated | relid=0 | w=27
  3177. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the ribonucleotide reductase, m2 b gene (rrm2b, 604712.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribonucleotide reductase, m2 b gene (rrm2b, 604712.0001) | rel=r_associated | relid=0 | w=27
  3178. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the ring finger protein 216 gene (rnf216, 609948.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ring finger protein 216 gene (rnf216, 609948.0001) | rel=r_associated | relid=0 | w=27
  3179. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the rp9 gene (rp9, 607331.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rp9 gene (rp9, 607331.0002) | rel=r_associated | relid=0 | w=27
  3180. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the rpgrip1-like gene (rpgrip1l, 610937.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the rpgrip1-like gene (rpgrip1l, 610937.0011) | rel=r_associated | relid=0 | w=27
  3181. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the s. cerevisiae homolog of mediator of rna polymerase ii transcription, subunit 25 gene (med25, 610197.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the s. cerevisiae homolog of mediator of rna polymerase ii transcription, subunit 25 gene (med25, 610197.0001). | rel=r_associated | relid=0 | w=27
  3182. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the s. cerevisiae homolog of trna splicing endonuclease 54 (tsen54, 608755.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the s. cerevisiae homolog of trna splicing endonuclease 54 (tsen54, 608755.0001) | rel=r_associated | relid=0 | w=27
  3183. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the semaphorin 4a gene (sema4a, 607292.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the semaphorin 4a gene (sema4a, 607292.0001) | rel=r_associated | relid=0 | w=27
  3184. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the septin 12 gene (sept12, 611562.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the septin 12 gene (sept12, 611562.0001) | rel=r_associated | relid=0 | w=27
  3185. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the serpin peptidase inhibitor, clade a, member 6 gene (serpina6, 122500.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the serpin peptidase inhibitor, clade a, member 6 gene (serpina6, 122500.0001) | rel=r_associated | relid=0 | w=27
  3186. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the serpin peptidase inhibitor, clade b (ovalbumin), member 7 gene (serpinb7, 603357.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the serpin peptidase inhibitor, clade b (ovalbumin), member 7 gene (serpinb7, 603357.0001) | rel=r_associated | relid=0 | w=27
  3187. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the sideroflexin 4 gene (sfxn4, 615564.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sideroflexin 4 gene (sfxn4, 615564.0001) | rel=r_associated | relid=0 | w=27
  3188. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the sigma nonopioid intracellular receptor 1 gene (sigmar1, 601978.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sigma nonopioid intracellular receptor 1 gene (sigmar1, 601978.0001) | rel=r_associated | relid=0 | w=27
  3189. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0001) | rel=r_associated | relid=0 | w=27
  3190. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 gene (cact, 613698.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 gene (cact, 613698.0001) | rel=r_associated | relid=0 | w=27
  3191. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene (slc25a4, 103220.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene (slc25a4, 103220.0005) | rel=r_associated | relid=0 | w=27
  3192. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the solute carrier family 25, member 38 gene (slc25a38, 610819.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25, member 38 gene (slc25a38, 610819.0001) | rel=r_associated | relid=0 | w=27
  3193. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the solute carrier family 26, member 4 gene (slc26a4, 605646.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 26, member 4 gene (slc26a4, 605646.0001) | rel=r_associated | relid=0 | w=27
  3194. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the solute carrier family 3 (cystine, dibasic, and neutral amino acid transporter), member 1 gene (slc3a1, 104614.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 3 (cystine, dibasic, and neutral amino acid transporter), member 1 gene (slc3a1, 104614.0001) | rel=r_associated | relid=0 | w=27
  3195. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the solute carrier family 5 (sodium iodide symporter), member 5 gene (slc5a5, 601843.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 5 (sodium iodide symporter), member 5 gene (slc5a5, 601843.0001) | rel=r_associated | relid=0 | w=27
  3196. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the solute carrier family 5 (sodium/glucose cotransporter), member 2 gene (slc5a2, 182381.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 5 (sodium/glucose cotransporter), member 2 gene (slc5a2, 182381.0001) | rel=r_associated | relid=0 | w=27
  3197. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the son of sevenless, drosophila, homolog 1 gene (sos1, 182530.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the son of sevenless, drosophila, homolog 1 gene (sos1, 182530.0001) | rel=r_associated | relid=0 | w=27
  3198. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the sonic hedgehog gene (shh, 600725.0016)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sonic hedgehog gene (shh, 600725.0016) | rel=r_associated | relid=0 | w=27
  3199. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the st3 beta-galactoside alpha-2,3-sialyltransferase 3 gene (st3gal3, 606494.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the st3 beta-galactoside alpha-2,3-sialyltransferase 3 gene (st3gal3, 606494.0003) | rel=r_associated | relid=0 | w=27
  3200. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605291.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605291.0001) | rel=r_associated | relid=0 | w=27
  3201. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the stt3, subunit of the oligosaccharyltransferase complex, s. cerevisiae, homolog of, b gene (stt3b, 608605.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the stt3, subunit of the oligosaccharyltransferase complex, s. cerevisiae, homolog of, b gene (stt3b, 608605.0001) | rel=r_associated | relid=0 | w=27
  3202. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the succinate dehydrogenase complex subunit b gene (sdhb, 185470.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the succinate dehydrogenase complex subunit b gene (sdhb, 185470.0001) | rel=r_associated | relid=0 | w=27
  3203. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the synaptic nuclear envelope protein 1 gene (syne2, 608442.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the synaptic nuclear envelope protein 1 gene (syne2, 608442.0001). | rel=r_associated | relid=0 | w=27
  3204. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the synaptic nuclear envelope protein-1 gene (syne1, 608441.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the synaptic nuclear envelope protein-1 gene (syne1, 608441.0001) | rel=r_associated | relid=0 | w=27
  3205. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the syntaxin 11 gene (stx11, 605014.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the syntaxin 11 gene (stx11, 605014.0001) | rel=r_associated | relid=0 | w=27
  3206. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the tbc1 domain family, member 7 gene (tbc1d7, 612655.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tbc1 domain family, member 7 gene (tbc1d7, 612655.0001) | rel=r_associated | relid=0 | w=27
  3207. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the tdp-glucose 4,6-dehydratase gene (tgds, 616146.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tdp-glucose 4,6-dehydratase gene (tgds, 616146.0001) | rel=r_associated | relid=0 | w=27
  3208. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the telomerase reverse transcriptase gene (tert, 187270.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the telomerase reverse transcriptase gene (tert, 187270.0001) | rel=r_associated | relid=0 | w=27
  3209. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the tenascin xb gene (tnxb, 600985.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tenascin xb gene (tnxb, 600985.0001) | rel=r_associated | relid=0 | w=27
  3210. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the tetratricopeptide repeat domain 21b gene (ttc21b, 612014.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tetratricopeptide repeat domain 21b gene (ttc21b, 612014.0004) | rel=r_associated | relid=0 | w=27
  3211. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the tho complex, subunit 6 gene (thoc6, 615403.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tho complex, subunit 6 gene (thoc6, 615403.0001) | rel=r_associated | relid=0 | w=27
  3212. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the thrombospondin-type laminin g domain and ear repeats gene (tspear, 612920.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thrombospondin-type laminin g domain and ear repeats gene (tspear, 612920.0001) | rel=r_associated | relid=0 | w=27
  3213. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the thyroglobulin gene (tg, 188450.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thyroglobulin gene (tg, 188450.0001) | rel=r_associated | relid=0 | w=27
  3214. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the thyroid-stimulating hormone, beta polypeptide gene (tshb, 188540.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the thyroid-stimulating hormone, beta polypeptide gene (tshb, 188540.0001) | rel=r_associated | relid=0 | w=27
  3215. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the tia1 cytotoxic granule-associated rna-binding protein gene (tia1, 603518.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tia1 cytotoxic granule-associated rna-binding protein gene (tia1, 603518.0001) | rel=r_associated | relid=0 | w=27
  3216. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0030)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0030) | rel=r_associated | relid=0 | w=27
  3217. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the transmembrane protein 237 (tmem237, 614423.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 237 (tmem237, 614423.0001) | rel=r_associated | relid=0 | w=27
  3218. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the transmembrane protein 240 gene (tmem240, 616101.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 240 gene (tmem240, 616101.0001) | rel=r_associated | relid=0 | w=27
  3219. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the transmembrane protein 70 gene (tmem70, 612418.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 70 gene (tmem70, 612418.0001) | rel=r_associated | relid=0 | w=27
  3220. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the transportin 3 gene (tnpo3, 610032.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transportin 3 gene (tnpo3, 610032.0001) | rel=r_associated | relid=0 | w=27
  3221. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the trk-fused gene (tfg, 602498.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the trk-fused gene (tfg, 602498.0001) | rel=r_associated | relid=0 | w=27
  3222. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the tubulin, beta-2a gene (tubb2a, 615101.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin, beta-2a gene (tubb2a, 615101.0001) | rel=r_associated | relid=0 | w=27
  3223. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the tubulin, beta-4a gene (tubb4a, 602662.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin, beta-4a gene (tubb4a, 602662.0001) | rel=r_associated | relid=0 | w=27
  3224. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the tumor protein p63 gene (tp63, 603273.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tumor protein p63 gene (tp63, 603273.0001) | rel=r_associated | relid=0 | w=27
  3225. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the tumor protein p73-like gene (tp73l, 603273.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tumor protein p73-like gene (tp73l, 603273.0011) | rel=r_associated | relid=0 | w=27
  3226. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the type 2 bone morphogenetic protein receptor gene (bmpr2, 600799.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the type 2 bone morphogenetic protein receptor gene (bmpr2, 600799.0001) | rel=r_associated | relid=0 | w=27
  3227. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the type iv, voltage-gated sodium channel, alpha-subunit gene (scn4a, 603967.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the type iv, voltage-gated sodium channel, alpha-subunit gene (scn4a, 603967.0009) | rel=r_associated | relid=0 | w=27
  3228. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the udp-gal:beta-gal beta-1,3-galactosyltransferase polypeptide 6 gene (b3galt6, 615291.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the udp-gal:beta-gal beta-1,3-galactosyltransferase polypeptide 6 gene (b3galt6, 615291.0001) | rel=r_associated | relid=0 | w=27
  3229. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the udp-gal:beta-gal beta-1,3-galactosyltransferase polypeptide 6 gene (b3galt6, 615291.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the udp-gal:beta-gal beta-1,3-galactosyltransferase polypeptide 6 gene (b3galt6, 615291.0007) | rel=r_associated | relid=0 | w=27
  3230. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the ush3a gene (ush3a, 606397.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ush3a gene (ush3a, 606397.0001) | rel=r_associated | relid=0 | w=27
  3231. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the voltage-gated sodium channel, type viii, alpha subunit gene (scn8a, 600702.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated sodium channel, type viii, alpha subunit gene (scn8a, 600702.0002) | rel=r_associated | relid=0 | w=27
  3232. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the voltage-gated sodium channel, type xi, alpha subunit gene (scn11a, 604385.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated sodium channel, type xi, alpha subunit gene (scn11a, 604385.0001) | rel=r_associated | relid=0 | w=27
  3233. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the voltage-gated, type x, alpha subunit gene (scn10a, 604427.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the voltage-gated, type x, alpha subunit gene (scn10a, 604427.0001) | rel=r_associated | relid=0 | w=27
  3234. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the von willebrand factor gene (vwf, 613160.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the von willebrand factor gene (vwf, 613160.0001) | rel=r_associated | relid=0 | w=27
  3235. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the was gene (was, 300392.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the was gene (was, 300392.0012) | rel=r_associated | relid=0 | w=27
  3236. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the wingless-type mmtv integration site family, member 5a gene (wnt5a, 164975.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wingless-type mmtv integration site family, member 5a gene (wnt5a, 164975.0001) | rel=r_associated | relid=0 | w=27
  3237. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the wiskott-aldrich syndrome protein gene (wasp, 301000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the wiskott-aldrich syndrome protein gene (wasp, 301000.0001) | rel=r_associated | relid=0 | w=27
  3238. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the zinc finger protein 423 gene (znf423, 604557.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger protein 423 gene (znf423, 604557.0001) | rel=r_associated | relid=0 | w=27
  3239. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation in the zinc finger- and btb domain-containing protein-42 (zbtb42, 613915.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger- and btb domain-containing protein-42 (zbtb42, 613915.0001) | rel=r_associated | relid=0 | w=27
  3240. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutation or trinucleotide repeat expansion (gaa)n in the frataxin gene (fxn, 606829.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation or trinucleotide repeat expansion (gaa)n in the frataxin gene (fxn, 606829.0001) | rel=r_associated | relid=0 | w=27
  3241. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the 5-alpha-reductase-2 gene (srd5a2, 607306.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the 5-alpha-reductase-2 gene (srd5a2, 607306.0001) | rel=r_associated | relid=0 | w=27
  3242. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the apolipoprotein lp(a) gene (lpa, 152200.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the apolipoprotein lp(a) gene (lpa, 152200.0001) | rel=r_associated | relid=0 | w=27
  3243. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0005) | rel=r_associated | relid=0 | w=27
  3244. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the beta-glucuronidase gene (gusb, 611499.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the beta-glucuronidase gene (gusb, 611499.0001) | rel=r_associated | relid=0 | w=27
  3245. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the cellular retinaldehyde-binding protein-1 gene (rlbp1, 180090.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cellular retinaldehyde-binding protein-1 gene (rlbp1, 180090.0004) | rel=r_associated | relid=0 | w=27
  3246. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the ceruloplasmin gene (cp, 117700.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the ceruloplasmin gene (cp, 117700.0001). | rel=r_associated | relid=0 | w=27
  3247. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the cholinergic receptor, nicotinic, alpha polypeptide-1 gene (chrna1, 100690.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cholinergic receptor, nicotinic, alpha polypeptide-1 gene (chrna1, 100690.0007) | rel=r_associated | relid=0 | w=27
  3248. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the cytochrome p450, subfamily i, dioxin-inducible, polypeptide 1 gene (cyp1b1, 601771.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the cytochrome p450, subfamily i, dioxin-inducible, polypeptide 1 gene (cyp1b1, 601771.0001) | rel=r_associated | relid=0 | w=27
  3249. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the glycosylceramidase gene (galc, 606890.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the glycosylceramidase gene (galc, 606890.0001) | rel=r_associated | relid=0 | w=27
  3250. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the homolog of the mouse noggin gene (nog, 602991.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the homolog of the mouse noggin gene (nog, 602991.0006) | rel=r_associated | relid=0 | w=27
  3251. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the low density lipoprotein receptor-related protein-5 gene (lrp5, 603506.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the low density lipoprotein receptor-related protein-5 gene (lrp5, 603506.0001) | rel=r_associated | relid=0 | w=27
  3252. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the mucolipin-1 gene (mcoln1, 605248.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the mucolipin-1 gene (mcoln1, 605248.0001) | rel=r_associated | relid=0 | w=27
  3253. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the myeloperoxidase gene (mpo, 606989.0001).
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the myeloperoxidase gene (mpo, 606989.0001). | rel=r_associated | relid=0 | w=27
  3254. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the phd finger protein 6 gene (phf6, 300414.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the phd finger protein 6 gene (phf6, 300414.0001) | rel=r_associated | relid=0 | w=27
  3255. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the prion protein gene (prnp, 176640.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the prion protein gene (prnp, 176640.0001) | rel=r_associated | relid=0 | w=27
  3256. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the sequestosome 1 gene (sqstm1, 601530.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the sequestosome 1 gene (sqstm1, 601530.0001) | rel=r_associated | relid=0 | w=27
  3257. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the survival of motor neuron 1 gene (smn1, 600354.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the survival of motor neuron 1 gene (smn1, 600354.0011) | rel=r_associated | relid=0 | w=27
  3258. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the transforming growth factor, beta-induced, 68kd gene (tgfbi, 601692.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the transforming growth factor, beta-induced, 68kd gene (tgfbi, 601692.0004) | rel=r_associated | relid=0 | w=27
  3259. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the triggering receptor expressed on myeloid cells-2 gene (trem2, 605086.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the triggering receptor expressed on myeloid cells-2 gene (trem2, 605086.0001) | rel=r_associated | relid=0 | w=27
  3260. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the tubulin-specific chaperone e gene (tbce, 604934.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the tubulin-specific chaperone e gene (tbce, 604934.0001) | rel=r_associated | relid=0 | w=27
  3261. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by mutations in the tumor necrosis factor receptor superfamily, member 11a (tnfrsf11a, 603499.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutations in the tumor necrosis factor receptor superfamily, member 11a (tnfrsf11a, 603499.0002) | rel=r_associated | relid=0 | w=27
  3262. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:caused by palindrome-mediated interchromosomal insertions on chromosome xq27.1
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by palindrome-mediated interchromosomal insertions on chromosome xq27.1 | rel=r_associated | relid=0 | w=27
  3263. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:contiguous gene deletion of at least 16mb encompassing 39 genes on 13q14
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene deletion of at least 16mb encompassing 39 genes on 13q14 | rel=r_associated | relid=0 | w=27
  3264. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:contiguous gene deletion syndrome caused by deletion (3.4 kb) of chromosome xq28
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene deletion syndrome caused by deletion (3.4 kb) of chromosome xq28 | rel=r_associated | relid=0 | w=27
  3265. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:contiguous gene syndrome caused by deletion of 91.3kb on chromosome 11p11.2 involving the creb3l1 (616215) and dgkz (601441) genes
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by deletion of 91.3kb on chromosome 11p11.2 involving the creb3l1 (616215) and dgkz (601441) genes | rel=r_associated | relid=0 | w=27
  3266. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:contiguous gene syndrome caused by duplication (1.5 - 3.0 mb) of chromosome 22q11.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by duplication (1.5 - 3.0 mb) of chromosome 22q11.2 | rel=r_associated | relid=0 | w=27
  3267. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility conferred by allele 2 of the dinucleotide repeat in the dopamine receptor drd5 gene (126453.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by allele 2 of the dinucleotide repeat in the dopamine receptor drd5 gene (126453.0001) | rel=r_associated | relid=0 | w=27
  3268. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility conferred by mutation in the breast cancer 1 gene (brca1, 113705.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the breast cancer 1 gene (brca1, 113705.0001) | rel=r_associated | relid=0 | w=27
  3269. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility conferred by mutation in the butyrophilin-like protein 2 gene (btnl2, 606000.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the butyrophilin-like protein 2 gene (btnl2, 606000.0001) | rel=r_associated | relid=0 | w=27
  3270. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility conferred by mutation in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0018) | rel=r_associated | relid=0 | w=27
  3271. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility conferred by mutation in the complement factor i gene (cfi, 217030.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the complement factor i gene (cfi, 217030.0004) | rel=r_associated | relid=0 | w=27
  3272. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility conferred by mutation in the ef-hand domain (c-terminal)-containing protein 1 gene (efhc1, 608815.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the ef-hand domain (c-terminal)-containing protein 1 gene (efhc1, 608815.0001) | rel=r_associated | relid=0 | w=27
  3273. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility conferred by mutation in the methyl-cpg binding protein-2 gene (mecp2, 300005.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the methyl-cpg binding protein-2 gene (mecp2, 300005.0011) | rel=r_associated | relid=0 | w=27
  3274. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility conferred by mutation in the nucleotide-binding oligomerization domain protein 2 gene (nod2, 605956.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the nucleotide-binding oligomerization domain protein 2 gene (nod2, 605956.0001) | rel=r_associated | relid=0 | w=27
  3275. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility conferred by mutation in the promoter of the nitric oxide synthase-1 gene (nos1, 163731.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the promoter of the nitric oxide synthase-1 gene (nos1, 163731.0001) | rel=r_associated | relid=0 | w=27
  3276. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility conferred by polymorphisms in the brain-derived neurotrophic factor gene (bdnf, 113505.0002 and 113505.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by polymorphisms in the brain-derived neurotrophic factor gene (bdnf, 113505.0002 and 113505.0003) | rel=r_associated | relid=0 | w=27
  3277. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:susceptibility to sle caused by mutation in the receptor for fc fragment of igg, low affinity iia gene (fcgr2a, 146790.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility to sle caused by mutation in the receptor for fc fragment of igg, low affinity iia gene (fcgr2a, 146790.0001) | rel=r_associated | relid=0 | w=27
  3278. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> en:translocation of cellular oncogene c-abl (189980) to the bcr gene on chromosome 22 resulting in chimeric brc-abl gene
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:translocation of cellular oncogene c-abl (189980) to the bcr gene on chromosome 22 resulting in chimeric brc-abl gene | rel=r_associated | relid=0 | w=27
  3279. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 27 / 0.628 -> syndrome
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=syndrome | rel=r_associated | relid=0 | w=27
  3280. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 26 / 0.605 -> chromosome
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=chromosome | rel=r_associated | relid=0 | w=26
  3281. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 25 / 0.581 -> gène
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=gène | rel=r_associated | relid=0 | w=25
  3282. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:balanced reciprocal translocation between chromosomes x and 15
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:balanced reciprocal translocation between chromosomes x and 15 | rel=r_associated | relid=0 | w=20
  3283. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by 1 to 3.8-mb duplication on chromosome 2q31.1
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by 1 to 3.8-mb duplication on chromosome 2q31.1 | rel=r_associated | relid=0 | w=20
  3284. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by deletion of a 32.5-kb regulatory region (xysr) -640 to -607 kb upstream of the sry-box-9 gene (sox9, 608160.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by deletion of a 32.5-kb regulatory region (xysr) -640 to -607 kb upstream of the sry-box-9 gene (sox9, 608160.0018) | rel=r_associated | relid=0 | w=20
  3285. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in gene encoding cystein-rich pdz domain-binding protein (cript, 604594.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in gene encoding cystein-rich pdz domain-binding protein (cript, 604594.0001) | rel=r_associated | relid=0 | w=20
  3286. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the 104-kd centrosomal protein gene (cep104, 616690.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 104-kd centrosomal protein gene (cep104, 616690.0001) | rel=r_associated | relid=0 | w=20
  3287. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the 120-kd centrosomal protein gene (cep120, 613446.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the 120-kd centrosomal protein gene (cep120, 613446.0001) | rel=r_associated | relid=0 | w=20
  3288. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the actin, alpha, skeletal muscle 1 gene (acta1, 102610.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the actin, alpha, skeletal muscle 1 gene (acta1, 102610.0018) | rel=r_associated | relid=0 | w=20
  3289. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the adhesion g protein-coupled receptor e2 gene (adgre2, 606100)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the adhesion g protein-coupled receptor e2 gene (adgre2, 606100) | rel=r_associated | relid=0 | w=20
  3290. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the alanyl-trna synthetase gene (aars, 601065.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alanyl-trna synthetase gene (aars, 601065.0003) | rel=r_associated | relid=0 | w=20
  3291. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the alpha-1 gap junction protein gene (gja1, 121014.0024)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1 gap junction protein gene (gja1, 121014.0024) | rel=r_associated | relid=0 | w=20
  3292. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the alpha-1 type xvii collagen gene (col17a1, 113811.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-1 type xvii collagen gene (col17a1, 113811.0015) | rel=r_associated | relid=0 | w=20
  3293. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the alpha-2 actinin gene (actn2, 102573.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-2 actinin gene (actn2, 102573.0001) | rel=r_associated | relid=0 | w=20
  3294. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the alpha-3 integrin gene (itga3, 605025.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-3 integrin gene (itga3, 605025.0001) | rel=r_associated | relid=0 | w=20
  3295. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the alpha-fetoprotein gene (afp, 104150.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-fetoprotein gene (afp, 104150.0001) | rel=r_associated | relid=0 | w=20
  3296. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the alpha-fetoprotein gene (afp, 104150.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the alpha-fetoprotein gene (afp, 104150.0002) | rel=r_associated | relid=0 | w=20
  3297. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the ankyrin 1 gene (ank1, 612641.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ankyrin 1 gene (ank1, 612641.0001) | rel=r_associated | relid=0 | w=20
  3298. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the bbs2 gene (bbs2, 606151.0018)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the bbs2 gene (bbs2, 606151.0018) | rel=r_associated | relid=0 | w=20
  3299. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the c. elegans mab21 homolog-like 2 gene (mab21l2, 604357.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the c. elegans mab21 homolog-like 2 gene (mab21l2, 604357.0001) | rel=r_associated | relid=0 | w=20
  3300. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the centromeric protein f gene (cenpf, 600236.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the centromeric protein f gene (cenpf, 600236.0001) | rel=r_associated | relid=0 | w=20
  3301. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the cholinergic receptor, nicotinic, beta polypeptide 1 gene (chrnb1, 100710.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cholinergic receptor, nicotinic, beta polypeptide 1 gene (chrnb1, 100710.0001) | rel=r_associated | relid=0 | w=20
  3302. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the chromosome 21 open reading frame-2 gene (c21orf2, 603191.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the chromosome 21 open reading frame-2 gene (c21orf2, 603191.0001) | rel=r_associated | relid=0 | w=20
  3303. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the collagen ii, alpha-polypeptide gene (col2a1, 120140.0055)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen ii, alpha-polypeptide gene (col2a1, 120140.0055) | rel=r_associated | relid=0 | w=20
  3304. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the collagen, type vi, alpha-3 gene (col6a3, 120250.0007)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the collagen, type vi, alpha-3 gene (col6a3, 120250.0007) | rel=r_associated | relid=0 | w=20
  3305. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the cytochrome c oxidase assembly factor 6 gene (coa6, 614772.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome c oxidase assembly factor 6 gene (coa6, 614772.0001) | rel=r_associated | relid=0 | w=20
  3306. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the cytochrome p450, family 4, subfamily v, polypeptide-2 gene (cyp4v2, 608614.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the cytochrome p450, family 4, subfamily v, polypeptide-2 gene (cyp4v2, 608614.0001) | rel=r_associated | relid=0 | w=20
  3307. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the dedicator of cytokinesis 2 gene (dock2, 603122.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the dedicator of cytokinesis 2 gene (dock2, 603122.0001) | rel=r_associated | relid=0 | w=20
  3308. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the endoplasmic reticulum membrane protein complex, subunit 1 gene (emc1, 616846.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the endoplasmic reticulum membrane protein complex, subunit 1 gene (emc1, 616846.0002) | rel=r_associated | relid=0 | w=20
  3309. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the eukaryotic translation elongation factor 1, alpha-2 gene (eef1a2, 602959.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the eukaryotic translation elongation factor 1, alpha-2 gene (eef1a2, 602959.0001) | rel=r_associated | relid=0 | w=20
  3310. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the ferm domain-containing protein 4a gene (frmd4a, 616305.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ferm domain-containing protein 4a gene (frmd4a, 616305.0001) | rel=r_associated | relid=0 | w=20
  3311. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0015)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0015) | rel=r_associated | relid=0 | w=20
  3312. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the follicle-stimulating hormone, beta-polypeptide gene (fshb, 136530.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the follicle-stimulating hormone, beta-polypeptide gene (fshb, 136530.0001) | rel=r_associated | relid=0 | w=20
  3313. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the guanine nucleotide-binding protein, alpha-transducing activity polypeptide-1 gene (gnat1, 139330.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the guanine nucleotide-binding protein, alpha-transducing activity polypeptide-1 gene (gnat1, 139330.0003) | rel=r_associated | relid=0 | w=20
  3314. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the homolog of drosophila twist-2 gene (twist2, 607556.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of drosophila twist-2 gene (twist2, 607556.0005) | rel=r_associated | relid=0 | w=20
  3315. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the homolog of the c. elegans unc80 gene (unc80, 612636.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the c. elegans unc80 gene (unc80, 612636.0001) | rel=r_associated | relid=0 | w=20
  3316. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the homolog of the drosophila sine oculis homeo box 1 gene (six1, 601205.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the drosophila sine oculis homeo box 1 gene (six1, 601205.0003) | rel=r_associated | relid=0 | w=20
  3317. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the homolog of the e. coli muts, 6 gene (msh6, 600678.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the e. coli muts, 6 gene (msh6, 600678.0001) | rel=r_associated | relid=0 | w=20
  3318. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the homolog of the s. cerevisiae coenzyme q4 gene (coq4, 612898.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae coenzyme q4 gene (coq4, 612898.0001) | rel=r_associated | relid=0 | w=20
  3319. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the homolog of the s. cerevisiae precursor mrna-processing factor 8 gene (prpf8, 607300.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the homolog of the s. cerevisiae precursor mrna-processing factor 8 gene (prpf8, 607300.0001) | rel=r_associated | relid=0 | w=20
  3320. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the human homolog of the drosophila suppressor of fused gene (sufu, 607035.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the human homolog of the drosophila suppressor of fused gene (sufu, 607035.0003) | rel=r_associated | relid=0 | w=20
  3321. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the ikaros family zinc finger 1 gene (ikzf1, 603023.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ikaros family zinc finger 1 gene (ikzf1, 603023.0001) | rel=r_associated | relid=0 | w=20
  3322. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the interferon induced with helicase c domain 1 gene (ifih1, 606951.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interferon induced with helicase c domain 1 gene (ifih1, 606951.0009) | rel=r_associated | relid=0 | w=20
  3323. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the interferon, alpha, beta, and omega, receptor 2 gene (irnar2, 602376.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interferon, alpha, beta, and omega, receptor 2 gene (irnar2, 602376.0002) | rel=r_associated | relid=0 | w=20
  3324. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the interleukin 17 receptor c gene (ir17rc, 610925.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the interleukin 17 receptor c gene (ir17rc, 610925.0001) | rel=r_associated | relid=0 | w=20
  3325. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the inwardly rectifying potassium channel, subfamily j, member 6 gene (kcnj6, 600877.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the inwardly rectifying potassium channel, subfamily j, member 6 gene (kcnj6, 600877.0001) | rel=r_associated | relid=0 | w=20
  3326. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the iq motif- and sec7 domain-containing protein 2 (iqsec2, 300522.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the iq motif- and sec7 domain-containing protein 2 (iqsec2, 300522.0001) | rel=r_associated | relid=0 | w=20
  3327. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the k(lysine) acetyltransferase 6a gene (kat6a, 601408.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the k(lysine) acetyltransferase 6a gene (kat6a, 601408.0001) | rel=r_associated | relid=0 | w=20
  3328. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the kiaa0568 gene (kiaa0586, 610178.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the kiaa0568 gene (kiaa0586, 610178.0006) | rel=r_associated | relid=0 | w=20
  3329. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0011)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0011) | rel=r_associated | relid=0 | w=20
  3330. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the mitochondrial enoyl-coa hydratase, short-chain, 1 gene (echs1, 602292.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the mitochondrial enoyl-coa hydratase, short-chain, 1 gene (echs1, 602292.0001) | rel=r_associated | relid=0 | w=20
  3331. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the myosin vi gene (myo6, 600970.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the myosin vi gene (myo6, 600970.0001) | rel=r_associated | relid=0 | w=20
  3332. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the non-pou domain-containing octamer-binding protein gene (nono, 300084.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the non-pou domain-containing octamer-binding protein gene (nono, 300084.0001) | rel=r_associated | relid=0 | w=20
  3333. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the oxysterol-binding protein-like protein 2 gene (osbpl2, 606731.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the oxysterol-binding protein-like protein 2 gene (osbpl2, 606731.0001) | rel=r_associated | relid=0 | w=20
  3334. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the peptidyl-trna hydrolase 2 gene (ptrh2, 608625.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the peptidyl-trna hydrolase 2 gene (ptrh2, 608625.0001) | rel=r_associated | relid=0 | w=20
  3335. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the phosphatidylinositol glycan, class y gene (pigy, 610662.0001) creation date : cassandra l. kniffin : 2/11/2016
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphatidylinositol glycan, class y gene (pigy, 610662.0001) creation date : cassandra l. kniffin : 2/11/2016 | rel=r_associated | relid=0 | w=20
  3336. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the phosphoserine phosphatase gene (psph, 172480.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the phosphoserine phosphatase gene (psph, 172480.0001) | rel=r_associated | relid=0 | w=20
  3337. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the piezo1 ion channel gene (piezo1, 611184.0009)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the piezo1 ion channel gene (piezo1, 611184.0009) | rel=r_associated | relid=0 | w=20
  3338. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the platelet-derived growth factor receptor, beta polypeptide gene (pdgfrb, 173410.0006)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the platelet-derived growth factor receptor, beta polypeptide gene (pdgfrb, 173410.0006) | rel=r_associated | relid=0 | w=20
  3339. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 2 gene (plekhg2, 611893.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 2 gene (plekhg2, 611893.0001) | rel=r_associated | relid=0 | w=20
  3340. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the polynucleotide kinase 3-prime phosphatase gene (pnkp, 605610.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the polynucleotide kinase 3-prime phosphatase gene (pnkp, 605610.0002) | rel=r_associated | relid=0 | w=20
  3341. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the post-gpi attachment to proteins 1 gene (pgap1, 611655.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the post-gpi attachment to proteins 1 gene (pgap1, 611655.0001) | rel=r_associated | relid=0 | w=20
  3342. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the potassium voltage-gated channel, shal-related subfamily member-3 gene (kcnd3, 605411.0005)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the potassium voltage-gated channel, shal-related subfamily member-3 gene (kcnd3, 605411.0005) | rel=r_associated | relid=0 | w=20
  3343. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the receptor-associated protein of the synapse, 43-kd gene (rapsn, 601592.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the receptor-associated protein of the synapse, 43-kd gene (rapsn, 601592.0001) | rel=r_associated | relid=0 | w=20
  3344. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the retinol-binding protein-4 gene (rbp4, 180250.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the retinol-binding protein-4 gene (rbp4, 180250.0004) | rel=r_associated | relid=0 | w=20
  3345. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the ribosomal protein l26 gene (rpl26, 603704.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ribosomal protein l26 gene (rpl26, 603704.0001) | rel=r_associated | relid=0 | w=20
  3346. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the sequestosome 1 gene (sqstm1, 601530.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sequestosome 1 gene (sqstm1, 601530.0001) | rel=r_associated | relid=0 | w=20
  3347. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the sh3 and px domains-containing protein 2b gene (sh3pxd2b, 613293.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the sh3 and px domains-containing protein 2b gene (sh3pxd2b, 613293.0001) | rel=r_associated | relid=0 | w=20
  3348. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the signal transducer and activator of transcription 2 (stat2, 600556.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the signal transducer and activator of transcription 2 (stat2, 600556.0001) | rel=r_associated | relid=0 | w=20
  3349. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0023)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0023) | rel=r_associated | relid=0 | w=20
  3350. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, folate), member 32 gene (slc25a32, 610815.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, folate), member 32 gene (slc25a32, 610815.0001) | rel=r_associated | relid=0 | w=20
  3351. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the t-box 4 gene (tbx4, 601719.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the t-box 4 gene (tbx4, 601719.0001) | rel=r_associated | relid=0 | w=20
  3352. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the t-type voltage-dependent calcium channel, alpha-1g subunit gene (cacna1g, 604065.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the t-type voltage-dependent calcium channel, alpha-1g subunit gene (cacna1g, 604065.0001) | rel=r_associated | relid=0 | w=20
  3353. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the teneurin transmembrane protein 4 gene (tenm4, 610084.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the teneurin transmembrane protein 4 gene (tenm4, 610084.0001) | rel=r_associated | relid=0 | w=20
  3354. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the transducin-like enhancer of split 6 gene (tle6, 612399.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transducin-like enhancer of split 6 gene (tle6, 612399.0001) | rel=r_associated | relid=0 | w=20
  3355. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the transmembrane anterior posterior transformation-1 gene (tapt1, 612758.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane anterior posterior transformation-1 gene (tapt1, 612758.0001) | rel=r_associated | relid=0 | w=20
  3356. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the transmembrane protein 216 gene (tmem216, 613277.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the transmembrane protein 216 gene (tmem216, 613277.0002) | rel=r_associated | relid=0 | w=20
  3357. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the tubulin-gamma complex-associated protein 4 gene (tubgcp4, 609610.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin-gamma complex-associated protein 4 gene (tubgcp4, 609610.0001) | rel=r_associated | relid=0 | w=20
  3358. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the tubulin, beta-4a gene (tubb4a, 602662.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the tubulin, beta-4a gene (tubb4a, 602662.0002) | rel=r_associated | relid=0 | w=20
  3359. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the ubiquitin-specific protease 9 gene, x-linked (usp9x, 300072.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the ubiquitin-specific protease 9 gene, x-linked (usp9x, 300072.0004) | rel=r_associated | relid=0 | w=20
  3360. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the uncoupling protein-3 gene (ucp3, 602044.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the uncoupling protein-3 gene (ucp3, 602044.0001) | rel=r_associated | relid=0 | w=20
  3361. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the whirlin gene (whrn, 607928.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the whirlin gene (whrn, 607928.0002) | rel=r_associated | relid=0 | w=20
  3362. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the zic family member 3 gene (zic3, 300265.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zic family member 3 gene (zic3, 300265.0001) | rel=r_associated | relid=0 | w=20
  3363. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by mutation in the zinc finger protein 408 gene (znf408, 616454.0003)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by mutation in the zinc finger protein 408 gene (znf408, 616454.0003) | rel=r_associated | relid=0 | w=20
  3364. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:caused by somatic mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:caused by somatic mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0001) | rel=r_associated | relid=0 | w=20
  3365. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:contiguous gene deletion of 91.6 kb to 4.74 mb on chromosome 16p13.2
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene deletion of 91.6 kb to 4.74 mb on chromosome 16p13.2 | rel=r_associated | relid=0 | w=20
  3366. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:contiguous gene syndrome caused by duplication (700-kb) of chromosome 14q32
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:contiguous gene syndrome caused by duplication (700-kb) of chromosome 14q32 | rel=r_associated | relid=0 | w=20
  3367. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:susceptibility conferred by mutation in the forkhead box e1 gene (foxe1, 602617.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the forkhead box e1 gene (foxe1, 602617.0004) | rel=r_associated | relid=0 | w=20
  3368. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:susceptibility conferred by mutation in the nk2 homeobox 1 gene (nkx2-1, 600635.0012)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the nk2 homeobox 1 gene (nkx2-1, 600635.0012) | rel=r_associated | relid=0 | w=20
  3369. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:susceptibility conferred by mutation in the solute carrier family 12 (potassium/chloride transporter), member 5 gene (slc12a5, 606726.0004)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the solute carrier family 12 (potassium/chloride transporter), member 5 gene (slc12a5, 606726.0004) | rel=r_associated | relid=0 | w=20
  3370. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:susceptibility conferred by mutation in the tumor necrosis factor receptor superfamily, member 11a gene (tnfrsf11a, 603499.0002)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the tumor necrosis factor receptor superfamily, member 11a gene (tnfrsf11a, 603499.0002) | rel=r_associated | relid=0 | w=20
  3371. en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) -- r_associated #0: 20 / 0.465 -> en:susceptibility conferred by mutation in the uncoupling protein-2 gene (ucp2, 601693.0001)
    n1=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | n2=en:susceptibility conferred by mutation in the uncoupling protein-2 gene (ucp2, 601693.0001) | rel=r_associated | relid=0 | w=20
≈ 3371 relations entrantes

  1. en:caused by mutation in the protease inhibitor 1 gene (pi, 107400.0001) --- r_associated #0: 46 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protease inhibitor 1 gene (pi, 107400.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=46
  2. en:caused by mutation in the interleukin 7 receptor gene (il7r, 146661.0001) --- r_associated #0: 45 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interleukin 7 receptor gene (il7r, 146661.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=45
  3. en:caused by mutation in the major facilitator superfamily domain-containing protein-8 gene (mfsd8, 611124.0001) --- r_associated #0: 44 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the major facilitator superfamily domain-containing protein-8 gene (mfsd8, 611124.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=44
  4. en:caused by mutation in the beta-1-galactosidase gene (glb, 230500.0003) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1-galactosidase gene (glb, 230500.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  5. en:caused by mutation in the calpain 3 gene (capn3, 114240.0001) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calpain 3 gene (capn3, 114240.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  6. en:caused by mutation in the complement component 4a gene (c4a, 120810.0001) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement component 4a gene (c4a, 120810.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  7. en:caused by mutation in the cyclin d2 gene (ccnd2, 123833.0001) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclin d2 gene (ccnd2, 123833.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  8. en:caused by mutation in the dopamine beta-hydroxylase gene (dbh, 609312.0002) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dopamine beta-hydroxylase gene (dbh, 609312.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  9. en:caused by mutation in the establishment of cohesion 1 homolog 2 gene (esco2, 609353.0001) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the establishment of cohesion 1 homolog 2 gene (esco2, 609353.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  10. en:caused by mutation in the homeo box gene expressed in es cells (hesx1, 601802.0001) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeo box gene expressed in es cells (hesx1, 601802.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  11. en:caused by mutation in the homolog of the e. coli muts 6 gene (msh6, 600678.0012) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the e. coli muts 6 gene (msh6, 600678.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  12. en:caused by mutation in the pseudouridine synthase-1 gene (pus1, 608109.0001) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pseudouridine synthase-1 gene (pus1, 608109.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  13. en:caused by mutation in the ribonucleotide reductase, m2 b gene (rrm2b, 604712.0006) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribonucleotide reductase, m2 b gene (rrm2b, 604712.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  14. en:caused by mutation in the v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 4 gene (erbb4, 600543.0001) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 4 gene (erbb4, 600543.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  15. en:caused by mutations in the tumor necrosis factor ligand superfamily, member 5 gene (tnfsf5, 308230.0001) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the tumor necrosis factor ligand superfamily, member 5 gene (tnfsf5, 308230.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  16. en:susceptibility conferred by mutation in the forkhead box e1 gene (foxe1, 602617.0004) --- r_associated #0: 43 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the forkhead box e1 gene (foxe1, 602617.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=43
  17. en:caused by expanded cag trinucleotide repeats in the beta subunit of the protein phosphatase 2 gene (ppp2r2b, 604325.0001) --- r_associated #0: 42 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by expanded cag trinucleotide repeats in the beta subunit of the protein phosphatase 2 gene (ppp2r2b, 604325.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=42
  18. en:caused by mutation in the coiled-coil domain-containing protein 8 gene (ccdc8, 614145.0001) --- r_associated #0: 42 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil domain-containing protein 8 gene (ccdc8, 614145.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=42
  19. en:caused by mutation in the gene encoding desmoglein-1 (dsg1, 125670.0001) --- r_associated #0: 42 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding desmoglein-1 (dsg1, 125670.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=42
  20. en:caused by mutation in the gtp cyclohydrolase i gene (gch1, 600225.0001) --- r_associated #0: 42 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gtp cyclohydrolase i gene (gch1, 600225.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=42
  21. en:caused by mutation in the homolog of the drosophila sine oculis homeo box 1 gene (six1, 601205.0003) --- r_associated #0: 42 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila sine oculis homeo box 1 gene (six1, 601205.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=42
  22. en:caused by mutation in the glyceronephosphate o-acyltransferase gene (gnpat, 602744.0001) --- r_associated #0: 41 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glyceronephosphate o-acyltransferase gene (gnpat, 602744.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=41
  23. en:caused by mutation in the homolog of the mouse hydrocephalus-inducing gene (hydin, 610812.0001) --- r_associated #0: 41 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse hydrocephalus-inducing gene (hydin, 610812.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=41
  24. en:caused by mutation in the pr-domain containing protein-5 gene (prdm5, 614161.0001) --- r_associated #0: 41 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pr-domain containing protein-5 gene (prdm5, 614161.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=41
  25. en:caused by mutation in the cyld gene (605018.0003) --- r_associated #0: 40 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyld gene (605018.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=40
  26. en:caused by mutation in the manan-binding lectin serine protease-1 gene (masp1, 600521.0001) --- r_associated #0: 40 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the manan-binding lectin serine protease-1 gene (masp1, 600521.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=40
  27. en:caused by mutation in the mitochondrial ribosomal protein s16 (mrps16, 609204.0001) --- r_associated #0: 40 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial ribosomal protein s16 (mrps16, 609204.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=40
  28. en:caused by mutation in the prosaposin gene (psap, 176801.0009). --- r_associated #0: 40 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prosaposin gene (psap, 176801.0009). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=40
  29. en:caused by mutation in the scavenger receptor class f, member 2 gene (scarf2, 613619.0001) --- r_associated #0: 40 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the scavenger receptor class f, member 2 gene (scarf2, 613619.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=40
  30. en:caused by mutation in the stromalin-3 gene (stag3, 608489.0001) --- r_associated #0: 40 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the stromalin-3 gene (stag3, 608489.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=40
  31. en:caused by mutations in cartilage oligomeric matrix protein (comp, 600310.0001) --- r_associated #0: 40 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in cartilage oligomeric matrix protein (comp, 600310.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=40
  32. en:caused by mutation in the chromatin licensing and dna replication factor 1 gene (cdt1, 605525.0001) --- r_associated #0: 39 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromatin licensing and dna replication factor 1 gene (cdt1, 605525.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=39
  33. en:caused by mutation in the cyclin-dependent kinase 6 gene (cdk6, 603368.0001) --- r_associated #0: 39 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclin-dependent kinase 6 gene (cdk6, 603368.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=39
  34. en:caused by mutation in the homolog 1 of drosophila notch gene (notch1, 190198.0003) --- r_associated #0: 39 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog 1 of drosophila notch gene (notch1, 190198.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=39
  35. en:caused by mutation in the homolog of drosophila twist-2 gene (twist2, 607556.0005) --- r_associated #0: 39 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of drosophila twist-2 gene (twist2, 607556.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=39
  36. en:caused by mutation in the prickle-like 2 gene (prickle2, 608501.0001) --- r_associated #0: 39 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prickle-like 2 gene (prickle2, 608501.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=39
  37. en:contiguous gene syndrome caused by duplication (700-kb) of chromosome 14q32 --- r_associated #0: 39 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by duplication (700-kb) of chromosome 14q32 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=39
  38. en:caused by mutation in the cat eye syndrome chromosome region, candidate 1 gene (cecr1, 607575.0010) --- r_associated #0: 38 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cat eye syndrome chromosome region, candidate 1 gene (cecr1, 607575.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=38
  39. en:caused by mutation in the kaptin gene (kptn, 615620.0001) --- r_associated #0: 38 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kaptin gene (kptn, 615620.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=38
  40. en:caused by mutation in the ring finger protein 216 gene (rnf216, 609948.0001) --- r_associated #0: 38 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ring finger protein 216 gene (rnf216, 609948.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=38
  41. en:caused by mutation in the udp-gal:beta-gal beta-1,3-galactosyltransferase polypeptide 6 gene (b3galt6, 615291.0007) --- r_associated #0: 38 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the udp-gal:beta-gal beta-1,3-galactosyltransferase polypeptide 6 gene (b3galt6, 615291.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=38
  42. en:caused by mutation in the uncoupling protein-3 gene (ucp3, 602044.0001) --- r_associated #0: 38 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the uncoupling protein-3 gene (ucp3, 602044.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=38
  43. en:caused by mutations in the udp-galactose-4-epimerase gene, 'severe' form (gale, 606953.0008) --- r_associated #0: 38 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the udp-galactose-4-epimerase gene, 'severe' form (gale, 606953.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=38
  44. en:caused by mutation in the guanylate cyclase 2c gene (gucy2c, 601330.0001) --- r_associated #0: 37 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the guanylate cyclase 2c gene (gucy2c, 601330.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=37
  45. en:caused by mutation in the lipase n gene (lipn, 613924.0001) --- r_associated #0: 37 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lipase n gene (lipn, 613924.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=37
  46. en:caused by mutation in the peroxisome biogenesis factor-1 gene (pex1, 602136.0001) --- r_associated #0: 37 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor-1 gene (pex1, 602136.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=37
  47. en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0006) --- r_associated #0: 37 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=37
  48. en:caused by mutation in the protein-tyrosine phosphatase, nonreceptor-type, 14 gene (ptpn14, 603155.0001) --- r_associated #0: 37 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein-tyrosine phosphatase, nonreceptor-type, 14 gene (ptpn14, 603155.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=37
  49. en:caused by mutation in the runt-related transcription factor 1 gene (runx1, 151385.0001) --- r_associated #0: 37 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the runt-related transcription factor 1 gene (runx1, 151385.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=37
  50. en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0003) --- r_associated #0: 37 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=37
  51. en:caused by mutation in the traf3-interacting protein-2 gene (traf3ip2, 607043.0002) --- r_associated #0: 37 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the traf3-interacting protein-2 gene (traf3ip2, 607043.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=37
  52. en:susceptibility conferred by mutation in the cyclin-dependent kinase-4 gene (cdk4, 123829.0001) --- r_associated #0: 37 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the cyclin-dependent kinase-4 gene (cdk4, 123829.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=37
  53. en:caused by mutation in the 11-beta-hydroxysteroid dehydrogenase, type ii gene (hsd11b2, 614232.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 11-beta-hydroxysteroid dehydrogenase, type ii gene (hsd11b2, 614232.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  54. en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0012) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  55. en:caused by mutation in the beta-ureidopropionase gene (upb1, 606673.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-ureidopropionase gene (upb1, 606673.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  56. en:caused by mutation in the cadherin 3 gene (cdh3, 114021.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cadherin 3 gene (cdh3, 114021.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  57. en:caused by mutation in the chromosome 12 open reading frame 65 gene (c12orf65, 613541.0003) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 12 open reading frame 65 gene (c12orf65, 613541.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  58. en:caused by mutation in the chromosome 19 open reading frame 12 gene (c19orf12, 614297.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 19 open reading frame 12 gene (c19orf12, 614297.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  59. en:caused by mutation in the complex i, subunit nd4 gene (mtnd4, 516003.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complex i, subunit nd4 gene (mtnd4, 516003.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  60. en:caused by mutation in the d-2-hydroxyglutarate dehydrogenase gene (d2hgd, 609186.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the d-2-hydroxyglutarate dehydrogenase gene (d2hgd, 609186.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  61. en:caused by mutation in the delta-aminolevulinate synthase 2 gene (alas2, 301300.0015) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the delta-aminolevulinate synthase 2 gene (alas2, 301300.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  62. en:caused by mutation in the desmoplakin gene (dsp, 125647.0003) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the desmoplakin gene (dsp, 125647.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  63. en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0014) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  64. en:caused by mutation in the hcls1-associated protein x1 (hax1, 605998.0001). --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hcls1-associated protein x1 (hax1, 605998.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  65. en:caused by mutation in the homolog of the s. cerevisiae meiotic recombination 11 a gene (mre11a, 600814.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae meiotic recombination 11 a gene (mre11a, 600814.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  66. en:caused by mutation in the interleukin-1 receptor antagonist gene (il1rn, 147679.0002) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interleukin-1 receptor antagonist gene (il1rn, 147679.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  67. en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0002) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  68. en:caused by mutation in the mhc class ii transactivator gene (mhc2ta, 600005.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mhc class ii transactivator gene (mhc2ta, 600005.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  69. en:caused by mutation in the platelet-derived growth factor, beta polypeptide gene (pdgfb, 190040.0003) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the platelet-derived growth factor, beta polypeptide gene (pdgfb, 190040.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  70. en:caused by mutation in the proteasome maturation protein gene (pomp, 613386.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the proteasome maturation protein gene (pomp, 613386.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  71. en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, glutamate), member 22 gene (slc25a22, 609302.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, glutamate), member 22 gene (slc25a22, 609302.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  72. en:caused by mutation in the solute carrier family 39 (zinc transporter), member 13 gene (slc39a13, 608735.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 39 (zinc transporter), member 13 gene (slc39a13, 608735.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  73. en:caused by mutation in the t-box 15 gene (tbx15, 604127.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the t-box 15 gene (tbx15, 604127.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  74. en:caused by mutation in the telomerase rna component gene (terc, 602322.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the telomerase rna component gene (terc, 602322.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  75. en:caused by mutation in the trf1-interacting nuclear factor 2 gene (tinf2, 604319.0002) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the trf1-interacting nuclear factor 2 gene (tinf2, 604319.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  76. en:caused by mutation in the udp-n-acetyl-alpha-d-galactosamine:polypeptide n-acetylgalactosaminyltransferase 3 gene (galnt3, 601756.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the udp-n-acetyl-alpha-d-galactosamine:polypeptide n-acetylgalactosaminyltransferase 3 gene (galnt3, 601756.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  77. en:caused by mutations in the 1-acylglycerol-3-phosphate o-acyltransferase 2 gene (agpat2, 603100.0001). --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the 1-acylglycerol-3-phosphate o-acyltransferase 2 gene (agpat2, 603100.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  78. en:caused by mutations in the platelet glycoprotein iiia gene (itgb3, 173470.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the platelet glycoprotein iiia gene (itgb3, 173470.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  79. en:caused by mutations in the succinate dehydrogenase complex subunit c gene (sdhc, 602413.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the succinate dehydrogenase complex subunit c gene (sdhc, 602413.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  80. en:caused by mutations in the tumor protein 63 gene (tp63, 603273.0012) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the tumor protein 63 gene (tp63, 603273.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  81. en:contiguous gene deletion syndrome caused by deletion (650kb-3.7mb) of 17p11.2 --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene deletion syndrome caused by deletion (650kb-3.7mb) of 17p11.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  82. en:susceptibility conferred by mutation in the breast cancer 2 gene (brca2, 600185.0001) --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the breast cancer 2 gene (brca2, 600185.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  83. en:susceptibility conferred by mutation in the kinesin family member 1b gene (kif1b, 605995.0002). --- r_associated #0: 36 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the kinesin family member 1b gene (kif1b, 605995.0002). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=36
  84. en:caused by mutation in the 120-kd centrosomal protein gene (cep120, 613446.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 120-kd centrosomal protein gene (cep120, 613446.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  85. en:caused by mutation in the aarf domain-containing kinase 3 gene (adck3, 606980.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aarf domain-containing kinase 3 gene (adck3, 606980.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  86. en:caused by mutation in the adhesion g protein-coupled receptor e2 gene (adgre2, 606100) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adhesion g protein-coupled receptor e2 gene (adgre2, 606100) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  87. en:caused by mutation in the c-type lectin domain family 7, member a gene (clec7a, 606264.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the c-type lectin domain family 7, member a gene (clec7a, 606264.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  88. en:caused by mutation in the carbohydrate synthase 1 gene (chsy1, 608123.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carbohydrate synthase 1 gene (chsy1, 608123.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  89. en:caused by mutation in the chloride intracellular channel 2 gene (clic2, 300138.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chloride intracellular channel 2 gene (clic2, 300138.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  90. en:caused by mutation in the cholinergic receptor, nicotinic, beta polypeptide 1 gene (chrnb1, 100710.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, beta polypeptide 1 gene (chrnb1, 100710.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  91. en:caused by mutation in the cholinergic receptor, nicotinic, beta polypeptide-1 gene (chrnb1, 100710.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, beta polypeptide-1 gene (chrnb1, 100710.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  92. en:caused by mutation in the coagulation factor vii gene (f7, 613878.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coagulation factor vii gene (f7, 613878.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  93. en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0005) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  94. en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 6 gene (dnajb6, 611332.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 6 gene (dnajb6, 611332.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  95. en:caused by mutation in the endothelin receptor type b gene (ednrb, 131244.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endothelin receptor type b gene (ednrb, 131244.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  96. en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0015) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  97. en:caused by mutation in the fras1 gene (fras1, 607830.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fras1 gene (fras1, 607830.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  98. en:caused by mutation in the fras1-related extracellular matrix protein 2 gene (frem2, 608945.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fras1-related extracellular matrix protein 2 gene (frem2, 608945.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  99. en:caused by mutation in the gene encoding exophilin-5 (exph5, 612878.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding exophilin-5 (exph5, 612878.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  100. en:caused by mutation in the gli-kruppel family member gli3 gene (gli3, 165240.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gli-kruppel family member gli3 gene (gli3, 165240.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  101. en:caused by mutation in the guanine nucleotide-binding protein, alpha-transducing activity polypeptide-1 gene (gnat1, 139330.0003) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the guanine nucleotide-binding protein, alpha-transducing activity polypeptide-1 gene (gnat1, 139330.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  102. en:caused by mutation in the interferon induced with helicase c domain 1 gene (ifih1, 606951.0009) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interferon induced with helicase c domain 1 gene (ifih1, 606951.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  103. en:caused by mutation in the low density lipoprotein receptor-related protein 2 gene (lrp2, 600073.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the low density lipoprotein receptor-related protein 2 gene (lrp2, 600073.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  104. en:caused by mutation in the mitochondrial complex i, subunit nd6 gene (mtnd6, 516006.0002) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial complex i, subunit nd6 gene (mtnd6, 516006.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  105. en:caused by mutation in the mitochondrial transfer rna cysteine gene (mttc, 590020.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial transfer rna cysteine gene (mttc, 590020.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  106. en:caused by mutation in the mlc1 gene (mlc1, 605908.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mlc1 gene (mlc1, 605908.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  107. en:caused by mutation in the non-pou domain-containing octamer-binding protein gene (nono, 300084.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the non-pou domain-containing octamer-binding protein gene (nono, 300084.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  108. en:caused by mutation in the origin recognition complex, subunit 4, gene (orc4, 603056.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the origin recognition complex, subunit 4, gene (orc4, 603056.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  109. en:caused by mutation in the perlecan gene (hspg2, 142461.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the perlecan gene (hspg2, 142461.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  110. en:caused by mutation in the phosphatidylinositol glycan, class y gene (pigy, 610662.0001) creation date : cassandra l. kniffin : 2/11/2016 --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol glycan, class y gene (pigy, 610662.0001) creation date : cassandra l. kniffin : 2/11/2016 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  111. en:caused by mutation in the phosphatidylserine synthase 1 gene (ptdss1, 612792.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylserine synthase 1 gene (ptdss1, 612792.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  112. en:caused by mutation in the platelet-derived growth factor receptor, beta polypeptide gene (pdgfrb, 173410.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the platelet-derived growth factor receptor, beta polypeptide gene (pdgfrb, 173410.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  113. en:caused by mutation in the protein kinase c, delta gene (prkcd, 176977.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein kinase c, delta gene (prkcd, 176977.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  114. en:caused by mutation in the receptor expression-enhancing protein 1 gene (reep1, 609139.0006) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the receptor expression-enhancing protein 1 gene (reep1, 609139.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  115. en:caused by mutation in the rho guanine nucleotide exchange factor 9 gene (arhgef9, 300429.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rho guanine nucleotide exchange factor 9 gene (arhgef9, 300429.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  116. en:caused by mutation in the signal transducer and activator of transcription 3 gene (stat3, 102582.0008) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the signal transducer and activator of transcription 3 gene (stat3, 102582.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  117. en:caused by mutation in the solute carrier family 10 (sodium/bile acid cotransporter family), member 2 gene (slc10a2, 601295.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 10 (sodium/bile acid cotransporter family), member 2 gene (slc10a2, 601295.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  118. en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, folate), member 32 gene (slc25a32, 610815.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, folate), member 32 gene (slc25a32, 610815.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  119. en:caused by mutation in the solute carrier family 5 (sodium iodide symporter), member 5 gene (slc5a5, 601843.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 5 (sodium iodide symporter), member 5 gene (slc5a5, 601843.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  120. en:caused by mutation in the succinate dehydrogenase complex assembly factor 1 gene (sdhaf1, 612848.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the succinate dehydrogenase complex assembly factor 1 gene (sdhaf1, 612848.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  121. en:caused by mutation in the synaptotagmin 14 gene (syt14, 610949.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the synaptotagmin 14 gene (syt14, 610949.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  122. en:caused by mutation in the t-box 4 gene (tbx4, 601719.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the t-box 4 gene (tbx4, 601719.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  123. en:caused by mutation in the telo2-interacting protein 2 gene (tti2, 614426.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the telo2-interacting protein 2 gene (tti2, 614426.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  124. en:caused by mutation in the thyroid-stimulating hormone, beta polypeptide gene (tshb, 188540.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thyroid-stimulating hormone, beta polypeptide gene (tshb, 188540.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  125. en:caused by mutation in the transmembrane protein 216 gene (tmem216, 613277.0002) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 216 gene (tmem216, 613277.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  126. en:caused by mutation in the valyl-trna synthetase 2 gene (vars2, 612802.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the valyl-trna synthetase 2 gene (vars2, 612802.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  127. en:caused by mutation in the vesicle-associated membrane protein 1 gene (vamp1, 185880.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the vesicle-associated membrane protein 1 gene (vamp1, 185880.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  128. en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0005) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  129. en:caused by mutation in the zinc finger protein 408 gene (znf408, 616454.0003) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger protein 408 gene (znf408, 616454.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  130. en:caused by mutations in the coagulation factor viii gene (f8, 306700.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the coagulation factor viii gene (f8, 306700.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  131. en:caused by mutations in the holocarbyoxylase synthetase gene (hlcs, 253270.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the holocarbyoxylase synthetase gene (hlcs, 253270.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  132. en:caused by mutations in the nijmegen breakage syndrome gene (nbs1, 602667.0001) --- r_associated #0: 35 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the nijmegen breakage syndrome gene (nbs1, 602667.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=35
  133. en:caused by 1 to 3.8-mb duplication on chromosome 2q31.1 --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by 1 to 3.8-mb duplication on chromosome 2q31.1 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  134. en:caused by deletion of a 32.5-kb regulatory region (xysr) -640 to -607 kb upstream of the sry-box-9 gene (sox9, 608160.0018) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion of a 32.5-kb regulatory region (xysr) -640 to -607 kb upstream of the sry-box-9 gene (sox9, 608160.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  135. en:caused by mutation in alkaline phosphatase gene (alpl, 171760.0003) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in alkaline phosphatase gene (alpl, 171760.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  136. en:caused by mutation in gene encoding cystein-rich pdz domain-binding protein (cript, 604594.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in gene encoding cystein-rich pdz domain-binding protein (cript, 604594.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  137. en:caused by mutation in the alpha-fetoprotein gene (afp, 104150.0002) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-fetoprotein gene (afp, 104150.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  138. en:caused by mutation in the beta-carotene 15,15-prime-monooxygenase 1 gene (bcmo1, 605748.0001). --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-carotene 15,15-prime-monooxygenase 1 gene (bcmo1, 605748.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  139. en:caused by mutation in the bmp binding endothelial regulator gene (bmper, 608699.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bmp binding endothelial regulator gene (bmper, 608699.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  140. en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0024) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0024) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  141. en:caused by mutation in the dedicator of cytokinesis 7 gene (dock7, 615730.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dedicator of cytokinesis 7 gene (dock7, 615730.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  142. en:caused by mutation in the dermatan sulfate epimerase gene (dse, 605942.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dermatan sulfate epimerase gene (dse, 605942.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  143. en:caused by mutation in the doublecortin domain-containing protein 2 gene (dcdc2, 605755.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the doublecortin domain-containing protein 2 gene (dcdc2, 605755.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  144. en:caused by mutation in the ectodysplasin anhidrotic receptor gene (edar, 604095.0005) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ectodysplasin anhidrotic receptor gene (edar, 604095.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  145. en:caused by mutation in the glutamate decarboxylase 1 gene (gad1, 605363.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutamate decarboxylase 1 gene (gad1, 605363.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  146. en:caused by mutation in the glycyl trna synthetase gene (gars, 600287.0002) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycyl trna synthetase gene (gars, 600287.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  147. en:caused by mutation in the growth factor-independent 1b gene (gfi1b, 604383.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the growth factor-independent 1b gene (gfi1b, 604383.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  148. en:caused by mutation in the ikaros family zinc finger 1 gene (ikzf1, 603023.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ikaros family zinc finger 1 gene (ikzf1, 603023.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  149. en:caused by mutation in the lipopolysaccharide-induced tumor necrosis factor-alpha factor gene (litaf, 603795.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lipopolysaccharide-induced tumor necrosis factor-alpha factor gene (litaf, 603795.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  150. en:caused by mutation in the microcephalin gene (mcph1, 607117.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the microcephalin gene (mcph1, 607117.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  151. en:caused by mutation in the mitochondrial apoptogenic protein 1 gene (apopt1, 616003.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial apoptogenic protein 1 gene (apopt1, 616003.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  152. en:caused by mutation in the mitochondrial elongation factor g1 gene (gfm1, 606639.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial elongation factor g1 gene (gfm1, 606639.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  153. en:caused by mutation in the mmaa gene (mmaa, 607481.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mmaa gene (mmaa, 607481.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  154. en:caused by mutation in the oligophrenin 1 gene (ophn1, 300127.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the oligophrenin 1 gene (ophn1, 300127.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  155. en:caused by mutation in the peptidyl-prolyl isomerase b gene (ppib, 123841.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peptidyl-prolyl isomerase b gene (ppib, 123841.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  156. en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 2 gene (plekhg2, 611893.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 2 gene (plekhg2, 611893.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  157. en:caused by mutation in the retinoblastoma-binding protein 8 gene (rbbp8, 604124.0003) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the retinoblastoma-binding protein 8 gene (rbbp8, 604124.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  158. en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0023) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0023) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  159. en:caused by mutation in the steroid 5-alpha-reductase 3 gene (srd5a3, 611715.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the steroid 5-alpha-reductase 3 gene (srd5a3, 611715.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  160. en:caused by mutation in the t-type voltage-dependent calcium channel, alpha-1g subunit gene (cacna1g, 604065.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the t-type voltage-dependent calcium channel, alpha-1g subunit gene (cacna1g, 604065.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  161. en:caused by mutation in the teneurin transmembrane protein 4 gene (tenm4, 610084.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the teneurin transmembrane protein 4 gene (tenm4, 610084.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  162. en:caused by mutation in the thiamine pyrophosphokinase gene (tpk1, 606370.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thiamine pyrophosphokinase gene (tpk1, 606370.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  163. en:caused by mutation in the tolloid-like 1 gene (tll1, 606742.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tolloid-like 1 gene (tll1, 606742.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  164. en:caused by mutation in the transmembrane anterior posterior transformation-1 gene (tapt1, 612758.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane anterior posterior transformation-1 gene (tapt1, 612758.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  165. en:caused by mutation in the ubiquitin-protein ligase e3b gene (ube3b, 608047.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquitin-protein ligase e3b gene (ube3b, 608047.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  166. en:caused by mutation in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0005) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  167. en:caused by mutation in the uromodulin gene (umod, 191845.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the uromodulin gene (umod, 191845.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  168. en:caused by mutation in the voltage-gated potassium channel, kqt-like subfamily, member 2 gene (kcnq2, 602235.0007) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated potassium channel, kqt-like subfamily, member 2 gene (kcnq2, 602235.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  169. en:caused by mutation in the zinc finger protein-141 gene (znf141, 194648.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger protein-141 gene (znf141, 194648.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  170. en:caused by mutations in the nhs gene (nhs, 300457.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the nhs gene (nhs, 300457.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  171. en:caused by mutations in the thyroid peroxidase gene (tpo, 606765.0001) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the thyroid peroxidase gene (tpo, 606765.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  172. en:caused by somatic mutation in the janus kinase 2 gene (jak2, 147796) --- r_associated #0: 34 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the janus kinase 2 gene (jak2, 147796) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=34
  173. en:caused by mutation in the 72-kd signal recognition particle gene (srp72. 602122.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 72-kd signal recognition particle gene (srp72. 602122.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  174. en:caused by mutation in the alanyl-trna synthetase gene (aars, 601065.0003) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alanyl-trna synthetase gene (aars, 601065.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  175. en:caused by mutation in the alpha-1 gap junction protein gene (gja1, 121014.0024) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1 gap junction protein gene (gja1, 121014.0024) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  176. en:caused by mutation in the alpha-1 type xvii collagen gene (col17a1, 113811.0015) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1 type xvii collagen gene (col17a1, 113811.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  177. en:caused by mutation in the alpha-fetoprotein gene (afp, 104150.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-fetoprotein gene (afp, 104150.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  178. en:caused by mutation in the ankyrin 1 gene (ank1, 612641.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ankyrin 1 gene (ank1, 612641.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  179. en:caused by mutation in the bbs5 gene (bbs5, 603650.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bbs5 gene (bbs5, 603650.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  180. en:caused by mutation in the c. elegans mab21 homolog-like 2 gene (mab21l2, 604357.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the c. elegans mab21 homolog-like 2 gene (mab21l2, 604357.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  181. en:caused by mutation in the caspase recruitment domain-containing protein 11 gene (card11, 607210.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the caspase recruitment domain-containing protein 11 gene (card11, 607210.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  182. en:caused by mutation in the chromosome 2 open reading frame 64 gene (c2orf64, 613920.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 2 open reading frame 64 gene (c2orf64, 613920.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  183. en:caused by mutation in the connexin-32 gene (gjb1, 304040.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the connexin-32 gene (gjb1, 304040.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  184. en:caused by mutation in the cytochrome c oxidase assembly factor 6 gene (coa6, 614772.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase assembly factor 6 gene (coa6, 614772.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  185. en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0004). --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0004). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  186. en:caused by mutation in the fibroblast growth factor-16 gene (fgf16, 300827.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor-16 gene (fgf16, 300827.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  187. en:caused by mutation in the fumarylacetoacetase gene (fah, 613871.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fumarylacetoacetase gene (fah, 613871.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  188. en:caused by mutation in the glutaryl-coa dehydrogenase gene (gcdh, 608801.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutaryl-coa dehydrogenase gene (gcdh, 608801.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  189. en:caused by mutation in the hepatocyte cell adhesion molecule gene (hepacam, 611642.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hepatocyte cell adhesion molecule gene (hepacam, 611642.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  190. en:caused by mutation in the homolog of the drosophila twist 2 gene (twist2, 607556.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila twist 2 gene (twist2, 607556.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  191. en:caused by mutation in the malin gene (nhlrc1, 608072.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the malin gene (nhlrc1, 608072.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  192. en:caused by mutation in the matrix metalloproteinase-20 gene (mmp20, 604629.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the matrix metalloproteinase-20 gene (mmp20, 604629.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  193. en:caused by mutation in the mediator complex subunit 13-like gene (med13l, 608771.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mediator complex subunit 13-like gene (med13l, 608771.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  194. en:caused by mutation in the methyl-cpg-binding protein-2 gene (mecp2, 300005.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methyl-cpg-binding protein-2 gene (mecp2, 300005.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  195. en:caused by mutation in the neurofibromin-2 gene (nf2, 607379.0017) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neurofibromin-2 gene (nf2, 607379.0017) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  196. en:caused by mutation in the patatin-like phospholipase domain-containing protein 6 (pnpla6, 603197.0004) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the patatin-like phospholipase domain-containing protein 6 (pnpla6, 603197.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  197. en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0004) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  198. en:caused by mutation in the post-gpi attachment to proteins 1 gene (pgap1, 611655.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the post-gpi attachment to proteins 1 gene (pgap1, 611655.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  199. en:caused by mutation in the retinol dehydrogenase 12 gene (rdh12, 608830.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the retinol dehydrogenase 12 gene (rdh12, 608830.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  200. en:caused by mutation in the serpin peptidase inhibitor, clade e, member 1 gene (serpine1, 173360.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the serpin peptidase inhibitor, clade e, member 1 gene (serpine1, 173360.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  201. en:caused by mutation in the solute carrier family 12 (sodium/chloride transporter), member 6 gene (slc12a6, 604878.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 12 (sodium/chloride transporter), member 6 gene (slc12a6, 604878.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  202. en:caused by mutation in the solute carrier family 12 (sodium/potassium/chloride transporters), member 1 gene (slc12a1, 600839.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 12 (sodium/potassium/chloride transporters), member 1 gene (slc12a1, 600839.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  203. en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0019) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0019) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  204. en:caused by mutation in the tropomyosin 2 gene (tpm2, 190990.0004) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tropomyosin 2 gene (tpm2, 190990.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  205. en:caused by mutations in homolog 3 of the drosophila 'roundabout' gene (robo3, 608630.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in homolog 3 of the drosophila 'roundabout' gene (robo3, 608630.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  206. en:susceptibility conferred by mutation in the alpha-2-macroglobulin gene (a2m, 103950.0005) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the alpha-2-macroglobulin gene (a2m, 103950.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  207. en:susceptibility conferred by mutation in the melanocortin 2 receptor accessory protein 2 gene (mrap2, 615410.0001) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the melanocortin 2 receptor accessory protein 2 gene (mrap2, 615410.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  208. en:susceptibility conferred by mutation in the tumor necrosis factor receptor superfamily, member 11a gene (tnfrsf11a, 603499.0002) --- r_associated #0: 32 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the tumor necrosis factor receptor superfamily, member 11a gene (tnfrsf11a, 603499.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=32
  209. en:caused by 750kb to 2.7mb deletion of chromosome 19q13.11 --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by 750kb to 2.7mb deletion of chromosome 19q13.11 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  210. en:caused by mutation in homolog of the c. elegans suppressor of clear gene (shoc2, 602775.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in homolog of the c. elegans suppressor of clear gene (shoc2, 602775.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  211. en:caused by mutation in the 104-kd centrosomal protein gene (cep104, 616690.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 104-kd centrosomal protein gene (cep104, 616690.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  212. en:caused by mutation in the alpha-2 actinin gene (actn2, 102573.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-2 actinin gene (actn2, 102573.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  213. en:caused by mutation in the atp synthase, h+ transporting, mitochondrial f1 complex, alpha subunit 1 (atp5a1, 164360.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp synthase, h+ transporting, mitochondrial f1 complex, alpha subunit 1 (atp5a1, 164360.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  214. en:caused by mutation in the bbs2 gene (bbs2, 606151.0018) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bbs2 gene (bbs2, 606151.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  215. en:caused by mutation in the beta-2b tubulin gene (tubb2b, 612850.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-2b tubulin gene (tubb2b, 612850.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  216. en:caused by mutation in the beta-3 laminin gene (lamb3, 150310.0017) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-3 laminin gene (lamb3, 150310.0017) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  217. en:caused by mutation in the cathepsin f gene (ctsf, 603539.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cathepsin f gene (ctsf, 603539.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  218. en:caused by mutation in the ccm2 gene (ccm2, 607929.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ccm2 gene (ccm2, 607929.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  219. en:caused by mutation in the coagulation factor v gene (f5, 612309.0004) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coagulation factor v gene (f5, 612309.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  220. en:caused by mutation in the cwf19-like protein 1 gene (cwf19l1, 616120.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cwf19-like protein 1 gene (cwf19l1, 616120.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  221. en:caused by mutation in the doublecortin gene (dcx, 300121.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the doublecortin gene (dcx, 300121.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  222. en:caused by mutation in the euchromatic histone methyltransferase-1 gene (ehmt1, 607001.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the euchromatic histone methyltransferase-1 gene (ehmt1, 607001.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  223. en:caused by mutation in the family with sequence similarity 20, member a gene (fam20a, 611062.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the family with sequence similarity 20, member a gene (fam20a, 611062.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  224. en:caused by mutation in the ferm domain-containing protein 4a gene (frmd4a, 616305.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ferm domain-containing protein 4a gene (frmd4a, 616305.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  225. en:caused by mutation in the hexokinase 1 gene (hk1, 142600.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hexokinase 1 gene (hk1, 142600.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  226. en:caused by mutation in the homolog of the e. coli muts 2 gene (msh2, 120435.0006) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the e. coli muts 2 gene (msh2, 120435.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  227. en:caused by mutation in the homolog of the s. cerevisiae coenzyme q4 gene (coq4, 612898.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae coenzyme q4 gene (coq4, 612898.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  228. en:caused by mutation in the hps1 gene (hps1, 203300) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hps1 gene (hps1, 203300) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  229. en:caused by mutation in the insulin gene (ins, 176730.0014) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the insulin gene (ins, 176730.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  230. en:caused by mutation in the k(lysine) acetyltransferase 6a gene (kat6a, 601408.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the k(lysine) acetyltransferase 6a gene (kat6a, 601408.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  231. en:caused by mutation in the l-arginine:glycine amidinotransferase gene (gatm, 602360.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the l-arginine:glycine amidinotransferase gene (gatm, 602360.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  232. en:caused by mutation in the myosin vi gene (myo6, 600970.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin vi gene (myo6, 600970.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  233. en:caused by mutation in the opa3 gene (opa3, 606580.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the opa3 gene (opa3, 606580.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  234. en:caused by mutation in the piezo1 ion channel gene (piezo1, 611184.0009) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the piezo1 ion channel gene (piezo1, 611184.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  235. en:caused by mutation in the platelet-derived growth factor receptor, beta polypeptide gene (pdgfrb, 173410.0006) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the platelet-derived growth factor receptor, beta polypeptide gene (pdgfrb, 173410.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  236. en:caused by mutation in the polyribonucleotide nucleotidyltransferase 1 gene (pnpt1, 610316.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polyribonucleotide nucleotidyltransferase 1 gene (pnpt1, 610316.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  237. en:caused by mutation in the potassium voltage-gated channel, shal-related subfamily member-3 gene (kcnd3, 605411.0005) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, shal-related subfamily member-3 gene (kcnd3, 605411.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  238. en:caused by mutation in the receptor-associated protein of the synapse, 43-kd gene (rapsn, 601592.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the receptor-associated protein of the synapse, 43-kd gene (rapsn, 601592.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  239. en:caused by mutation in the sedlin gene (sedl, 300202.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sedlin gene (sedl, 300202.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  240. en:caused by mutation in the septin 12 gene (sept12, 611562.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the septin 12 gene (sept12, 611562.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  241. en:caused by mutation in the sequestosome 1 gene (sqstm1, 601530.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sequestosome 1 gene (sqstm1, 601530.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  242. en:caused by mutation in the stt3, subunit of the oligosaccharyltransferase complex, s. cerevisiae, homolog of, a gene (stt3a, 601134.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the stt3, subunit of the oligosaccharyltransferase complex, s. cerevisiae, homolog of, a gene (stt3a, 601134.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  243. en:caused by mutation in the tenascin c gene (tnc, 187380.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tenascin c gene (tnc, 187380.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  244. en:caused by mutation in the testis/liver gamma-2 subunit of phosphorylase kinase gene (phkg2, 172471.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the testis/liver gamma-2 subunit of phosphorylase kinase gene (phkg2, 172471.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  245. en:caused by mutation in the tetratricopeptide repeat domain-containing protein 8 gene (ttc8, 608132.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tetratricopeptide repeat domain-containing protein 8 gene (ttc8, 608132.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  246. en:caused by mutation in the transducin-like enhancer of split 6 gene (tle6, 612399.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transducin-like enhancer of split 6 gene (tle6, 612399.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  247. en:caused by mutation in the tubulin, beta-4a gene (tubb4a, 602662.0002) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin, beta-4a gene (tubb4a, 602662.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  248. en:caused by mutation in the tubulin-gamma complex-associated protein 4 gene (tubgcp4, 609610.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin-gamma complex-associated protein 4 gene (tubgcp4, 609610.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  249. en:caused by mutation in the v-ha-ras harvey rat sarcoma viral oncogene homolog gene (hras, 190020.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-ha-ras harvey rat sarcoma viral oncogene homolog gene (hras, 190020.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  250. en:caused by mutation in the wolframin gene (wfs1, 222300.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wolframin gene (wfs1, 222300.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  251. en:caused by mutation in the wolframin gene (wfs1, 606201.0020) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wolframin gene (wfs1, 606201.0020) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  252. en:caused by mutations in the beta-2 integrin gene (itgb2, 600065.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the beta-2 integrin gene (itgb2, 600065.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  253. en:caused by mutations in the cartilage-derived morphogenetic protein-1 gene (cdmp1, 601146.0005) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cartilage-derived morphogenetic protein-1 gene (cdmp1, 601146.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  254. en:caused by mutations in the galactosamine-6-sulfatase gene (galns, 612222.0001). --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the galactosamine-6-sulfatase gene (galns, 612222.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  255. en:caused by somatic mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  256. en:susceptibility conferred by mutation in the complement factor h gene (chf, 134370.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the complement factor h gene (chf, 134370.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  257. en:susceptibility conferred by mutation in the dopamine receptor d3 gene (drd3, 126451.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the dopamine receptor d3 gene (drd3, 126451.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  258. en:susceptibility conferred by mutation in the lysyl oxidase-like 1 gene (loxl1, 153456.0001) --- r_associated #0: 31 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the lysyl oxidase-like 1 gene (loxl1, 153456.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=31
  259. en:a contiguous gene syndrome caused by mutations in the zinc finger transcription factor trps1 (trps1, 604386) and the exostosin 1 gene (ext1, 133700) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome caused by mutations in the zinc finger transcription factor trps1 (trps1, 604386) and the exostosin 1 gene (ext1, 133700) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  260. en:associated with mutation in the p53 tumor protein gene (tp53, 191170.0006) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:associated with mutation in the p53 tumor protein gene (tp53, 191170.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  261. en:balanced reciprocal translocation between chromosomes x and 15 --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:balanced reciprocal translocation between chromosomes x and 15 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  262. en:caused by 1-mb duplication on chromosome 2q31.1 --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by 1-mb duplication on chromosome 2q31.1 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  263. en:caused by a (cctg)n repeat expansion in the zinc finger protein 9 gene (znf9, 116955.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a (cctg)n repeat expansion in the zinc finger protein 9 gene (znf9, 116955.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  264. en:caused by a 1.75 mb deletion at 15q24 --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a 1.75 mb deletion at 15q24 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  265. en:caused by a trinucleotide repeat expansion (ctg)n in the dystrophia myotonica-protein kinase gene (dmpk, 605377.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a trinucleotide repeat expansion (ctg)n in the dystrophia myotonica-protein kinase gene (dmpk, 605377.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  266. en:caused by contiguous gene duplication (chrx:135.6-136.1, grch37) on xq26.3 --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by contiguous gene duplication (chrx:135.6-136.1, grch37) on xq26.3 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  267. en:caused by deletion of at least 600kb in 10q26.2 --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion of at least 600kb in 10q26.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  268. en:caused by duplication of the methyl-cp6-binding protein 2 gene (mecp2, 300005.0030) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of the methyl-cp6-binding protein 2 gene (mecp2, 300005.0030) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  269. en:caused by expanded cag trinucleotide repeats in the alpha-1a calcium channel subunit gene (cacna1a, 601011.0007) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by expanded cag trinucleotide repeats in the alpha-1a calcium channel subunit gene (cacna1a, 601011.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  270. en:caused by fusion of the ret protooncogene (164761) with tif1g (605769), d10s170 (601985), ele1 (601984), and prkar1a (188830) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by fusion of the ret protooncogene (164761) with tif1g (605769), d10s170 (601985), ele1 (601984), and prkar1a (188830) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  271. en:caused by interstitial or terminal deletion of chromosome 18q --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by interstitial or terminal deletion of chromosome 18q | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  272. en:caused by mutation in alpha-galactosidase a gene (gla, 300644.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in alpha-galactosidase a gene (gla, 300644.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  273. en:caused by mutation in glycogen synthase 1 gene (gys1, 138570.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in glycogen synthase 1 gene (gys1, 138570.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  274. en:caused by mutation in the 15-alpha-hydroxyprostaglandin dehydrogenase gene (hpgd, 601688.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 15-alpha-hydroxyprostaglandin dehydrogenase gene (hpgd, 601688.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  275. en:caused by mutation in the 155-kd nucleoporin gene (nup155, 606694.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 155-kd nucleoporin gene (nup155, 606694.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  276. en:caused by mutation in the 164-kd centrosomal protein gene (cep164, 614848.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 164-kd centrosomal protein gene (cep164, 614848.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  277. en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase 4 gene (hsd17b4, 601860.0008) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase 4 gene (hsd17b4, 601860.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  278. en:caused by mutation in the abelson helper integration site 1 gene (ahi1, 608894.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the abelson helper integration site 1 gene (ahi1, 608894.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  279. en:caused by mutation in the adenylosuccinate lyase gene (adsl, 608222.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenylosuccinate lyase gene (adsl, 608222.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  280. en:caused by mutation in the aggrecan-1 gene (agc1, 155760.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aggrecan-1 gene (agc1, 155760.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  281. en:caused by mutation in the alanine-glyoxylate aminotransferase gene (agxt, 604285.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alanine-glyoxylate aminotransferase gene (agxt, 604285.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  282. en:caused by mutation in the aldehyde dehydrogenase 7 family, member a1 gene (aldh7a1, 107323.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aldehyde dehydrogenase 7 family, member a1 gene (aldh7a1, 107323.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  283. en:caused by mutation in the alpha subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0015). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0015). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  284. en:caused by mutation in the alpha-1 actinin gene (actn1, 102565.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1 actinin gene (actn1, 102565.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  285. en:caused by mutation in the alpha-1-subunit of the voltage-gated type ii sodium channel gene (scn2a, 182390.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1-subunit of the voltage-gated type ii sodium channel gene (scn2a, 182390.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  286. en:caused by mutation in the alpha-1d subunit of the l-type voltage-dependent calcium channel gene (cacna1d, 114206.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1d subunit of the l-type voltage-dependent calcium channel gene (cacna1d, 114206.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  287. en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  288. en:caused by mutation in the alpha-stimulatory subunit of the guanine nucleotide-binding protein gene (gnas1, 139320.0011) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-stimulatory subunit of the guanine nucleotide-binding protein gene (gnas1, 139320.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  289. en:caused by mutation in the aminoacylase-1 gene (acy1, 104620.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aminoacylase-1 gene (acy1, 104620.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  290. en:caused by mutation in the ankyrin repeat and sterile alpha motif domains-containing protein gene 6 (anks6, 615370.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ankyrin repeat and sterile alpha motif domains-containing protein gene 6 (anks6, 615370.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  291. en:caused by mutation in the arginase gene (arg1, 207800.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the arginase gene (arg1, 207800.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  292. en:caused by mutation in the arylhydrocarbon-interacting receptor protein-like 1 gene (aipl1, 604392.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the arylhydrocarbon-interacting receptor protein-like 1 gene (aipl1, 604392.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  293. en:caused by mutation in the atlastin gene (spg3a, 606439.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atlastin gene (spg3a, 606439.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  294. en:caused by mutation in the atp-binding cassette, subfamily b, member 11 gene (abcb11, 603201.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily b, member 11 gene (abcb11, 603201.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  295. en:caused by mutation in the atp-binding cassette, subfamily b, member 11 gene (abcb11, 603201.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily b, member 11 gene (abcb11, 603201.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  296. en:caused by mutation in the atp-binding cassette, subfamily b, member 6 gene (abcb6, 605452.0008) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily b, member 6 gene (abcb6, 605452.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  297. en:caused by mutation in the atp-binding cassette, subfamily c, member 9 gene (abcc9, 601439.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily c, member 9 gene (abcc9, 601439.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  298. en:caused by mutation in the atp/gtp-binding protein-like-1 gene (agbl1, 615496.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp/gtp-binding protein-like-1 gene (agbl1, 615496.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  299. en:caused by mutation in the atpase, ca(2+)-transporting, type 2c, member 1 gene (atp2c1, 604384.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, ca(2+)-transporting, type 2c, member 1 gene (atp2c1, 604384.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  300. en:caused by mutation in the atpase, cu(2+)-transporting, alpha polypeptide (atp7a, 300011.0015) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, cu(2+)-transporting, alpha polypeptide (atp7a, 300011.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  301. en:caused by mutation in the atpase, cu++ transporting, alpha polypeptide gene (atp7a, 300011.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, cu++ transporting, alpha polypeptide gene (atp7a, 300011.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  302. en:caused by mutation in the bbs2 gene (bbs2, 606151.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bbs2 gene (bbs2, 606151.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  303. en:caused by mutation in the bestrophin 1 gene (best1, 607854.0020) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bestrophin 1 gene (best1, 607854.0020) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  304. en:caused by mutation in the beta-a2 crystallin gene (cryba2, 600836.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-a2 crystallin gene (cryba2, 600836.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  305. en:caused by mutation in the beta-galactosidase gene (glb1, 611458.0009) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-galactosidase gene (glb1, 611458.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  306. en:caused by mutation in the beta-synuclein gene (sncb, 602569.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-synuclein gene (sncb, 602569.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  307. en:caused by mutation in the biogenesis of lysosome-related organelles complex 1, subunit 3 gene (bloc1s3, 609762.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the biogenesis of lysosome-related organelles complex 1, subunit 3 gene (bloc1s3, 609762.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  308. en:caused by mutation in the biotinidase gene (btd, 253260.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the biotinidase gene (btd, 253260.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  309. en:caused by mutation in the branched chain keto acid dehydrogenase e1, alpha polypeptide gene (bckdha, 608348.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the branched chain keto acid dehydrogenase e1, alpha polypeptide gene (bckdha, 608348.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  310. en:caused by mutation in the brca1-associated c-terminal helicase 1 gene (brip1, 605882.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the brca1-associated c-terminal helicase 1 gene (brip1, 605882.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  311. en:caused by mutation in the breast cancer type 2 gene (brca2, 600185.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the breast cancer type 2 gene (brca2, 600185.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  312. en:caused by mutation in the bruton agammaglobulinemia tyrosine kinase gene (btk, 300300.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bruton agammaglobulinemia tyrosine kinase gene (btk, 300300.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  313. en:caused by mutation in the c2 calcium-dependent domain-containing protein 3 gene (c2cd3, 615944.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the c2 calcium-dependent domain-containing protein 3 gene (c2cd3, 615944.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  314. en:caused by mutation in the cadherin 23 gene (cdh23, 605516.0005) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cadherin 23 gene (cdh23, 605516.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  315. en:caused by mutation in the calcium channel, voltage-dependent, p/q type, alpha 1a subunit gene (cacna1a, 601011.0005) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calcium channel, voltage-dependent, p/q type, alpha 1a subunit gene (cacna1a, 601011.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  316. en:caused by mutation in the calcium- and integrin-binding protein 2 gene (cib2, 605564.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calcium- and integrin-binding protein 2 gene (cib2, 605564.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  317. en:caused by mutation in the calreticulin-3 gene (calr3, 611414.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calreticulin-3 gene (calr3, 611414.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  318. en:caused by mutation in the caspase recruitment domain-containing protein 14 gene (card14, 607211.0006) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the caspase recruitment domain-containing protein 14 gene (card14, 607211.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  319. en:caused by mutation in the caveolin 1 gene (cav1, 601047.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the caveolin 1 gene (cav1, 601047.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  320. en:caused by mutation in the caveolin 3 gene (cav3, 601253.0007) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the caveolin 3 gene (cav3, 601253.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  321. en:caused by mutation in the cd59 antigen gene (cd59, 107271.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd59 antigen gene (cd59, 107271.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  322. en:caused by mutation in the cd79a antigen gene (cd79a, 112205.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd79a antigen gene (cd79a, 112205.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  323. en:caused by mutation in the centromeric protein f gene (cenpf, 600236.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the centromeric protein f gene (cenpf, 600236.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  324. en:caused by mutation in the chloride channel 2 gene (clcn2, 600570.0006) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chloride channel 2 gene (clcn2, 600570.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  325. en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0005) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  326. en:caused by mutation in the chloride channel 7 gene (clcn7, 602727.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chloride channel 7 gene (clcn7, 602727.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  327. en:caused by mutation in the chromosome 12 open reading frame 62 gene (c12orf62, 614478.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 12 open reading frame 62 gene (c12orf62, 614478.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  328. en:caused by mutation in the chromosome 15 open reading frame 41 gene (c15orf41, 615626.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 15 open reading frame 41 gene (c15orf41, 615626.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  329. en:caused by mutation in the chromosome 8 open reading frame 37 gene (c8orf37, 614477.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 8 open reading frame 37 gene (c8orf37, 614477.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  330. en:caused by mutation in the coagulation factor ii gene (f2, 176930.0009) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coagulation factor ii gene (f2, 176930.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  331. en:caused by mutation in the coiled-coil domain-containing protein 103 (ccdc103, 614677.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil domain-containing protein 103 (ccdc103, 614677.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  332. en:caused by mutation in the coiled-coil domain-containing protein 111 gene (ccdc111, 615421.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil domain-containing protein 111 gene (ccdc111, 615421.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  333. en:caused by mutation in the collagen and calcium-binding egf domain-containing protein 1 gene (ccbe1, 612753.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen and calcium-binding egf domain-containing protein 1 gene (ccbe1, 612753.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  334. en:caused by mutation in the collagen iv, alpha-1 polypeptide gene (col4a1, 120130.0003) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen iv, alpha-1 polypeptide gene (col4a1, 120130.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  335. en:caused by mutation in the complement component 3 gene (c3, 120700.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement component 3 gene (c3, 120700.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  336. en:caused by mutation in the component x gene of the pyruvate dehydrogenase complex (pdhx, 608769.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the component x gene of the pyruvate dehydrogenase complex (pdhx, 608769.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  337. en:caused by mutation in the coronin 1a gene (coro1a, 605000.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coronin 1a gene (coro1a, 605000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  338. en:caused by mutation in the cystinosin gene (ctns, 219800.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cystinosin gene (ctns, 219800.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  339. en:caused by mutation in the cytochrome b(-245) alpha subunit gene (cyba, 608508.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome b(-245) alpha subunit gene (cyba, 608508.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  340. en:caused by mutation in the cytochrome p450, subfamily iid6 gene (cyp2d6, 124030.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450, subfamily iid6 gene (cyp2d6, 124030.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  341. en:caused by mutation in the dedicator of cytokinesis 2 gene (dock2, 603122.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dedicator of cytokinesis 2 gene (dock2, 603122.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  342. en:caused by mutation in the dedicator of cytokinesis 8 gene (dock8, 611432.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dedicator of cytokinesis 8 gene (dock8, 611432.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  343. en:caused by mutation in the deformed epidermal autoregulatory factor 1 homolog gene (deaf1, 602635.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the deformed epidermal autoregulatory factor 1 homolog gene (deaf1, 602635.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  344. en:caused by mutation in the delta-1 phospholipase c gene (plcd1, 602142.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the delta-1 phospholipase c gene (plcd1, 602142.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  345. en:caused by mutation in the desmin gene (des, 125660.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the desmin gene (des, 125660.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  346. en:caused by mutation in the dihydropyrimidinase gene (dpys, 613326.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dihydropyrimidinase gene (dpys, 613326.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  347. en:caused by mutation in the downstream of tyrosine kinase 7 gene (dok7, 610285.0009). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the downstream of tyrosine kinase 7 gene (dok7, 610285.0009). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  348. en:caused by mutation in the dual oxidase 2 gene (duox2, 606759.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dual oxidase 2 gene (duox2, 606759.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  349. en:caused by mutation in the dual oxidase maturation factor 2 gene (duoxa2, 612772.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dual oxidase maturation factor 2 gene (duoxa2, 612772.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  350. en:caused by mutation in the dysferlin gene (dys, 603009.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dysferlin gene (dys, 603009.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  351. en:caused by mutation in the dystrobrevin-binding protein 1 gene (dtnbp1, 607145.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dystrobrevin-binding protein 1 gene (dtnbp1, 607145.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  352. en:caused by mutation in the early growth response-2 gene (egr2, 129010.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the early growth response-2 gene (egr2, 129010.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  353. en:caused by mutation in the early growth response-2 gene (egr2, 129010.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the early growth response-2 gene (egr2, 129010.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  354. en:caused by mutation in the elongation of very long chain fatty acids-like 4 gene (elovl4, 605512.0005) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the elongation of very long chain fatty acids-like 4 gene (elovl4, 605512.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  355. en:caused by mutation in the elongation of very long chain fatty acids-like 4 gene (elovl4, 605512.0007) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the elongation of very long chain fatty acids-like 4 gene (elovl4, 605512.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  356. en:caused by mutation in the embryonic skeletal muscle myosin heavy chain 3 gene (myh3, 160720.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the embryonic skeletal muscle myosin heavy chain 3 gene (myh3, 160720.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  357. en:caused by mutation in the enolase 3 gene (eno3, 131370.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the enolase 3 gene (eno3, 131370.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  358. en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 1 gene (eif2b1, 606686.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 1 gene (eif2b1, 606686.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  359. en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 2 gene (eif2b2, 606454.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 2 gene (eif2b2, 606454.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  360. en:caused by mutation in the excision repair cross complementing rodent repair deficiency, complementation group 6 gene (ercc6, 133540.0007) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the excision repair cross complementing rodent repair deficiency, complementation group 6 gene (ercc6, 133540.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  361. en:caused by mutation in the excision-repair cross-complementing group 3 gene (ercc3, 133510.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the excision-repair cross-complementing group 3 gene (ercc3, 133510.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  362. en:caused by mutation in the excision-repair cross-complementing group 4 gene (ercc4, 133520.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the excision-repair cross-complementing group 4 gene (ercc4, 133520.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  363. en:caused by mutation in the fas-associated via death domain gene (fadd, 602457.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fas-associated via death domain gene (fadd, 602457.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  364. en:caused by mutation in the feline leukemia virus subgroup c receptor 1 gene (flvcr1, 609144.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the feline leukemia virus subgroup c receptor 1 gene (flvcr1, 609144.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  365. en:caused by mutation in the fibroblast growth factor 5 gene (fgf5, 165190.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor 5 gene (fgf5, 165190.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  366. en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0008) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  367. en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  368. en:caused by mutation in the follicle-stimulating hormone, beta-polypeptide gene (fshb, 136530.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the follicle-stimulating hormone, beta-polypeptide gene (fshb, 136530.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  369. en:caused by mutation in the folliculin gene (flcn, 607273.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the folliculin gene (flcn, 607273.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  370. en:caused by mutation in the forkhead transcription factor foxl2 gene (foxl2, 605597.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead transcription factor foxl2 gene (foxl2, 605597.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  371. en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0006). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0006). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  372. en:caused by mutation in the fxyd domain-containing ion transport regulator 2 gene (fxyd2, 601814.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fxyd domain-containing ion transport regulator 2 gene (fxyd2, 601814.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  373. en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606598.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606598.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  374. en:caused by mutation in the gap junction protein, alpha-1 gene (gja1, 121014.0021) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gap junction protein, alpha-1 gene (gja1, 121014.0021) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  375. en:caused by mutation in the gdp-mannose pyrophosphorylase b gene (gmppb, 615320.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gdp-mannose pyrophosphorylase b gene (gmppb, 615320.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  376. en:caused by mutation in the gene encoding a disintegrin and metalloproteinase domain-10 (adam10, 602192.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding a disintegrin and metalloproteinase domain-10 (adam10, 602192.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  377. en:caused by mutation in the glucose-6-phosphate transporter 1 gene (g6pt1, 602671.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glucose-6-phosphate transporter 1 gene (g6pt1, 602671.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  378. en:caused by mutation in the glutamate-cysteine ligase, catalytic subunit gene (gclc, 606857.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutamate-cysteine ligase, catalytic subunit gene (gclc, 606857.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  379. en:caused by mutation in the glutathione peroxidase-4 gene (gpx4, 138322.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutathione peroxidase-4 gene (gpx4, 138322.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  380. en:caused by mutation in the glyoxylate reductase/hydroxypyruvate reductase gene (grhpr, 604296.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glyoxylate reductase/hydroxypyruvate reductase gene (grhpr, 604296.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  381. en:caused by mutation in the granulin precursor gene (grn, 138945.0015) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the granulin precursor gene (grn, 138945.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  382. en:caused by mutation in the grhl2 gene (608576.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the grhl2 gene (608576.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  383. en:caused by mutation in the growth/differentiation factor 5 gene (gd5, 601146.0005) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the growth/differentiation factor 5 gene (gd5, 601146.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  384. en:caused by mutation in the heat-shock 27-kd protein (hspb1, 602195.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heat-shock 27-kd protein (hspb1, 602195.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  385. en:caused by mutation in the heat-shock 60-kd protein 1 gene (hspd1, 118190.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heat-shock 60-kd protein 1 gene (hspd1, 118190.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  386. en:caused by mutation in the homeobox a13 gene (hoxa13, 142959.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeobox a13 gene (hoxa13, 142959.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  387. en:caused by mutation in the homolog of mouse peripherin 2 gene --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of mouse peripherin 2 gene | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  388. en:caused by mutation in the homolog of s. cerevisiae precursor mrna-processing factor-4 gene (prpf4, 607795.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of s. cerevisiae precursor mrna-processing factor-4 gene (prpf4, 607795.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  389. en:caused by mutation in the homolog of the drosophila fat tumor suppressor 4 gene (fat4, 612411.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila fat tumor suppressor 4 gene (fat4, 612411.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  390. en:caused by mutation in the homolog of the e. coli elac 2 gene (elac2, 605367.0006) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the e. coli elac 2 gene (elac2, 605367.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  391. en:caused by mutation in the homolog of the mouse mpv17 gene (mpv17, 136960.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse mpv17 gene (mpv17, 136960.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  392. en:caused by mutation in the homolog of the mouse noggin gene (nog, 602991.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse noggin gene (nog, 602991.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  393. en:caused by mutation in the homolog of the mouse stimulated by retinoic acid-6 gene (stra6, 610745.0007) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse stimulated by retinoic acid-6 gene (stra6, 610745.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  394. en:caused by mutation in the homolog of the s. cerevisiae, cytochrome c oxidase 20 gene (cox20, 614698.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae, cytochrome c oxidase 20 gene (cox20, 614698.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  395. en:caused by mutation in the homolog of the yeast vacuolar protein sorting 37 gene (vps37a, 609927.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the yeast vacuolar protein sorting 37 gene (vps37a, 609927.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  396. en:caused by mutation in the hormone-sensitive lipase gene (lipe, 151750.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hormone-sensitive lipase gene (lipe, 151750.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  397. en:caused by mutation in the immunoglobulin kappa constant region gene (igkc, 147200.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the immunoglobulin kappa constant region gene (igkc, 147200.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  398. en:caused by mutation in the inositol 1,4,5-triphosphate receptor 1 gene (itpr1, 147265.0003) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inositol 1,4,5-triphosphate receptor 1 gene (itpr1, 147265.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  399. en:caused by mutation in the integrin, alpha-8 gene (itga8, 604063.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the integrin, alpha-8 gene (itga8, 604063.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  400. en:caused by mutation in the inversin gene (invs, 243305.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inversin gene (invs, 243305.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  401. en:caused by mutation in the iq motif- and sec7 domain-containing protein 2 (iqsec2, 300522.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the iq motif- and sec7 domain-containing protein 2 (iqsec2, 300522.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  402. en:caused by mutation in the isovaleryl co-a dehydrogenase gene (ivd, 607036.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the isovaleryl co-a dehydrogenase gene (ivd, 607036.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  403. en:caused by mutation in the junctophilin-2 gene (jph2, 605267.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the junctophilin-2 gene (jph2, 605267.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  404. en:caused by mutation in the kelch repeat and btb/poz domains-containing protein 13 gene (kbtbd13, 613727.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kelch repeat and btb/poz domains-containing protein 13 gene (kbtbd13, 613727.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  405. en:caused by mutation in the keratin 1 gene (krt1, 139350.0014) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 1 gene (krt1, 139350.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  406. en:caused by mutation in the keratin 5 gene (krt5, 148040.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 5 gene (krt5, 148040.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  407. en:caused by mutation in the keratin 6a gene (krt6a, 148041.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 6a gene (krt6a, 148041.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  408. en:caused by mutation in the keratin 74 gene (krt74, 608248.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 74 gene (krt74, 608248.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  409. en:caused by mutation in the keratin 74 gene (krt74, 608248.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 74 gene (krt74, 608248.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  410. en:caused by mutation in the keratin-13 gene (krt13, 148065.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin-13 gene (krt13, 148065.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  411. en:caused by mutation in the kiaa0568 gene (kiaa0586, 610178.0006) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kiaa0568 gene (kiaa0586, 610178.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  412. en:caused by mutation in the kinesin family member 1a gene (kif1a, 601255.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 1a gene (kif1a, 601255.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  413. en:caused by mutation in the kinesin family member 1a gene (kif1a, 601255.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 1a gene (kif1a, 601255.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  414. en:caused by mutation in the kinesin heavy chain member 2a (kif2a, 602591.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin heavy chain member 2a (kif2a, 602591.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  415. en:caused by mutation in the kizuna centrosomal protein gene (kiz, 615757.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kizuna centrosomal protein gene (kiz, 615757.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  416. en:caused by mutation in the laforin gene (epm2a, 607566.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the laforin gene (epm2a, 607566.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  417. en:caused by mutation in the leucine-rich repeat- and sterile alpha motif-containing 1 gene (lrsam1, 610933.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucine-rich repeat- and sterile alpha motif-containing 1 gene (lrsam1, 610933.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  418. en:caused by mutation in the leucyl-trna synthetase 2 gene (lars2, 604544.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucyl-trna synthetase 2 gene (lars2, 604544.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  419. en:caused by mutation in the lim homeo box gene 4 (lhx4, 602146.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lim homeo box gene 4 (lhx4, 602146.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  420. en:caused by mutation in the limbin gene (evc2, 607261.0009) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the limbin gene (evc2, 607261.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  421. en:caused by mutation in the lipopolysaccharide-responsive, beige-like anchor protein (lrba, 606453.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lipopolysaccharide-responsive, beige-like anchor protein (lrba, 606453.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  422. en:caused by mutation in the lmbr1 domain-containing protein 1 gene (lmbrd1, 612625.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lmbr1 domain-containing protein 1 gene (lmbrd1, 612625.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  423. en:caused by mutation in the long-chain base subunit 1 of the serine palmitoyltransferase gene (sptlc1, 605712.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the long-chain base subunit 1 of the serine palmitoyltransferase gene (sptlc1, 605712.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  424. en:caused by mutation in the lyr motif-containing protein 7 gene (lyrm7, 615831.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lyr motif-containing protein 7 gene (lyrm7, 615831.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  425. en:caused by mutation in the mads box transcription enhancer factor 2, polypeptide a gene (mef2a, 600660.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mads box transcription enhancer factor 2, polypeptide a gene (mef2a, 600660.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  426. en:caused by mutation in the matrin-3 gene (matr3, 164017.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the matrin-3 gene (matr3, 164017.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  427. en:caused by mutation in the matrix metalloproteinase 2 gene (mmp2, 120360.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the matrix metalloproteinase 2 gene (mmp2, 120360.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  428. en:caused by mutation in the melanophilin gene (mlph, 606526.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the melanophilin gene (mlph, 606526.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  429. en:caused by mutation in the member-5 subfamily-j inwardly rectifying potassium channel gene (kcnj5, 600734.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the member-5 subfamily-j inwardly rectifying potassium channel gene (kcnj5, 600734.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  430. en:caused by mutation in the member-5 subfamily-j inwardly rectifying potassium channel gene (kcnj5, 600734.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the member-5 subfamily-j inwardly rectifying potassium channel gene (kcnj5, 600734.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  431. en:caused by mutation in the membrane-spanning 4 domains, subfamily a, member 1 gene (ms4a1, 112210.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the membrane-spanning 4 domains, subfamily a, member 1 gene (ms4a1, 112210.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  432. en:caused by mutation in the methionine sulfoxide reductase b3 gene (msrb3, 613719.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methionine sulfoxide reductase b3 gene (msrb3, 613719.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  433. en:caused by mutation in the methionine synthase gene (mtr, 156570.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methionine synthase gene (mtr, 156570.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  434. en:caused by mutation in the methionyl-trna synthetase 2 gene (mars2, 609728.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methionyl-trna synthetase 2 gene (mars2, 609728.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  435. en:caused by mutation in the methylmalonyl-coa epimerase gene (mcee, 608419.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methylmalonyl-coa epimerase gene (mcee, 608419.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  436. en:caused by mutation in the methylmalonyl-coa mutase gene (mut, 251000.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methylmalonyl-coa mutase gene (mut, 251000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  437. en:caused by mutation in the methyltransferase-like 23 gene (mettl23, 615262.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methyltransferase-like 23 gene (mettl23, 615262.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  438. en:caused by mutation in the mitochondrial ribosomal protein l3 gene (mrpl3, 607118.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial ribosomal protein l3 gene (mrpl3, 607118.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  439. en:caused by mutation in the mitochondrial transfer rna serine 1 gene (mtts1, 590080.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial transfer rna serine 1 gene (mtts1, 590080.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  440. en:caused by mutation in the mitochondrial transfer rna, mitochondrial, serine, 1 gene (mtts1, 590080.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial transfer rna, mitochondrial, serine, 1 gene (mtts1, 590080.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  441. en:caused by mutation in the mitochondrial trna (lysine) gene (mttk, 590060.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial trna (lysine) gene (mttk, 590060.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  442. en:caused by mutation in the mitochondrial ts translation elongation factor gene (tsfm, 604723.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial ts translation elongation factor gene (tsfm, 604723.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  443. en:caused by mutation in the mitochondrion-associated apoptosis-inducing factor 1 gene (aifm1, 300169.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrion-associated apoptosis-inducing factor 1 gene (aifm1, 300169.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  444. en:caused by mutation in the mitogen-activated protein kinase kinase 1 gene (map2k1, 176872.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitogen-activated protein kinase kinase 1 gene (map2k1, 176872.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  445. en:caused by mutation in the mks1 gene (mks1, 609883.0006) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mks1 gene (mks1, 609883.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  446. en:caused by mutation in the monoamine oxidase a gene (maoa, 309850.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the monoamine oxidase a gene (maoa, 309850.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  447. en:caused by mutation in the mothers against decapentaplegic, drosophila homolog of, 4 gene (smad4, 600993.0007) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mothers against decapentaplegic, drosophila homolog of, 4 gene (smad4, 600993.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  448. en:caused by mutation in the muscarinic cholinergic receptor-3 gene (chrm3, 118494.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the muscarinic cholinergic receptor-3 gene (chrm3, 118494.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  449. en:caused by mutation in the myeloid/lymphoid or mixed lineage leukemia gene (mll, 159555.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myeloid/lymphoid or mixed lineage leukemia gene (mll, 159555.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  450. en:caused by mutation in the myogenic factor 6 gene (myf6, 159991.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myogenic factor 6 gene (myf6, 159991.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  451. en:caused by mutation in the myosin viia gene (myo7a, 276903.0007) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin viia gene (myo7a, 276903.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  452. en:caused by mutation in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  453. en:caused by mutation in the n-acetylglutamate synthase gene (nags, 608300.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the n-acetylglutamate synthase gene (nags, 608300.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  454. en:caused by mutation in the n-myc downstream regulated gene-1 (ndrg1, 605262.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the n-myc downstream regulated gene-1 (ndrg1, 605262.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  455. en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 6 gene (ndufs6, 603848.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 6 gene (ndufs6, 603848.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  456. en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex 10 gene (ndufa10, 603835.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex 10 gene (ndufa10, 603835.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  457. en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex, assembly factor 1 gene (ndufaf1, 606934.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex, assembly factor 1 gene (ndufaf1, 606934.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  458. en:caused by mutation in the natriuretic peptide receptor 2 gene (npr2, 108961) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the natriuretic peptide receptor 2 gene (npr2, 108961) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  459. en:caused by mutation in the neural retina leucine zipper gene (nrl, 162080.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neural retina leucine zipper gene (nrl, 162080.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  460. en:caused by mutation in the neurobeachin-like 2 gene (nbeal2, 614169.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neurobeachin-like 2 gene (nbeal2, 614169.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  461. en:caused by mutation in the neutrophil cytosolic factor-1 gene, p47-phox (ncf1, 608512.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neutrophil cytosolic factor-1 gene, p47-phox (ncf1, 608512.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  462. en:caused by mutation in the nipa-like domain-containing 4 gene (nipal4, 609383.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nipa-like domain-containing 4 gene (nipal4, 609383.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  463. en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  464. en:caused by mutation in the npc1 gene (npc1, 607623.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the npc1 gene (npc1, 607623.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  465. en:caused by mutation in the nuclear receptor subfamily 3, group c, member 2 gene (nr3c2, 600983.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear receptor subfamily 3, group c, member 2 gene (nr3c2, 600983.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  466. en:caused by mutation in the nuclear-encoded mitochondrial dna polymerase-gamma gene (polg, 174763.0008) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear-encoded mitochondrial dna polymerase-gamma gene (polg, 174763.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  467. en:caused by mutation in the orai calcium release-activated calcium modulator 1 gene (orai1, 610277.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the orai calcium release-activated calcium modulator 1 gene (orai1, 610277.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  468. en:caused by mutation in the parathyroid hormone receptor-1 gene (pthr1, 168468.0012) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the parathyroid hormone receptor-1 gene (pthr1, 168468.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  469. en:caused by mutation in the parathyroid hormone-like hormone gene (pthlh, 168470.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the parathyroid hormone-like hormone gene (pthlh, 168470.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  470. en:caused by mutation in the periaxin gene (prx, 605725.0005) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the periaxin gene (prx, 605725.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  471. en:caused by mutation in the peroxisome biogenesis factor-2 gene (pex2, 170993.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor-2 gene (pex2, 170993.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  472. en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  473. en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory, 1 gene (pik3r1, 171833.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory, 1 gene (pik3r1, 171833.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  474. en:caused by mutation in the phosphatidylinositol-3-phosphate 5-kinase, type iii gene (pip5k3, 609414.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol-3-phosphate 5-kinase, type iii gene (pip5k3, 609414.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  475. en:caused by mutation in the phosphoglucomutase-3 gene (pgm3, 172100.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoglucomutase-3 gene (pgm3, 172100.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  476. en:caused by mutation in the phospholipase c, beta-1 gene (plcb1, 607120.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phospholipase c, beta-1 gene (plcb1, 607120.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  477. en:caused by mutation in the platelet glycoprotein vi gene (gp6, 605546.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the platelet glycoprotein vi gene (gp6, 605546.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  478. en:caused by mutation in the platelet-activating factor acetylhydrolase, isoform 1b, alpha subunit gene (pafah1b1, 601545.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the platelet-activating factor acetylhydrolase, isoform 1b, alpha subunit gene (pafah1b1, 601545.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  479. en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 5 gene (plekhg5, 611101.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 5 gene (plekhg5, 611101.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  480. en:caused by mutation in the podocin gene (nphs2, 604766.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the podocin gene (nphs2, 604766.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  481. en:caused by mutation in the polymerase i, rna, subunit d gene (polr1d, 613715.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polymerase i, rna, subunit d gene (polr1d, 613715.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  482. en:caused by mutation in the post-gpi attachment to proteins 2 gene (pgap2, 615187.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the post-gpi attachment to proteins 2 gene (pgap2, 615187.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  483. en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 1 gene (kcnj1, 600359.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 1 gene (kcnj1, 600359.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  484. en:caused by mutation in the potassium voltage-gated channel, isk-related family, member 2 gene (kcne2, 603796.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, isk-related family, member 2 gene (kcne2, 603796.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  485. en:caused by mutation in the presenilin-1 gene (psen1, 104311.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the presenilin-1 gene (psen1, 104311.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  486. en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase (lysine hydroxylase) 2 gene (plod2, 601865.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase (lysine hydroxylase) 2 gene (plod2, 601865.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  487. en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene (plod3, 603066.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 gene (plod3, 603066.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  488. en:caused by mutation in the prodynorphin gene (pdyn, 131340.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prodynorphin gene (pdyn, 131340.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  489. en:caused by mutation in the proline/serine/threonine phosphatase-interacting protein 1 (pstpip1, 606347.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the proline/serine/threonine phosphatase-interacting protein 1 (pstpip1, 606347.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  490. en:caused by mutation in the protein kinase c, gamma polypeptide gene (prkcg, 176980.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein kinase c, gamma polypeptide gene (prkcg, 176980.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  491. en:caused by mutation in the protein o-mannosyltransferase 2 gene (pomt2, 607439.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein o-mannosyltransferase 2 gene (pomt2, 607439.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  492. en:caused by mutation in the protein-o-mannose kinase gene (pomk, 615247.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein-o-mannose kinase gene (pomk, 615247.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  493. en:caused by mutation in the protoporphyrinogen oxidase gene (ppox, 600923.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protoporphyrinogen oxidase gene (ppox, 600923.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  494. en:caused by mutation in the purinergic receptor p2x, ligand-gated ion channel, 2 gene (p2rx2, 600844.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the purinergic receptor p2x, ligand-gated ion channel, 2 gene (p2rx2, 600844.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  495. en:caused by mutation in the ras and rab interactor 2 gene (rin2, 610222.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ras and rab interactor 2 gene (rin2, 610222.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  496. en:caused by mutation in the receptor-interacting serine-threonine kinase-4 gene (ripk4, 605706.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the receptor-interacting serine-threonine kinase-4 gene (ripk4, 605706.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  497. en:caused by mutation in the recombination signal-binding protein for immunoglobulin kappa j region gene (rbpj, 147183.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the recombination signal-binding protein for immunoglobulin kappa j region gene (rbpj, 147183.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  498. en:caused by mutation in the retinoblastoma-binding protein-8 gene (rbbp8, 604124.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the retinoblastoma-binding protein-8 gene (rbbp8, 604124.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  499. en:caused by mutation in the retinoic acid-induced gene 1 (rai1, 607642.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the retinoic acid-induced gene 1 (rai1, 607642.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  500. en:caused by mutation in the ribonuclease h2, subunit b gene (rnaseh2b, 610326.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribonuclease h2, subunit b gene (rnaseh2b, 610326.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  501. en:caused by mutation in the ribonuclease t2 gene (rnaset2, 612944.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribonuclease t2 gene (rnaset2, 612944.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  502. en:caused by mutation in the ribosomal protein sa gene (rpsa, 150370.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribosomal protein sa gene (rpsa, 150370.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  503. en:caused by mutation in the ring finger protein 168 gene (rnf168, 612688.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ring finger protein 168 gene (rnf168, 612688.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  504. en:caused by mutation in the rna, u4, small nuclear, at-ac form gene (rnu4atac, 601428.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rna, u4, small nuclear, at-ac form gene (rnu4atac, 601428.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  505. en:caused by mutation in the rna-binding motif protein 10 gene (rbm10, 300080.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rna-binding motif protein 10 gene (rbm10, 300080.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  506. en:caused by mutation in the runt-related transcription factor 2 gene (runx2, 600211.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the runt-related transcription factor 2 gene (runx2, 600211.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  507. en:caused by mutation in the sacsin gene (sacs, 604490.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sacsin gene (sacs, 604490.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  508. en:caused by mutation in the sam domain- and hd domain-containing protein 1 gene (samhd1, 606754.0011) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sam domain- and hd domain-containing protein 1 gene (samhd1, 606754.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  509. en:caused by mutation in the serine protease inhibitor, kazal-type-1 gene (spink1, 167790.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the serine protease inhibitor, kazal-type-1 gene (spink1, 167790.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  510. en:caused by mutation in the shh (600725) regulatory element in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0010) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the shh (600725) regulatory element in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  511. en:caused by mutation in the short/branched-chain acyl-coa dehydrogenase gene (acadsb, 600301.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the short/branched-chain acyl-coa dehydrogenase gene (acadsb, 600301.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  512. en:caused by mutation in the sideroflexin 4 gene (sfxn4, 615564.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sideroflexin 4 gene (sfxn4, 615564.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  513. en:caused by mutation in the snf2-related cbp activatory protein gene (srcap, 611421.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the snf2-related cbp activatory protein gene (srcap, 611421.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  514. en:caused by mutation in the sodium channel, nonvoltage-gated 1, beta gene (scnn1b, 600760.0009) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sodium channel, nonvoltage-gated 1, beta gene (scnn1b, 600760.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  515. en:caused by mutation in the sodium channel, nonvoltage-gated 1, gamma gene (scnn1g, 600761.0005) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sodium channel, nonvoltage-gated 1, gamma gene (scnn1g, 600761.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  516. en:caused by mutation in the solute carrier family 17 (sodium phosphate cotransporter), member 3 gene (slc17a3, 611034.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 17 (sodium phosphate cotransporter), member 3 gene (slc17a3, 611034.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  517. en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  518. en:caused by mutation in the solute carrier family 35, cmp-sialic acid transporter, member 1 gene (slc35a1, 605634.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 35, cmp-sialic acid transporter, member 1 gene (slc35a1, 605634.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  519. en:caused by mutation in the spectrin repeat-containing nuclear envelope protein 4 gene (syne4, 615535.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the spectrin repeat-containing nuclear envelope protein 4 gene (syne4, 615535.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  520. en:caused by mutation in the sry-box-10 gene (sox10, 602229.0006) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sry-box-10 gene (sox10, 602229.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  521. en:caused by mutation in the stam-binding protein gene (stambp, 606247.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the stam-binding protein gene (stambp, 606247.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  522. en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605921.0008) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605921.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  523. en:caused by mutation in the succinate dehydrogenase complex, subunit a, flavoprotein gene (sdha, 600857.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the succinate dehydrogenase complex, subunit a, flavoprotein gene (sdha, 600857.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  524. en:caused by mutation in the superkiller viralicidic activity 2-like, s. cerevisiae homolog gene (skiv2l, 600478.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the superkiller viralicidic activity 2-like, s. cerevisiae homolog gene (skiv2l, 600478.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  525. en:caused by mutation in the synaptic nuclear envelope protein 1 gene (syne1, 608441.0008). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the synaptic nuclear envelope protein 1 gene (syne1, 608441.0008). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  526. en:caused by mutation in the synaptic nuclear envelope protein-1 gene (syne1, 608441.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the synaptic nuclear envelope protein-1 gene (syne1, 608441.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  527. en:caused by mutation in the synaptonemal complex protein-3 gene (sycp3, 604759.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the synaptonemal complex protein-3 gene (sycp3, 604759.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  528. en:caused by mutation in the synaptophysin gene (syp, 313475.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the synaptophysin gene (syp, 313475.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  529. en:caused by mutation in the tbc1 domain family, member 20 gene (tbc1d20, 611663.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tbc1 domain family, member 20 gene (tbc1d20, 611663.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  530. en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0007) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  531. en:caused by mutation in the tectonin beta-propeller repeat-containing protein 2 gene (tecpr2, 615000.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tectonin beta-propeller repeat-containing protein 2 gene (tecpr2, 615000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  532. en:caused by mutation in the testis-specific protein-like 1 gene (tspyl1, 604714.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the testis-specific protein-like 1 gene (tspyl1, 604714.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  533. en:caused by mutation in the tetraspanin-12 gene (tspan12, 613138.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tetraspanin-12 gene (tspan12, 613138.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  534. en:caused by mutation in the tetratricopeptide repeat domain-containing protein-7a gene (ttc7a, 609332.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tetratricopeptide repeat domain-containing protein-7a gene (ttc7a, 609332.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  535. en:caused by mutation in the threonyl-trna synthetase 2 gene (tars2, 612805.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the threonyl-trna synthetase 2 gene (tars2, 612805.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  536. en:caused by mutation in the thyroglobulin gene (tg, 188450.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thyroglobulin gene (tg, 188450.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  537. en:caused by mutation in the thyroid-stimulating hormone receptor gene (tshr, 603372.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thyroid-stimulating hormone receptor gene (tshr, 603372.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  538. en:caused by mutation in the transcription factor ap2-alpha gene (tfap2a, 107580.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transcription factor ap2-alpha gene (tfap2a, 107580.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  539. en:caused by mutation in the transforming growth factor, beta receptor ii, 70-80kd gene (tgfbr2, 190182.0008) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transforming growth factor, beta receptor ii, 70-80kd gene (tgfbr2, 190182.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  540. en:caused by mutation in the transient receptor potential cation channel, subfamily a, member 1 gene (trpa1, 604775.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transient receptor potential cation channel, subfamily a, member 1 gene (trpa1, 604775.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  541. en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0030) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0030) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  542. en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0013) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  543. en:caused by mutation in the trna nucleotidyltransferase, cca-adding, 1 gene (trnt1, 612907.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the trna nucleotidyltransferase, cca-adding, 1 gene (trnt1, 612907.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  544. en:caused by mutation in the tuberin gene (tsc2, 191092.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tuberin gene (tsc2, 191092.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  545. en:caused by mutation in the tubulin, alpha-8 gene (tuba8, 605472.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin, alpha-8 gene (tuba8, 605472.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  546. en:caused by mutation in the tubulin-specific chaperone e gene (tcbe, 604934.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin-specific chaperone e gene (tcbe, 604934.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  547. en:caused by mutation in the tumor protein p53 gene (tp53, 191170.0023) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tumor protein p53 gene (tp53, 191170.0023) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  548. en:caused by mutation in the tumor-associated calcium signal transducer 2 gene (tacstd2, 137290.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tumor-associated calcium signal transducer 2 gene (tacstd2, 137290.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  549. en:caused by mutation in the ubiquinol-cytochrome c reductase-protein gene (uqcrb, 191330.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquinol-cytochrome c reductase-protein gene (uqcrb, 191330.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  550. en:caused by mutation in the ubiquitin-specific protease 9 gene, x-linked (usp9x, 300072.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquitin-specific protease 9 gene, x-linked (usp9x, 300072.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  551. en:caused by mutation in the uridine diphosphate glycosyltransferase 1 gene (ugt1, 191740.0005) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the uridine diphosphate glycosyltransferase 1 gene (ugt1, 191740.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  552. en:caused by mutation in the v-akt murine thymoma viral oncogene homolog 3 gene (akt3, 611223.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-akt murine thymoma viral oncogene homolog 3 gene (akt3, 611223.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  553. en:caused by mutation in the v-ha-ras harvey rat sarcoma viral oncogene homolog gene (hras, 190020.0017) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-ha-ras harvey rat sarcoma viral oncogene homolog gene (hras, 190020.0017) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  554. en:caused by mutation in the voltage-gated potassium channel, shaw-related subfamily, member 1 gene (kcnc1, 176258.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated potassium channel, shaw-related subfamily, member 1 gene (kcnc1, 176258.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  555. en:caused by mutation in the voltage-gated sodium channel type i, alpha polypeptide gene (scn1a, 182389.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated sodium channel type i, alpha polypeptide gene (scn1a, 182389.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  556. en:caused by mutation in the voltage-gated sodium channel, type ix, alpha subunit gene (scn9a, 603415.0005) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated sodium channel, type ix, alpha subunit gene (scn9a, 603415.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  557. en:caused by mutation in the von willebrand-cleaving protease gene (adamts13, 604134.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the von willebrand-cleaving protease gene (adamts13, 604134.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  558. en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  559. en:caused by mutations in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  560. en:caused by mutations in the beta-1 transforming growth factor gene (tgfb1, 190180.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the beta-1 transforming growth factor gene (tgfb1, 190180.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  561. en:caused by mutations in the cd40 gene (tnfrsf5, 109535.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cd40 gene (tnfrsf5, 109535.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  562. en:caused by mutations in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  563. en:caused by mutations in the cystatin c gene (cst3, 604312.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cystatin c gene (cst3, 604312.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  564. en:caused by mutations in the cystinosis gene (ctns, 219800.0008) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cystinosis gene (ctns, 219800.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  565. en:caused by mutations in the cytochrome p450, subfamily xxviia, polypeptide 1 gene (cyp27a1, 213700.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cytochrome p450, subfamily xxviia, polypeptide 1 gene (cyp27a1, 213700.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  566. en:caused by mutations in the dentin sialophosphoprotein gene (dspp, 125485.0004) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the dentin sialophosphoprotein gene (dspp, 125485.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  567. en:caused by mutations in the exostosin 1 gene (ext1, 133700.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the exostosin 1 gene (ext1, 133700.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  568. en:caused by mutations in the glycine n-methyltransferase gene (gnmt, 606628.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the glycine n-methyltransferase gene (gnmt, 606628.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  569. en:caused by mutations in the myeloperoxidase gene (mpo, 606989.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the myeloperoxidase gene (mpo, 606989.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  570. en:caused by mutations in the neurofibromin gene (nf1, 162200.0010) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the neurofibromin gene (nf1, 162200.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  571. en:caused by mutations in the parathyoid hormone receptor 1 gene (pthr1, 168468.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the parathyoid hormone receptor 1 gene (pthr1, 168468.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  572. en:caused by mutations in the peroxisomal acyl-coa oxidase gene (acox1, 609751.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the peroxisomal acyl-coa oxidase gene (acox1, 609751.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  573. en:caused by mutations in the seipin gene (bscl2, 606158.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the seipin gene (bscl2, 606158.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  574. en:caused by mutations in the solute carrier family 17 (sodium phosphate), member 5 gene (slc17a5, 604322.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the solute carrier family 17 (sodium phosphate), member 5 gene (slc17a5, 604322.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  575. en:caused by mutations in the solute carrier family 4, sodium bicarbonate cotransporter, member 4 gene (slc4a4, 603345.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the solute carrier family 4, sodium bicarbonate cotransporter, member 4 gene (slc4a4, 603345.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  576. en:caused by mutations in the tumor necrosis factor receptor superfamily, member 11a (tnfrsf11a, 603499.0002) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the tumor necrosis factor receptor superfamily, member 11a (tnfrsf11a, 603499.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  577. en:caused by mutations in the udp-galaltose-4-epimerase gene, 'mild' form (gale, 606953.0001). --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the udp-galaltose-4-epimerase gene, 'mild' form (gale, 606953.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  578. en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0021) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0021) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  579. en:caused by mutations in the wnt1-inducible signalling pathways protein 3 (wisp3, 603400.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the wnt1-inducible signalling pathways protein 3 (wisp3, 603400.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  580. en:caused by partial duplication of mtdna --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by partial duplication of mtdna | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  581. en:caused by postzygotic somatic mosaic mutation in the phosphatidylinositol 3-kinase, catalytic, alpha polypeptide gene (pik3ca, 171834.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by postzygotic somatic mosaic mutation in the phosphatidylinositol 3-kinase, catalytic, alpha polypeptide gene (pik3ca, 171834.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  582. en:caused by somatic mutation in the guanine nucleotide-binding protein, alpha-stimulating activity polypeptide 1 gene (gnas1, 139320.0008) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the guanine nucleotide-binding protein, alpha-stimulating activity polypeptide 1 gene (gnas1, 139320.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  583. en:caused by somatic mutation in the v-ki-ras2 kirsten rat sarcoma viral oncogene homolog gene (kras, 190070.0005) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the v-ki-ras2 kirsten rat sarcoma viral oncogene homolog gene (kras, 190070.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  584. en:contiguous gene deletion of 91.6 kb to 4.74 mb on chromosome 16p13.2 --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene deletion of 91.6 kb to 4.74 mb on chromosome 16p13.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  585. en:contiguous gene deletion syndrome caused by deletion (3.5mb) of 1q32-q44 --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene deletion syndrome caused by deletion (3.5mb) of 1q32-q44 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  586. en:contiguous gene syndrome involving deletion of 2.63 mb on chromosome 5q12 --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome involving deletion of 2.63 mb on chromosome 5q12 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  587. en:contiguous gene syndrome involving deletions of the collagen, type iv, alpha-5 (col4a5, 303630) and collagen, type iv, alpha-6 (col4a6, 303631) genes --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome involving deletions of the collagen, type iv, alpha-5 (col4a5, 303630) and collagen, type iv, alpha-6 (col4a6, 303631) genes | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  588. en:linked to a locus at 16q. --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:linked to a locus at 16q. | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  589. en:susceptibility conferred by mutation in the neurofilament, heavy polypeptide gene (nefh, 162230.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the neurofilament, heavy polypeptide gene (nefh, 162230.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  590. en:susceptibility conferred by mutation in the neuroligin-4 gene (nlgn4, 300427.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the neuroligin-4 gene (nlgn4, 300427.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  591. en:susceptibility conferred by somatic mutation in the calreticulin gene (calr, 109091.0001) --- r_associated #0: 30 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by somatic mutation in the calreticulin gene (calr, 109091.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=30
  592. en:bcl2 gene on chromosome 18q21 is juxtaposed to igh gene at 14q32, resulting chimeric bcl2-igh mrna is expressed blocking apoptosis --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:bcl2 gene on chromosome 18q21 is juxtaposed to igh gene at 14q32, resulting chimeric bcl2-igh mrna is expressed blocking apoptosis | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  593. en:cause by mutation in the homolog of the s. cerevisiae alg2 gene (alg2, 607905.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:cause by mutation in the homolog of the s. cerevisiae alg2 gene (alg2, 607905.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  594. en:caused by a trinucleotide repeat expansion cag(n) in the androgen receptor gene (ar, 313700.0014) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a trinucleotide repeat expansion cag(n) in the androgen receptor gene (ar, 313700.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  595. en:caused by chromosome 14 paternal uniparental disomy --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by chromosome 14 paternal uniparental disomy | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  596. en:caused by duplication of 8q22.1-qter and deletion of 8pter-p23.1 --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of 8q22.1-qter and deletion of 8pter-p23.1 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  597. en:caused by imprinting defect on chromosome 14q32 --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by imprinting defect on chromosome 14q32 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  598. en:caused by interstitial duplication (3.7mb) of 17p11.2 --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by interstitial duplication (3.7mb) of 17p11.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  599. en:caused by mutation in galactose-1-phosphate uridyltransferase gene (galt, 230400.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in galactose-1-phosphate uridyltransferase gene (galt, 230400.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  600. en:caused by mutation in the 3-prime repair exonuclease 1 gene (trex1, 606609.0008) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 3-prime repair exonuclease 1 gene (trex1, 606609.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  601. en:caused by mutation in the 4-hydroxyphenylpyruvate dioxygenase gene (hpd, 609695.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 4-hydroxyphenylpyruvate dioxygenase gene (hpd, 609695.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  602. en:caused by mutation in the 41-kd centrosomal protein gene (cep41, 610523.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 41-kd centrosomal protein gene (cep41, 610523.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  603. en:caused by mutation in the 45-kd receptor-associated protein of the synapse (rapsyn, 601592.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 45-kd receptor-associated protein of the synapse (rapsyn, 601592.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  604. en:caused by mutation in the 5-oxoprolinase gene (oplah, 614243.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 5-oxoprolinase gene (oplah, 614243.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  605. en:caused by mutation in the 83-kd centrosomal protein gene (cep83, 615847.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 83-kd centrosomal protein gene (cep83, 615847.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  606. en:caused by mutation in the a disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 17 gene (adamts17, 607511.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the a disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 17 gene (adamts17, 607511.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  607. en:caused by mutation in the abnormal spindle-like, microcephaly-associated gene (aspm, 605481.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the abnormal spindle-like, microcephaly-associated gene (aspm, 605481.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  608. en:caused by mutation in the acyl-coa dehydrogenase-9 gene (acad9, 611103.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the acyl-coa dehydrogenase-9 gene (acad9, 611103.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  609. en:caused by mutation in the acylglycerol kinase gene (agk, 610345.0010) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the acylglycerol kinase gene (agk, 610345.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  610. en:caused by mutation in the adaptor-related protein complex 1, sigma-1 subunit gene (ap1s1, 603531.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adaptor-related protein complex 1, sigma-1 subunit gene (ap1s1, 603531.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  611. en:caused by mutation in the adaptor-related protein complex 4, sigma-1 subunit (ap4s1, 607243.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adaptor-related protein complex 4, sigma-1 subunit (ap4s1, 607243.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  612. en:caused by mutation in the adenine phosphoribosyltransferase gene (aprt, 102600.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenine phosphoribosyltransferase gene (aprt, 102600.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  613. en:caused by mutation in the adp-ribosylation factor guanine nucleotide exchange factor 2 gene (arfgef2, 605371.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adp-ribosylation factor guanine nucleotide exchange factor 2 gene (arfgef2, 605371.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  614. en:caused by mutation in the aladin gene (aaas, 605378.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aladin gene (aaas, 605378.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  615. en:caused by mutation in the alanyl-trna synthetase gene (aars, 601065.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alanyl-trna synthetase gene (aars, 601065.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  616. en:caused by mutation in the aldehyde dehydrogenase 5 family, member a1 gene (aldh5a1, 610045.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aldehyde dehydrogenase 5 family, member a1 gene (aldh5a1, 610045.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  617. en:caused by mutation in the alms1 gene (alms1, 606844.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alms1 gene (alms1, 606844.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  618. en:caused by mutation in the alpha subunit of the nonvoltage-gated sodium channel 1 gene (scnn1a, 600228.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha subunit of the nonvoltage-gated sodium channel 1 gene (scnn1a, 600228.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  619. en:caused by mutation in the alpha-1,4-glucosidase gene (gaa, 606800.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1,4-glucosidase gene (gaa, 606800.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  620. en:caused by mutation in the alpha-1s subunit of l-type voltage-dependent calcium channel gene (cacna1s, 114208.0001). --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1s subunit of l-type voltage-dependent calcium channel gene (cacna1s, 114208.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  621. en:caused by mutation in the alpha-3 integrin gene (itga3, 605025.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-3 integrin gene (itga3, 605025.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  622. en:caused by mutation in the alpha-mannosidase gene (man2b1, 609458.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-mannosidase gene (man2b1, 609458.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  623. en:caused by mutation in the alpha-methylacyl-coa racemase gene (amacr, 604489.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-methylacyl-coa racemase gene (amacr, 604489.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  624. en:caused by mutation in the alpha-subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0003) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  625. en:caused by mutation in the amelogenin gene (amelx, 300391.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the amelogenin gene (amelx, 300391.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  626. en:caused by mutation in the amyloid beta (a4) precursor protein gene (app, 104760.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the amyloid beta (a4) precursor protein gene (app, 104760.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  627. en:caused by mutation in the angiopoietin-like 4 gene (angptl4, 605910.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the angiopoietin-like 4 gene (angptl4, 605910.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  628. en:caused by mutation in the anoctamin 10 gene (ano10, 613726.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the anoctamin 10 gene (ano10, 613726.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  629. en:caused by mutation in the apolipoprotein b gene (apob, 107730.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the apolipoprotein b gene (apob, 107730.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  630. en:caused by mutation in the aquaporin 7 gene (aqp7, 602974.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aquaporin 7 gene (aqp7, 602974.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  631. en:caused by mutation in the atpase family gene 3-like 2 gene (afg3l2, 604581.0010) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase family gene 3-like 2 gene (afg3l2, 604581.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  632. en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0006) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  633. en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0010) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  634. en:caused by mutation in the autoimmune regulator gene (aire, 607358.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the autoimmune regulator gene (aire, 607358.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  635. en:caused by mutation in the avian sarcoma viral (v-ski) oncogene homolog gene (ski, 164780.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the avian sarcoma viral (v-ski) oncogene homolog gene (ski, 164780.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  636. en:caused by mutation in the bbs protein complex-interacting protein 1 gene (bbip1, 613605.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bbs protein complex-interacting protein 1 gene (bbip1, 613605.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  637. en:caused by mutation in the bbs1 gene (bbs1, 209901.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bbs1 gene (bbs1, 209901.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  638. en:caused by mutation in the beta actin gene (actb, 102630.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta actin gene (actb, 102630.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  639. en:caused by mutation in the beta retinoic acid receptor (rarb, 180220.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta retinoic acid receptor (rarb, 180220.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  640. en:caused by mutation in the beta-1,4-galactosyltransferase gene (b4galt1, 137060.0001). --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1,4-galactosyltransferase gene (b4galt1, 137060.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  641. en:caused by mutation in the beta-1-galactosidase gene (glb1, 230500.0004) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1-galactosidase gene (glb1, 230500.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  642. en:caused by mutation in the beta-sarcoglycan gene (sgcb, 600900.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-sarcoglycan gene (sgcb, 600900.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  643. en:caused by mutation in the bone morphogenetic protein 2 gene (bmp2, 112261.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bone morphogenetic protein 2 gene (bmp2, 112261.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  644. en:caused by mutation in the breast cancer type 1 gene (brca1, 113705.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the breast cancer type 1 gene (brca1, 113705.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  645. en:caused by mutation in the bromodomain-and wd repeat domain-containing protein 3 gene (brwd3, 300553.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bromodomain-and wd repeat domain-containing protein 3 gene (brwd3, 300553.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  646. en:caused by mutation in the c20orf7 gene (612360.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the c20orf7 gene (612360.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  647. en:caused by mutation in the cadherin-1 gene (cdh1, 192090.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cadherin-1 gene (cdh1, 192090.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  648. en:caused by mutation in the calcium-activated nucleotidase 1 gene (cant1, 613165.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calcium-activated nucleotidase 1 gene (cant1, 613165.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  649. en:caused by mutation in the calmodulin-2 gene (calm2, 114182.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calmodulin-2 gene (calm2, 114182.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  650. en:caused by mutation in the carbohydrate sulfotransferase 3 gene (chst3, 603799.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carbohydrate sulfotransferase 3 gene (chst3, 603799.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  651. en:caused by mutation in the carbonic anhydrase viii gene (ca8, 114815.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carbonic anhydrase viii gene (ca8, 114815.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  652. en:caused by mutation in the cardiac myosin-binding protein-c gene (mybpc3, 600958.0024) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cardiac myosin-binding protein-c gene (mybpc3, 600958.0024) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  653. en:caused by mutation in the cartilage-associated protein gene (crtap, 605497.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cartilage-associated protein gene (crtap, 605497.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  654. en:caused by mutation in the caspase 8 gene (casp8, 601763.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the caspase 8 gene (casp8, 601763.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  655. en:caused by mutation in the cathepsin c gene (ctsc, 602365.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cathepsin c gene (ctsc, 602365.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  656. en:caused by mutation in the ccctc-binding factor gene (ctcf, 604167.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ccctc-binding factor gene (ctcf, 604167.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  657. en:caused by mutation in the cd3 antigen, epsilon subunit gene (cd3e, 186830.0003) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd3 antigen, epsilon subunit gene (cd3e, 186830.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  658. en:caused by mutation in the cd79b antigen gene (cd79b, 147245.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd79b antigen gene (cd79b, 147245.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  659. en:caused by mutation in the centromeric protein j gene (cenpj, 609279.0004) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the centromeric protein j gene (cenpj, 609279.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  660. en:caused by mutation in the choline acetyltransferase gene (chat, 118490.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the choline acetyltransferase gene (chat, 118490.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  661. en:caused by mutation in the chromosome 19 open reading frame 12 gene (c19orf12, 614297.0006) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 19 open reading frame 12 gene (c19orf12, 614297.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  662. en:caused by mutation in the class 4 pou domain transcription factor 3 gene (pou4f3, 602460.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the class 4 pou domain transcription factor 3 gene (pou4f3, 602460.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  663. en:caused by mutation in the coagulation factor xii gene (f12, 610619.0006) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coagulation factor xii gene (f12, 610619.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  664. en:caused by mutation in the coiled-coil domain-containing protein 88c gene (ccdc88c, 611204.0004) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil domain-containing protein 88c gene (ccdc88c, 611204.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  665. en:caused by mutation in the coiled-coil-helix-coiled-coil helix domain-containing protein 10 gene (chchd10, 615903.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil-helix-coiled-coil helix domain-containing protein 10 gene (chchd10, 615903.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  666. en:caused by mutation in the coiled-coil-helix-coiled-coil-helix domain-containing protein 10 gene (chchd10, 615903.0004) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil-helix-coiled-coil-helix domain-containing protein 10 gene (chchd10, 615903.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  667. en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  668. en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0014). --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0014). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  669. en:caused by mutation in the collagen, type iv, alpha-1 gene (col4a1, 120130.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type iv, alpha-1 gene (col4a1, 120130.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  670. en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  671. en:caused by mutation in the complement component 2 gene (c2, 613927.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement component 2 gene (c2, 613927.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  672. en:caused by mutation in the component of oligomeric golgi complex 6 gene (cog6, 606977.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the component of oligomeric golgi complex 6 gene (cog6, 606977.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  673. en:caused by mutation in the controller of the opn1lw and opn1mw genes (300824) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the controller of the opn1lw and opn1mw genes (300824) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  674. en:caused by mutation in the cryptic-protein gene (cfc1, 605194.0004) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cryptic-protein gene (cfc1, 605194.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  675. en:caused by mutation in the cyld gene (605018.0005) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyld gene (605018.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  676. en:caused by mutation in the cytochrome b-245, beta polypeptide gene (cybb, 300481.0022) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome b-245, beta polypeptide gene (cybb, 300481.0022) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  677. en:caused by mutation in the cytochrome b5 reductase 3 gene (cyb5r3, 613213.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome b5 reductase 3 gene (cyb5r3, 613213.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  678. en:caused by mutation in the cytochrome c oxidase iii gene (mtco3, 516050.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase iii gene (mtco3, 516050.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  679. en:caused by mutation in the cytochrome c oxidase subunit ii gene (mtco2, 516040.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase subunit ii gene (mtco2, 516040.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  680. en:caused by mutation in the cytochrome c oxidase subunit vib, polypeptide 1 gene (cox6b1, 124089.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase subunit vib, polypeptide 1 gene (cox6b1, 124089.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  681. en:caused by mutation in the cytochrome c oxidase, subunit iv, isoform 2 gene (cox4i2, 607976.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase, subunit iv, isoform 2 gene (cox4i2, 607976.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  682. en:caused by mutation in the cytochrome c oxidase, subunit via, polypeptide 1 gene (cox6a1, 602072.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase, subunit via, polypeptide 1 gene (cox6a1, 602072.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  683. en:caused by mutation in the cytochrome p450, subfamily xxvic, polypeptide 1 gene (cyp26c1, 608428.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450, subfamily xxvic, polypeptide 1 gene (cyp26c1, 608428.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  684. en:caused by mutation in the dep domain-containing protein 5 gene (depdc, 614191.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dep domain-containing protein 5 gene (depdc, 614191.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  685. en:caused by mutation in the desmin gene (des, 125660.0018) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the desmin gene (des, 125660.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  686. en:caused by mutation in the dihydroorotate dehydrogenase gene (dhodh, 126064.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dihydroorotate dehydrogenase gene (dhodh, 126064.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  687. en:caused by mutation in the dna polymerase, epsilon gene (pole, 174762.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna polymerase, epsilon gene (pole, 174762.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  688. en:caused by mutation in the dynamin 1-like gene (dnm1l, 603850.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynamin 1-like gene (dnm1l, 603850.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  689. en:caused by mutation in the dynein, cytoplasmic 1, heavy chain 1 gene (dync1h1, 600112.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynein, cytoplasmic 1, heavy chain 1 gene (dync1h1, 600112.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  690. en:caused by mutation in the e homolog of the drosophila nk2 transcription factor (nkx2e, 600584.0004) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the e homolog of the drosophila nk2 transcription factor (nkx2e, 600584.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  691. en:caused by mutation in the edar-associated death domain gene (edaradd, 606603.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the edar-associated death domain gene (edaradd, 606603.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  692. en:caused by mutation in the enteric smooth muscle actin gamma-2 gene (actg2, 102545.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the enteric smooth muscle actin gamma-2 gene (actg2, 102545.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  693. en:caused by mutation in the erythropoeitin receptor gene (epor, 133171.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the erythropoeitin receptor gene (epor, 133171.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  694. en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 4 gene (eif2b4, 606687.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 4 gene (eif2b4, 606687.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  695. en:caused by mutation in the evc gene (evc, 604831.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the evc gene (evc, 604831.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  696. en:caused by mutation in the excision-repair cross-complementing group 4 gene (ercc4, 133520.0004) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the excision-repair cross-complementing group 4 gene (ercc4, 133520.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  697. en:caused by mutation in the eyes absent-1 gene (eya1, 601653.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eyes absent-1 gene (eya1, 601653.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  698. en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0055) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0055) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  699. en:caused by mutation in the fibroblast growth factor 3 gene (fgf3, 164950.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor 3 gene (fgf3, 164950.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  700. en:caused by mutation in the filamin a gene (flna, 300017.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the filamin a gene (flna, 300017.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  701. en:caused by mutation in the fmr1 gene (fmr1, 309550.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fmr1 gene (fmr1, 309550.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  702. en:caused by mutation in the forkhead, drosophila, homolog-like 7 gene (foxc1, 601090.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead, drosophila, homolog-like 7 gene (foxc1, 601090.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  703. en:caused by mutation in the gata-binding protein-1 gene (gata1, 305371.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein-1 gene (gata1, 305371.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  704. en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0007) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  705. en:caused by mutation in the gene encoding peripheral myelin protein-22 (pmp22, 601097.0004) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding peripheral myelin protein-22 (pmp22, 601097.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  706. en:caused by mutation in the glutaredoxin 5 gene (glrx5, 609588.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutaredoxin 5 gene (glrx5, 609588.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  707. en:caused by mutation in the golgi snap receptor complex member 2 gene (gosr2, 604027.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the golgi snap receptor complex member 2 gene (gosr2, 604027.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  708. en:caused by mutation in the guanine nucleotide-binding protein, alpha-activating activity polypeptide, olfactory type gene (gnal, 139312.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the guanine nucleotide-binding protein, alpha-activating activity polypeptide, olfactory type gene (gnal, 139312.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  709. en:caused by mutation in the h19 gene (h19, 103280.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the h19 gene (h19, 103280.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  710. en:caused by mutation in the heat-shock 27-kd protein 3 gene (hspb3, 604624.0001). --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heat-shock 27-kd protein 3 gene (hspb3, 604624.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  711. en:caused by mutation in the hemoglobin gamma b gene (hbg2, 142250.0026) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hemoglobin gamma b gene (hbg2, 142250.0026) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  712. en:caused by mutation in the heparan-alpha-glucosaminide n-acetyltransferase gene (hgsnat, 610453.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heparan-alpha-glucosaminide n-acetyltransferase gene (hgsnat, 610453.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  713. en:caused by mutation in the hepatic growth factor gene (hgf, 142409.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hepatic growth factor gene (hgf, 142409.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  714. en:caused by mutation in the hexose-6-phosphate dehydrogenase gene (h6pd, 138090.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hexose-6-phosphate dehydrogenase gene (h6pd, 138090.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  715. en:caused by mutation in the homolog of chlamydomonas intraflagellar transport 172 gene (ift172, 607386.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of chlamydomonas intraflagellar transport 172 gene (ift172, 607386.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  716. en:caused by mutation in the homolog of mouse newborn ovary homeobox gene (nobox, 610934.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of mouse newborn ovary homeobox gene (nobox, 610934.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  717. en:caused by mutation in the homolog of s. cerevisiae fig4 gene (fig4, 609390.0009) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of s. cerevisiae fig4 gene (fig4, 609390.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  718. en:caused by mutation in the homolog of the drosophila atonal 7 gene (atoh7, 609875.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila atonal 7 gene (atoh7, 609875.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  719. en:caused by mutation in the homolog of the drosophila dicer 1 gene (dicer1, 606241.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila dicer 1 gene (dicer1, 606241.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  720. en:caused by mutation in the homolog of the drosophila muscle segment homeo box-2 gene (msx2, 123101.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila muscle segment homeo box-2 gene (msx2, 123101.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  721. en:caused by mutation in the homolog of the drosophila orthodenticle 2 gene (otx2, 600038.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila orthodenticle 2 gene (otx2, 600038.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  722. en:caused by mutation in the homolog of the mouse itchy gene (itch, 606409.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse itchy gene (itch, 606409.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  723. en:caused by mutation in the homolog of the s. cerevisiae alg11 gene (alg11, 613666.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae alg11 gene (alg11, 613666.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  724. en:caused by mutation in the homolog of the s. cerevisiae precursor mrna-processing factor 8 gene (prpf8, 607300.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae precursor mrna-processing factor 8 gene (prpf8, 607300.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  725. en:caused by mutation in the homolog of the s. cerevisiae sco2 gene (sco2, 604272.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae sco2 gene (sco2, 604272.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  726. en:caused by mutation in the hps5 gene (hps5, 607521) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hps5 gene (hps5, 607521) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  727. en:caused by mutation in the human homolog a of the s. cerevisiae sec23 gene (sec23a, 610511.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the human homolog a of the s. cerevisiae sec23 gene (sec23a, 610511.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  728. en:caused by mutation in the human homolog of the s. cerevisiae sil1 gene (608005.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the human homolog of the s. cerevisiae sil1 gene (608005.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  729. en:caused by mutation in the hyperpolarization-activated cyclic nucleotide-gated potassium channel 4 gene (hcn4, 605206.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hyperpolarization-activated cyclic nucleotide-gated potassium channel 4 gene (hcn4, 605206.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  730. en:caused by mutation in the inositol 1,4,5-triphosphate receptor, type 1 gene (itpr1, 147265) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inositol 1,4,5-triphosphate receptor, type 1 gene (itpr1, 147265) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  731. en:caused by mutation in the integrin, beta-3 gene (itgb3, 173470.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the integrin, beta-3 gene (itgb3, 173470.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  732. en:caused by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0003) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  733. en:caused by mutation in the interferon regulatory factor 8 gene (irf8, 601565.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interferon regulatory factor 8 gene (irf8, 601565.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  734. en:caused by mutation in the interleukin 10 receptor, alpha gene (il10ra, 146933.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interleukin 10 receptor, alpha gene (il10ra, 146933.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  735. en:caused by mutation in the interleukin 21 gene (il21, 605384.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interleukin 21 gene (il21, 605384.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  736. en:caused by mutation in the inverted formin 2 gene (inf2, 610982.0006) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inverted formin 2 gene (inf2, 610982.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  737. en:caused by mutation in the isoleucyl-trna synthetase 2 gene (iars2, 612801.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the isoleucyl-trna synthetase 2 gene (iars2, 612801.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  738. en:caused by mutation in the janus kinase 3 gene (jak3, 600173.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the janus kinase 3 gene (jak3, 600173.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  739. en:caused by mutation in the k(lysine) acetyltransferase 6b gene (kat6b, 605880.0005) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the k(lysine) acetyltransferase 6b gene (kat6b, 605880.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  740. en:caused by mutation in the keratin 1 gene (krt1, 139350.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 1 gene (krt1, 139350.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  741. en:caused by mutation in the keratin 14 gene (krt14, 148066.0005) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 14 gene (krt14, 148066.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  742. en:caused by mutation in the keratin-6c gene (krt6c, 612315.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin-6c gene (krt6c, 612315.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  743. en:caused by mutation in the kiaa1033 gene (kiaa1033, 615748.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kiaa1033 gene (kiaa1033, 615748.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  744. en:caused by mutation in the kiaa2022 gene (300524.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kiaa2022 gene (300524.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  745. en:caused by mutation in the kiss1 metastasis suppressor gene (kiss1, 603286.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kiss1 metastasis suppressor gene (kiss1, 603286.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  746. en:caused by mutation in the l-2-hydroxyglutarate dehydrogenase gene (l2hgdh, 609584.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the l-2-hydroxyglutarate dehydrogenase gene (l2hgdh, 609584.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  747. en:caused by mutation in the laminin, alpha-1 gene (lama1, 150320.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the laminin, alpha-1 gene (lama1, 150320.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  748. en:caused by mutation in the leucine zipper-like transcriptional regulator 1 gene (lztr1, 600574.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucine zipper-like transcriptional regulator 1 gene (lztr1, 600574.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  749. en:caused by mutation in the leucine-rich repeat kinase 2 gene (lrrk2, 609007.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucine-rich repeat kinase 2 gene (lrrk2, 609007.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  750. en:caused by mutation in the lipase h gene (liph, 607365.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lipase h gene (liph, 607365.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  751. en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0011) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  752. en:caused by mutation in the lyr motif-containing protein 4 gene (lyrm4, 613311.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lyr motif-containing protein 4 gene (lyrm4, 613311.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  753. en:caused by mutation in the male germ cell-associated kinase gene (mak, 154235.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the male germ cell-associated kinase gene (mak, 154235.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  754. en:caused by mutation in the mannosyl (alpha-1,6-)-glycoprotein beta-1,2-n-acetylglucosaminyltransferase gene (mgat2, 602616.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mannosyl (alpha-1,6-)-glycoprotein beta-1,2-n-acetylglucosaminyltransferase gene (mgat2, 602616.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  755. en:caused by mutation in the matrix gla protein gene (mgp, 154870.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the matrix gla protein gene (mgp, 154870.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  756. en:caused by mutation in the mer tyrosine kinase protooncogene (mertk, 604705.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mer tyrosine kinase protooncogene (mertk, 604705.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  757. en:caused by mutation in the metabotropic glutamate receptor 1 gene (grm1, 604473.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the metabotropic glutamate receptor 1 gene (grm1, 604473.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  758. en:caused by mutation in the methionine adenosyltransferase 1 gene (mat1a, 610550.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methionine adenosyltransferase 1 gene (mat1a, 610550.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  759. en:caused by mutation in the micro rna 17 host gene (mir17hg, 609415) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the micro rna 17 host gene (mir17hg, 609415) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  760. en:caused by mutation in the micro rna 2861 gene (mir2861, 613405.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the micro rna 2861 gene (mir2861, 613405.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  761. en:caused by mutation in the microtubule-associated tau protein gene (mapt, 157140.0011) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the microtubule-associated tau protein gene (mapt, 157140.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  762. en:caused by mutation in the mitochondrial glutamic acid transfer rna gene (mtte, 590025.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial glutamic acid transfer rna gene (mtte, 590025.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  763. en:caused by mutation in the mitochondrial ribosomal protein s22 gene (mrps22, 605810.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial ribosomal protein s22 gene (mrps22, 605810.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  764. en:caused by mutation in the mitochondrial rna-processing endoribonuclease gene (rmrp, 157660.0009) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial rna-processing endoribonuclease gene (rmrp, 157660.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  765. en:caused by mutation in the mitochondrial transfer rna-leucine gene (mttl1, 590050.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial transfer rna-leucine gene (mttl1, 590050.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  766. en:caused by mutation in the mmachc gene (mmachc gene 609831.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mmachc gene (mmachc gene 609831.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  767. en:caused by mutation in the mouse homolog of the nodal gene (nodal, 601265.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mouse homolog of the nodal gene (nodal, 601265.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  768. en:caused by mutation in the mucosa-associated lymphoid tissue lymphoma translocation gene 1 (malt1, 604860.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mucosa-associated lymphoid tissue lymphoma translocation gene 1 (malt1, 604860.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  769. en:caused by mutation in the multiple epidermal growth factor-like domains 10 gene (megf10, 612453.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the multiple epidermal growth factor-like domains 10 gene (megf10, 612453.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  770. en:caused by mutation in the multiple pdz domain protein gene (mpdz, 603785.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the multiple pdz domain protein gene (mpdz, 603785.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  771. en:caused by mutation in the muscle glycogen phosphorylase gene (pygm, 608455.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the muscle glycogen phosphorylase gene (pygm, 608455.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  772. en:caused by mutation in the myosin heavy chain 3 gene (myh3, 160720.0005) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin heavy chain 3 gene (myh3, 160720.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  773. en:caused by mutation in the myosin ie gene (myo1e, 601479.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin ie gene (myo1e, 601479.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  774. en:caused by mutation in the myosin light chain kinase gene (mylk, 600922.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin light chain kinase gene (mylk, 600922.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  775. en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, gamma subunit gene (gnptg, 607838.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, gamma subunit gene (gnptg, 607838.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  776. en:caused by mutation in the n-deacetylase/n-sulfotransferase 1 gene (ndst1, 600853.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the n-deacetylase/n-sulfotransferase 1 gene (ndst1, 600853.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  777. en:caused by mutation in the nad(p)h steroid dehydrogenase-like protein (nsdhl, 300275.0007) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nad(p)h steroid dehydrogenase-like protein (nsdhl, 300275.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  778. en:caused by mutation in the nadh dehydrogenase (ubiquinone) flavoprotein 2 gene (ndufv2, 600532.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) flavoprotein 2 gene (ndufv2, 600532.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  779. en:caused by mutation in the nadh dehydrogenase, subunit 2 gene (mtnd2, 516001.0006) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase, subunit 2 gene (mtnd2, 516001.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  780. en:caused by mutation in the natriuretic peptide receptor b gene (npr2, 108961.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the natriuretic peptide receptor b gene (npr2, 108961.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  781. en:caused by mutation in the nebulin gene (neb, 160650.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nebulin gene (neb, 160650.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  782. en:caused by mutation in the neurexin 1 gene (nrxn1, 600565.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neurexin 1 gene (nrxn1, 600565.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  783. en:caused by mutation in the neuronal nicotinic cholinergic receptor, alpha polypeptide 2 gene (chrna2, 118502.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neuronal nicotinic cholinergic receptor, alpha polypeptide 2 gene (chrna2, 118502.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  784. en:caused by mutation in the never-in-mitosis gene a-related kinase-2 gene (nek2, 604043.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the never-in-mitosis gene a-related kinase-2 gene (nek2, 604043.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  785. en:caused by mutation in the nlr family, caspase recruitment domain-containing 4 gene (nlrc4, 606831.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nlr family, caspase recruitment domain-containing 4 gene (nlrc4, 606831.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  786. en:caused by mutation in the nlr family, pyrin-domain containing 3 gene (nlrp3, 606416.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nlr family, pyrin-domain containing 3 gene (nlrp3, 606416.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  787. en:caused by mutation in the nlr family, pyrin-domain containing 3 gene (nlrp3, 606416.0004) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nlr family, pyrin-domain containing 3 gene (nlrp3, 606416.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  788. en:caused by mutation in the nuclear receptor subfamily 2, group e, member 3 gene (nr2e3, 604485.0006) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear receptor subfamily 2, group e, member 3 gene (nr2e3, 604485.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  789. en:caused by mutation in the origin recognition complex, subunit 1, gene (orc1, 601902.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the origin recognition complex, subunit 1, gene (orc1, 601902.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  790. en:caused by mutation in the paired box gene 6 gene (pax6, 607108.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the paired box gene 6 gene (pax6, 607108.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  791. en:caused by mutation in the patatin-like phospholipase domain-containing protein 2 gene (pnpla2, 609059.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the patatin-like phospholipase domain-containing protein 2 gene (pnpla2, 609059.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  792. en:caused by mutation in the peptidyl-trna hydrolase 2 gene (ptrh2, 608625.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peptidyl-trna hydrolase 2 gene (ptrh2, 608625.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  793. en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  794. en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 1 gene (pik3r1, 171833.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 1 gene (pik3r1, 171833.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  795. en:caused by mutation in the phosphatidylinositol glycan, class v gene (pigv, 610274.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol glycan, class v gene (pigv, 610274.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  796. en:caused by mutation in the phosphodiesterase 8b gene (pde8b, 603390.0002). --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphodiesterase 8b gene (pde8b, 603390.0002). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  797. en:caused by mutation in the phospholipase c, gamma-2 gene (plcg2, 600220.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phospholipase c, gamma-2 gene (plcg2, 600220.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  798. en:caused by mutation in the phosphoserine aminotransferase-1 gene (psat1, 610936.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoserine aminotransferase-1 gene (psat1, 610936.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  799. en:caused by mutation in the plasma cholesteryl ester transfer protein gene (cetp, 118470.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the plasma cholesteryl ester transfer protein gene (cetp, 118470.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  800. en:caused by mutation in the polyhomeotic-like 1 gene (phc1, 602978.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polyhomeotic-like 1 gene (phc1, 602978.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  801. en:caused by mutation in the potassium voltage-gated channel, isk-related subfamily, member 1 gene (kcne1, 176261.0003) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, isk-related subfamily, member 1 gene (kcne1, 176261.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  802. en:caused by mutation in the potassium voltage-gated channel, shaker-related subfamily, member 1 gene (kcna1, 176260.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, shaker-related subfamily, member 1 gene (kcna1, 176260.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  803. en:caused by mutation in the prenyl diphosphate synthase, subunit 1 gene (pdss1, 607429.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prenyl diphosphate synthase, subunit 1 gene (pdss1, 607429.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  804. en:caused by mutation in the presenilin-1 gene (psen1, 104311.0027) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the presenilin-1 gene (psen1, 104311.0027) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  805. en:caused by mutation in the prion protein gene (prnp, 176640.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prion protein gene (prnp, 176640.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  806. en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase gene (pomgnt1, 606822.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase gene (pomgnt1, 606822.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  807. en:caused by mutation in the protein-o-mannose kinase gene (pomk, 615247.0003) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein-o-mannose kinase gene (pomk, 615247.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  808. en:caused by mutation in the protocadherin 19 gene (pcdh19, 300460.0001). --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protocadherin 19 gene (pcdh19, 300460.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  809. en:caused by mutation in the protocadherin-15 gene (pcdh15, 605514.0006) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protocadherin-15 gene (pcdh15, 605514.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  810. en:caused by mutation in the pulmonary-associated surfactant protein a2 gene (sftpa2, 178642.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pulmonary-associated surfactant protein a2 gene (sftpa2, 178642.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  811. en:caused by mutation in the purine-rich element-binding protein a gene (pura, 600473.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the purine-rich element-binding protein a gene (pura, 600473.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  812. en:caused by mutation in the putative protein o-mannosyltransferase 2 gene (pomt2, 607439.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the putative protein o-mannosyltransferase 2 gene (pomt2, 607439.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  813. en:caused by mutation in the pyrin domain-containing-1 of the nlr family gene (nlrp1, 606626.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pyrin domain-containing-1 of the nlr family gene (nlrp1, 606626.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  814. en:caused by mutation in the rab3 gtpase-activating protein (noncatalytic) subunit 2 gene (rab3gap2, 609275.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rab3 gtpase-activating protein (noncatalytic) subunit 2 gene (rab3gap2, 609275.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  815. en:caused by mutation in the ranbp-type and c3hc4-type zinc finger-containing 1 gene (rbck1, 610924.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ranbp-type and c3hc4-type zinc finger-containing 1 gene (rbck1, 610924.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  816. en:caused by mutation in the ras guanyl nucleotide-releasing protein 2 gene (rasgrp2, 605577.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ras guanyl nucleotide-releasing protein 2 gene (rasgrp2, 605577.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  817. en:caused by mutation in the receptor expression-enhancing protein-1 gene (reep1, 609139.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the receptor expression-enhancing protein-1 gene (reep1, 609139.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  818. en:caused by mutation in the receptor for the fc fragment of igg, low affinity iiia (fcgr3a, 146740.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the receptor for the fc fragment of igg, low affinity iiia (fcgr3a, 146740.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  819. en:caused by mutation in the recombinase activating gene 2 (rag2, 179616.0003) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the recombinase activating gene 2 (rag2, 179616.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  820. en:caused by mutation in the ret protooncogene (ret, 164761.0014) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ret protooncogene (ret, 164761.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  821. en:caused by mutation in the retina and anterior neural fold homeobox gene (rax, 601881.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the retina and anterior neural fold homeobox gene (rax, 601881.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  822. en:caused by mutation in the rho gdp-dissociation inhibitor alpha gene (arhgdia, 601925.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rho gdp-dissociation inhibitor alpha gene (arhgdia, 601925.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  823. en:caused by mutation in the rhodopsin gene (rho, 180380.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rhodopsin gene (rho, 180380.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  824. en:caused by mutation in the rna-binding motif protein 8a gene (rbm8a, 605313.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rna-binding motif protein 8a gene (rbm8a, 605313.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  825. en:caused by mutation in the rna-specific adenosine deaminase gene (adar, 146920.0007) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rna-specific adenosine deaminase gene (adar, 146920.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  826. en:caused by mutation in the rpgrip1-like gene (rpgrip1l, 610937.0005). --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rpgrip1-like gene (rpgrip1l, 610937.0005). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  827. en:caused by mutation in the semaphorin 4a gene (sema4a, 607292.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the semaphorin 4a gene (sema4a, 607292.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  828. en:caused by mutation in the serpin peptidase inhibitor, clade b (ovalbumin), member 7 gene (serpinb7, 603357.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the serpin peptidase inhibitor, clade b (ovalbumin), member 7 gene (serpinb7, 603357.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  829. en:caused by mutation in the seryl-trna synthetase 2 gene (sars2, 612804.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the seryl-trna synthetase 2 gene (sars2, 612804.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  830. en:caused by mutation in the sialyltransferase-9 gene (siat9, 604402.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sialyltransferase-9 gene (siat9, 604402.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  831. en:caused by mutation in the signal transducer and activator of transcription 2 (stat2, 600556.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the signal transducer and activator of transcription 2 (stat2, 600556.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  832. en:caused by mutation in the signal transducer and activator of transcription-3 gene (stat3, 102582.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the signal transducer and activator of transcription-3 gene (stat3, 102582.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  833. en:caused by mutation in the skeletal muscle alpha-1 actin gene (acta1, 102610.0011) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the skeletal muscle alpha-1 actin gene (acta1, 102610.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  834. en:caused by mutation in the solute carrier family 16, member 1 gene (slc16a1, 600682.0003) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 16, member 1 gene (slc16a1, 600682.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  835. en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0018) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  836. en:caused by mutation in the solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene (slc25a19, 606521.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19 gene (slc25a19, 606521.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  837. en:caused by mutation in the solute carrier family 25, member 19 gene (mitochondrial thiamine pyrophosphate carrier) (slc25a19, 606521.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25, member 19 gene (mitochondrial thiamine pyrophosphate carrier) (slc25a19, 606521.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  838. en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 222600.0005) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 222600.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  839. en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 606718.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 606718.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  840. en:caused by mutation in the solute carrier family 46 (folate transporter), member 1 gene (slc46a1, 611672.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 46 (folate transporter), member 1 gene (slc46a1, 611672.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  841. en:caused by mutation in the solute carrier family 5 (sodium/glucose cotransporter), member 2 gene (slc5a2, 182381.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 5 (sodium/glucose cotransporter), member 2 gene (slc5a2, 182381.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  842. en:caused by mutation in the sonic hedgehog gene (shh, 600725.0016) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sonic hedgehog gene (shh, 600725.0016) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  843. en:caused by mutation in the sorting nexin 10 gene (snx10, 614780.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sorting nexin 10 gene (snx10, 614780.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  844. en:caused by mutation in the sparc-related modular calcium-binding 1 gene (smoc1, 608488.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sparc-related modular calcium-binding 1 gene (smoc1, 608488.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  845. en:caused by mutation in the spermine synthase gene (sms, 300105.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the spermine synthase gene (sms, 300105.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  846. en:caused by mutation in the sprouty-related evh1 domain-containing protein 1 gene (spred1, 609291.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sprouty-related evh1 domain-containing protein 1 gene (spred1, 609291.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  847. en:caused by mutation in the swi/snf related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene (smarca2, 600014.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the swi/snf related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 gene (smarca2, 600014.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  848. en:caused by mutation in the swi/snf-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, dead/h box-containing, 1 gene (smarcad1, 612761.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the swi/snf-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, dead/h box-containing, 1 gene (smarcad1, 612761.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  849. en:caused by mutation in the synaptic ras gtpase activating protein 1 gene (syngap1, 603384.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the synaptic ras gtpase activating protein 1 gene (syngap1, 603384.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  850. en:caused by mutation in the synaptotagmin-2 gene (syt2, 600104.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the synaptotagmin-2 gene (syt2, 600104.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  851. en:caused by mutation in the syntaxin-binding protein 1 gene (stxbp1, 602926.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the syntaxin-binding protein 1 gene (stxbp1, 602926.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  852. en:caused by mutation in the tenascin xb gene (tnxb, 600985.0006) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tenascin xb gene (tnxb, 600985.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  853. en:caused by mutation in the tetratricopeptide repeat domain 19 gene (ttc19, 613814.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tetratricopeptide repeat domain 19 gene (ttc19, 613814.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  854. en:caused by mutation in the thioredoxin-like 4a gene (txnl4a, 611595.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thioredoxin-like 4a gene (txnl4a, 611595.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  855. en:caused by mutation in the thromboxane a synthase-1 gene (tbxas1, 274180.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thromboxane a synthase-1 gene (tbxas1, 274180.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  856. en:caused by mutation in the thymidine phosphorylase gene (tymp, 131222.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thymidine phosphorylase gene (tymp, 131222.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  857. en:caused by mutation in the thyroid transcription factor 1 gene (titf1, 600635.0005) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thyroid transcription factor 1 gene (titf1, 600635.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  858. en:caused by mutation in the titin gene (ttn, 188840.0012) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the titin gene (ttn, 188840.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  859. en:caused by mutation in the trafficking protein particle complex, subunit 9 gene (trappc9, 611966.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the trafficking protein particle complex, subunit 9 gene (trappc9, 611966.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  860. en:caused by mutation in the transglutaminase 6 gene (tgm6, 613900.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transglutaminase 6 gene (tgm6, 613900.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  861. en:caused by mutation in the transglutaminase-5 gene (tgm5, 603805.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transglutaminase-5 gene (tgm5, 603805.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  862. en:caused by mutation in the transmembrane protein 138 gene (tmem138, 614459.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 138 gene (tmem138, 614459.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  863. en:caused by mutation in the transmembrane protein 142a gene (tmem142a, 610277.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 142a gene (tmem142a, 610277.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  864. en:caused by mutation in the transmembrane protein 231 gene (tmem231, 614949.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 231 gene (tmem231, 614949.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  865. en:caused by mutation in the transmembrane protein 240 gene (tmem240, 616101.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 240 gene (tmem240, 616101.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  866. en:caused by mutation in the tripartite motif-containing protein 2 gene (trim2, 614141.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tripartite motif-containing protein 2 gene (trim2, 614141.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  867. en:caused by mutation in the tropomyosin-3 gene (tpm3, 191030.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tropomyosin-3 gene (tpm3, 191030.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  868. en:caused by mutation in the tubulin beta-3 gene (tubb3, 602661.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin beta-3 gene (tubb3, 602661.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  869. en:caused by mutation in the tubulin tyrosine ligase-like family member 5 gene (ttll5, 612268.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin tyrosine ligase-like family member 5 gene (ttll5, 612268.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  870. en:caused by mutation in the tubulin-gamma complex-associated protein 6 gene (tubgcp6, 610053.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin-gamma complex-associated protein 6 gene (tubgcp6, 610053.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  871. en:caused by mutation in the tumor protein p63 gene (tp63, 603273.0007) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tumor protein p63 gene (tp63, 603273.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  872. en:caused by mutation in the type v collagen, alpha-1 gene (col5a1, 120215.0005) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the type v collagen, alpha-1 gene (col5a1, 120215.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  873. en:caused by mutation in the tyrosine kinase 2 gene (tyk2, 176941.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tyrosine kinase 2 gene (tyk2, 176941.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  874. en:caused by mutation in the tyrosyl-trna synthetase gene (yars, 603623.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tyrosyl-trna synthetase gene (yars, 603623.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  875. en:caused by mutation in the ubiquinol-cytochrome c reductase complex assembly factor 2 gene (uqcc2, 614461.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquinol-cytochrome c reductase complex assembly factor 2 gene (uqcc2, 614461.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  876. en:caused by mutation in the ubiquitin-protein ligase e3 component n-recognin 1 gene (ubr1, 605981.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquitin-protein ligase e3 component n-recognin 1 gene (ubr1, 605981.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  877. en:caused by mutation in the upf3, b, yeast homolog gene (upf3b, 300298.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the upf3, b, yeast homolog gene (upf3b, 300298.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  878. en:caused by mutation in the uracil-dna glycosylase gene (ung, 191525.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the uracil-dna glycosylase gene (ung, 191525.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  879. en:caused by mutation in the urocanase domain-containing protein 1 gene (uroc1, 613012.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the urocanase domain-containing protein 1 gene (uroc1, 613012.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  880. en:caused by mutation in the v-ki-ras2 kirsten rat sarcoma 2 viral oncogene homolog gene (kras, 190070.0009) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-ki-ras2 kirsten rat sarcoma 2 viral oncogene homolog gene (kras, 190070.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  881. en:caused by mutation in the v-raf-1 murine leukemia viral oncogene homolog-1 gene (raf1, 164760.0005) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-raf-1 murine leukemia viral oncogene homolog-1 gene (raf1, 164760.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  882. en:caused by mutation in the voltage-gated potassium channel, shaw-related subfamily, member 3 gene (kcnc3, 176264.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated potassium channel, shaw-related subfamily, member 3 gene (kcnc3, 176264.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  883. en:caused by mutation in the voltage-gated sodium channel, type xi, alpha subunit gene (scn11a, 604385.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated sodium channel, type xi, alpha subunit gene (scn11a, 604385.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  884. en:caused by mutation in the wd repeat-containing protein 45 gene (wdr45, 300526.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein 45 gene (wdr45, 300526.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  885. en:caused by mutation in the wfs1 gene (wfs1, 606201.0032) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wfs1 gene (wfs1, 606201.0032) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  886. en:caused by mutation in the x-linked small muscle protein gene (smpx, 300226.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the x-linked small muscle protein gene (smpx, 300226.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  887. en:caused by mutation in the zinc finger c4h2 domain-containing protein gene (zc4h2, 300897.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger c4h2 domain-containing protein gene (zc4h2, 300897.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  888. en:caused by mutation in the zinc finger e box-binding homeobox 2 gene (zeb2, 605802.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger e box-binding homeobox 2 gene (zeb2, 605802.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  889. en:caused by mutation in the zinc finger mynd domain-containing protein 11 gene (zmynd11, 608668.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger mynd domain-containing protein 11 gene (zmynd11, 608668.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  890. en:caused by mutation in the zinc finger protein 644 gene (znf644, 614159.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger protein 644 gene (znf644, 614159.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  891. en:caused by mutation in the zinc finger protein of cerebellum 2 gene (zic2, 603073.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger protein of cerebellum 2 gene (zic2, 603073.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  892. en:caused by mutation in the zinc finger- and btb domain-containing protein 24 gene (zbtb24, 614064.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger- and btb domain-containing protein 24 gene (zbtb24, 614064.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  893. en:caused by mutation in zinc finger mynd-containing protein-15 gene (zmynd15, 614312.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in zinc finger mynd-containing protein-15 gene (zmynd15, 614312.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  894. en:caused by mutation or trinucleotide repeat expansion (gaa)n in the frataxin gene (fxn, 606829.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation or trinucleotide repeat expansion (gaa)n in the frataxin gene (fxn, 606829.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  895. en:caused by mutations in the 5-alpha-reductase-2 gene (srd5a2, 607306.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the 5-alpha-reductase-2 gene (srd5a2, 607306.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  896. en:caused by mutations in the butrylcholinesterase gene (bche, 177400.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the butrylcholinesterase gene (bche, 177400.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  897. en:caused by mutations in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0002) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  898. en:caused by mutations in the cysteine-rich protein with egf-like domain 1 gene (creld1, 607170.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cysteine-rich protein with egf-like domain 1 gene (creld1, 607170.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  899. en:caused by mutations in the delta-1-pyrroline-5-carboxylate dehydrogenase gene (p5cdh, 606811.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the delta-1-pyrroline-5-carboxylate dehydrogenase gene (p5cdh, 606811.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  900. en:caused by mutations in the desmoplakin gene (dsp, 125647.0004) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the desmoplakin gene (dsp, 125647.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  901. en:caused by mutations in the excision-repair cross-complementing group 8 gene (ercc8, 609412.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the excision-repair cross-complementing group 8 gene (ercc8, 609412.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  902. en:caused by mutations in the flj90130 gene (flj90130, 607461.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the flj90130 gene (flj90130, 607461.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  903. en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0003) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  904. en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0006) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  905. en:caused by mutations in the heparan sulfate sulfatase gene (sgsh, 605270.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the heparan sulfate sulfatase gene (sgsh, 605270.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  906. en:caused by mutations in the homolog of the mouse noggin gene (nog, 602991.0006) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the homolog of the mouse noggin gene (nog, 602991.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  907. en:caused by mutations in the indian hedgehog gene (ihh, 600726.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the indian hedgehog gene (ihh, 600726.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  908. en:caused by mutations in the keratin 17 gene (krt17, 148069.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the keratin 17 gene (krt17, 148069.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  909. en:caused by mutations in the liver phosphorylase alpha-2 subunit gene (phka2, 306000.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the liver phosphorylase alpha-2 subunit gene (phka2, 306000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  910. en:caused by mutations in the marvel domain-containing protein 2 gene (marveld2, 610572.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the marvel domain-containing protein 2 gene (marveld2, 610572.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  911. en:caused by mutations in the menin gene (men1, 131100.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the menin gene (men1, 131100.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  912. en:caused by mutations in the myelin protein zero gene (mpz, 159440.0016) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the myelin protein zero gene (mpz, 159440.0016) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  913. en:caused by mutations in the otoferlin gene (otof, 603681.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the otoferlin gene (otof, 603681.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  914. en:caused by mutations in the parafibromin gene (hrpt2, 607393.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the parafibromin gene (hrpt2, 607393.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  915. en:caused by mutations in the pkhd1 gene (606702.0001). --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the pkhd1 gene (606702.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  916. en:caused by mutations in the protein tyrosine kinase-binding protein gene (tyrobp, 604142.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the protein tyrosine kinase-binding protein gene (tyrobp, 604142.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  917. en:caused by mutations in the ras-associated protein rab27a gene (rab27a, 603868.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the ras-associated protein rab27a gene (rab27a, 603868.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  918. en:caused by mutations in the recombinase activating gene 2 (rag2, 179616.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the recombinase activating gene 2 (rag2, 179616.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  919. en:caused by mutations in the ryanodine receptor 1 gene (ryr1, 180901.0003) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the ryanodine receptor 1 gene (ryr1, 180901.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  920. en:caused by mutations in the secreted ly6/upar-related protein 1 gene (slurp1, 606119.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the secreted ly6/upar-related protein 1 gene (slurp1, 606119.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  921. en:caused by mutations in the selenoprotein n-1 gene (sepn1, 606210.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the selenoprotein n-1 gene (sepn1, 606210.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  922. en:caused by mutations in the tubulin-specific chaperone e gene (tbce, 604934.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the tubulin-specific chaperone e gene (tbce, 604934.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  923. en:caused by mutations in the xylosylprotein 4-beta-galactosyltransferase, polypeptide 7 gene (b4galt7, 604327.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the xylosylprotein 4-beta-galactosyltransferase, polypeptide 7 gene (b4galt7, 604327.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  924. en:caused by simultaneous homozygous mutations in both the chloride channel, kidney, a gene (clcnka, 602024.0001) and chloride channel, kidney, b gene (clcnkb, 602023.0008) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by simultaneous homozygous mutations in both the chloride channel, kidney, a gene (clcnka, 602024.0001) and chloride channel, kidney, b gene (clcnkb, 602023.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  925. en:caused by somatic mutation in the phosphatidylinositol glycan, class a gene (piga, 311770.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the phosphatidylinositol glycan, class a gene (piga, 311770.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  926. en:caused by translocation disrupting the fibulin-1 gene (fbln1, 135820) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by translocation disrupting the fibulin-1 gene (fbln1, 135820) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  927. en:contiguous gene deletion syndrome caused by microdeletion (43-490kb) of chromosome 11q13 --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene deletion syndrome caused by microdeletion (43-490kb) of chromosome 11q13 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  928. en:contiguous gene syndrome caused by 6-mb duplication of 15q11-q13 --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by 6-mb duplication of 15q11-q13 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  929. en:contiguous gene syndrome caused by deletion (2.2 mb) of chromosome 17q23.1-q23 --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by deletion (2.2 mb) of chromosome 17q23.1-q23 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  930. en:contiguous gene syndrome caused by deletion (580kb-22.5mb) of 3q13.31 --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by deletion (580kb-22.5mb) of 3q13.31 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  931. en:contiguous gene syndrome caused by deletion of 7.1 to 8.7mb of 16p12.2-p11.2 --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by deletion of 7.1 to 8.7mb of 16p12.2-p11.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  932. en:contiguous gene syndrome caused by duplication (269kb) on 9q21.11 including the tight junction protein 2 (tjp2, 607709) gene and the family with sequence similarity 189, member a2 (fam189a2, 607710) gene --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by duplication (269kb) on 9q21.11 including the tight junction protein 2 (tjp2, 607709) gene and the family with sequence similarity 189, member a2 (fam189a2, 607710) gene | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  933. en:contiguous gene syndrome involving mutation of genes on 7q11.2 --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome involving mutation of genes on 7q11.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  934. en:microdeletion of 15q11 in 70% of patients confirmed by fluorescent in situ hybridization --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:microdeletion of 15q11 in 70% of patients confirmed by fluorescent in situ hybridization | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  935. en:supernumerary inv dup(22)(q11) chromosome, occasionally due to interstitial duplication of 22q11 --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:supernumerary inv dup(22)(q11) chromosome, occasionally due to interstitial duplication of 22q11 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  936. en:susceptibility conferred by mutation in the complement factor b gene (cfb, 138470.0005) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the complement factor b gene (cfb, 138470.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  937. en:susceptibility conferred by mutation in the ef-hand domain (c-terminal)-containing protein 1 gene (efhc1, 608815.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the ef-hand domain (c-terminal)-containing protein 1 gene (efhc1, 608815.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  938. en:susceptibility conferred by mutation in the homolog of the s. cerevisiae coq2 gene (coq2, 609825.0006). --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the homolog of the s. cerevisiae coq2 gene (coq2, 609825.0006). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  939. en:susceptibility conferred by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0013) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  940. en:susceptibility conferred by mutation in the nk2 homeobox 1 gene (nkx2-1, 600635.0012) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the nk2 homeobox 1 gene (nkx2-1, 600635.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  941. en:susceptibility conferred by mutation in the transmembrane 4 l6 family, member 20 gene (tm4sf20, 615404.0001) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the transmembrane 4 l6 family, member 20 gene (tm4sf20, 615404.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  942. en:susceptibility conferred by mutation in the voltage-dependent calcium channel, l type, alpha-1s subunit gene (cacna1s, 114208.0005) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the voltage-dependent calcium channel, l type, alpha-1s subunit gene (cacna1s, 114208.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  943. en:susceptibility conferred by somatic mutation in the homolog of the myeloproliferative leukemia virus gene (mpl, 159530.0011) --- r_associated #0: 29 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by somatic mutation in the homolog of the myeloproliferative leukemia virus gene (mpl, 159530.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=29
  944. en:2p21del syndrome is a contiguous gene syndrome caused by 179kb deletion containing the slc3a1 (104614), prepl (609557), ppm1b (603770), and c2orf34 (609559) genes --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:2p21del syndrome is a contiguous gene syndrome caused by 179kb deletion containing the slc3a1 (104614), prepl (609557), ppm1b (603770), and c2orf34 (609559) genes | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  945. en:a contiguous gene syndrome caused by deletion of 2.2 to 10.6mb of terminal 1p36 --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome caused by deletion of 2.2 to 10.6mb of terminal 1p36 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  946. en:caused by a 1.35-mb duplication of chromosome 1q21 --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a 1.35-mb duplication of chromosome 1q21 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  947. en:caused by a 5.1-mb duplication of chromosome xq27.3-q28 --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a 5.1-mb duplication of chromosome xq27.3-q28 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  948. en:caused by an sva retrotransposon insertion in an intron of the tata-binding protein-associated factor-1 gene (taf1, 313650.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by an sva retrotransposon insertion in an intron of the tata-binding protein-associated factor-1 gene (taf1, 313650.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  949. en:caused by contiguous gene deletion of imprinted region of 11p15.5 --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by contiguous gene deletion of imprinted region of 11p15.5 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  950. en:caused by duplication of 72 kb of 5q23.2 including at a minimum the lamin b1 gene (lmnb1, 150340.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of 72 kb of 5q23.2 including at a minimum the lamin b1 gene (lmnb1, 150340.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  951. en:caused by mutation in a disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 10 gene (adamts10, 608990.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in a disintegrin-like and metalloproteinase with thrombospondin type 1 motif, 10 gene (adamts10, 608990.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  952. en:caused by mutation in both the opsin 1, long-wave-sensitive (red cone pigment) gene (opn1lw, 300822.0001) and opsin 1, medium-wave-sensitive (green cone pigment) gene (opn1mw, 300821.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in both the opsin 1, long-wave-sensitive (red cone pigment) gene (opn1lw, 300822.0001) and opsin 1, medium-wave-sensitive (green cone pigment) gene (opn1mw, 300821.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  953. en:caused by mutation in cartilage oligomeric matrix protein (comp, 600310.0005) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in cartilage oligomeric matrix protein (comp, 600310.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  954. en:caused by mutation in the 135-kd centrosomal protein gene (cep135, 611423.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 135-kd centrosomal protein gene (cep135, 611423.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  955. en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase x gene (hsd17b10, 300256.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase x gene (hsd17b10, 300256.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  956. en:caused by mutation in the 3-prime repair exonuclease 1 gene (trex1, 606609.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 3-prime repair exonuclease 1 gene (trex1, 606609.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  957. en:caused by mutation in the 3-prime repair exonuclease-1 gene (trex1, 606609.0005) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 3-prime repair exonuclease-1 gene (trex1, 606609.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  958. en:caused by mutation in the 4-aminobutyrate aminotransferase gene (abat, 137150.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 4-aminobutyrate aminotransferase gene (abat, 137150.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  959. en:caused by mutation in the 5-prime nucleotidase, cytosolic ii gene (nt5c2, 600417.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 5-prime nucleotidase, cytosolic ii gene (nt5c2, 600417.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  960. en:caused by mutation in the acetylglucosaminyltransferase-like protein gene (large, 603590.0003) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the acetylglucosaminyltransferase-like protein gene (large, 603590.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  961. en:caused by mutation in the actin, alpha, cardiac muscle gene (actc1, 102540.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the actin, alpha, cardiac muscle gene (actc1, 102540.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  962. en:caused by mutation in the activin receptor-like kinase gene (alk1, 601284.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the activin receptor-like kinase gene (alk1, 601284.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  963. en:caused by mutation in the adamts-like 4 gene (adamtsl4, 610113.0003) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adamts-like 4 gene (adamtsl4, 610113.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  964. en:caused by mutation in the adaptor-related protein complex 4, epsilon-1 subunit gene (ap4e1, 607244.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adaptor-related protein complex 4, epsilon-1 subunit gene (ap4e1, 607244.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  965. en:caused by mutation in the additional sex combs-like 1 gene (asxl1, 612990.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the additional sex combs-like 1 gene (asxl1, 612990.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  966. en:caused by mutation in the adenosine deaminase, rna-specific gene (adar, 601059.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenosine deaminase, rna-specific gene (adar, 601059.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  967. en:caused by mutation in the af4/fmr2 family, member 2 gene (aff2, 300806.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the af4/fmr2 family, member 2 gene (aff2, 300806.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  968. en:caused by mutation in the aldolase a, fructose-bisphosphatase gene (aldoa, 103850.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aldolase a, fructose-bisphosphatase gene (aldoa, 103850.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  969. en:caused by mutation in the alpha subunit of the voltage-gated sodium channel type ix gene (scn9a, 603415.0019) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha subunit of the voltage-gated sodium channel type ix gene (scn9a, 603415.0019) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  970. en:caused by mutation in the alpha-1 subunit of the thyroid hormone receptor gene (thra, 190120.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1 subunit of the thyroid hormone receptor gene (thra, 190120.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  971. en:caused by mutation in the alpha-2 subunit of collagen type ix gene (col9a2, 120260.0006) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-2 subunit of collagen type ix gene (col9a2, 120260.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  972. en:caused by mutation in the alpha-b crystallin gene (cryab, 123590.0006) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-b crystallin gene (cryab, 123590.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  973. en:caused by mutation in the alpha-synuclein gene (snca, 163890.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-synuclein gene (snca, 163890.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  974. en:caused by mutation in the alsin gene (als2, 606352.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alsin gene (als2, 606352.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  975. en:caused by mutation in the ankyrin repeat domain-containing protein 26 gene (ankrd26, 610855.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ankyrin repeat domain-containing protein 26 gene (ankrd26, 610855.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  976. en:caused by mutation in the anoctamin 3 gene (ano3, 610110.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the anoctamin 3 gene (ano3, 610110.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  977. en:caused by mutation in the apolipoprotein c-ii gene (apoc2, 608083.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the apolipoprotein c-ii gene (apoc2, 608083.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  978. en:caused by mutation in the asparagine synthetase gene (asns, 108370.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the asparagine synthetase gene (asns, 108370.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  979. en:caused by mutation in the ataxia-telangiectasia and rad3-related gene (atr, 601215.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ataxia-telangiectasia and rad3-related gene (atr, 601215.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  980. en:caused by mutation in the atp synthase 6 gene (mtap6, 516060.0003) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp synthase 6 gene (mtap6, 516060.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  981. en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0016) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0016) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  982. en:caused by mutation in the atpase, h+ transporting, lysosomal, accessory protein-2 gene (atp6ap2, 300556.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, h+ transporting, lysosomal, accessory protein-2 gene (atp6ap2, 300556.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  983. en:caused by mutation in the atpase, h+ transporting, lysosomal, beta polypeptide, 58kd gene (atp6b1, 192132.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, h+ transporting, lysosomal, beta polypeptide, 58kd gene (atp6b1, 192132.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  984. en:caused by mutation in the b-cell adhesion molecule gene (bcam, 612773.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the b-cell adhesion molecule gene (bcam, 612773.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  985. en:caused by mutation in the b-cell linker protein gene (blnk, 604515.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the b-cell linker protein gene (blnk, 604515.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  986. en:caused by mutation in the bcl2-associated athanogene 3 gene (bag3, 603883.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bcl2-associated athanogene 3 gene (bag3, 603883.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  987. en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  988. en:caused by mutation in the beta-1,3-glucosyltransferase gene (b3galtl, 610308.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1,3-glucosyltransferase gene (b3galtl, 610308.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  989. en:caused by mutation in the beta-4 gap junction protein gene (gjb4, 605425.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-4 gap junction protein gene (gjb4, 605425.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  990. en:caused by mutation in the bone morphogenetic receptor, type ii gene (bmpr2, 600799.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bone morphogenetic receptor, type ii gene (bmpr2, 600799.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  991. en:caused by mutation in the brain protein 44-like gene (brp44l, 614738.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the brain protein 44-like gene (brp44l, 614738.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  992. en:caused by mutation in the brca1-associated atm activator 1 gene (brat1, 614506.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the brca1-associated atm activator 1 gene (brat1, 614506.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  993. en:caused by mutation in the brca1-associated protein 1 (bap1, 603089.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the brca1-associated protein 1 (bap1, 603089.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  994. en:caused by mutation in the btb/poz domain-containing protein 12 (btbd12, 613278.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the btb/poz domain-containing protein 12 (btbd12, 613278.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  995. en:caused by mutation in the calsequestrin-2 gene (casq2, 114251.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calsequestrin-2 gene (casq2, 114251.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  996. en:caused by mutation in the catalytic subunit of the dolichyl-phosphate mannosyltransferase 1 gene (dpm1, 603503.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the catalytic subunit of the dolichyl-phosphate mannosyltransferase 1 gene (dpm1, 603503.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  997. en:caused by mutation in the cathepsin c gene (ctsc, 602365.0006) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cathepsin c gene (ctsc, 602365.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  998. en:caused by mutation in the ceramide synthase 1 gene (cers1, 606919.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ceramide synthase 1 gene (cers1, 606919.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  999. en:caused by mutation in the chloride intracellular channel-5 gene (clic5, 607293.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chloride intracellular channel-5 gene (clic5, 607293.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1000. en:caused by mutation in the chromosome 10 open reading frame 2 gene (c10orf2, 606075.0016) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 10 open reading frame 2 gene (c10orf2, 606075.0016) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1001. en:caused by mutation in the chromosome 2 open reading frame 25 gene (c2orf25, 611935.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 2 open reading frame 25 gene (c2orf25, 611935.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1002. en:caused by mutation in the chromosome 5 open reading frame 42 gene (c5orf42, 614571.0007) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 5 open reading frame 42 gene (c5orf42, 614571.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1003. en:caused by mutation in the coagulation factor ii gene (f2, 176930.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coagulation factor ii gene (f2, 176930.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1004. en:caused by mutation in the coenzyme a synthase gene (coasy, 609855.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coenzyme a synthase gene (coasy, 609855.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1005. en:caused by mutation in the coiled-coil and c2 domain-containing 1a gene (cc2d1a, 610055.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil and c2 domain-containing 1a gene (cc2d1a, 610055.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1006. en:caused by mutation in the coiled-coil and c2 domains-containing protein 2a (cc2d2a, 612013.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil and c2 domains-containing protein 2a (cc2d2a, 612013.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1007. en:caused by mutation in the coiled-coil domain-containing protein 78 gene (ccdc78, 614666.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil domain-containing protein 78 gene (ccdc78, 614666.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1008. en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0004) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1009. en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0039) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0039) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1010. en:caused by mutation in the collagen ii, alpha-polypeptide gene (col2a1, 120140.0055) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-polypeptide gene (col2a1, 120140.0055) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1011. en:caused by mutation in the collagen iv, alpha-1 polypeptide gene (col4a1, 120130.0007) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen iv, alpha-1 polypeptide gene (col4a1, 120130.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1012. en:caused by mutation in the collagen type viii alpha-2 gene (col8a2, 120252.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen type viii alpha-2 gene (col8a2, 120252.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1013. en:caused by mutation in the collagen vi, alpha-1 polypeptide gene (col6a1, 120220.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen vi, alpha-1 polypeptide gene (col6a1, 120220.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1014. en:caused by mutation in the collagen x, alpha-1 polypeptide gene (col10a1, 120110.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen x, alpha-1 polypeptide gene (col10a1, 120110.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1015. en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1016. en:caused by mutation in the collagen xvii, alpha-1 polypeptide gene (col17a2, 113811.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen xvii, alpha-1 polypeptide gene (col17a2, 113811.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1017. en:caused by mutation in the collagen, type iv, alpha-6 gene (col4a6, 303631.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type iv, alpha-6 gene (col4a6, 303631.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1018. en:caused by mutation in the complement factor i gene (cfi, 217030.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement factor i gene (cfi, 217030.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1019. en:caused by mutation in the contactin 2 gene (cntn2, 190197.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the contactin 2 gene (cntn2, 190197.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1020. en:caused by mutation in the cullin 4b gene (cul4b, 300304.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cullin 4b gene (cul4b, 300304.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1021. en:caused by mutation in the cyclin-dependent kinase inhibitor-1b gene (cdkn1b, 600778.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclin-dependent kinase inhibitor-1b gene (cdkn1b, 600778.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1022. en:caused by mutation in the cyld gene (605018.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyld gene (605018.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1023. en:caused by mutation in the cystatin a gene (csta, 184600.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cystatin a gene (csta, 184600.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1024. en:caused by mutation in the cytochrome b of complex iii gene (mtcyb, 516020.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome b of complex iii gene (mtcyb, 516020.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1025. en:caused by mutation in the cytochrome b5a gene (cyb5a, 613218.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome b5a gene (cyb5a, 613218.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1026. en:caused by mutation in the cytochrome c oxidase subunit iii gene (mtco3, 516050.0004) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase subunit iii gene (mtco3, 516050.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1027. en:caused by mutation in the cytochrome c oxidase, subunit viib gene (cox7b, 300885.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase, subunit viib gene (cox7b, 300885.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1028. en:caused by mutation in the cytochrome p450, family 4, subfamily v, polypeptide-2 gene (cyp4v2, 608614.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450, family 4, subfamily v, polypeptide-2 gene (cyp4v2, 608614.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1029. en:caused by mutation in the cytochrome p450, subfamily xib, polypeptide 1 gene (cyp11b1, 610613.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450, subfamily xib, polypeptide 1 gene (cyp11b1, 610613.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1030. en:caused by mutation in the ddb1- and cul4-associated factor 17 gene (dcaf17, 612515.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ddb1- and cul4-associated factor 17 gene (dcaf17, 612515.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1031. en:caused by mutation in the dead box polypeptide 59 gene (ddx59, 615464.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dead box polypeptide 59 gene (ddx59, 615464.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1032. en:caused by mutation in the delta-4-3-oxosteroid 5-beta-reductase gene (akr1d1, 604741.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the delta-4-3-oxosteroid 5-beta-reductase gene (akr1d1, 604741.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1033. en:caused by mutation in the desmoglein 4 gene (dsg4, 607892.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the desmoglein 4 gene (dsg4, 607892.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1034. en:caused by mutation in the dj1 gene (602533.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dj1 gene (602533.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1035. en:caused by mutation in the dna methyl-transferase 3b gene (dnmt3b, 602900.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna methyl-transferase 3b gene (dnmt3b, 602900.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1036. en:caused by mutation in the dna polymerase, epsilon gene (pole, 174762.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna polymerase, epsilon gene (pole, 174762.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1037. en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 6 gene (dnajc6, 608375.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 6 gene (dnajc6, 608375.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1038. en:caused by mutation in the dual-specificity tyrosine phosphorylation-regulated kinase 1b gene (dyrk1b, 604556.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dual-specificity tyrosine phosphorylation-regulated kinase 1b gene (dyrk1b, 604556.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1039. en:caused by mutation in the dynactin 1 gene (dctn1, 601143.0006) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynactin 1 gene (dctn1, 601143.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1040. en:caused by mutation in the dynactin-1 gene (dctn1, 601143.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynactin-1 gene (dctn1, 601143.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1041. en:caused by mutation in the dynein axonemal heavy chain 11 gene (dnah11, 603339.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynein axonemal heavy chain 11 gene (dnah11, 603339.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1042. en:caused by mutation in the dynein, axonemal, light chain 4 gene (dnal4, 610565.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynein, axonemal, light chain 4 gene (dnal4, 610565.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1043. en:caused by mutation in the dynein, cytoplasmic 1, heavy chain 1 gene (dync1h1, 600112.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynein, cytoplasmic 1, heavy chain 1 gene (dync1h1, 600112.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1044. en:caused by mutation in the dynein, cytoplasmic 2, heavy chain 1 gene (dync2h1, 603297.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynein, cytoplasmic 2, heavy chain 1 gene (dync2h1, 603297.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1045. en:caused by mutation in the elastin gene (eln, 130160.0008) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the elastin gene (eln, 130160.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1046. en:caused by mutation in the elmo/ced12 domain-containing protein 3 gene (elmod3, 615427.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the elmo/ced12 domain-containing protein 3 gene (elmod3, 615427.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1047. en:caused by mutation in the enamelin gene (enam, 606585.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the enamelin gene (enam, 606585.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1048. en:caused by mutation in the endoplasmic reticulum membrane protein complex, subunit 1 gene (emc1, 616846.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endoplasmic reticulum membrane protein complex, subunit 1 gene (emc1, 616846.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1049. en:caused by mutation in the ets variant gene 6 (etv, 600618.0003) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ets variant gene 6 (etv, 600618.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1050. en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 5 gene (eif2b5, 603945.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 5 gene (eif2b5, 603945.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1051. en:caused by mutation in the exosome component 3 gene (exosc3, 606489.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the exosome component 3 gene (exosc3, 606489.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1052. en:caused by mutation in the f-box only protein 7 gene (fbxo7, 605648.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the f-box only protein 7 gene (fbxo7, 605648.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1053. en:caused by mutation in the family with sequence similarity 134, member b gene (fam134b, 613114.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the family with sequence similarity 134, member b gene (fam134b, 613114.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1054. en:caused by mutation in the fas ligand gene (fasl, 134638.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fas ligand gene (fasl, 134638.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1055. en:caused by mutation in the feline leukemia virus subgroup c receptor 2 gene (flvcr2, 610865.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the feline leukemia virus subgroup c receptor 2 gene (flvcr2, 610865.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1056. en:caused by mutation in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1057. en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0028) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0028) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1058. en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0043) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0043) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1059. en:caused by mutation in the fibronectin-like domain-containing leucine-rich transmembrane protein 3 gene (flrt3, 604808.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibronectin-like domain-containing leucine-rich transmembrane protein 3 gene (flrt3, 604808.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1060. en:caused by mutation in the fibulin 5 gene (fbln5, 604580.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibulin 5 gene (fbln5, 604580.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1061. en:caused by mutation in the forkhead box g1 gene (foxg1, 164874.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead box g1 gene (foxg1, 164874.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1062. en:caused by mutation in the formin 2 gene (fmn2, 606373.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the formin 2 gene (fmn2, 606373.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1063. en:caused by mutation in the frizzled 4 gene (fzd4, 604579.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the frizzled 4 gene (fzd4, 604579.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1064. en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0004) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1065. en:caused by mutation in the fyve and coiled-coil domain containing-1 gene (fyco1, 607182.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fyve and coiled-coil domain containing-1 gene (fyco1, 607182.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1066. en:caused by mutation in the g-protein, alpha-stimulating 1 gene (gnas1, 139320.0035) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the g-protein, alpha-stimulating 1 gene (gnas1, 139320.0035) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1067. en:caused by mutation in the gamma g hemoglobin gene (hbg2, 142250.0025) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma g hemoglobin gene (hbg2, 142250.0025) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1068. en:caused by mutation in the gamma-2 phospholipase c gene (plcg2, 600220.0004). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma-2 phospholipase c gene (plcg2, 600220.0004). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1069. en:caused by mutation in the gamma-b crystallin gene (crygb, 123670.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma-b crystallin gene (crygb, 123670.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1070. en:caused by mutation in the gata-binding protein 1 gene (gata1, 305371.0008) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein 1 gene (gata1, 305371.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1071. en:caused by mutation in the gata-binding protein-2 gene (gata2, 137295.0009) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein-2 gene (gata2, 137295.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1072. en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1073. en:caused by mutation in the glutamine:fructose-6-phosphate aminotransferase 1 gene (gfpt1, 138292.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutamine:fructose-6-phosphate aminotransferase 1 gene (gfpt1, 138292.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1074. en:caused by mutation in the glycerate kinase gene (glyctk, 610516.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycerate kinase gene (glyctk, 610516.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1075. en:caused by mutation in the glycogen branching enzyme gene (gbe1, 607839.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycogen branching enzyme gene (gbe1, 607839.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1076. en:caused by mutation in the glycogenin-1 gene (gyg1, 603942.0003) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycogenin-1 gene (gyg1, 603942.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1077. en:caused by mutation in the guanine nucleotide-binding protein (g-protein), alpha-inhibiting activity polypeptide-3 gene (gnai3, 139370.0001]) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the guanine nucleotide-binding protein (g-protein), alpha-inhibiting activity polypeptide-3 gene (gnai3, 139370.0001]) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1078. en:caused by mutation in the hemoglobin beta gene (hbb, 141900.0437) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hemoglobin beta gene (hbb, 141900.0437) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1079. en:caused by mutation in the hepatic lipase gene (lipc, 151670.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hepatic lipase gene (lipc, 151670.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1080. en:caused by mutation in the histidyl-trna synthetase gene (hars, 142810.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the histidyl-trna synthetase gene (hars, 142810.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1081. en:caused by mutation in the homeobox b1 gene (hoxb1, 142968.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeobox b1 gene (hoxb1, 142968.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1082. en:caused by mutation in the homeobox-hb9 gene (hlxb9, 142994.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeobox-hb9 gene (hlxb9, 142994.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1083. en:caused by mutation in the homolog of chlamydomonas poc1 centriolar protein-b gene (poc1b, 614784.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of chlamydomonas poc1 centriolar protein-b gene (poc1b, 614784.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1084. en:caused by mutation in the homolog of the chlamydomonas radial spoke head 1 gene (rsph1, 609314.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the chlamydomonas radial spoke head 1 gene (rsph1, 609314.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1085. en:caused by mutation in the homolog of the drosophila diaphanous, 3, gene (diaph3, 614567.0001). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila diaphanous, 3, gene (diaph3, 614567.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1086. en:caused by mutation in the homolog of the drosophila discs large 3 gene (dlg3, 300189.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila discs large 3 gene (dlg3, 300189.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1087. en:caused by mutation in the homolog of the drosophila jagunal 1 gene (jagn1, 616012.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila jagunal 1 gene (jagn1, 616012.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1088. en:caused by mutation in the homolog of the drosophila mothers against decapentaplegic 9 gene (smad9, 603295.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila mothers against decapentaplegic 9 gene (smad9, 603295.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1089. en:caused by mutation in the homolog of the drosophila suppressor of fused gene (sufu, 607035.0007) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila suppressor of fused gene (sufu, 607035.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1090. en:caused by mutation in the homolog of the e. coli dnaj subfamily c member 19 gene (dnajc19, 608977.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the e. coli dnaj subfamily c member 19 gene (dnajc19, 608977.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1091. en:caused by mutation in the homolog of the e. coli muts, 6 gene (msh6, 600678.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the e. coli muts, 6 gene (msh6, 600678.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1092. en:caused by mutation in the homolog of the mouse peripherin 2 gene (prph2, 179605.0021) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse peripherin 2 gene (prph2, 179605.0021) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1093. en:caused by mutation in the homolog of the s. cerevisiae brf1 gene (brf1, 604902.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae brf1 gene (brf1, 604902.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1094. en:caused by mutation in the homolog of the s. cerevisiae coq2 gene (coq2, 609825.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae coq2 gene (coq2, 609825.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1095. en:caused by mutation in the homolog of the s. cerevisiae minichromosome maintenance 4 gene (mcm4, 602638.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae minichromosome maintenance 4 gene (mcm4, 602638.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1096. en:caused by mutation in the homolog of the s. cerevisiae mitochondrial translation optimization 1 gene (mto1, 614667.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae mitochondrial translation optimization 1 gene (mto1, 614667.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1097. en:caused by mutation in the homolog of the s. cerevisiae nfu1 iron-sulfur cluster scaffold gene (nfu1, 608100.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae nfu1 iron-sulfur cluster scaffold gene (nfu1, 608100.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1098. en:caused by mutation in the homolog of the s. cerevisiae precursor rna-processing factor 31 gene (prpf31, 606419.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae precursor rna-processing factor 31 gene (prpf31, 606419.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1099. en:caused by mutation in the homolog of the yeast vacuolar protein sorting 35 gene (vps35, 601501.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the yeast vacuolar protein sorting 35 gene (vps35, 601501.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1100. en:caused by mutation in the human homolog of the drosophila 'patched' gene 1 (ptch1, 601309.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the human homolog of the drosophila 'patched' gene 1 (ptch1, 601309.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1101. en:caused by mutation in the immunoglobulin mu gene (ighm, 147020.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the immunoglobulin mu gene (ighm, 147020.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1102. en:caused by mutation in the immunoglobulin-binding protein-1 gene (igbp1, 300139.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the immunoglobulin-binding protein-1 gene (igbp1, 300139.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1103. en:caused by mutation in the indian hedgehog gene (ihh, 600726.0005) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the indian hedgehog gene (ihh, 600726.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1104. en:caused by mutation in the insulin-like growth factor-1 receptor gene (igf1r, 147370.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the insulin-like growth factor-1 receptor gene (igf1r, 147370.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1105. en:caused by mutation in the integrin, alpha-2b gene (itga2b, 607759.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the integrin, alpha-2b gene (itga2b, 607759.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1106. en:caused by mutation in the integrin, beta-3 gene (itgb3, 173470.0018) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the integrin, beta-3 gene (itgb3, 173470.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1107. en:caused by mutation in the interleukin 21 receptor gene (il21r, 605383.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interleukin 21 receptor gene (il21r, 605383.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1108. en:caused by mutation in the interleukin-17 receptor d gene (il17rd, 606807.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interleukin-17 receptor d gene (il17rd, 606807.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1109. en:caused by mutation in the intestinal sodium/glucose transporter gene (slc5a1, 182380.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the intestinal sodium/glucose transporter gene (slc5a1, 182380.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1110. en:caused by mutation in the isoprenoid synthase domain-containing protein gene (ispd, 614631.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the isoprenoid synthase domain-containing protein gene (ispd, 614631.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1111. en:caused by mutation in the keratin 1 gene (krt1, 139350.0005) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 1 gene (krt1, 139350.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1112. en:caused by mutation in the keratin 10 gene (krt10, 148080.0014) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 10 gene (krt10, 148080.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1113. en:caused by mutation in the keratin 86 gene (krt86, 601928.0001). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 86 gene (krt86, 601928.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1114. en:caused by mutation in the klotho gene (kl, 604824.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the klotho gene (kl, 604824.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1115. en:caused by mutation in the kn motif- and ankyrin repeat domain-containing protein 2 gene (kank2, 614610.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kn motif- and ankyrin repeat domain-containing protein 2 gene (kank2, 614610.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1116. en:caused by mutation in the krev interaction trapped 1 gene (krit1 604214.0001). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the krev interaction trapped 1 gene (krit1 604214.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1117. en:caused by mutation in the l-3-hydroxyacyl-coa dehydrogenase gene (had, 601609.0001). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the l-3-hydroxyacyl-coa dehydrogenase gene (had, 601609.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1118. en:caused by mutation in the lamin a/c gene (lmna, 150330.0020) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin a/c gene (lmna, 150330.0020) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1119. en:caused by mutation in the lamin a/c gene (lmna, 150330.0021) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin a/c gene (lmna, 150330.0021) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1120. en:caused by mutation in the lamin a/c gene (lmna, 150330.0022) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin a/c gene (lmna, 150330.0022) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1121. en:caused by mutation in the laminin beta-3 gene (lamb3, 150310.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the laminin beta-3 gene (lamb3, 150310.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1122. en:caused by mutation in the laminin, gamma-3 gene (lamc3, 604349.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the laminin, gamma-3 gene (lamc3, 604349.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1123. en:caused by mutation in the leptin gene (lep, 164160.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leptin gene (lep, 164160.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1124. en:caused by mutation in the leucine-rich ppr motif-containing protein gene (lrpprc, 607544.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucine-rich ppr motif-containing protein gene (lrpprc, 607544.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1125. en:caused by mutation in the lipoic acid synthase gene (lias, 607031.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lipoic acid synthase gene (lias, 607031.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1126. en:caused by mutation in the makorin-3 gene (mkrn3, 603856.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the makorin-3 gene (mkrn3, 603856.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1127. en:caused by mutation in the mannosyl-oligosaccharide glucosidase gene (mogs, 601336.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mannosyl-oligosaccharide glucosidase gene (mogs, 601336.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1128. en:caused by mutation in the melanocortin-2 receptor accessory protein gene (mrap, 609196.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the melanocortin-2 receptor accessory protein gene (mrap, 609196.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1129. en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0006) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1130. en:caused by mutation in the methyl-cpg-binding domain protein 5 gene (mbd5, 611472.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methyl-cpg-binding domain protein 5 gene (mbd5, 611472.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1131. en:caused by mutation in the methyl-cpg-binding protein 2 gene (mecp2, 300005.0009). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methyl-cpg-binding protein 2 gene (mecp2, 300005.0009). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1132. en:caused by mutation in the mitochondrial aconitase gene (aco2, 100850.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial aconitase gene (aco2, 100850.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1133. en:caused by mutation in the mitochondrial phenylalanyl-trna synthetase 2 gene (fars2, 611592.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial phenylalanyl-trna synthetase 2 gene (fars2, 611592.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1134. en:caused by mutation in the mitochondrial rna-processing endoribonuclease (rmrp, 157660.0018) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial rna-processing endoribonuclease (rmrp, 157660.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1135. en:caused by mutation in the mitofusin 2 gene (mfn2, 608507.00001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitofusin 2 gene (mfn2, 608507.00001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1136. en:caused by mutation in the mmab gene (mmab, 607568.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mmab gene (mmab, 607568.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1137. en:caused by mutation in the myelin protein zero gene (mpz, 159440.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1138. en:caused by mutation in the myozenin 2 gene (myoz2, 605602.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myozenin 2 gene (myoz2, 605602.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1139. en:caused by mutation in the nadh dehydrogenase, subunit 6 gene (mtnd6, 516006.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase, subunit 6 gene (mtnd6, 516006.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1140. en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 10 gene (ndufa10, 603835.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 10 gene (ndufa10, 603835.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1141. en:caused by mutation in the nephrin gene (nphs1, 602716.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nephrin gene (nphs1, 602716.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1142. en:caused by mutation in the neurogenin 3 gene (neurog3, 604882.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neurogenin 3 gene (neurog3, 604882.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1143. en:caused by mutation in the nicotinamide nucleotide transhydrogenase gene (nnt, 607878.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nicotinamide nucleotide transhydrogenase gene (nnt, 607878.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1144. en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0021) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0021) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1145. en:caused by mutation in the nuclear receptor subfamily 3, group c, member 1 gene (nr3c1, 138040.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear receptor subfamily 3, group c, member 1 gene (nr3c1, 138040.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1146. en:caused by mutation in the nuclear receptor subfamily 5, group a, member 1 gene (nr5a1, 184757.0016) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear receptor subfamily 5, group a, member 1 gene (nr5a1, 184757.0016) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1147. en:caused by mutation in the nuclear-encoded mitochondrial thymidine kinase gene (tk2, 188250.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear-encoded mitochondrial thymidine kinase gene (tk2, 188250.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1148. en:caused by mutation in the ofd1 gene (ofd1, 300170.0007). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ofd1 gene (ofd1, 300170.0007). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1149. en:caused by mutation in the ofd1 protein gene (ofd1, 300170.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ofd1 protein gene (ofd1, 300170.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1150. en:caused by mutation in the ornithine transcarbamylase gene (otc, 311250.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ornithine transcarbamylase gene (otc, 311250.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1151. en:caused by mutation in the otogelin-like protein gene (otogl, 614925.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the otogelin-like protein gene (otogl, 614925.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1152. en:caused by mutation in the p21-activated kinase 3 gene (pak3, 300142.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the p21-activated kinase 3 gene (pak3, 300142.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1153. en:caused by mutation in the paired-like homeobox 2b gene (phox2b, 603851.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the paired-like homeobox 2b gene (phox2b, 603851.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1154. en:caused by mutation in the palladin gene (pldn, 604310.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the palladin gene (pldn, 604310.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1155. en:caused by mutation in the pancreas transcription factor 1, alpha subunit gene (ptf1a, 607094.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pancreas transcription factor 1, alpha subunit gene (ptf1a, 607094.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1156. en:caused by mutation in the paraplegin gene (spg7, 602783.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the paraplegin gene (spg7, 602783.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1157. en:caused by mutation in the peroxisome biogenesis factor-12 gene (pex12, 601758.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor-12 gene (pex12, 601758.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1158. en:caused by mutation in the peroxisome proliferator-activated receptor-gamma gene (pparg, 601487.0007) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome proliferator-activated receptor-gamma gene (pparg, 601487.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1159. en:caused by mutation in the phenylalanine hydroxylase gene (pah, 261600.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phenylalanine hydroxylase gene (pah, 261600.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1160. en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 2 gene (pik3r2, 603157.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 2 gene (pik3r2, 603157.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1161. en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 5 gene (pik3r5, 611317.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 5 gene (pik3r5, 611317.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1162. en:caused by mutation in the phosphatidylinositol glycan, class a gene (piga, 311770.0011) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol glycan, class a gene (piga, 311770.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1163. en:caused by mutation in the phosphatidylinositol glycan, class t gene (pigt, 610272.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol glycan, class t gene (pigt, 610272.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1164. en:caused by mutation in the phosphodiesterase-6g, cgmp-specific, rod, gamma gene (pde6g, 180073.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphodiesterase-6g, cgmp-specific, rod, gamma gene (pde6g, 180073.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1165. en:caused by mutation in the poliovirus receptor-like 1 gene (pvrl1, 600644.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the poliovirus receptor-like 1 gene (pvrl1, 600644.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1166. en:caused by mutation in the poliovirus receptor-like 1 gene (pvrl1, 600644.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the poliovirus receptor-like 1 gene (pvrl1, 600644.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1167. en:caused by mutation in the poly-u-binding splicing factor, 60kd gene (puf60, 604819.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the poly-u-binding splicing factor, 60kd gene (puf60, 604819.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1168. en:caused by mutation in the polymerase (dna-directed), delta 1, catalytic subunit gene (pold1, 174761.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polymerase (dna-directed), delta 1, catalytic subunit gene (pold1, 174761.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1169. en:caused by mutation in the polyribonucleotide nucleotidyltransferase 1 gene (pnpt1, 610316.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polyribonucleotide nucleotidyltransferase 1 gene (pnpt1, 610316.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1170. en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 2 gene (kcnj2, 600681.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 2 gene (kcnj2, 600681.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1171. en:caused by mutation in the pr domain-containing protein-16 gene (prdm16, 605557.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pr domain-containing protein-16 gene (prdm16, 605557.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1172. en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase gene (plod, 153454.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the procollagen-lysine, 2-oxoglutarate 5-dioxygenase gene (plod, 153454.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1173. en:caused by mutation in the prokineticin receptor-2 gene (prokr2, 607123.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prokineticin receptor-2 gene (prokr2, 607123.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1174. en:caused by mutation in the protease inhibitor 12 gene (pi12, 602445.0001). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protease inhibitor 12 gene (pi12, 602445.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1175. en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase 1 gene (pomgnt1, 606822.0013) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase 1 gene (pomgnt1, 606822.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1176. en:caused by mutation in the pterin-4-alpha-carbinolamine dehydratase 1 gene (pcbd1, 126090.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pterin-4-alpha-carbinolamine dehydratase 1 gene (pcbd1, 126090.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1177. en:caused by mutation in the pyrroline-5-carboxylate reductase 1 gene (pycr1, 179035.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pyrroline-5-carboxylate reductase 1 gene (pycr1, 179035.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1178. en:caused by mutation in the pyruvate carboxylase gene (pc, 608786.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pyruvate carboxylase gene (pc, 608786.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1179. en:caused by mutation in the ran-binding protein 2 gene (ranbp2, 601181.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ran-binding protein 2 gene (ranbp2, 601181.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1180. en:caused by mutation in the rearranged during transfection protooncogene (ret, 164761.0045) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rearranged during transfection protooncogene (ret, 164761.0045) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1181. en:caused by mutation in the receptor tyrosine kinase-like orphan receptor 2 gene (ror2, 602337.0004) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the receptor tyrosine kinase-like orphan receptor 2 gene (ror2, 602337.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1182. en:caused by mutation in the regulatory factor x, 6 gene (rfx6, 612659.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the regulatory factor x, 6 gene (rfx6, 612659.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1183. en:caused by mutation in the renin gene (ren, 179820.0004) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the renin gene (ren, 179820.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1184. en:caused by mutation in the retinol dehydrogenase 11 gene (rdh11, 607849.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the retinol dehydrogenase 11 gene (rdh11, 607849.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1185. en:caused by mutation in the rho guanine nucleotide exchange factor-6 gene (300267.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rho guanine nucleotide exchange factor-6 gene (300267.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1186. en:caused by mutation in the rho guanine-nucleotide exchange factor-10 gene (arhgef10, 608136.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rho guanine-nucleotide exchange factor-10 gene (arhgef10, 608136.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1187. en:caused by mutation in the ribose 5-phosphate isomerase a gene (rpia, 180430.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribose 5-phosphate isomerase a gene (rpia, 180430.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1188. en:caused by mutation in the ribosomal protein l26 gene (rpl26, 603704.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribosomal protein l26 gene (rpl26, 603704.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1189. en:caused by mutation in the ribosomal protein s29 gene (rps29, 603633.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribosomal protein s29 gene (rps29, 603633.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1190. en:caused by mutation in the ribosomal protein s6 kinase, 90kd, polypeptide 3 gene (rps6ka3, 300075.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribosomal protein s6 kinase, 90kd, polypeptide 3 gene (rps6ka3, 300075.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1191. en:caused by mutation in the ring finger protein 125 gene (rnf125, 610432.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ring finger protein 125 gene (rnf125, 610432.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1192. en:caused by mutation in the ryanodine receptor-2 gene (ryr2, 180902.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ryanodine receptor-2 gene (ryr2, 180902.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1193. en:caused by mutation in the s. cerevisiae homolog of mediator of rna polymerase ii transcription, subunit 25 gene (med25, 610197.0001). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the s. cerevisiae homolog of mediator of rna polymerase ii transcription, subunit 25 gene (med25, 610197.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1194. en:caused by mutation in the s. cerevisiae homolog of the required for meiotic nuclear division 1 gene (rmnd1, 614917.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the s. cerevisiae homolog of the required for meiotic nuclear division 1 gene (rmnd1, 614917.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1195. en:caused by mutation in the sal-like 4 gene (sall4, 607323.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sal-like 4 gene (sall4, 607323.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1196. en:caused by mutation in the secreted modular calcium-binding protein 2 gene (smoc2, 607223.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the secreted modular calcium-binding protein 2 gene (smoc2, 607223.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1197. en:caused by mutation in the serine active site-containing protein 1 (serac1, 614725.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the serine active site-containing protein 1 (serac1, 614725.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1198. en:caused by mutation in the serine protease inhibitor, kazal type, 5 gene (spink5, 605010.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the serine protease inhibitor, kazal type, 5 gene (spink5, 605010.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1199. en:caused by mutation in the serpin peptidase inhibitor, clade h, member 1 (serpinh1, 600943.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the serpin peptidase inhibitor, clade h, member 1 (serpinh1, 600943.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1200. en:caused by mutation in the set-binding factor 1 gene (sbf1, 603560.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the set-binding factor 1 gene (sbf1, 603560.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1201. en:caused by mutation in the set-binding protein 1 gene (setbp1, 611060.0006) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the set-binding protein 1 gene (setbp1, 611060.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1202. en:caused by mutation in the sodium channel, voltage-gated, type ix, alpha subunit gene (scn9a, 603415.0018) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sodium channel, voltage-gated, type ix, alpha subunit gene (scn9a, 603415.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1203. en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0008) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 1 gene (slc2a1, 138140.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1204. en:caused by mutation in the solute carrier family 22, member 1-like gene (slc22a1l, 602631.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 22, member 1-like gene (slc22a1l, 602631.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1205. en:caused by mutation in the solute carrier family 25 (mitochondrial carrier) member 4 gene (slc25a4, 103220.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier) member 4 gene (slc25a4, 103220.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1206. en:caused by mutation in the solute carrier family 26, member 4 gene (slc26a4, 605646.0004) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 26, member 4 gene (slc26a4, 605646.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1207. en:caused by mutation in the solute carrier family 33 (acetyl-coa transporter), member 1 gene (slc33a1, 603690.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 33 (acetyl-coa transporter), member 1 gene (slc33a1, 603690.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1208. en:caused by mutation in the solute carrier family 35, member c1 gene (slc35c1, 605881.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 35, member c1 gene (slc35c1, 605881.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1209. en:caused by mutation in the solute carrier family 35, member d1 gene (slc25d1, 610804.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 35, member d1 gene (slc25d1, 610804.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1210. en:caused by mutation in the solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene (slc7a7, 603593.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 gene (slc7a7, 603593.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1211. en:caused by mutation in the spectrin beta-1 gene (sptb, 182870.0010) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the spectrin beta-1 gene (sptb, 182870.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1212. en:caused by mutation in the speg complex locus gene (speg, 615950.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the speg complex locus gene (speg, 615950.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1213. en:caused by mutation in the sry (sex determining region y)-box 2 gene (sox2, 184427.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sry (sex determining region y)-box 2 gene (sox2, 184427.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1214. en:caused by mutation in the sry-box-10 gene (sox10, 602229.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sry-box-10 gene (sox10, 602229.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1215. en:caused by mutation in the subunit 1 phosphatase of the c-terminal domain of rna polymerase ii subunit a gene (ctdp1, 604927.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the subunit 1 phosphatase of the c-terminal domain of rna polymerase ii subunit a gene (ctdp1, 604927.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1216. en:caused by mutation in the superoxide dismutase-1 gene (sod-1, 147450.0001) susceptibility conferred by mutation in the angiogenin gene (ang, 105850.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the superoxide dismutase-1 gene (sod-1, 147450.0001) susceptibility conferred by mutation in the angiogenin gene (ang, 105850.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1217. en:caused by mutation in the surfeit 1 gene (surf1, 185620.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the surfeit 1 gene (surf1, 185620.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1218. en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1219. en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a, member 4 gene (smarca4, 603254.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily a, member 4 gene (smarca4, 603254.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1220. en:caused by mutation in the syntaxin 1b gene (stx1b, 601485.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the syntaxin 1b gene (stx1b, 601485.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1221. en:caused by mutation in the tachykinin-3 gene (tac3, 162330.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tachykinin-3 gene (tac3, 162330.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1222. en:caused by mutation in the taf2 ran polymerase ii, tata box-binding protein-associated factor, 150kd gene (taf2, 604912.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the taf2 ran polymerase ii, tata box-binding protein-associated factor, 150kd gene (taf2, 604912.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1223. en:caused by mutation in the telethonin gene (tcap, 604488.0001). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the telethonin gene (tcap, 604488.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1224. en:caused by mutation in the telomerase rna component gene (terc, 602322.0004) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the telomerase rna component gene (terc, 602322.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1225. en:caused by mutation in the tetratricopeptide repeat domain 21b gene (ttc21b, 612014.0004) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tetratricopeptide repeat domain 21b gene (ttc21b, 612014.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1226. en:caused by mutation in the thyroid hormone receptor interactor 11 gene (trip11, 604505.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thyroid hormone receptor interactor 11 gene (trip11, 604505.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1227. en:caused by mutation in the transforming growth factor, beta-induced, 68kd gene (tgfbi, 601692.0005) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transforming growth factor, beta-induced, 68kd gene (tgfbi, 601692.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1228. en:caused by mutation in the translational activator of mitochondrially encoded cytochrome c oxidase subunit 1 gene (taco1, 612958.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the translational activator of mitochondrially encoded cytochrome c oxidase subunit 1 gene (taco1, 612958.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1229. en:caused by mutation in the transmembrane mucin 1 gene (muc1, 158340.0001). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane mucin 1 gene (muc1, 158340.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1230. en:caused by mutation in the transmembrane protein 126a gene (tmem126a, 612988.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 126a gene (tmem126a, 612988.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1231. en:caused by mutation in the transmembrane protein 15 gene (tmem15, 610746.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 15 gene (tmem15, 610746.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1232. en:caused by mutation in the transmembrane protein 16e gene (tmem16e, 608662.0003) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 16e gene (tmem16e, 608662.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1233. en:caused by mutation in the transmembrane protein 231 gene (tmem231, 614949.0003) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 231 gene (tmem231, 614949.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1234. en:caused by mutation in the tropomyosin 2 gene (tpm2, 190990.0002) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tropomyosin 2 gene (tpm2, 190990.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1235. en:caused by mutation in the tumor necrosis factor receptor superfamily member 1a gene (tnfrsf1a, 191190.0001). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tumor necrosis factor receptor superfamily member 1a gene (tnfrsf1a, 191190.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1236. en:caused by mutation in the twinkle gene (c10orf2, 606075.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the twinkle gene (c10orf2, 606075.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1237. en:caused by mutation in the type iv, voltage-gated sodium channel, alpha-subunit gene (scn4a, 603967.0009) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the type iv, voltage-gated sodium channel, alpha-subunit gene (scn4a, 603967.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1238. en:caused by mutation in the tyrosinase-related protein 1 gene (tyrp1, 115501.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tyrosinase-related protein 1 gene (tyrp1, 115501.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1239. en:caused by mutation in the ubiquinol-cytochrome c reductase core protein ii gene (uqcr2, 191329.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquinol-cytochrome c reductase core protein ii gene (uqcr2, 191329.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1240. en:caused by mutation in the uridine diphosphate glycosyltransferase 1 gene (ugt1, 191740.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the uridine diphosphate glycosyltransferase 1 gene (ugt1, 191740.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1241. en:caused by mutation in the v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog (maf, 177075.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog (maf, 177075.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1242. en:caused by mutation in the vascular endothelial growth factor c gene (vegfc, 601528.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the vascular endothelial growth factor c gene (vegfc, 601528.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1243. en:caused by mutation in the voltage-dependent p/q type calcium channel alpha-1a subunit gene (cacna1a, 601011.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-dependent p/q type calcium channel alpha-1a subunit gene (cacna1a, 601011.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1244. en:caused by mutation in the von willebrand factor gene (vwf, 613160.0015) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the von willebrand factor gene (vwf, 613160.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1245. en:caused by mutation in the wt1 gene (wt1, 607102.0010) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wt1 gene (wt1, 607102.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1246. en:caused by mutation in the ww domain-containing oxidoreductase gene (wwox, 605131.0004) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ww domain-containing oxidoreductase gene (wwox, 605131.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1247. en:caused by mutation in the zeta-chain-associated protein kinase 70 gene (zap70, 176947.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zeta-chain-associated protein kinase 70 gene (zap70, 176947.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1248. en:caused by mutation in the zinc finger- and btb domain-containing protein-42 (zbtb42, 613915.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger- and btb domain-containing protein-42 (zbtb42, 613915.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1249. en:caused by mutation in the zinc metalloproteinase ste24 gene (zmpste24, 606480.0003) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc metalloproteinase ste24 gene (zmpste24, 606480.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1250. en:caused by mutations in lecithin:cholesterol acyltransferase gene (lcat, 606967.0005). --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in lecithin:cholesterol acyltransferase gene (lcat, 606967.0005). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1251. en:caused by mutations in merlin (nf2, 101000.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in merlin (nf2, 101000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1252. en:caused by mutations in the acid lysosomal sphingomyelin phosphodiesterase-1 gene (smpd1, 607608.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the acid lysosomal sphingomyelin phosphodiesterase-1 gene (smpd1, 607608.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1253. en:caused by mutations in the aldehyde dehydrogenase 3 family, member a2 gene (aldh3a2, 270200.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the aldehyde dehydrogenase 3 family, member a2 gene (aldh3a2, 270200.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1254. en:caused by mutations in the bcl6 corepressor gene (bcor, 300485.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the bcl6 corepressor gene (bcor, 300485.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1255. en:caused by mutations in the caspase 10 gene (casp10, 601762.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the caspase 10 gene (casp10, 601762.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1256. en:caused by mutations in the cystic fibrosis transmembrane conductance regulator gene (cftr, 602421.0005) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cystic fibrosis transmembrane conductance regulator gene (cftr, 602421.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1257. en:caused by mutations in the dna polymerase gamma gene (polg, 174763.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the dna polymerase gamma gene (polg, 174763.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1258. en:caused by mutations in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0010) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1259. en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the growth/differentiation factor-5 gene (gdf5, 601146.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1260. en:caused by mutations in the mitofusin 2 gene (mfn2, 608507.0009) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the mitofusin 2 gene (mfn2, 608507.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1261. en:caused by mutations in the mucolipin-1 gene (mcoln1, 605248.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the mucolipin-1 gene (mcoln1, 605248.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1262. en:caused by mutations in the n(5,10)-methylenetetrahydrofolate reductase gene (mthfr, 607093.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the n(5,10)-methylenetetrahydrofolate reductase gene (mthfr, 607093.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1263. en:caused by mutations in the nad(p)h steroid dehydrogenase-like protein gene (nsdhl, 300275.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the nad(p)h steroid dehydrogenase-like protein gene (nsdhl, 300275.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1264. en:caused by mutations in the peroxisomal biogenesis factor-7 gene (pex7, 601757.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the peroxisomal biogenesis factor-7 gene (pex7, 601757.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1265. en:caused by mutations in the phd finger protein 6 gene (phf6, 300414.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the phd finger protein 6 gene (phf6, 300414.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1266. en:caused by mutations in the plectin 1 gene (plec1, 601282.0005) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the plectin 1 gene (plec1, 601282.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1267. en:caused by mutations in the pyrin gene (mefv, 608107.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the pyrin gene (mefv, 608107.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1268. en:caused by mutations in the sclerostin gene (sost, 605740.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the sclerostin gene (sost, 605740.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1269. en:caused by mutations in the sequestosome 1 gene (sqstm1, 601530.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the sequestosome 1 gene (sqstm1, 601530.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1270. en:caused by mutations in the sh2 domain protein 1a gene (sh2d1a, 300490.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the sh2 domain protein 1a gene (sh2d1a, 300490.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1271. en:caused by mutations in the t-box 4 gene (tbx4, 601719.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the t-box 4 gene (tbx4, 601719.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1272. en:caused by solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene (slc24a1, 603617.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 gene (slc24a1, 603617.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1273. en:caused by somatic mutation in the phosphatidylinositol 3-kinase, catalytic, alpha polypeptide gene (pik3ca, 171834.0003) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the phosphatidylinositol 3-kinase, catalytic, alpha polypeptide gene (pik3ca, 171834.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1274. en:contiguous gene deletion syndrome caused by deletion (3.4 kb) of chromosome xq28 --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene deletion syndrome caused by deletion (3.4 kb) of chromosome xq28 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1275. en:rare cases secondary to chromosome translocation --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:rare cases secondary to chromosome translocation | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1276. en:susceptibility conferred by mutation in the adaptor-related protein complex 1, sigma-3 subunit gene (ap1s3, 615781.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the adaptor-related protein complex 1, sigma-3 subunit gene (ap1s3, 615781.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1277. en:susceptibility conferred by mutation in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0018) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1278. en:susceptibility conferred by mutation in the complement factor i gene (cfi, 217030.0010) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the complement factor i gene (cfi, 217030.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1279. en:susceptibility conferred by mutation in the gamma-aminobutyric acid receptor, delta gene (gabrd, 137163.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the gamma-aminobutyric acid receptor, delta gene (gabrd, 137163.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1280. en:susceptibility conferred by mutation in the methyl-cpg binding protein-2 gene (mecp2, 300005.0011) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the methyl-cpg binding protein-2 gene (mecp2, 300005.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1281. en:susceptibility conferred by mutation in the phosphatidylinositol glycan, class t gene (pigt, 610272.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the phosphatidylinositol glycan, class t gene (pigt, 610272.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1282. en:susceptibility conferred by mutation in the promoter of the nitric oxide synthase-1 gene (nos1, 163731.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the promoter of the nitric oxide synthase-1 gene (nos1, 163731.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1283. en:susceptibility conferred by mutation in the protection of telomeres 1 gene (pot1, 606478.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the protection of telomeres 1 gene (pot1, 606478.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1284. en:susceptibility conferred by mutation in the soluble adenylyl cyclase gene (sac, 605205.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the soluble adenylyl cyclase gene (sac, 605205.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1285. en:susceptibility conferred by mutation in the uncoupling protein-2 gene (ucp2, 601693.0001) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the uncoupling protein-2 gene (ucp2, 601693.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1286. en:susceptibility conferred by polymorphisms in the brain-derived neurotrophic factor gene (bdnf, 113505.0002 and 113505.0003) --- r_associated #0: 28 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by polymorphisms in the brain-derived neurotrophic factor gene (bdnf, 113505.0002 and 113505.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=28
  1287. en:a contiguous gene deletion syndrome caused by a deletion (3.9 mb) of chromosome 2p16.1-p15 --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene deletion syndrome caused by a deletion (3.9 mb) of chromosome 2p16.1-p15 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1288. en:a contiguous gene syndrome caused by deletion of the alpha-1 hemoglobin (141800) and alpha-2 hemoglobin (141850) genes --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome caused by deletion of the alpha-1 hemoglobin (141800) and alpha-2 hemoglobin (141850) genes | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1289. en:cause by mutation in the anthrax toxin receptor 1 gene (antxr1, 606410.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:cause by mutation in the anthrax toxin receptor 1 gene (antxr1, 606410.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1290. en:caused by a deletion of 11q23 --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a deletion of 11q23 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1291. en:caused by a trinucleotide repeat expansion (cag)n in the tata box-binding protein gene (tbp, 600075.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a trinucleotide repeat expansion (cag)n in the tata box-binding protein gene (tbp, 600075.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1292. en:caused by by mutations in the prophet of pit1, paired-like homeodomain transcription factor gene (prop1, 601538.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by by mutations in the prophet of pit1, paired-like homeodomain transcription factor gene (prop1, 601538.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1293. en:caused by deletion (1.7mb) of 1q41-q42 --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion (1.7mb) of 1q41-q42 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1294. en:caused by deletion of 6-12mb on 3pter-p25 --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion of 6-12mb on 3pter-p25 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1295. en:caused by duplication of 120-527kb on 17p13.3 --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of 120-527kb on 17p13.3 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1296. en:caused by mutation in serine protease 56 gene (prss56, 613858.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in serine protease 56 gene (prss56, 613858.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1297. en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase x gene (hsd17b10, 300256.0004) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 17-beta-hydroxysteroid dehydrogenase x gene (hsd17b10, 300256.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1298. en:caused by mutation in the 290-kd centrosomal protein gene (cep290, 610142.0004). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 290-kd centrosomal protein gene (cep290, 610142.0004). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1299. en:caused by mutation in the 33-kd acidic cluster protein gene (acp33, 608181.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 33-kd acidic cluster protein gene (acp33, 608181.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1300. en:caused by mutation in the acid beta glucosidase gene (gba, 606463.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the acid beta glucosidase gene (gba, 606463.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1301. en:caused by mutation in the acid beta-glucosidase gene (gba, 606463.0006) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the acid beta-glucosidase gene (gba, 606463.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1302. en:caused by mutation in the actin, alpha, skeletal muscle 1 gene (acta1, 102610.0018) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the actin, alpha, skeletal muscle 1 gene (acta1, 102610.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1303. en:caused by mutation in the actin, alpha-2, smooth muscle, aorta gene (acta2, 102620.0004) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the actin, alpha-2, smooth muscle, aorta gene (acta2, 102620.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1304. en:caused by mutation in the activin a receptor, type i gene (acvr1, 102576.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the activin a receptor, type i gene (acvr1, 102576.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1305. en:caused by mutation in the adamts-like protein 2 gene (adamtsl2, 612277.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adamts-like protein 2 gene (adamtsl2, 612277.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1306. en:caused by mutation in the adenosine deaminase gene (ada, 102700.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenosine deaminase gene (ada, 102700.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1307. en:caused by mutation in the adult folate receptor 1 gene (folr1, 136430.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adult folate receptor 1 gene (folr1, 136430.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1308. en:caused by mutation in the alanyl-trna synthetase 2 gene (aars2, 612035.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alanyl-trna synthetase 2 gene (aars2, 612035.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1309. en:caused by mutation in the aldehyde dehydrogenase 18 family, member a1 gene (aldh18a1, 138250.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aldehyde dehydrogenase 18 family, member a1 gene (aldh18a1, 138250.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1310. en:caused by mutation in the aldolase b, fructose-bisphosphate gene (aldob, 612724.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aldolase b, fructose-bisphosphate gene (aldob, 612724.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1311. en:caused by mutation in the alpha-1 gap junction protein gene (gja1, 121014.0016) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1 gap junction protein gene (gja1, 121014.0016) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1312. en:caused by mutation in the alpha-11 guanine nucleotide-binding protein gene (gna11, 139313.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-11 guanine nucleotide-binding protein gene (gna11, 139313.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1313. en:caused by mutation in the alpha-dystrobrevin gene (dtna, 601239.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-dystrobrevin gene (dtna, 601239.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1314. en:caused by mutation in the alpha-n-acetylgalactosaminidase gene (naga, 104170.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-n-acetylgalactosaminidase gene (naga, 104170.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1315. en:caused by mutation in the androgen receptor gene (ar, 313700.0020) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the androgen receptor gene (ar, 313700.0020) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1316. en:caused by mutation in the ankyrin 2 gene (ank2, 106410.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ankyrin 2 gene (ank2, 106410.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1317. en:caused by mutation in the anoctamin 5 gene gene (ano5, 608662.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the anoctamin 5 gene gene (ano5, 608662.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1318. en:caused by mutation in the anthrax toxin receptor 2 gene (antxr2, 608041.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the anthrax toxin receptor 2 gene (antxr2, 608041.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1319. en:caused by mutation in the arginine vasopressin receptor-2 gene (avpr2, 300538.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the arginine vasopressin receptor-2 gene (avpr2, 300538.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1320. en:caused by mutation in the arylsulfatase b gene (arsb, 611542.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the arylsulfatase b gene (arsb, 611542.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1321. en:caused by mutation in the asparaginyl-trna synthetase 2 gene (nars2, 612803.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the asparaginyl-trna synthetase 2 gene (nars2, 612803.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1322. en:caused by mutation in the aspartyl-trna synthetase 2 gene (dars2, 610956.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aspartyl-trna synthetase 2 gene (dars2, 610956.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1323. en:caused by mutation in the at-hook dna-binding motif-containing protein 1 gene (ahdc1, 615790.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the at-hook dna-binding motif-containing protein 1 gene (ahdc1, 615790.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1324. en:caused by mutation in the atpase, ca++ dependent, slow-twitch, cardiac muscle-2 gene (atp2a2, 108740.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, ca++ dependent, slow-twitch, cardiac muscle-2 gene (atp2a2, 108740.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1325. en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, class i, type 8b, member 1 gene (atp8b1, 602397.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1326. en:caused by mutation in the atpase, na+k+ transporting, alpha-2 polypeptide gene (atp1a2, 182340.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, na+k+ transporting, alpha-2 polypeptide gene (atp1a2, 182340.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1327. en:caused by mutation in the atpase, na+k+ transporting, alpha-3 polypeptide gene (atp1a3, 182350.0009) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, na+k+ transporting, alpha-3 polypeptide gene (atp1a3, 182350.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1328. en:caused by mutation in the axonemal dynein assembly factor 3 gene (dnaaf3, 614566.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the axonemal dynein assembly factor 3 gene (dnaaf3, 614566.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1329. en:caused by mutation in the bbs12 gene (bbs12, 610683.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bbs12 gene (bbs12, 610683.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1330. en:caused by mutation in the bbs4 gene (bbs4, 600374.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bbs4 gene (bbs4, 600374.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1331. en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0008) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1332. en:caused by mutation in the beta-1 catenin gene (ctnnb1, 116806.0017) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1 catenin gene (ctnnb1, 116806.0017) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1333. en:caused by mutation in the beta-1 galactosidase gene (glb1, 611458.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1 galactosidase gene (glb1, 611458.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1334. en:caused by mutation in the beta-3 transforming growth factor gene (tgfb3, 190230.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-3 transforming growth factor gene (tgfb3, 190230.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1335. en:caused by mutation in the beta-mannosidase gene (manba, 609489.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-mannosidase gene (manba, 609489.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1336. en:caused by mutation in the bone morphogenetic protein receptor, type 1b gene (bmpr1b, 603248.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bone morphogenetic protein receptor, type 1b gene (bmpr1b, 603248.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1337. en:caused by mutation in the bone morphogenetic protein-1 gene (bmp1, 112264.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bone morphogenetic protein-1 gene (bmp1, 112264.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1338. en:caused by mutation in the brca2 gene (brca2, 600185.0027) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the brca2 gene (brca2, 600185.0027) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1339. en:caused by mutation in the c1q- and tumor necrosis factor-related protein 5 gene (c1qtnf5, 608752.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the c1q- and tumor necrosis factor-related protein 5 gene (c1qtnf5, 608752.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1340. en:caused by mutation in the calcium-activated large conductance potassium channel subfamily m, alpha member 1 gene (kcnma1, 600150.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calcium-activated large conductance potassium channel subfamily m, alpha member 1 gene (kcnma1, 600150.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1341. en:caused by mutation in the calcium-binding protein 2 gene (cabp2, 607314.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calcium-binding protein 2 gene (cabp2, 607314.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1342. en:caused by mutation in the camp-dependent regulatory subunit 1 of protein kinase a gene (prkar1a, 188830.0015) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the camp-dependent regulatory subunit 1 of protein kinase a gene (prkar1a, 188830.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1343. en:caused by mutation in the carboxypeptidase a6 gene (cpa6, 609562.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carboxypeptidase a6 gene (cpa6, 609562.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1344. en:caused by mutation in the cardiac muscle alpha actin gene (actc1, 102540.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cardiac muscle alpha actin gene (actc1, 102540.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1345. en:caused by mutation in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0009) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1346. en:caused by mutation in the caveolin-1 gene (cav1, 601047.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the caveolin-1 gene (cav1, 601047.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1347. en:caused by mutation in the centrosome spindle pole-associated protein 1 gene (cspp1, 611654.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the centrosome spindle pole-associated protein 1 gene (cspp1, 611654.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1348. en:caused by mutation in the chromodomain helicase dna-binding protein 7 gene (chd7, 608892.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromodomain helicase dna-binding protein 7 gene (chd7, 608892.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1349. en:caused by mutation in the cln8 gene (cln8, 607837.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cln8 gene (cln8, 607837.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1350. en:caused by mutation in the coagulation factor 2 gene (f2, 176930.0009) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coagulation factor 2 gene (f2, 176930.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1351. en:caused by mutation in the coagulation factor v gene (f5, 612309.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coagulation factor v gene (f5, 612309.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1352. en:caused by mutation in the codanin 1 gene (cdan1, 607465.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the codanin 1 gene (cdan1, 607465.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1353. en:caused by mutation in the coiled-coil-helix-coiled-coil-helix domain-containing protein 10 gene (chchd10, 615903.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil-helix-coiled-coil-helix domain-containing protein 10 gene (chchd10, 615903.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1354. en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1355. en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0018) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1356. en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0009). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0009). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1357. en:caused by mutation in the collagen vi, alpha-3 polypeptide gene (col6a3, 120250.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen vi, alpha-3 polypeptide gene (col6a3, 120250.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1358. en:caused by mutation in the collagen, type vi, alpha-3 gene (col6a3, 120250.0007) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type vi, alpha-3 gene (col6a3, 120250.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1359. en:caused by mutation in the colony-stimulating factor 1 receptor gene (csf1r, 164770.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the colony-stimulating factor 1 receptor gene (csf1r, 164770.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1360. en:caused by mutation in the complement component-8, beta polypeptide gene (c8b, 120960.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement component-8, beta polypeptide gene (c8b, 120960.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1361. en:caused by mutation in the complement factor d gene (cfd, 134350.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement factor d gene (cfd, 134350.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1362. en:caused by mutation in the complement factor h gene (cfh, 134370.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement factor h gene (cfh, 134370.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1363. en:caused by mutation in the coproporphyrinogen oxidase gene (cpo, 612732.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coproporphyrinogen oxidase gene (cpo, 612732.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1364. en:caused by mutation in the cystathionine beta-synthase gene (cbs, 613381.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cystathionine beta-synthase gene (cbs, 613381.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1365. en:caused by mutation in the delta-aminolevulinate dehydratase gene (alad, 125270.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the delta-aminolevulinate dehydratase gene (alad, 125270.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1366. en:caused by mutation in the delta-aminolevulinate synthase 2 gene (alas2, 301300.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the delta-aminolevulinate synthase 2 gene (alas2, 301300.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1367. en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1368. en:caused by mutation in the desmoglein 1 gene (dsg1, 125670.0008) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the desmoglein 1 gene (dsg1, 125670.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1369. en:caused by mutation in the desmoglein 2 gene (dsg2, 125671.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the desmoglein 2 gene (dsg2, 125671.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1370. en:caused by mutation in the dicarbonyl/l-xylulose reductase gene (dcxr, 608347.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dicarbonyl/l-xylulose reductase gene (dcxr, 608347.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1371. en:caused by mutation in the dihydrolipoamide acetyltransferase gene (dlat, 608770.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dihydrolipoamide acetyltransferase gene (dlat, 608770.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1372. en:caused by mutation in the dihydropyrimidine dehydrogenase gene (dpyd, 612779.0001). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dihydropyrimidine dehydrogenase gene (dpyd, 612779.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1373. en:caused by mutation in the distal-less homeobox-5 gene (dlx5, 600028.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the distal-less homeobox-5 gene (dlx5, 600028.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1374. en:caused by mutation in the dna methyltransferase 3a gene (dnmt3a, 602769.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna methyltransferase 3a gene (dnmt3a, 602769.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1375. en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 3 gene (dnajc3, 601184.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 3 gene (dnajc3, 601184.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1376. en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 5 gene (dnajc5, 611203.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dnaj/hsp40 homolog, subfamily c, member 5 gene (dnajc5, 611203.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1377. en:caused by mutation in the dolichyl-phosphate n-acetylglucosamine phosphotransferase gene (dpagt1, 191350.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dolichyl-phosphate n-acetylglucosamine phosphotransferase gene (dpagt1, 191350.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1378. en:caused by mutation in the drosophila homolog of the mothers against decapentaplegic, 4 gene (smad4, 600993.0015) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the drosophila homolog of the mothers against decapentaplegic, 4 gene (smad4, 600993.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1379. en:caused by mutation in the dynein, axonemal, intermediate chain 1 gene (dnai1, 604366.0001). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynein, axonemal, intermediate chain 1 gene (dnai1, 604366.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1380. en:caused by mutation in the dysferlin gene (dysf, 603009.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dysferlin gene (dysf, 603009.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1381. en:caused by mutation in the endothelin-3 gene (edn3, 131242.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endothelin-3 gene (edn3, 131242.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1382. en:caused by mutation in the ephrin b1 gene (efnb1, 300035.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ephrin b1 gene (efnb1, 300035.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1383. en:caused by mutation in the epsilon-sarcoglycan gene (sgce, 604149.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the epsilon-sarcoglycan gene (sgce, 604149.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1384. en:caused by mutation in the ets2 repressor factor gene (erf, 611888.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ets2 repressor factor gene (erf, 611888.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1385. en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 3 gene (eif2b3, 606273.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation initiation factor 2b, subunit 3 gene (eif2b3, 606273.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1386. en:caused by mutation in the eukaryotic translation initiation factor 4-gamma, 1 gene (eif4g1, 600495.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation initiation factor 4-gamma, 1 gene (eif4g1, 600495.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1387. en:caused by mutation in the excision-repair cross-complementing group 6 gene (ercc6, 609413.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the excision-repair cross-complementing group 6 gene (ercc6, 609413.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1388. en:caused by mutation in the extracellular matrix protein 1 gene (ecm1, 602201.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the extracellular matrix protein 1 gene (ecm1, 602201.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1389. en:caused by mutation in the f-box and leucine-rich repeat protein 4 gene (fbxl4, 605654.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the f-box and leucine-rich repeat protein 4 gene (fbxl4, 605654.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1390. en:caused by mutation in the f-box only protein 38 gene (fbxo38, 608533.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the f-box only protein 38 gene (fbxo38, 608533.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1391. en:caused by mutation in the factor xiii alpha subunit (f13a1, 134570.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the factor xiii alpha subunit (f13a1, 134570.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1392. en:caused by mutation in the family with sequence similarity 83, member h gene (fam83h, 611927.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the family with sequence similarity 83, member h gene (fam83h, 611927.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1393. en:caused by mutation in the fancd2/fanci-associated nuclease 1 gene (fan1, 613534.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fancd2/fanci-associated nuclease 1 gene (fan1, 613534.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1394. en:caused by mutation in the fermitin family (drosophila) homolog 3 gene (fermt3, 607901.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fermitin family (drosophila) homolog 3 gene (fermt3, 607901.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1395. en:caused by mutation in the ferrochelatase gene (fech, 177000.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ferrochelatase gene (fech, 177000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1396. en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibrillin 1 gene (fbn1, 134797.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1397. en:caused by mutation in the fibrillin 2 gene (fbn2, 121050.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibrillin 2 gene (fbn2, 121050.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1398. en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0040) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0040) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1399. en:caused by mutation in the fibroblast growth factor 10 gene (fgf10, 602115.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor 10 gene (fgf10, 602115.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1400. en:caused by mutation in the fibroblast growth factor 23 gene (fgf23, 605380.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor 23 gene (fgf23, 605380.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1401. en:caused by mutation in the fibroblast growth factor receptor 1 gene (fgfr1, 136350.0011) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor 1 gene (fgfr1, 136350.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1402. en:caused by mutation in the fibroblast growth factor receptor 1 gene (fgfr1, 136350.0030) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor 1 gene (fgfr1, 136350.0030) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1403. en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1404. en:caused by mutation in the fibroblast growth factor-10 gene (fgf10, 602115.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor-10 gene (fgf10, 602115.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1405. en:caused by mutation in the fibronectin 1 gene (fn1, 135600.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibronectin 1 gene (fn1, 135600.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1406. en:caused by mutation in the filamin a gene (flna, 300017.0025) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the filamin a gene (flna, 300017.0025) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1407. en:caused by mutation in the filamin b gene (flnb, 603381.0004) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the filamin b gene (flnb, 603381.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1408. en:caused by mutation in the fk506-binding protein-14 gene (fkbp14, 614505.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fk506-binding protein-14 gene (fkbp14, 614505.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1409. en:caused by mutation in the folliculin gene (flcn, 607273.0009) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the folliculin gene (flcn, 607273.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1410. en:caused by mutation in the forkhead box c2 gene (foxc2, 602402.0007) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead box c2 gene (foxc2, 602402.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1411. en:caused by mutation in the forkhead box p3 gene (foxp3, 300292.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead box p3 gene (foxp3, 300292.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1412. en:caused by mutation in the fukutin gene (fktn, 607440.0005) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fukutin gene (fktn, 607440.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1413. en:caused by mutation in the fukutin gene (fktn, 607440.0009) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fukutin gene (fktn, 607440.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1414. en:caused by mutation in the galactokinase 1 gene (galk1, 604313.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the galactokinase 1 gene (galk1, 604313.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1415. en:caused by mutation in the gamma-aminobutyric acid receptor, gamma-2 gene (gabrg2, 137164.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma-aminobutyric acid receptor, gamma-2 gene (gabrg2, 137164.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1416. en:caused by mutation in the gap junction alpha-12 gene (gja12, 608803.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gap junction alpha-12 gene (gja12, 608803.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1417. en:caused by mutation in the gdp-mannose pyrophosphorylase a gene (gmppa, 615495.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gdp-mannose pyrophosphorylase a gene (gmppa, 615495.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1418. en:caused by mutation in the gene encoding alpha-b crystallin (cryab, 123590.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding alpha-b crystallin (cryab, 123590.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1419. en:caused by mutation in the gene encoding the beaded filament structural protein 2 (bfsp2, 603212.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding the beaded filament structural protein 2 (bfsp2, 603212.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1420. en:caused by mutation in the glutamate-ammonia ligase gene (glul, 138290.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutamate-ammonia ligase gene (glul, 138290.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1421. en:caused by mutation in the glycerol-3-phosphate dehydrogenase 1 gene (gpd1, 138420.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycerol-3-phosphate dehydrogenase 1 gene (gpd1, 138420.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1422. en:caused by mutation in the glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 gene (gpihbp1, 612757.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 gene (gpihbp1, 612757.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1423. en:caused by mutation in the glypican 6 gene (gpc6, 604404.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glypican 6 gene (gpc6, 604404.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1424. en:caused by mutation in the grainyhead-like-3 gene (grhl3, 608317.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the grainyhead-like-3 gene (grhl3, 608317.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1425. en:caused by mutation in the growth/differentiation factor-5 gene (gdf5, 601146.0013) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the growth/differentiation factor-5 gene (gdf5, 601146.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1426. en:caused by mutation in the guanine nucleotide-binding protein, alpha-stimulating activity polypeptide gene (gnas, 139320.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the guanine nucleotide-binding protein, alpha-stimulating activity polypeptide gene (gnas, 139320.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1427. en:caused by mutation in the guanine nucleotide-binding protein, beta-4 gene (gnb4, 610863.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the guanine nucleotide-binding protein, beta-4 gene (gnb4, 610863.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1428. en:caused by mutation in the guanylate cyclase 2d, membrane, retina-specific gene (gucy2d, 600179.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the guanylate cyclase 2d, membrane, retina-specific gene (gucy2d, 600179.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1429. en:caused by mutation in the heat-shock 60kd protein 1 gene (hspd1, 118190.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heat-shock 60kd protein 1 gene (hspd1, 118190.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1430. en:caused by mutation in the heparan sulfate 6-o-sulfotransferase-1 gene (hs6st1, 604846.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heparan sulfate 6-o-sulfotransferase-1 gene (hs6st1, 604846.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1431. en:caused by mutation in the heparanase-2 gene (hpse2, 613469.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heparanase-2 gene (hpse2, 613469.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1432. en:caused by mutation in the hepatocyte nuclear factor 4-alpha gene (hnf4a, 600281.0008) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hepatocyte nuclear factor 4-alpha gene (hnf4a, 600281.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1433. en:caused by mutation in the heterogeneous nuclear ribonucleoprotein d-like protein gene (hnrnpdl, 607137.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heterogeneous nuclear ribonucleoprotein d-like protein gene (hnrnpdl, 607137.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1434. en:caused by mutation in the histidyl-trna synthetase 2 gene (hars2, 600783.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the histidyl-trna synthetase 2 gene (hars2, 600783.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1435. en:caused by mutation in the homolog of drosophila sprouty-4 gene (spry4, 607984.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of drosophila sprouty-4 gene (spry4, 607984.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1436. en:caused by mutation in the homolog of s. cerevisiae cell division cycle 6 gene (cdc6, 602627.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of s. cerevisiae cell division cycle 6 gene (cdc6, 602627.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1437. en:caused by mutation in the homolog of the c. elegans unc80 gene (unc80, 612636.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the c. elegans unc80 gene (unc80, 612636.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1438. en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 140 gene (ift140, 614620.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 140 gene (ift140, 614620.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1439. en:caused by mutation in the homolog of the drosophila bicaudal d, 2 gene (bicd2, 609797.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila bicaudal d, 2 gene (bicd2, 609797.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1440. en:caused by mutation in the homolog of the drosophila dicer 1 gene (dicer1, 606241.0007). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila dicer 1 gene (dicer1, 606241.0007). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1441. en:caused by mutation in the homolog of the drosophila sine oculis-binding protein gene (sobp, 613667.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila sine oculis-binding protein gene (sobp, 613667.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1442. en:caused by mutation in the homolog of the mouse monogenic, audiogenic seizure susceptibility 1 gene (mass1, 602851.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse monogenic, audiogenic seizure susceptibility 1 gene (mass1, 602851.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1443. en:caused by mutation in the homolog of the mouse noggin gene (nog, 602991.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse noggin gene (nog, 602991.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1444. en:caused by mutation in the homolog of the mouse t brachyury gene (t, 601397.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse t brachyury gene (t, 601397.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1445. en:caused by mutation in the homolog of the s. cerevisiae alg3 gene (alg3, 608750.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae alg3 gene (alg3, 608750.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1446. en:caused by mutation in the homolog of the s. cerevisiae pet100 gene (pet100, 614770.0001). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae pet100 gene (pet100, 614770.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1447. en:caused by mutation in the homolog of the s. cerevisiae sec23 gene b (sec23b, 610512.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae sec23 gene b (sec23b, 610512.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1448. en:caused by mutation in the homolog of the yeast vacuolar protein sorting 13 gene (vps13b, 607817.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the yeast vacuolar protein sorting 13 gene (vps13b, 607817.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1449. en:caused by mutation in the homolog of the yeast vacuolar protein sorting 45 gene (vps45, 610035.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the yeast vacuolar protein sorting 45 gene (vps45, 610035.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1450. en:caused by mutation in the human homolog of the drosophila suppressor of fused gene (sufu, 607035.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the human homolog of the drosophila suppressor of fused gene (sufu, 607035.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1451. en:caused by mutation in the hydroxymethylbilane synthase gene (hmbs, 176000.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hydroxymethylbilane synthase gene (hmbs, 176000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1452. en:caused by mutation in the hyperpolarization-activated cyclic nucleotide-gated potassium channel (hcn1, 602780.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hyperpolarization-activated cyclic nucleotide-gated potassium channel (hcn1, 602780.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1453. en:caused by mutation in the immediate-early response 3-interacting protein 1 (ier3ip1, 609382.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the immediate-early response 3-interacting protein 1 (ier3ip1, 609382.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1454. en:caused by mutation in the inositol polyphosphate-5-phosphatase, 72-kd gene (inpp5e, 613037.0002). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inositol polyphosphate-5-phosphatase, 72-kd gene (inpp5e, 613037.0002). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1455. en:caused by mutation in the integrin, alpha-2b gene (itga2b, 607759.0017) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the integrin, alpha-2b gene (itga2b, 607759.0017) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1456. en:caused by mutation in the interferon-induced transmembrane protein 5 gene (ifitm5, 614757.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interferon-induced transmembrane protein 5 gene (ifitm5, 614757.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1457. en:caused by mutation in the interphotoreceptor matrix proteoglycan 2 gene (impg2, 607056.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interphotoreceptor matrix proteoglycan 2 gene (impg2, 607056.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1458. en:caused by mutation in the intestinal zinc-specific transporter gene (slc39a4, 607059.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the intestinal zinc-specific transporter gene (slc39a4, 607059.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1459. en:caused by mutation in the iq motif-containing protein b1 gene (iqcb1, 609237.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the iq motif-containing protein b1 gene (iqcb1, 609237.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1460. en:caused by mutation in the keratin 10 gene (krt10, 148080.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 10 gene (krt10, 148080.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1461. en:caused by mutation in the keratin 17 gene (krt17, 148069.0004) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 17 gene (krt17, 148069.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1462. en:caused by mutation in the keratin 5 gene (krt5, 148040.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 5 gene (krt5, 148040.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1463. en:caused by mutation in the keratin 81 gene (krt81, 602153.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 81 gene (krt81, 602153.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1464. en:caused by mutation in the ketohexokinase gene (khk, 614058.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ketohexokinase gene (khk, 614058.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1465. en:caused by mutation in the kiaa1279 gene (kiaa1279, 609367.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kiaa1279 gene (kiaa1279, 609367.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1466. en:caused by mutation in the kidney chloride channel b gene (clcnkb, 602023.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kidney chloride channel b gene (clcnkb, 602023.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1467. en:caused by mutation in the kinesin family member 21a gene (kif21a, 608283.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 21a gene (kif21a, 608283.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1468. en:caused by mutation in the lactate dehydrogenase a gene (ldha, 150000.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lactate dehydrogenase a gene (ldha, 150000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1469. en:caused by mutation in the lamin b receptor (lbr, 600024.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin b receptor (lbr, 600024.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1470. en:caused by mutation in the latent transforming growth factor-beta-binding protein 3 gene (ltbp3, 602090.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the latent transforming growth factor-beta-binding protein 3 gene (ltbp3, 602090.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1471. en:caused by mutation in the low density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0015) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the low density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1472. en:caused by mutation in the low density lipoprotein receptor-related protein-6 gene (lrp6, 603507.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the low density lipoprotein receptor-related protein-6 gene (lrp6, 603507.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1473. en:caused by mutation in the low-density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0014) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the low-density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1474. en:caused by mutation in the major facilitator superfamily domain-containing protein-8 gene (mfsd8, 611124.0008) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the major facilitator superfamily domain-containing protein-8 gene (mfsd8, 611124.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1475. en:caused by mutation in the mastermind-like domain containing 1 gene (mamld1, 300120.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mastermind-like domain containing 1 gene (mamld1, 300120.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1476. en:caused by mutation in the microtubule-associated serine/threonine kinase-like gene (mastl, 608221.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the microtubule-associated serine/threonine kinase-like gene (mastl, 608221.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1477. en:caused by mutation in the mitochondrial complex i, subunit nd6 gene (mtnd6, 516006.0005) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial complex i, subunit nd6 gene (mtnd6, 516006.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1478. en:caused by mutation in the mitochondrial enoyl-coa hydratase, short-chain, 1 gene (echs1, 602292.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial enoyl-coa hydratase, short-chain, 1 gene (echs1, 602292.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1479. en:caused by mutation in the mitochondrial genome maintenance exonuclease 1 gene (mgme1, 615076.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial genome maintenance exonuclease 1 gene (mgme1, 615076.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1480. en:caused by mutation in the mitochondrial lon peptidase-1 gene (lonp1, 605490.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial lon peptidase-1 gene (lonp1, 605490.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1481. en:caused by mutation in the molybdenum cofactor synthesis gene 2 (mocs2, 603708.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the molybdenum cofactor synthesis gene 2 (mocs2, 603708.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1482. en:caused by mutation in the myelin protein zero gene (mpz, 159440.0013) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1483. en:caused by mutation in the myelin protein zero gene (mpz, 159440.0021) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0021) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1484. en:caused by mutation in the myosin 5a gene (myo5a, 160777.0004) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin 5a gene (myo5a, 160777.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1485. en:caused by mutation in the myosin va gene (myo5a, 160777.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin va gene (myo5a, 160777.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1486. en:caused by mutation in the myosin, heavy chain 9, non-muscle gene (myh9, 160775.0005) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin, heavy chain 9, non-muscle gene (myh9, 160775.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1487. en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 3 gene (ndufs3, 603846.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 3 gene (ndufs3, 603846.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1488. en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex 11 gene (ndufa11, 612638.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex 11 gene (ndufa11, 612638.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1489. en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 2 gene (ndufa2, 602137.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 2 gene (ndufa2, 602137.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1490. en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 beta subcomplex 9 gene (ndufb9, 601445.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 beta subcomplex 9 gene (ndufb9, 601445.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1491. en:caused by mutation in the nerve growth factor-beta gene (ngfb, 162030.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nerve growth factor-beta gene (ngfb, 162030.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1492. en:caused by mutation in the neurotrophic tyrosine kinase receptor, type 1, gene (ntrk1, 191315.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neurotrophic tyrosine kinase receptor, type 1, gene (ntrk1, 191315.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1493. en:caused by mutation in the nuclear factor of kappa light chain gene enhancer in b cells inhibitor alpha gene (nfkbia, 164008.0001). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear factor of kappa light chain gene enhancer in b cells inhibitor alpha gene (nfkbia, 164008.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1494. en:caused by mutation in the oxysterol-binding protein-like protein 2 gene (osbpl2, 606731.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the oxysterol-binding protein-like protein 2 gene (osbpl2, 606731.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1495. en:caused by mutation in the paired box gene 3 (pax3, 606597.0009) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the paired box gene 3 (pax3, 606597.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1496. en:caused by mutation in the paired-like homeodomain transcription factor-1 gene (pitx1, 602149.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the paired-like homeodomain transcription factor-1 gene (pitx1, 602149.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1497. en:caused by mutation in the paired-like homeodomain transcription factor-3 gene (pitx3, 602669.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the paired-like homeodomain transcription factor-3 gene (pitx3, 602669.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1498. en:caused by mutation in the parathyroid hormone-responsive b1 gene (pthb1, 607968.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the parathyroid hormone-responsive b1 gene (pthb1, 607968.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1499. en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0010) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1500. en:caused by mutation in the phosphoribosylpyrophosphate synthetase 1 gene (prps1, 311850.0011) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoribosylpyrophosphate synthetase 1 gene (prps1, 311850.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1501. en:caused by mutation in the phosphoserine aminotransferase 1 gene (psat1, 610936.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoserine aminotransferase 1 gene (psat1, 610936.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1502. en:caused by mutation in the piezo1 ion channel gene (piezo1, 611184.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the piezo1 ion channel gene (piezo1, 611184.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1503. en:caused by mutation in the polymerase i, rna, subunit c gene (polr1c, 610060.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polymerase i, rna, subunit c gene (polr1c, 610060.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1504. en:caused by mutation in the polynucleotide kinase 3-prime phosphatase gene (pnkp, 605610.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polynucleotide kinase 3-prime phosphatase gene (pnkp, 605610.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1505. en:caused by mutation in the post-gpi attachment to proteins 1 gene (pgap1, 611655.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the post-gpi attachment to proteins 1 gene (pgap1, 611655.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1506. en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 13 gene (kcnj13, 603208.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 13 gene (kcnj13, 603208.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1507. en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 2 gene (kcnq2, 602235.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 2 gene (kcnq2, 602235.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1508. en:caused by mutation in the prion protein gene (prnp, 176640.0010) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prion protein gene (prnp, 176640.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1509. en:caused by mutation in the prokineticin-2 gene (prok2, 607002.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prokineticin-2 gene (prok2, 607002.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1510. en:caused by mutation in the propionyl coenzyme a carboxylase, beta polypeptide gene (pccb, 232050.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the propionyl coenzyme a carboxylase, beta polypeptide gene (pccb, 232050.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1511. en:caused by mutation in the prosaposin gene (psap, 176801.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prosaposin gene (psap, 176801.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1512. en:caused by mutation in the proteasome subunit, beta-type, 8 gene (psmb8, 177046.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the proteasome subunit, beta-type, 8 gene (psmb8, 177046.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1513. en:caused by mutation in the protein s gene (pros1, 176880.0010) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein s gene (pros1, 176880.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1514. en:caused by mutation in the protein s gene (psa, 176880.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein s gene (psa, 176880.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1515. en:caused by mutation in the purinergic receptor p2y, g protein-coupled, 12 gene (p2ry12, 600515.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the purinergic receptor p2y, g protein-coupled, 12 gene (p2ry12, 600515.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1516. en:caused by mutation in the rab escort protein 1 gene (chm, 300390.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rab escort protein 1 gene (chm, 300390.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1517. en:caused by mutation in the ras-associated protein rab18 gene (rab18, 602207.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ras-associated protein rab18 gene (rab18, 602207.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1518. en:caused by mutation in the recq protein-like 2 gene (recql2, 604611.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the recq protein-like 2 gene (recql2, 604611.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1519. en:caused by mutation in the regulatory factor x, 5 gene (rfx5, 601863.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the regulatory factor x, 5 gene (rfx5, 601863.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1520. en:caused by mutation in the regulatory factor x, ankyrin repeat-containing gene (rfxank, 603200.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the regulatory factor x, ankyrin repeat-containing gene (rfxank, 603200.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1521. en:caused by mutation in the renin gene (ren, 179820.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the renin gene (ren, 179820.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1522. en:caused by mutation in the ribosomal protein s19 gene (rps19, 603474.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribosomal protein s19 gene (rps19, 603474.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1523. en:caused by mutation in the rna-binding motif protein 28 gene (rbm28, 612074.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rna-binding motif protein 28 gene (rbm28, 612074.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1524. en:caused by mutation in the s-antigen gene (sag, 181031.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the s-antigen gene (sag, 181031.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1525. en:caused by mutation in the s. cerevisiae homolog of mediator of rna polymerase ii transcription, subunit 12 gene (med12, 300188.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the s. cerevisiae homolog of mediator of rna polymerase ii transcription, subunit 12 gene (med12, 300188.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1526. en:caused by mutation in the sar1, s. cerevisiae, homolog b gene (sar1b, 607690.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sar1, s. cerevisiae, homolog b gene (sar1b, 607690.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1527. en:caused by mutation in the sepiapterin reductase gene (spr, 182125.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sepiapterin reductase gene (spr, 182125.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1528. en:caused by mutation in the serine protease inhibitor, kunitz-type, 2 gene (spint2, 605124.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the serine protease inhibitor, kunitz-type, 2 gene (spint2, 605124.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1529. en:caused by mutation in the sh3 and cystein-rich domains 3 gene (stac3, 615521.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sh3 and cystein-rich domains 3 gene (stac3, 615521.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1530. en:caused by mutation in the sh3 and px domains-containing protein 2b gene (sh3pxd2b, 613293.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sh3 and px domains-containing protein 2b gene (sh3pxd2b, 613293.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1531. en:caused by mutation in the shugoshin-like-1 gene (sgol1, 609168.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the shugoshin-like-1 gene (sgol1, 609168.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1532. en:caused by mutation in the slit- and ntrk-like family, member 1 gene (slitrk1, 609678.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the slit- and ntrk-like family, member 1 gene (slitrk1, 609678.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1533. en:caused by mutation in the smad nuclear interacting protein-1 gene (snip1, 608241.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the smad nuclear interacting protein-1 gene (snip1, 608241.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1534. en:caused by mutation in the solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene (slc24a4, 609840.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 gene (slc24a4, 609840.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1535. en:caused by mutation in the solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 gene (slc24a5, 609802.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 gene (slc24a5, 609802.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1536. en:caused by mutation in the solute carrier family 3 (cystine, dibasic, and neutral amino acid transporter), member 1 gene (slc3a1, 104614.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 3 (cystine, dibasic, and neutral amino acid transporter), member 1 gene (slc3a1, 104614.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1537. en:caused by mutation in the solute carrier family 35 (udp-galactose transporter), member 2 gene (slc35a2, 314375.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 35 (udp-galactose transporter), member 2 gene (slc35a2, 314375.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1538. en:caused by mutation in the solute carrier family 9, isoform a3, regulatory factor 1 gene (slc9a3r1, 604990.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 9, isoform a3, regulatory factor 1 gene (slc9a3r1, 604990.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1539. en:caused by mutation in the solute carrier family 9, isoform a6 gene (slc9a6, 300231.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 9, isoform a6 gene (slc9a6, 300231.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1540. en:caused by mutation in the spastin gene (spg4, 604277.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the spastin gene (spg4, 604277.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1541. en:caused by mutation in the special at-rich sequence-binding protein 2 gene (satb2, 608148.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the special at-rich sequence-binding protein 2 gene (satb2, 608148.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1542. en:caused by mutation in the st3 beta-galactoside alpha-2,3-sialyltransferase 3 gene (st3gal3, 606494.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the st3 beta-galactoside alpha-2,3-sialyltransferase 3 gene (st3gal3, 606494.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1543. en:caused by mutation in the steroid 5-alpha-reductase 3 gene (srd5a3, 611715.0006). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the steroid 5-alpha-reductase 3 gene (srd5a3, 611715.0006). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1544. en:caused by mutation in the sulfite oxidase gene (suox, 606887.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sulfite oxidase gene (suox, 606887.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1545. en:caused by mutation in the surfactant pulmonary-associated protein c gene (sftpc, 178620.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the surfactant pulmonary-associated protein c gene (sftpc, 178620.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1546. en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily b, member 1 gene (smarcb1, 601607.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily b, member 1 gene (smarcb1, 601607.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1547. en:caused by mutation in the synapsin-1 gene (syn1, 313440.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the synapsin-1 gene (syn1, 313440.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1548. en:caused by mutation in the synaptic nuclear envelope protein 1 gene (syne2, 608442.0001). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the synaptic nuclear envelope protein 1 gene (syne2, 608442.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1549. en:caused by mutation in the synaptojanin-1 gene (synj1, 604297.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the synaptojanin-1 gene (synj1, 604297.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1550. en:caused by mutation in the t-cell receptor alpha chain constant region gene (trac, 186880.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the t-cell receptor alpha chain constant region gene (trac, 186880.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1551. en:caused by mutation in the tachykinin receptor-3 gene (tac3r, 162332.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tachykinin receptor-3 gene (tac3r, 162332.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1552. en:caused by mutation in the tectonic family member 3 gene (tctn3, 613847.0006) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tectonic family member 3 gene (tctn3, 613847.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1553. en:caused by mutation in the tectonic family, member 3 gene (tctn3, 613847.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tectonic family, member 3 gene (tctn3, 613847.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1554. en:caused by mutation in the thrombopoietin gene (thpo, 600044.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thrombopoietin gene (thpo, 600044.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1555. en:caused by mutation in the transforming growth factor, beta-3 gene (tgfb3, 190230.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transforming growth factor, beta-3 gene (tgfb3, 190230.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1556. en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0006) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1557. en:caused by mutation in the transmembrane protein 5 gene (tmem5, 605862.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 5 gene (tmem5, 605862.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1558. en:caused by mutation in the transmembrane protein-43 gene (tmem43, 612048.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein-43 gene (tmem43, 612048.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1559. en:caused by mutation in the transthyretin gene (ttr, 176300.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transthyretin gene (ttr, 176300.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1560. en:caused by mutation in the trf1-interacting nuclear factor 2 gene (tinf2, 604319.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the trf1-interacting nuclear factor 2 gene (tinf2, 604319.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1561. en:caused by mutation in the triadin gene (trdn, 603283.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the triadin gene (trdn, 603283.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1562. en:caused by mutation in the trio- and f-actin-binding protein (triobp, 609761.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the trio- and f-actin-binding protein (triobp, 609761.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1563. en:caused by mutation in the triosephosphate isomerase-1 gene (tpi1, 190450.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the triosephosphate isomerase-1 gene (tpi1, 190450.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1564. en:caused by mutation in the tripartite motif-containing protein 32 gene (trim32, 602290.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tripartite motif-containing protein 32 gene (trim32, 602290.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1565. en:caused by mutation in the tubulin, beta-2a gene (tubb2a, 615101.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin, beta-2a gene (tubb2a, 615101.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1566. en:caused by mutation in the tubulin, beta-4a gene (tubb4a, 602662.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin, beta-4a gene (tubb4a, 602662.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1567. en:caused by mutation in the tumor protein p73-like gene (tp73l, 603273.0011) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tumor protein p73-like gene (tp73l, 603273.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1568. en:caused by mutation in the type ix, voltage-gated sodium channel, alpha subunit gene (scn9a, 603415.0008) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the type ix, voltage-gated sodium channel, alpha subunit gene (scn9a, 603415.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1569. en:caused by mutation in the ubiquinol-cytochrome c reductase complex assembly factor 3 gene (uqcc3, 616097.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquinol-cytochrome c reductase complex assembly factor 3 gene (uqcc3, 616097.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1570. en:caused by mutation in the usherin gene (ush2a, 608400.0001). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the usherin gene (ush2a, 608400.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1571. en:caused by mutation in the v-akt murine thymoma viral oncogene homolog-2 gene (akt2, 164731.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-akt murine thymoma viral oncogene homolog-2 gene (akt2, 164731.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1572. en:caused by mutation in the very low density lipoprotein receptor (vldlr, 192977.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the very low density lipoprotein receptor (vldlr, 192977.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1573. en:caused by mutation in the von willebrand factor gene (vwf, 613160.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the von willebrand factor gene (vwf, 613160.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1574. en:caused by mutation in the wd repeat-containing protein 35 gene (wdr35, 613602.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein 35 gene (wdr35, 613602.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1575. en:caused by mutation in the wd repeat-containing protein 60 gene (wdr60, 615462.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein 60 gene (wdr60, 615462.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1576. en:caused by mutation in the wd repeat-containing protein 73 gene (wdr73, 616144.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein 73 gene (wdr73, 616144.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1577. en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1578. en:caused by mutation in the wingless-type mmtv integration site family, member 10b gene (wnt10b, 601906.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wingless-type mmtv integration site family, member 10b gene (wnt10b, 601906.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1579. en:caused by mutation in the wingless-type mmtv integration site family, member 3 gene (wnt3, 165330.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wingless-type mmtv integration site family, member 3 gene (wnt3, 165330.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1580. en:caused by mutation in the wingless-type mmtv integration site family, member 7a gene (wnt7a, 601570.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wingless-type mmtv integration site family, member 7a gene (wnt7a, 601570.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1581. en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1582. en:caused by mutation in the zinc finger mynd domain-containing protein 10 (zmynd10, 607070.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger mynd domain-containing protein 10 (zmynd10, 607070.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1583. en:caused by mutation in the zinc finger protein 41 gene (znf41, 314995.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger protein 41 gene (znf41, 314995.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1584. en:caused by mutation in the zinc metalloproteinase ste24 gene (zmpste24, 606480.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc metalloproteinase ste24 gene (zmpste24, 606480.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1585. en:caused by mutation in type ix collagen, alpha-2 polypeptide gene (col9a2, 120260.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in type ix collagen, alpha-2 polypeptide gene (col9a2, 120260.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1586. en:caused by mutations in myeloproliferative leukemia virus oncogene (mpl, 159530.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in myeloproliferative leukemia virus oncogene (mpl, 159530.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1587. en:caused by mutations in the aspartoacylase gene (aspa, 271900.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the aspartoacylase gene (aspa, 271900.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1588. en:caused by mutations in the ataxin 7 gene (sca7, 607640.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the ataxin 7 gene (sca7, 607640.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1589. en:caused by mutations in the atp-binding cassette, subfamily b, member 7 gene (abcb7, 300135.0001). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the atp-binding cassette, subfamily b, member 7 gene (abcb7, 300135.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1590. en:caused by mutations in the calcium-sensing receptor gene (casr, 601199.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the calcium-sensing receptor gene (casr, 601199.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1591. en:caused by mutations in the canalicular multispecific organic anion transporter gene (abcc2, 601107.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the canalicular multispecific organic anion transporter gene (abcc2, 601107.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1592. en:caused by mutations in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the carnitine palmitoyltransferase ii gene (cpt2, 600650.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1593. en:caused by mutations in the cystathionase gene (cth, 607657.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cystathionase gene (cth, 607657.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1594. en:caused by mutations in the low density lipoprotein receptor gene (ldlr, 143890.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the low density lipoprotein receptor gene (ldlr, 143890.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1595. en:caused by mutations in the prion protein gene (prnp, 176640.0018) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the prion protein gene (prnp, 176640.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1596. en:caused by mutations in the procollagen i n-proteinase gene (adamts2, 604539.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the procollagen i n-proteinase gene (adamts2, 604539.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1597. en:caused by mutations in the req-like dna helicase type 4 gene (reql4, 603780.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the req-like dna helicase type 4 gene (reql4, 603780.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1598. en:caused by mutations in the solute carrier family 16, monocarboxylic acid transporter, member 1 gene (slc16a1, 600682.0001). --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the solute carrier family 16, monocarboxylic acid transporter, member 1 gene (slc16a1, 600682.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1599. en:caused by mutations in the solute carrier family 17 (sodium phosphate), member 5 gene (slc17a5, 604322.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the solute carrier family 17 (sodium phosphate), member 5 gene (slc17a5, 604322.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1600. en:caused by mutations in the succinate dehydrogenase complex subunit d gene (sdhd, 602690.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the succinate dehydrogenase complex subunit d gene (sdhd, 602690.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1601. en:caused by mutations in the t-box 5 gene (tbx5, 601620.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the t-box 5 gene (tbx5, 601620.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1602. en:caused by mutations in the vitamin d receptor gene (vdr, 601769.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the vitamin d receptor gene (vdr, 601769.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1603. en:caused by mutations in the zinc finger transcription factor trps1 (trps1, 604386.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the zinc finger transcription factor trps1 (trps1, 604386.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1604. en:caused by simultaneous heterozygous mutation in both the never in mitosis gene a-related kinase 1 gene (nek1, 604588.0003) and the dynein, cytoplasmic-2, heavy chain-1 gene (dyn2ch1, 603297.0016) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by simultaneous heterozygous mutation in both the never in mitosis gene a-related kinase 1 gene (nek1, 604588.0003) and the dynein, cytoplasmic-2, heavy chain-1 gene (dyn2ch1, 603297.0016) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1605. en:caused by simultaneous homozygous mutation in both the solute carrier organic anion transporter family, member 1b1 gene (slco1b1, 604843.0001) and the solute carrier organic anion transporter family, member 1b3 gene (slco1b3, 605495.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by simultaneous homozygous mutation in both the solute carrier organic anion transporter family, member 1b1 gene (slco1b1, 604843.0001) and the solute carrier organic anion transporter family, member 1b3 gene (slco1b3, 605495.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1606. en:caused by somatic mutation in the beta-1 catenin gene (ctnnb1, 116806.0006) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the beta-1 catenin gene (ctnnb1, 116806.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1607. en:caused by the glycogenin 1 gene (gyg1, 603942.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by the glycogenin 1 gene (gyg1, 603942.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1608. en:conferred by mutation in the dual serine/threonine and tyrosine protein kinase gene (dstyk, 612666.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:conferred by mutation in the dual serine/threonine and tyrosine protein kinase gene (dstyk, 612666.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1609. en:contiguous gene deletion of 12 mb encompassing 47 genes on 1p32-p31 --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene deletion of 12 mb encompassing 47 genes on 1p32-p31 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1610. en:contiguous gene deletion syndrome caused by deletion of 300 to 500 kb between bp1 and bp2 on 15q11.2 --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene deletion syndrome caused by deletion of 300 to 500 kb between bp1 and bp2 on 15q11.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1611. en:contiguous gene syndrome caused by duplication (1.5 - 3.0 mb) of chromosome 22q11.2 --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by duplication (1.5 - 3.0 mb) of chromosome 22q11.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1612. en:contiguous gene syndrome caused by homozygous deletion of approximately 122kb on chromosome 11p15-p14 --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by homozygous deletion of approximately 122kb on chromosome 11p15-p14 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1613. en:full trisomy 21, 94% --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:full trisomy 21, 94% | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1614. en:mutation in the axis inhibitor 2 gene (axin2, 604025.0003) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:mutation in the axis inhibitor 2 gene (axin2, 604025.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1615. en:resistance conferred by mutation in the potassium large conductance calcium-activated channel, subfamily m, beta member 1 gene (kcnmb1, 603951.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:resistance conferred by mutation in the potassium large conductance calcium-activated channel, subfamily m, beta member 1 gene (kcnmb1, 603951.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1616. en:susceptibility conferred by deletion that includes the complement factor h-related 1 gene (cfhr1, 134371.0001) and complement factor h-related 3 gene (cfhr3, 605366.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by deletion that includes the complement factor h-related 1 gene (cfhr1, 134371.0001) and complement factor h-related 3 gene (cfhr3, 605366.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1617. en:susceptibility conferred by mutation in the complement factor i gene (cfi, 217030.0004) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the complement factor i gene (cfi, 217030.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1618. en:susceptibility conferred by mutation in the dynactin 1 gene (dctn1, 601143.0002) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the dynactin 1 gene (dctn1, 601143.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1619. en:susceptibility conferred by mutation in the major histocompatibility complex, class i, c gene (hla-c, 142840.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the major histocompatibility complex, class i, c gene (hla-c, 142840.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1620. en:susceptibility conferred by mutation in the peripherin gene (prph, 170710.0001) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the peripherin gene (prph, 170710.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1621. en:susceptibility conferred by mutation in the tumor protein p53 gene (tp53, 191170.0042) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the tumor protein p53 gene (tp53, 191170.0042) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1622. en:susceptibility conferred by mutations in the mhc class ii transactivator gene (mhc2ta, 600005.0007) --- r_associated #0: 27 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutations in the mhc class ii transactivator gene (mhc2ta, 600005.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=27
  1623. en:(prph2, 179605.0008) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:(prph2, 179605.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1624. en:a contiguous gene syndrome caused by deletion of 180kb encompassing 18 genes on chromosome 17p13.1 --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome caused by deletion of 180kb encompassing 18 genes on chromosome 17p13.1 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1625. en:associated with snps in the b-cell cll/lymphoma 11a gene (bcl11a, 606557.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:associated with snps in the b-cell cll/lymphoma 11a gene (bcl11a, 606557.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1626. en:cause by mutation in the homolog of the s. cerevisiae alg2 gene (alg2, 607905.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:cause by mutation in the homolog of the s. cerevisiae alg2 gene (alg2, 607905.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1627. en:caused by a trinucleotide repeat expansion (ctg)n in the ataxin 8 opposite strand gene (atxn8os, 603680.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a trinucleotide repeat expansion (ctg)n in the ataxin 8 opposite strand gene (atxn8os, 603680.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1628. en:caused by deletion of 1.5mb on 3q29 encompassing 22 genes --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion of 1.5mb on 3q29 encompassing 22 genes | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1629. en:caused by deletion of 3.0-30.0mb on 14q11-q22 --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion of 3.0-30.0mb on 14q11-q22 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1630. en:caused by duplication of 186-260kb on 16p13.3 --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of 186-260kb on 16p13.3 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1631. en:caused by epigenetic changes of dna hypomethylation at the h19/igf2-imprinting control region (icr1, 616186) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by epigenetic changes of dna hypomethylation at the h19/igf2-imprinting control region (icr1, 616186) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1632. en:caused by fusion of the fip1-like 1 gene (fip1l1, 607686) and the platelet-derived growth factor receptor-alpha gene (pdgfra, 173490) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by fusion of the fip1-like 1 gene (fip1l1, 607686) and the platelet-derived growth factor receptor-alpha gene (pdgfra, 173490) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1633. en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0014) and the gap junction protein, beta-3 gene (gjb3, 603324.0011) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0014) and the gap junction protein, beta-3 gene (gjb3, 603324.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1634. en:caused by mutation in the 11-beta-hydroxysteroid dehydrogenase type 1 gene (hsd11b1, 600713.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 11-beta-hydroxysteroid dehydrogenase type 1 gene (hsd11b1, 600713.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1635. en:caused by mutation in the 65-kd yes-associated protein-1 gene (yap1, 606608.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 65-kd yes-associated protein-1 gene (yap1, 606608.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1636. en:caused by mutation in the acid beta-glucocerebrosidase gene (gba, 606643.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the acid beta-glucocerebrosidase gene (gba, 606643.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1637. en:caused by mutation in the activation-induced cytidine deaminase gene (aicda, 605257.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the activation-induced cytidine deaminase gene (aicda, 605257.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1638. en:caused by mutation in the adenosine kinase gene (adk, 102750.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenosine kinase gene (adk, 102750.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1639. en:caused by mutation in the aldehyde dehydrogenase 1 family, member a3 gene (aldh1a3, 600463.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aldehyde dehydrogenase 1 family, member a3 gene (aldh1a3, 600463.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1640. en:caused by mutation in the alkylglycerone-phosphate synthase gene (agps, 603051.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alkylglycerone-phosphate synthase gene (agps, 603051.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1641. en:caused by mutation in the alpha subunit of the voltage-gated sodium channel type i gene (scn1a, 182389.0007) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha subunit of the voltage-gated sodium channel type i gene (scn1a, 182389.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1642. en:caused by mutation in the alpha-tectorin gene (tecta, 602574.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-tectorin gene (tecta, 602574.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1643. en:caused by mutation in the aminoacyl-trna synthetase complex-interacting multifunctional protein 1 gene (aimp1, 603605.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aminoacyl-trna synthetase complex-interacting multifunctional protein 1 gene (aimp1, 603605.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1644. en:caused by mutation in the amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene (agl, 610860.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the amylo-1,6-glucosidase, 4-alpha-glucanotransferase gene (agl, 610860.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1645. en:caused by mutation in the amyloid precursor protein gene (app, 104760.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the amyloid precursor protein gene (app, 104760.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1646. en:caused by mutation in the androgen receptor gene (ar, 313700.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the androgen receptor gene (ar, 313700.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1647. en:caused by mutation in the apoptosis-inducing factor, mitochondrion-associated, 1 gene (aifm1, 300169.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the apoptosis-inducing factor, mitochondrion-associated, 1 gene (aifm1, 300169.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1648. en:caused by mutation in the ataxia-telangiectasia mutated gene (atm, 607585.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ataxia-telangiectasia mutated gene (atm, 607585.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1649. en:caused by mutation in the atlastin gtpase 3 gene (atl3, 609369.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atlastin gtpase 3 gene (atl3, 609369.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1650. en:caused by mutation in the atp-binding cassette, subfamily a, member 12 gene (abca12, 607800.0006) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily a, member 12 gene (abca12, 607800.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1651. en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1652. en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0005) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1653. en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1654. en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0012) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily c, member 8 gene (abcc8, 600509.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1655. en:caused by mutation in the atp-binding cassette, subfamily d, member 4 gene (abcd4, 603214.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily d, member 4 gene (abcd4, 603214.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1656. en:caused by mutation in the atp-binding cassette, subfamily g, member 8 gene (abcg8, 605460.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily g, member 8 gene (abcg8, 605460.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1657. en:caused by mutation in the atpase, cu++ transporting, alpha polypeptide gene (atp7a, 300011.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, cu++ transporting, alpha polypeptide gene (atp7a, 300011.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1658. en:caused by mutation in the atpase, cu++ transporting, beta polypeptide gene (atp7b, 277900.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, cu++ transporting, beta polypeptide gene (atp7b, 277900.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1659. en:caused by mutation in the atpase, na+k+ transporting, alpha-2 polypeptide gene (atp1a2, 182340.0005) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, na+k+ transporting, alpha-2 polypeptide gene (atp1a2, 182340.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1660. en:caused by mutation in the bbs10 gene (bbs10, 610148.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bbs10 gene (bbs10, 610148.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1661. en:caused by mutation in the beta subunit of the nonvoltage-gated sodium channel 1 gene (scnn1b, 600760.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta subunit of the nonvoltage-gated sodium channel 1 gene (scnn1b, 600760.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1662. en:caused by mutation in the beta-1 laminin gene (lamb1, 150240.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1 laminin gene (lamb1, 150240.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1663. en:caused by mutation in the beta-1,3-n-acetylgalactosaminyltransferase 2 gene (b3galnt2, 610194.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1,3-n-acetylgalactosaminyltransferase 2 gene (b3galnt2, 610194.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1664. en:caused by mutation in the beta-2 transforming growth factor gene (tgfb2, 190220.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-2 transforming growth factor gene (tgfb2, 190220.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1665. en:caused by mutation in the beta-2-microglobulin gene (b2m, 109700.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-2-microglobulin gene (b2m, 109700.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1666. en:caused by mutation in the beta-b3 crystallin gene (crybb3, 123630.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-b3 crystallin gene (crybb3, 123630.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1667. en:caused by mutation in the beta-tubulin gene (tubb, 191130.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-tubulin gene (tubb, 191130.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1668. en:caused by mutation in the biliverdin reductase a gene (blvra, 109750.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the biliverdin reductase a gene (blvra, 109750.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1669. en:caused by mutation in the brain-derived neurotrophic factor gene (bdnf, 113505.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the brain-derived neurotrophic factor gene (bdnf, 113505.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1670. en:caused by mutation in the bridging integrator 1 gene (bin1, 601248.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bridging integrator 1 gene (bin1, 601248.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1671. en:caused by mutation in the budding uninhibited by benzimidazoles 1 beta gene (bub1b, 602860.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the budding uninhibited by benzimidazoles 1 beta gene (bub1b, 602860.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1672. en:caused by mutation in the c8orf38 gene (c8orf38, 612392.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the c8orf38 gene (c8orf38, 612392.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1673. en:caused by mutation in the camp-dependent protein kinase, catalytic, gamma gene (prkacg, 176893.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the camp-dependent protein kinase, catalytic, gamma gene (prkacg, 176893.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1674. en:caused by mutation in the camp-dependent protein kinase, regulatory, type i, alpha gene (prkar1a, 188830.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the camp-dependent protein kinase, regulatory, type i, alpha gene (prkar1a, 188830.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1675. en:caused by mutation in the cancer susceptibility candidate 5 gene (casc5, 609173.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cancer susceptibility candidate 5 gene (casc5, 609173.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1676. en:caused by mutation in the carbonic anhydrase xii gene (ca12, 603263.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carbonic anhydrase xii gene (ca12, 603263.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1677. en:caused by mutation in the casein kinase 1, delta, gene (csnk1d, 600864.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the casein kinase 1, delta, gene (csnk1d, 600864.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1678. en:caused by mutation in the caspase recruitment domain-containing protein 11 gene (card11, 607210.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the caspase recruitment domain-containing protein 11 gene (card11, 607210.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1679. en:caused by mutation in the cathepsin c gene (ctsc, 602365.0012) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cathepsin c gene (ctsc, 602365.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1680. en:caused by mutation in the cd19 antigen gene (cd191, 107265.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd19 antigen gene (cd191, 107265.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1681. en:caused by mutation in the cdk5 regulatory subunit-associated protein 2 gene (cdk5rap2, 608201.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cdk5 regulatory subunit-associated protein 2 gene (cdk5rap2, 608201.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1682. en:caused by mutation in the centromeric protein e gene (cenpe, 117143.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the centromeric protein e gene (cenpe, 117143.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1683. en:caused by mutation in the centromeric protein j gene (cenpj, 609279.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the centromeric protein j gene (cenpj, 609279.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1684. en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1685. en:caused by mutation in the cholinergic receptor, nicotinic, alpha polypeptide-1, muscle gene (chrna1, 100690.0013) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, alpha polypeptide-1, muscle gene (chrna1, 100690.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1686. en:caused by mutation in the chromosome 21 open reading frame 59 gene (c21orf59, 615494.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 21 open reading frame 59 gene (c21orf59, 615494.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1687. en:caused by mutation in the chromosome 21 open reading frame-2 gene (c21orf2, 603191.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 21 open reading frame-2 gene (c21orf2, 603191.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1688. en:caused by mutation in the chromosome 5 open reading frame 42 gene (c5orf42, 614571.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 5 open reading frame 42 gene (c5orf42, 614571.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1689. en:caused by mutation in the claudin 16 gene (cldn16, 603959.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the claudin 16 gene (cldn16, 603959.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1690. en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0005) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1691. en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1692. en:caused by mutation in the collagen, type xxv, alpha-1 gene (col25a1, 610004.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type xxv, alpha-1 gene (col25a1, 610004.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1693. en:caused by mutation in the collagen, type xxvii, alpha-1 gene (col27a1, 608461.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type xxvii, alpha-1 gene (col27a1, 608461.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1694. en:caused by mutation in the complement factor h-related 5 gene (cfhr5, 608593.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement factor h-related 5 gene (cfhr5, 608593.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1695. en:caused by mutation in the complex i, subunit nd4l gene (mtnd4l, 516004.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complex i, subunit nd4l gene (mtnd4l, 516004.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1696. en:caused by mutation in the complex iv, cytochrome c oxidase subunit i gene (mtco1, 516030.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complex iv, cytochrome c oxidase subunit i gene (mtco1, 516030.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1697. en:caused by mutation in the creatine transporter gene (slc6a8, 300036.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the creatine transporter gene (slc6a8, 300036.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1698. en:caused by mutation in the cullin 3 gene (cul3, 603136.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cullin 3 gene (cul3, 603136.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1699. en:caused by mutation in the cyclin m2 gene (cnnm2, 607803.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclin m2 gene (cnnm2, 607803.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1700. en:caused by mutation in the cyclin o gene (ccno, 607752.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclin o gene (ccno, 607752.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1701. en:caused by mutation in the cyclin-dependent kinase inhibitor 1c gene (cdkn1c, 600856.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclin-dependent kinase inhibitor 1c gene (cdkn1c, 600856.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1702. en:caused by mutation in the cysteine- and glycine-rich protein 3 gene (csrp3, 600824.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cysteine- and glycine-rich protein 3 gene (csrp3, 600824.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1703. en:caused by mutation in the cytochrome c oxidase subunit 15 gene (cox15, 603646) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase subunit 15 gene (cox15, 603646) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1704. en:caused by mutation in the ddhd domain-containing protein 2 gene (ddhd2, 615003.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ddhd domain-containing protein 2 gene (ddhd2, 615003.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1705. en:caused by mutation in the dead/h box-11 gene (ddx11, 601150.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dead/h box-11 gene (ddx11, 601150.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1706. en:caused by mutation in the dehydrogenase e1 and transketolase domains-containing protein 1 (dhtkd1, 614984.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dehydrogenase e1 and transketolase domains-containing protein 1 (dhtkd1, 614984.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1707. en:caused by mutation in the desmoplakin gene (dsp, 125647.0008) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the desmoplakin gene (dsp, 125647.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1708. en:caused by mutation in the dihydrofolate reductase gene (dhfr, 126060.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dihydrofolate reductase gene (dhfr, 126060.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1709. en:caused by mutation in the dolichyl-phosphate mannosyltransferase 2, regulatory subunit gene (dpm2, 603564.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dolichyl-phosphate mannosyltransferase 2, regulatory subunit gene (dpm2, 603564.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1710. en:caused by mutation in the dolichyl-phosphate n-acetylglucosamine phosphotransferase gene (dpagt1, 191350.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dolichyl-phosphate n-acetylglucosamine phosphotransferase gene (dpagt1, 191350.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1711. en:caused by mutation in the dynein, axonemal, light chain 1 gene (dnal1, 610062.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynein, axonemal, light chain 1 gene (dnal1, 610062.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1712. en:caused by mutation in the ecto-5-prime nucleotidase gene (nt5e, 129190.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ecto-5-prime nucleotidase gene (nt5e, 129190.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1713. en:caused by mutation in the ectonucleotide pyrophosphatase/phosphodiesterase-1 gene (enpp1, 173335.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ectonucleotide pyrophosphatase/phosphodiesterase-1 gene (enpp1, 173335.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1714. en:caused by mutation in the edar-associated death domain gene (edaradd, 606603.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the edar-associated death domain gene (edaradd, 606603.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1715. en:caused by mutation in the egf-containing fibulin-like extracellular matrix protein-2 gene (efemp2, 604633.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the egf-containing fibulin-like extracellular matrix protein-2 gene (efemp2, 604633.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1716. en:caused by mutation in the erythrocytic protein 4.2 gene (epb42, 177070.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the erythrocytic protein 4.2 gene (epb42, 177070.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1717. en:caused by mutation in the estrogen receptor-1 gene (esr1, 133430.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the estrogen receptor-1 gene (esr1, 133430.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1718. en:caused by mutation in the eukaryotic translation elongation factor 1, alpha-2 gene (eef1a2, 602959.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation elongation factor 1, alpha-2 gene (eef1a2, 602959.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1719. en:caused by mutation in the eukaryotic translation initiation factor 4a, isoform 3, gene (eif4a3, 608546.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation initiation factor 4a, isoform 3, gene (eif4a3, 608546.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1720. en:caused by mutation in the evc gene (evc, 604831.0006) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the evc gene (evc, 604831.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1721. en:caused by mutation in the exosome component 8 gene (exosc8, 606019.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the exosome component 8 gene (exosc8, 606019.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1722. en:caused by mutation in the f-box only protein 31 gene (fbxo31, 609102.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the f-box only protein 31 gene (fbxo31, 609102.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1723. en:caused by mutation in the family with sequence similarity 123, member b gene (fam123b, 300647.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the family with sequence similarity 123, member b gene (fam123b, 300647.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1724. en:caused by mutation in the family with sequence similarity 20, member c gene (fam20c, 611061.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the family with sequence similarity 20, member c gene (fam20c, 611061.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1725. en:caused by mutation in the ferritin light chain gene (ftl, 134790.0018) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ferritin light chain gene (ftl, 134790.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1726. en:caused by mutation in the fez family zinc finger protein-1 gene (fezf1, 613301.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fez family zinc finger protein-1 gene (fezf1, 613301.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1727. en:caused by mutation in the fibrillin 2 gene (fbn2, 612570.0011) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibrillin 2 gene (fbn2, 612570.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1728. en:caused by mutation in the fibroblast growth factor gene-14 (fgf14, 601515.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor gene-14 (fgf14, 601515.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1729. en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0007) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1730. en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0015) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1731. en:caused by mutation in the filamin a gene (flna, 300017.0011) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the filamin a gene (flna, 300017.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1732. en:caused by mutation in the forkhead box p1 gene (foxp1, 605515.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead box p1 gene (foxp1, 605515.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1733. en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1734. en:caused by mutation in the g protein-coupled receptor 98 gene (gpr98, 602851.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the g protein-coupled receptor 98 gene (gpr98, 602851.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1735. en:caused by mutation in the gamma-1 actin gene (actg1, 102560.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma-1 actin gene (actg1, 102560.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1736. en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606598.0006) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606598.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1737. en:caused by mutation in the gap junction protein, beta-2, 26kd gene (gjb2, 121011.0012) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gap junction protein, beta-2, 26kd gene (gjb2, 121011.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1738. en:caused by mutation in the gap junction protein, beta-2, 26kd gene (gjb2, 121011.0015) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gap junction protein, beta-2, 26kd gene (gjb2, 121011.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1739. en:caused by mutation in the gata zinc finger domain-containing protein-1 gene (gatad1, 614518.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata zinc finger domain-containing protein-1 gene (gatad1, 614518.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1740. en:caused by mutation in the gata-binding protein 2 gene (gata2, 137295.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein 2 gene (gata2, 137295.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1741. en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0018) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein-4 gene (gata4, 600576.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1742. en:caused by mutation in the gene atp-binding cassette, subfamily a, member 5 gene (abca5, 612503.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene atp-binding cassette, subfamily a, member 5 gene (abca5, 612503.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1743. en:caused by mutation in the gene encoding growth/differentiation factor-2 (gdf2, 605120.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding growth/differentiation factor-2 (gdf2, 605120.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1744. en:caused by mutation in the gene encoding interleukin 10 receptor, beta (il10rb, 123889.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding interleukin 10 receptor, beta (il10rb, 123889.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1745. en:caused by mutation in the glycyl trna synthetase gene (gars, 600287.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycyl trna synthetase gene (gars, 600287.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1746. en:caused by mutation in the goosecoid homeobox gene (gsc, 138890.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the goosecoid homeobox gene (gsc, 138890.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1747. en:caused by mutation in the growth/differentiation factor 1 gene (gdf1, 602880.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the growth/differentiation factor 1 gene (gdf1, 602880.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1748. en:caused by mutation in the gtp cyclohydrolase 1 gene (gch1, 600225.0017) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gtp cyclohydrolase 1 gene (gch1, 600225.0017) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1749. en:caused by mutation in the gtp-binding protein 3 gene (gtpbp3, 608536.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gtp-binding protein 3 gene (gtpbp3, 608536.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1750. en:caused by mutation in the hamartin gene (tsc1, 605284.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hamartin gene (tsc1, 605284.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1751. en:caused by mutation in the hepatocyte nuclear factor-1-beta gene (tcf2, 189907.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hepatocyte nuclear factor-1-beta gene (tcf2, 189907.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1752. en:caused by mutation in the hexokinase-1 gene (hk1, 142600.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hexokinase-1 gene (hk1, 142600.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1753. en:caused by mutation in the high-mobility group box 3 gene (hmgb3, 300193.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the high-mobility group box 3 gene (hmgb3, 300193.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1754. en:caused by mutation in the histidine triad nucleotide-binding protein 1 gene (hint1, 601314.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the histidine triad nucleotide-binding protein 1 gene (hint1, 601314.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1755. en:caused by mutation in the histone deacetylase 8 gene (hdac8, 300269.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the histone deacetylase 8 gene (hdac8, 300269.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1756. en:caused by mutation in the homeobox d13 gene (hoxd13, 142989.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeobox d13 gene (hoxd13, 142989.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1757. en:caused by mutation in the homeobox d13 gene (hoxd13, 142989.0008). --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeobox d13 gene (hoxd13, 142989.0008). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1758. en:caused by mutation in the homolog of drosophila mindbomb-1 gene (mib1, 608677.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of drosophila mindbomb-1 gene (mib1, 608677.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1759. en:caused by mutation in the homolog of the a. nidulans nude 1 gene (nde1, 609449.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the a. nidulans nude 1 gene (nde1, 609449.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1760. en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 80 gene (ift80, 611177.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 80 gene (ift80, 611177.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1761. en:caused by mutation in the homolog of the drosophila achaete-scute complex, 1 gene (ascl1, 100790.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila achaete-scute complex, 1 gene (ascl1, 100790.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1762. en:caused by mutation in the homolog of the drosophila orthodenticle 2 gene (otx2, 600038.0006) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila orthodenticle 2 gene (otx2, 600038.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1763. en:caused by mutation in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1764. en:caused by mutation in the homolog of the s. cerevisiae coq6 gene (coq6, 614647.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae coq6 gene (coq6, 614647.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1765. en:caused by mutation in the homolog of the s. cerevisiae coq9 gene (coq9, 612837.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae coq9 gene (coq9, 612837.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1766. en:caused by mutation in the homolog of the s. cerevisiae fig4 gene (fig4, 609390.0016) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae fig4 gene (fig4, 609390.0016) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1767. en:caused by mutation in the homolog of the s. cerevisiae trna splicing endonuclease 54 gene (tsen54, 608755.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae trna splicing endonuclease 54 gene (tsen54, 608755.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1768. en:caused by mutation in the hps3 gene (hps3, 606118) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hps3 gene (hps3, 606118) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1769. en:caused by mutation in the hps6 gene (hps6, 607522) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hps6 gene (hps6, 607522) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1770. en:caused by mutation in the il2-inducible t-cell kinase gene (itk, 186973.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the il2-inducible t-cell kinase gene (itk, 186973.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1771. en:caused by mutation in the immunoglobulin lambda-like polypeptide 1 gene (igll1, 146770.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the immunoglobulin lambda-like polypeptide 1 gene (igll1, 146770.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1772. en:caused by mutation in the immunoglobulin mu-binding protein 2 gene (ighmbp2, 600502.0010) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the immunoglobulin mu-binding protein 2 gene (ighmbp2, 600502.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1773. en:caused by mutation in the immunoglobulin superfamily, member 1 gene (igsf1, 300137.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the immunoglobulin superfamily, member 1 gene (igsf1, 300137.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1774. en:caused by mutation in the inositol monophosphatase domain-containing protein 1 gene (impad1, 614010.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inositol monophosphatase domain-containing protein 1 gene (impad1, 614010.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1775. en:caused by mutation in the insulin-like growth factor-1 gene (igf1, 147440.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the insulin-like growth factor-1 gene (igf1, 147440.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1776. en:caused by mutation in the insulin-like growth factor-binding protein-7 gene (igfbp7, 602867.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the insulin-like growth factor-binding protein-7 gene (igfbp7, 602867.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1777. en:caused by mutation in the integral membrane protein-2b gene (itm2b, 603904.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the integral membrane protein-2b gene (itm2b, 603904.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1778. en:caused by mutation in the interferon, alpha, beta, and omega, receptor 2 gene (irnar2, 602376.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interferon, alpha, beta, and omega, receptor 2 gene (irnar2, 602376.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1779. en:caused by mutation in the interferon-induced helicase c domain-containing protein 1 gene (ifih1, 606951.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interferon-induced helicase c domain-containing protein 1 gene (ifih1, 606951.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1780. en:caused by mutation in the interleukin 17 receptor c gene (ir17rc, 610925.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interleukin 17 receptor c gene (ir17rc, 610925.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1781. en:caused by mutation in the interleukin receptor gamma chain gene (il2rg, 308380.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interleukin receptor gamma chain gene (il2rg, 308380.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1782. en:caused by mutation in the inwardly rectifying potassium channel, subfamily j, member 6 gene (kcnj6, 600877.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inwardly rectifying potassium channel, subfamily j, member 6 gene (kcnj6, 600877.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1783. en:caused by mutation in the iroquois homeobox protein-5 gene (irx5, 606195.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the iroquois homeobox protein-5 gene (irx5, 606195.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1784. en:caused by mutation in the isoprenoid synthase domain-containing protein gene (ispd, 614641.0014) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the isoprenoid synthase domain-containing protein gene (ispd, 614641.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1785. en:caused by mutation in the janus kinase 2 gene (jak2, 147796.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the janus kinase 2 gene (jak2, 147796.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1786. en:caused by mutation in the keratin 5 gene (krt5, 148040.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 5 gene (krt5, 148040.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1787. en:caused by mutation in the kinesin family member 11 gene (kif11, 148760.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 11 gene (kif11, 148760.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1788. en:caused by mutation in the kinesin family member 22 gene (kif22, 603213.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 22 gene (kif22, 603213.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1789. en:caused by mutation in the l-3-hydroxyacyl-coa dehydrogenase gene (hadh, 601609.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the l-3-hydroxyacyl-coa dehydrogenase gene (hadh, 601609.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1790. en:caused by mutation in the l1 cell adhesion molecule gene (l1cam, 308840.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the l1 cell adhesion molecule gene (l1cam, 308840.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1791. en:caused by mutation in the l1 cell adhesion molecule gene (l1cam, 308840.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the l1 cell adhesion molecule gene (l1cam, 308840.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1792. en:caused by mutation in the la ribonucleoprotein domain family, member 7 gene (larp7, 612026.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the la ribonucleoprotein domain family, member 7 gene (larp7, 612026.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1793. en:caused by mutation in the lamin a/c gene (lmna, 150330.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin a/c gene (lmna, 150330.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1794. en:caused by mutation in the laminin alpha-3 gene (lama3, 600805.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the laminin alpha-3 gene (lama3, 600805.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1795. en:caused by mutation in the laminin beta-2 gene (lamb2, 150325.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the laminin beta-2 gene (lamb2, 150325.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1796. en:caused by mutation in the lecithin retinol acyltransferase gene (lrat, 604863.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lecithin retinol acyltransferase gene (lrat, 604863.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1797. en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1798. en:caused by mutation in the lysosome associated membrane protein-2 gene (lamp2, 309060.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lysosome associated membrane protein-2 gene (lamp2, 309060.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1799. en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0008) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1800. en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1801. en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0009) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mevalonate kinase gene (mvk, 251170.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1802. en:caused by mutation in the mitochondrial complex i, subunit nd4 gene (mtnd4, 516003.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial complex i, subunit nd4 gene (mtnd4, 516003.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1803. en:caused by mutation in the mitochondrial methionyl-trna formyltransferase gene (mtfmt, 611766.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial methionyl-trna formyltransferase gene (mtfmt, 611766.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1804. en:caused by mutation in the mitochondrial transfer rna glutamine gene (mttq, 590030.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial transfer rna glutamine gene (mttq, 590030.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1805. en:caused by mutation in the mitochondrial transfer rna lysine gene (mttk, 590060.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial transfer rna lysine gene (mttk, 590060.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1806. en:caused by mutation in the mitochondrial trna serine 1 gene (mtts1, 590080.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial trna serine 1 gene (mtts1, 590080.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1807. en:caused by mutation in the mitochondrial trna-serine 2 gene (mtts2, 590085.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial trna-serine 2 gene (mtts2, 590085.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1808. en:caused by mutation in the mkks gene (mkks, 604896.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mkks gene (mkks, 604896.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1809. en:caused by mutation in the molybdenum cofactor synthesis gene 1 (mocs1, 603707.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the molybdenum cofactor synthesis gene 1 (mocs1, 603707.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1810. en:caused by mutation in the myelin protein zero gene (mpz, 159440.0017) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0017) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1811. en:caused by mutation in the myelin protein zero gene (mpz, 159440.0018) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1812. en:caused by mutation in the myosin, heavy chain 9, nonmuscle gene (myh9, 160775.0008) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin, heavy chain 9, nonmuscle gene (myh9, 160775.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1813. en:caused by mutation in the n-acetylglucosamine-6-sulfatase gene (gns, 607664.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the n-acetylglucosamine-6-sulfatase gene (gns, 607664.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1814. en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 1 gene (ndufs1, 157655.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 1 gene (ndufs1, 157655.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1815. en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 3 gene (ndufv3, 603846.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 3 gene (ndufv3, 603846.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1816. en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 4 gene (ndufs4, 602694.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 4 gene (ndufs4, 602694.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1817. en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 7 gene (ndufs7, 601825.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 7 gene (ndufs7, 601825.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1818. en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 8 gene (ndufs8, 602141.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 8 gene (ndufs8, 602141.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1819. en:caused by mutation in the nata catalytic subunit n-alpha-acetyltransferase-10 gene (naa10, 300013.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nata catalytic subunit n-alpha-acetyltransferase-10 gene (naa10, 300013.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1820. en:caused by mutation in the natriuretic peptide precursor a gene (nppa, 108780.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the natriuretic peptide precursor a gene (nppa, 108780.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1821. en:caused by mutation in the natriuretic peptide precursor-a gene (nppa, 108780.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the natriuretic peptide precursor-a gene (nppa, 108780.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1822. en:caused by mutation in the nephrocystin 1 gene (nphp1, 607100.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nephrocystin 1 gene (nphp1, 607100.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1823. en:caused by mutation in the nephrocystin 4 gene (nphp4, 607215.0006) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nephrocystin 4 gene (nphp4, 607215.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1824. en:caused by mutation in the neurofilament light chain gene (nefl, 162280.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neurofilament light chain gene (nefl, 162280.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1825. en:caused by mutation in the ninein gene (nin, 608684.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ninein gene (nin, 608684.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1826. en:caused by mutation in the nonerythrocytic alpha-spectrin 1 gene (sptan1, 182810.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nonerythrocytic alpha-spectrin 1 gene (sptan1, 182810.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1827. en:caused by mutation in the nonerythrocytic beta-spectrin 2 gene (sptbn2, 604985.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nonerythrocytic beta-spectrin 2 gene (sptbn2, 604985.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1828. en:caused by mutation in the nonmuscle myosin heavy chain 14 gene (myh14, 608568.0006) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nonmuscle myosin heavy chain 14 gene (myh14, 608568.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1829. en:caused by mutation in the nuclear factor i/x gene (nfix, 164005.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear factor i/x gene (nfix, 164005.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1830. en:caused by mutation in the nuclear receptor binding set domain protein 1 (nsd1, 606681.0011) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear receptor binding set domain protein 1 (nsd1, 606681.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1831. en:caused by mutation in the nuclear-encoded mitochondrial deoxyguanosine kinase gene (dguok, 601465.0001). --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear-encoded mitochondrial deoxyguanosine kinase gene (dguok, 601465.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1832. en:caused by mutation in the nyctalopin gene (nyx, 300278.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nyctalopin gene (nyx, 300278.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1833. en:caused by mutation in the paired box homeotic gene 2 (pax2, 167409.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the paired box homeotic gene 2 (pax2, 167409.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1834. en:caused by mutation in the pancreas/duodenum homeobox protein 1 gene (pdx1, 600733.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pancreas/duodenum homeobox protein 1 gene (pdx1, 600733.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1835. en:caused by mutation in the pantothenate kinase-2 gene (pank2, 607157.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pantothenate kinase-2 gene (pank2, 607157.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1836. en:caused by mutation in the patatin-like phospholipase domain-containing protein 6 (pnpla6, 603197.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the patatin-like phospholipase domain-containing protein 6 (pnpla6, 603197.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1837. en:caused by mutation in the periaxin gene (prx, 605725.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the periaxin gene (prx, 605725.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1838. en:caused by mutation in the pericentrin 2 gene (pcnt2, 605925.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pericentrin 2 gene (pcnt2, 605925.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1839. en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0006) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peripheral myelin protein-22 gene (pmp22, 601097.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1840. en:caused by mutation in the peroxisome biogenesis factor-5 gene (pex5, 600414.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor-5 gene (pex5, 600414.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1841. en:caused by mutation in the peroxisome biogenesis factor-6 gene (pex6, 601498.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor-6 gene (pex6, 601498.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1842. en:caused by mutation in the phosphate regulating endopeptidase homolog, x-linked, gene (phex, 300550.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphate regulating endopeptidase homolog, x-linked, gene (phex, 300550.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1843. en:caused by mutation in the phosphatidylinositol glycan, class m gene (pigm, 610273.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol glycan, class m gene (pigm, 610273.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1844. en:caused by mutation in the phosphatidylinositol glycan, class w gene (pigw, 610275.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol glycan, class w gene (pigw, 610275.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1845. en:caused by mutation in the phosphoglucomutase-1 gene (pgm1, 171900.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoglucomutase-1 gene (pgm1, 171900.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1846. en:caused by mutation in the phosphoglycerate dehydrogenase gene (phgdh, 606879.0007) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoglycerate dehydrogenase gene (phgdh, 606879.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1847. en:caused by mutation in the phospholipase c, epsilon-1 gene (plce1, 608414.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phospholipase c, epsilon-1 gene (plce1, 608414.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1848. en:caused by mutation in the phosphoserine phosphatase gene (psph, 172480.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoserine phosphatase gene (psph, 172480.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1849. en:caused by mutation in the platelet glycoprotein ib, alpha polypeptide, gene (gp1ba, 606672.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the platelet glycoprotein ib, alpha polypeptide, gene (gp1ba, 606672.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1850. en:caused by mutation in the polymerase (dna-directed), delta 1, catalytic subunit gene (pold1, 174761.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polymerase (dna-directed), delta 1, catalytic subunit gene (pold1, 174761.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1851. en:caused by mutation in the polynucleotide kinase 3-prime phosphatase gene (pnkp, 605610.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polynucleotide kinase 3-prime phosphatase gene (pnkp, 605610.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1852. en:caused by mutation in the porcupine, drosophila, homolog of gene (porcn, 300651.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the porcupine, drosophila, homolog of gene (porcn, 300651.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1853. en:caused by mutation in the potassium channel tetramerization domain-containing 1 (kctd1, 613420.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium channel tetramerization domain-containing 1 (kctd1, 613420.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1854. en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 607542.0032) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 607542.0032) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1855. en:caused by mutation in the pou domain, class 3, transcription factor 4 gene (pou3f4, 300039.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pou domain, class 3, transcription factor 4 gene (pou3f4, 300039.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1856. en:caused by mutation in the prenyl diphosphate synthase, subunit 2 gene (pdss2, 610564.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prenyl diphosphate synthase, subunit 2 gene (pdss2, 610564.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1857. en:caused by mutation in the presenilin-2 gene (psen2, 600759.0008) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the presenilin-2 gene (psen2, 600759.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1858. en:caused by mutation in the presynaptic glycine transporter-2 gene (slc6a5, 604159.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the presynaptic glycine transporter-2 gene (slc6a5, 604159.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1859. en:caused by mutation in the protein c gene (proc, 612283.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein c gene (proc, 612283.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1860. en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1861. en:caused by mutation in the purine nucleoside phosphorylase gene (pnp, 164050.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the purine nucleoside phosphorylase gene (pnp, 164050.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1862. en:caused by mutation in the quinoid dihydropteridine reductase gene (qdpr, 612676.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the quinoid dihydropteridine reductase gene (qdpr, 612676.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1863. en:caused by mutation in the r-spondin family, member 4 gene (rspo4, 610573.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the r-spondin family, member 4 gene (rspo4, 610573.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1864. en:caused by mutation in the rab3 gtpase-activating protein subunit 2 gene (rab3gap2, 609275.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rab3 gtpase-activating protein subunit 2 gene (rab3gap2, 609275.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1865. en:caused by mutation in the rab6-interacting golgin gene (gorab, 607893.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rab6-interacting golgin gene (gorab, 607893.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1866. en:caused by mutation in the radixin gene (rdx, 179410.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the radixin gene (rdx, 179410.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1867. en:caused by mutation in the recombinase activating gene 1 (rag1, 179615.0005) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the recombinase activating gene 1 (rag1, 179615.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1868. en:caused by mutation in the retinal rod photoreceptor cgmp phosphodiesterase, beta subunit gene (pde6b, 180072.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the retinal rod photoreceptor cgmp phosphodiesterase, beta subunit gene (pde6b, 180072.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1869. en:caused by mutation in the retinol-binding protein-4 gene (rbp4, 180250.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the retinol-binding protein-4 gene (rbp4, 180250.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1870. en:caused by mutation in the retinoschisin gene (rs1, 300839.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the retinoschisin gene (rs1, 300839.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1871. en:caused by mutation in the ribonucleotide reductase, m2 b gene (rrm2b, 604712.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribonucleotide reductase, m2 b gene (rrm2b, 604712.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1872. en:caused by mutation in the rp1-like protein 1 gene (rp1l1, 608581.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rp1-like protein 1 gene (rp1l1, 608581.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1873. en:caused by mutation in the s. cerevisiae homolog of trna splicing endonuclease 54 (tsen54, 608755.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the s. cerevisiae homolog of trna splicing endonuclease 54 (tsen54, 608755.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1874. en:caused by mutation in the sclerostin gene (sost, 605740.0005) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sclerostin gene (sost, 605740.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1875. en:caused by mutation in the septin 9 gene (sept9, 604061.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the septin 9 gene (sept9, 604061.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1876. en:caused by mutation in the serine palmitoyltransferase, long-chain base subunit 2 gene (sptlc2, 605713.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the serine palmitoyltransferase, long-chain base subunit 2 gene (sptlc2, 605713.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1877. en:caused by mutation in the sh3 domain and tetratricopeptide repeat domain 2 gene (sh3tc2, 608206.0005) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sh3 domain and tetratricopeptide repeat domain 2 gene (sh3tc2, 608206.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1878. en:caused by mutation in the signal sequence receptor, delta gene (ssr4, 300090.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the signal sequence receptor, delta gene (ssr4, 300090.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1879. en:caused by mutation in the signal transducer and activator of transcription 1 gene (stat1, 600555.0008) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the signal transducer and activator of transcription 1 gene (stat1, 600555.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1880. en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 10 gene (slc2a10, 606145.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 2 (facilitated glucose transporter), member 10 gene (slc2a10, 606145.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1881. en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, aralar), member 12 gene (slc25a12, 603667.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, aralar), member 12 gene (slc25a12, 603667.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1882. en:caused by mutation in the solute carrier family 25 (mitochondrial citrate transporter), member 1 gene (slc25a1, 190315.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (mitochondrial citrate transporter), member 1 gene (slc25a1, 190315.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1883. en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 8 gene (slc26a8, 608480.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 26 (sulfate transporter), member 8 gene (slc26a8, 608480.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1884. en:caused by mutation in the solute carrier family 26, member 3 gene (slc26a3, 126650.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 26, member 3 gene (slc26a3, 126650.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1885. en:caused by mutation in the solute carrier family 34 (sodium phosphate cotransporter), member 1 gene (slc34a1, 182309.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 34 (sodium phosphate cotransporter), member 1 gene (slc34a1, 182309.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1886. en:caused by mutation in the solute carrier family 34 (sodium/phosphate cotransporter), member 1 gene (slc34a1, 182309.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 34 (sodium/phosphate cotransporter), member 1 gene (slc34a1, 182309.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1887. en:caused by mutation in the somatic cytochrome c gene (cycs, 123970.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the somatic cytochrome c gene (cycs, 123970.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1888. en:caused by mutation in the son of sevenless gene (sos1, 182530.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the son of sevenless gene (sos1, 182530.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1889. en:caused by mutation in the sonic hedgehog gene (shh, 600725.0014) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sonic hedgehog gene (shh, 600725.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1890. en:caused by mutation in the sprt-like n-terminal domain-protein gene (splrtn, 616086.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sprt-like n-terminal domain-protein gene (splrtn, 616086.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1891. en:caused by mutation in the sterile alpha motif domain-containing protein-9 gene (samd9, 610456.0001). --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sterile alpha motif domain-containing protein-9 gene (samd9, 610456.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1892. en:caused by mutation in the steroid sulfatase gene (sts, 300747.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the steroid sulfatase gene (sts, 300747.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1893. en:caused by mutation in the sterol 3-beta-hydroxysteroid-delta-5-desaturase gene (sc5dl, 602286.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sterol 3-beta-hydroxysteroid-delta-5-desaturase gene (sc5dl, 602286.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1894. en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605921.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605921.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1895. en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily 1, member 1 gene (smarce1, 603111.0002). --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily 1, member 1 gene (smarce1, 603111.0002). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1896. en:caused by mutation in the t-box 3 gene (tbx3, 601621.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the t-box 3 gene (tbx3, 601621.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1897. en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1898. en:caused by mutation in the tbc1 domain family, member 7 gene (tbc1d7, 612655.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tbc1 domain family, member 7 gene (tbc1d7, 612655.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1899. en:caused by mutation in the tectonic family, member 1 gene (tctn1, 609863.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tectonic family, member 1 gene (tctn1, 609863.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1900. en:caused by mutation in the transcription factor-12 gene (tcf12, 600480.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transcription factor-12 gene (tcf12, 600480.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1901. en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0006) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1902. en:caused by mutation in the trna-specific adenosine deaminase 3 gene (adat3, 615302.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the trna-specific adenosine deaminase 3 gene (adat3, 615302.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1903. en:caused by mutation in the type iii voltage-gated sodium channel beta subunit gene (scn3b, 608214.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the type iii voltage-gated sodium channel beta subunit gene (scn3b, 608214.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1904. en:caused by mutation in the type v collagen, alpha-2 gene (col5a2, 120190.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the type v collagen, alpha-2 gene (col5a2, 120190.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1905. en:caused by mutation in the ubiquitin protein ligase e3a gene (ube3a, 601623.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquitin protein ligase e3a gene (ube3a, 601623.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1906. en:caused by mutation in the ubiquitin-conjugating enzyme e2a gene (ube2a, 312180.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquitin-conjugating enzyme e2a gene (ube2a, 312180.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1907. en:caused by mutation in the uroporphyrinogen iii cosynthase gene (uros, 606938.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the uroporphyrinogen iii cosynthase gene (uros, 606938.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1908. en:caused by mutation in the uv-stimulated scaffold protein a gene (uvssa, 614632.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the uv-stimulated scaffold protein a gene (uvssa, 614632.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1909. en:caused by mutation in the v-maf musculoaponeurotic fibrosarcoma oncogene family, protein b gene (mafb, 608968.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-maf musculoaponeurotic fibrosarcoma oncogene family, protein b gene (mafb, 608968.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1910. en:caused by mutation in the vhl gene (vhl, 608537.0014) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the vhl gene (vhl, 608537.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1911. en:caused by mutation in the voltage-gated sodium channel 9 alpha-subunit gene (scn9a, 603415.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated sodium channel 9 alpha-subunit gene (scn9a, 603415.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1912. en:caused by mutation in the voltage-gated sodium channel, type viii, alpha subunit gene (scn8a, 600702.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated sodium channel, type viii, alpha subunit gene (scn8a, 600702.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1913. en:caused by mutation in the wd repeat-containing protein-35 gene (wdr35, 613602.0005) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein-35 gene (wdr35, 613602.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1914. en:caused by mutation in the wfs1 gene (606201) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wfs1 gene (606201) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1915. en:caused by mutation in the whirlin gene (whrn, 607928.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the whirlin gene (whrn, 607928.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1916. en:caused by mutation in the ww domain-containing oxidoreductase gene (wwox, 605131.0002) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ww domain-containing oxidoreductase gene (wwox, 605131.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1917. en:caused by mutation in the zic family member 3 gene (zic3, 300265.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zic family member 3 gene (zic3, 300265.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1918. en:caused by mutation in the zinc finger fyve domain-containing protein 26 (zfyve26, 612012.0001). --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger fyve domain-containing protein 26 (zfyve26, 612012.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1919. en:caused by mutation in the zinc finger protein 423 gene (znf423, 604557.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger protein 423 gene (znf423, 604557.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1920. en:caused by mutation in the zona pellucida glycoprotein-1 gene (zp1, 195000.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zona pellucida glycoprotein-1 gene (zp1, 195000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1921. en:caused by mutations in receptor tyrosine kinase-like orphan receptor 2 gene (ror2, 602337.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in receptor tyrosine kinase-like orphan receptor 2 gene (ror2, 602337.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1922. en:caused by mutations in the cellular retinaldehyde-binding protein-1 gene (rlbp1, 180090.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cellular retinaldehyde-binding protein-1 gene (rlbp1, 180090.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1923. en:caused by mutations in the cyclin-dependent kinase inhibitor 2a gene (cdkn2a, 600160.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cyclin-dependent kinase inhibitor 2a gene (cdkn2a, 600160.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1924. en:caused by mutations in the flj90140 gene (flj90130, 607461.0005) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the flj90140 gene (flj90130, 607461.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1925. en:caused by mutations in the homolog of the mouse noggin gene (nog, 602991.0013) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the homolog of the mouse noggin gene (nog, 602991.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1926. en:caused by mutations in the lim homeo box transcription factor 1, beta gene (lmx1b, 602575.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the lim homeo box transcription factor 1, beta gene (lmx1b, 602575.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1927. en:caused by mutations in the low density lipoprotein receptor-related protein-5 gene (lrp5, 603506.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the low density lipoprotein receptor-related protein-5 gene (lrp5, 603506.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1928. en:caused by mutations in the paired-like homeodomain transcription factor-2 gene (pitx2, 601542.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the paired-like homeodomain transcription factor-2 gene (pitx2, 601542.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1929. en:caused by mutations in the ret protoncogene (ret, 1645761.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the ret protoncogene (ret, 1645761.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1930. en:caused by mutations in the ryanodine receptor gene (ryr1, 180901.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the ryanodine receptor gene (ryr1, 180901.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1931. en:caused by mutations in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0009) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1932. en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0018). --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0018). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1933. en:caused by somatic deletion of 1 allele of the ribosomal protein s14 gene (rps14, 130620) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic deletion of 1 allele of the ribosomal protein s14 gene (rps14, 130620) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1934. en:caused by somatic mutation in the neuroblastoma ras viral oncogene homolog gene (nras, 164790.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the neuroblastoma ras viral oncogene homolog gene (nras, 164790.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1935. en:caused by trinucleotide repeat expansion (cgg)n in the fragile site mental retardation gene (fmr1, 309550.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by trinucleotide repeat expansion (cgg)n in the fragile site mental retardation gene (fmr1, 309550.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1936. en:caused by triplication of the alpha-synuclein gene (snca, 163890.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by triplication of the alpha-synuclein gene (snca, 163890.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1937. en:hcs is a contiguous gene syndrome caused by 23.8-75.5kb deletion containing the slc3a1 (104614) and prepl (609557) genes --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:hcs is a contiguous gene syndrome caused by 23.8-75.5kb deletion containing the slc3a1 (104614) and prepl (609557) genes | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1938. en:molecular basis --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:molecular basis | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1939. en:remainder of cases secondary to maternal disomy --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:remainder of cases secondary to maternal disomy | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1940. en:susceptibility associated with variants in the frizzled-related protein gene (frzb, 605083.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility associated with variants in the frizzled-related protein gene (frzb, 605083.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1941. en:susceptibility conferred by mutation in the breast cancer 1 gene (brca1, 113705.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the breast cancer 1 gene (brca1, 113705.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1942. en:susceptibility conferred by mutation in the cd46 antigen gene (cd46, 120920.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the cd46 antigen gene (cd46, 120920.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1943. en:susceptibility conferred by mutation in the homolog of the drosophila bicaudal c gene (bicc1, 614295.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the homolog of the drosophila bicaudal c gene (bicc1, 614295.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1944. en:susceptibility conferred by mutation in the inwardly rectifying potassium channel, subfamily j, member 18 gene (kcnj18, 613236.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the inwardly rectifying potassium channel, subfamily j, member 18 gene (kcnj18, 613236.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1945. en:susceptibility conferred by mutation in the nucleotide-binding oligomerization domain protein 2 gene (nod2, 605956.0001) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the nucleotide-binding oligomerization domain protein 2 gene (nod2, 605956.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1946. en:susceptibility conferred by mutation in the solute carrier family 12 (potassium/chloride transporter), member 5 gene (slc12a5, 606726.0004) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the solute carrier family 12 (potassium/chloride transporter), member 5 gene (slc12a5, 606726.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1947. en:susceptibility conferred by mutation in the transforming growth factor-beta receptor, type i gene (tgfbr1, 190181.0009). --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the transforming growth factor-beta receptor, type i gene (tgfbr1, 190181.0009). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1948. en:susceptibility conferred by mutations in the matrilin-3 gene (matn3, 602109.0003) --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutations in the matrilin-3 gene (matn3, 602109.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1949. en:translocation 21, 3.3% --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:translocation 21, 3.3% | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1950. en:translocation of cellular oncogene c-abl (189980) to the bcr gene on chromosome 22 resulting in chimeric brc-abl gene --- r_associated #0: 26 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:translocation of cellular oncogene c-abl (189980) to the bcr gene on chromosome 22 resulting in chimeric brc-abl gene | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=26
  1951. en:a contiguous gene deletion syndrome involving deletion of 1.4mb on chromosome 17q11.2 --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene deletion syndrome involving deletion of 1.4mb on chromosome 17q11.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1952. en:a contiguous gene syndrome caused by deletion of the friend leukemia virus integration 1 gene (fli1, 193067) and perhaps other genes in 11q23 --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome caused by deletion of the friend leukemia virus integration 1 gene (fli1, 193067) and perhaps other genes in 11q23 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1953. en:a contiguous gene syndrome involving deletion of the digeorge syndrome chromosome region (dgcr) involving mutations in tup-like enhancer of split 1 (tuple1, 600237) and digeorge critical region gene 2 (dgcr2, 600594) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome involving deletion of the digeorge syndrome chromosome region (dgcr) involving mutations in tup-like enhancer of split 1 (tuple1, 600237) and digeorge critical region gene 2 (dgcr2, 600594) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1954. en:associated with mutation in the beta-1 catenin gene (ctnnb1, 116806.0013) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:associated with mutation in the beta-1 catenin gene (ctnnb1, 116806.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1955. en:caused by a 260-kb duplication on chromosome 11q12.2-11q12.3. --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a 260-kb duplication on chromosome 11q12.2-11q12.3. | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1956. en:caused by a deletion of chromosome 9p --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a deletion of chromosome 9p | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1957. en:caused by a trinucleotide repeat expansion (cag)n in the huntingtin gene (htt, 613004.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a trinucleotide repeat expansion (cag)n in the huntingtin gene (htt, 613004.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1958. en:caused by a trinucleotide repeat expansion cag(n) in the junctophilin-3 gene (jph3, 605268.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a trinucleotide repeat expansion cag(n) in the junctophilin-3 gene (jph3, 605268.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1959. en:caused by deletion (4.06 mb) of chromosome 14q22.1-q22.3 --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion (4.06 mb) of chromosome 14q22.1-q22.3 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1960. en:caused by deletion of 1.0-2.5mb on chromosome 17q12 --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion of 1.0-2.5mb on chromosome 17q12 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1961. en:caused by duplication of 1.0-2.5mb on chromosome 17q12 --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of 1.0-2.5mb on chromosome 17q12 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1962. en:caused by duplication of 294 kb to 2.7 mb including the prkaca gene on chromosome 19p13 --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of 294 kb to 2.7 mb including the prkaca gene on chromosome 19p13 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1963. en:caused by duplication of at least 325kb on 10q24 --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of at least 325kb on 10q24 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1964. en:caused by expanded cag trinucleotide repeats in the ataxin-2 gene (atx2, 601517.0001). --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by expanded cag trinucleotide repeats in the ataxin-2 gene (atx2, 601517.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1965. en:caused by mutation in cyclin-dependent kinase inhibitor 2a (cdkn2a, 600160.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in cyclin-dependent kinase inhibitor 2a (cdkn2a, 600160.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1966. en:caused by mutation in subunit a of the neuronal voltage-gated sodium channel gene (scn1a, 182389.0012) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in subunit a of the neuronal voltage-gated sodium channel gene (scn1a, 182389.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1967. en:caused by mutation in the 5-hydroxytryptamine receptor-1a gene (htr1a, 109760.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 5-hydroxytryptamine receptor-1a gene (htr1a, 109760.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1968. en:caused by mutation in the abhydrolase domain containing-5 gene (abhd5, 604780.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the abhydrolase domain containing-5 gene (abhd5, 604780.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1969. en:caused by mutation in the activity-dependent neuroprotector homeobox gene (adnp, 611386.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the activity-dependent neuroprotector homeobox gene (adnp, 611386.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1970. en:caused by mutation in the adenomatous polyposis coli gene (apc, 611731.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenomatous polyposis coli gene (apc, 611731.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1971. en:caused by mutation in the adenylate cyclase-1, brain gene (adcy1, 103072.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenylate cyclase-1, brain gene (adcy1, 103072.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1972. en:caused by mutation in the alkaline phosphatase gene (alpl, 171760.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alkaline phosphatase gene (alpl, 171760.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1973. en:caused by mutation in the alpha subunit of the hydroxyacyl-coa dehydrogenase/3-ketoacyl-coa thiolase/enoyl-coa hydratase (hadha, 600890.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha subunit of the hydroxyacyl-coa dehydrogenase/3-ketoacyl-coa thiolase/enoyl-coa hydratase (hadha, 600890.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1974. en:caused by mutation in the alpha-4 laminin gene (lama4, 600133.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-4 laminin gene (lama4, 600133.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1975. en:caused by mutation in the alsin gene (als2, 606352.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alsin gene (als2, 606352.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1976. en:caused by mutation in the arginine vasopressin receptor 2 gene (avpr2, 300538.0021) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the arginine vasopressin receptor 2 gene (avpr2, 300538.0021) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1977. en:caused by mutation in the arginyl-trna synthetase 1 gene (rars, 107820.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the arginyl-trna synthetase 1 gene (rars, 107820.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1978. en:caused by mutation in the arylsulfatase a gene (arsa, 607574.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the arylsulfatase a gene (arsa, 607574.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1979. en:caused by mutation in the ataxia-telangiectasia and rad3-related gene (atr, 601215.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ataxia-telangiectasia and rad3-related gene (atr, 601215.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1980. en:caused by mutation in the atlastin-1 gene (atl1, 606439.0010) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atlastin-1 gene (atl1, 606439.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1981. en:caused by mutation in the atp-binding cassette, subfamily c, member 9 gene (abcc9, 601439.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily c, member 9 gene (abcc9, 601439.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1982. en:caused by mutation in the atp-binding cassette, subfamily d, member 1 gene (abcd1, 300371.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily d, member 1 gene (abcd1, 300371.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1983. en:caused by mutation in the atpase, class i, type 8a, member 2 gene (atp8a2, 605870.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, class i, type 8a, member 2 gene (atp8a2, 605870.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1984. en:caused by mutation in the b-cell receptor-associated protein 31 gene (bcap31, 300398.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the b-cell receptor-associated protein 31 gene (bcap31, 300398.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1985. en:caused by mutation in the barrier-to-autointegration factor-1 gene (banf1, 603811.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the barrier-to-autointegration factor-1 gene (banf1, 603811.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1986. en:caused by mutation in the basic helix-loop-helix domain-containing protein class b, 3 gene (bhlhb3, 606200.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the basic helix-loop-helix domain-containing protein class b, 3 gene (bhlhb3, 606200.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1987. en:caused by mutation in the beta filamin b gene (flnb, 603381.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta filamin b gene (flnb, 603381.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1988. en:caused by mutation in the branched chain keto acid dehydrogenase e1, beta polypeptide gene (bckdhb, 248611.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the branched chain keto acid dehydrogenase e1, beta polypeptide gene (bckdhb, 248611.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1989. en:caused by mutation in the bruton tyrosine kinase gene (btk, 300300.0004) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bruton tyrosine kinase gene (btk, 300300.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1990. en:caused by mutation in the c homolog of the s. cerevisiae rad51 gene (rad51c, 602774.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the c homolog of the s. cerevisiae rad51 gene (rad51c, 602774.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1991. en:caused by mutation in the cadherin 23 gene (cdh23, 605516.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cadherin 23 gene (cdh23, 605516.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1992. en:caused by mutation in the calcium-sensing receptor gene (casr, 601199.0004) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calcium-sensing receptor gene (casr, 601199.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1993. en:caused by mutation in the cbp/p300-interacting transactivator, with glu/asp-rich c-terminal domain, 2 gene (cited2, 602937.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cbp/p300-interacting transactivator, with glu/asp-rich c-terminal domain, 2 gene (cited2, 602937.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1994. en:caused by mutation in the cd3 antigen, delta subunit gene (cd3d, 186790.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd3 antigen, delta subunit gene (cd3d, 186790.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1995. en:caused by mutation in the cd3 antigen, gamma subunit gene (cd3g, 186740.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd3 antigen, gamma subunit gene (cd3g, 186740.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1996. en:caused by mutation in the cd8 antigen, alpha polypeptide gene (cd8a, 186910.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd8 antigen, alpha polypeptide gene (cd8a, 186910.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1997. en:caused by mutation in the ceramide synthase 3 gene (cers3, 615276.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ceramide synthase 3 gene (cers3, 615276.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1998. en:caused by mutation in the chmp family, member 1a gene (chmp1a, 164010.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chmp family, member 1a gene (chmp1a, 164010.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  1999. en:caused by mutation in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2000. en:caused by mutation in the chondroitin sulfate proteoglycan-2 gene (cspg2, 118661.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chondroitin sulfate proteoglycan-2 gene (cspg2, 118661.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2001. en:caused by mutation in the chordin-like-1 gene (chrdl1, 300350.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chordin-like-1 gene (chrdl1, 300350.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2002. en:caused by mutation in the chromosome 12 open reading frame 57 gene (c12orf57, 615140.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 12 open reading frame 57 gene (c12orf57, 615140.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2003. en:caused by mutation in the chromosome 16 open reading frame 57 gene (c16orf57, 613276.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 16 open reading frame 57 gene (c16orf57, 613276.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2004. en:caused by mutation in the cln3 gene (cln3, 607042.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cln3 gene (cln3, 607042.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2005. en:caused by mutation in the cofilin 2 gene (cfl2, 601443.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cofilin 2 gene (cfl2, 601443.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2006. en:caused by mutation in the coiled-coil domain-containing protein 151 gene (ccdc151, 615956.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil domain-containing protein 151 gene (ccdc151, 615956.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2007. en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0017) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0017) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2008. en:caused by mutation in the collagen vi, alpha-2 polypeptide gene (col6a2, 120240.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen vi, alpha-2 polypeptide gene (col6a2, 120240.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2009. en:caused by mutation in the collectin 11 gene (612502.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collectin 11 gene (612502.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2010. en:caused by mutation in the complement component receptor 2 gene (cr2, 120650.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement component receptor 2 gene (cr2, 120650.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2011. en:caused by mutation in the conserved telomere maintenance component 1 gene (ctc1, 613129.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the conserved telomere maintenance component 1 gene (ctc1, 613129.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2012. en:caused by mutation in the contactin 1 gene (cntn1, 600016.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the contactin 1 gene (cntn1, 600016.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2013. en:caused by mutation in the cyclic nucleotide-gated channel, beta-3 gene (cngb3, 605080.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclic nucleotide-gated channel, beta-3 gene (cngb3, 605080.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2014. en:caused by mutation in the cytochrome b(-245) beta subunit gene (cybb, 300481.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome b(-245) beta subunit gene (cybb, 300481.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2015. en:caused by mutation in the cytochrome c oxidase subunit i gene (mtco1, 516030.0004) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase subunit i gene (mtco1, 516030.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2016. en:caused by mutation in the cytochrome c1 gene (cyc1, 123980.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c1 gene (cyc1, 123980.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2017. en:caused by mutation in the ddhd domain-containing protein 1 gene (ddhd1, 614603.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ddhd domain-containing protein 1 gene (ddhd1, 614603.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2018. en:caused by mutation in the dehydrodolichyl diphosphate synthase gene (dhdds, 608172.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dehydrodolichyl diphosphate synthase gene (dhdds, 608172.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2019. en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2020. en:caused by mutation in the deoxyribonuclease i-like 3 gene (dnase1l3, 602244.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the deoxyribonuclease i-like 3 gene (dnase1l3, 602244.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2021. en:caused by mutation in the dihydrolipoamide branched chain transacylase gene (dbt, 248610.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dihydrolipoamide branched chain transacylase gene (dbt, 248610.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2022. en:caused by mutation in the distal-less homeobox-5 gene (dlx5, 600028.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the distal-less homeobox-5 gene (dlx5, 600028.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2023. en:caused by mutation in the dna polymerase-gamma gene (polg, 174763.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna polymerase-gamma gene (polg, 174763.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2024. en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 2 gene (dnajb2, 604139.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 2 gene (dnajb2, 604139.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2025. en:caused by mutation in the dyslexia susceptibility 1 candidate 1 gene (dyx1c1, 608706.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dyslexia susceptibility 1 candidate 1 gene (dyx1c1, 608706.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2026. en:caused by mutation in the dystonin gene (dst, 113810.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dystonin gene (dst, 113810.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2027. en:caused by mutation in the dystrophin-associated glycoprotein 1 gene (dag1, 128239.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dystrophin-associated glycoprotein 1 gene (dag1, 128239.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2028. en:caused by mutation in the ectodysplasin a gene (eda, 300451.0014) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ectodysplasin a gene (eda, 300451.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2029. en:caused by mutation in the ectonucleotide pyrophosphatase/phosphodiesterase-1 gene (enpp1, 173335.0020) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ectonucleotide pyrophosphatase/phosphodiesterase-1 gene (enpp1, 173335.0020) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2030. en:caused by mutation in the elg9, c. elegans, homolog of, 1 gene (egln1, 606425.0004) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the elg9, c. elegans, homolog of, 1 gene (egln1, 606425.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2031. en:caused by mutation in the epidermal growth factor gene (egfr, 131550.0007) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the epidermal growth factor gene (egfr, 131550.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2032. en:caused by mutation in the epididymal secretory protein he1 gene (npc1, 601015.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the epididymal secretory protein he1 gene (npc1, 601015.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2033. en:caused by mutation in the ethe1 gene (ethe1, 608451.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ethe1 gene (ethe1, 608451.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2034. en:caused by mutation in the eukaryotic translation elongation factor-2 gene (eef2, 130610.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation elongation factor-2 gene (eef2, 130610.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2035. en:caused by mutation in the excision-repair cross-complementing group 8 gene (ercc6, 609413.0009) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the excision-repair cross-complementing group 8 gene (ercc6, 609413.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2036. en:caused by mutation in the family with sequence similarity 111, member a, gene (fam111a, 615292.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the family with sequence similarity 111, member a, gene (fam111a, 615292.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2037. en:caused by mutation in the family with sequence similarity 126 gene, member a gene (fam126a, 610531.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the family with sequence similarity 126 gene, member a gene (fam126a, 610531.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2038. en:caused by mutation in the fat mass- and obesity-associated gene (fto, 610966.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fat mass- and obesity-associated gene (fto, 610966.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2039. en:caused by mutation in the fatty acyl coa reductase 1 gene (far1, 616107.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fatty acyl coa reductase 1 gene (far1, 616107.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2040. en:caused by mutation in the fibroblast growth factor 17 gene (fgf17, 603725.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor 17 gene (fgf17, 603725.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2041. en:caused by mutation in the fibroblast growth factor 20 gene (fgf20, 605558.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor 20 gene (fgf20, 605558.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2042. en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-1 gene (fgfr1, 136350.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2043. en:caused by mutation in the filamin b gene (flnb, 603381.0006) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the filamin b gene (flnb, 603381.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2044. en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0002). --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0002). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2045. en:caused by mutation in the fras1-related extracellular matrix protein 1 gene (frem1, 608944.0004) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fras1-related extracellular matrix protein 1 gene (frem1, 608944.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2046. en:caused by mutation in the gamma type 1 phosphatidylinositol 4-phosphate 5-kinase gene (pip5k1c, 606102.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma type 1 phosphatidylinositol 4-phosphate 5-kinase gene (pip5k1c, 606102.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2047. en:caused by mutation in the gamma-aminobutyric acid receptor, alpha-1 gene (137160.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma-aminobutyric acid receptor, alpha-1 gene (137160.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2048. en:caused by mutation in the gap junction protein, beta 2 gene (gjb2, 121011.0020) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gap junction protein, beta 2 gene (gjb2, 121011.0020) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2049. en:caused by mutation in the gap junction protein, beta-6 gene (gjb6, 604418.0004) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gap junction protein, beta-6 gene (gjb6, 604418.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2050. en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0006) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2051. en:caused by mutation in the gene encoding homolog of drosophila nanos-1 (nanos1, 608226.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding homolog of drosophila nanos-1 (nanos1, 608226.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2052. en:caused by mutation in the gli-kruppel family member 2 gene (gli2, 165230.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gli-kruppel family member 2 gene (gli2, 165230.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2053. en:caused by mutation in the glucose-6-phosphatase, catalytic gene (g6pc, 613742.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glucose-6-phosphatase, catalytic gene (g6pc, 613742.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2054. en:caused by mutation in the glucose-6-phosphatase, catalytic subunit 3 gene (g6pc3, 611045.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glucose-6-phosphatase, catalytic subunit 3 gene (g6pc3, 611045.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2055. en:caused by mutation in the glutaminyl-trna synthetase gene (qars, 603727.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutaminyl-trna synthetase gene (qars, 603727.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2056. en:caused by mutation in the glutamyl-trna synthetase 2 gene (ears2, 612799.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutamyl-trna synthetase 2 gene (ears2, 612799.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2057. en:caused by mutation in the glycine dehydrogenase gene (gldc, 238300.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycine dehydrogenase gene (gldc, 238300.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2058. en:caused by mutation in the glycogen branching enzyme gene (gbe1, 607839.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycogen branching enzyme gene (gbe1, 607839.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2059. en:caused by mutation in the gonadotropic-releasing hormone 1 gene (gnrh1, 152760.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gonadotropic-releasing hormone 1 gene (gnrh1, 152760.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2060. en:caused by mutation in the guanidinoacetate methyltransferase gene (gamt, 601240.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the guanidinoacetate methyltransferase gene (gamt, 601240.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2061. en:caused by mutation in the heat-shock 22-kd protein 8 gene (hspb8, 608014.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heat-shock 22-kd protein 8 gene (hspb8, 608014.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2062. en:caused by mutation in the heparin cofactor ii gene (hcf2, 142360.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heparin cofactor ii gene (hcf2, 142360.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2063. en:caused by mutation in the histone deacetylase 8 gene (hdac8, 300269.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the histone deacetylase 8 gene (hdac8, 300269.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2064. en:caused by mutation in the homolog of the drosophila fat tumor suppressor gene 4 (fat4, 612411.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila fat tumor suppressor gene 4 (fat4, 612411.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2065. en:caused by mutation in the homolog of the gle1, (s. cerevisiae) rna export mediator gene (gle1, 603371.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the gle1, (s. cerevisiae) rna export mediator gene (gle1, 603371.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2066. en:caused by mutation in the homolog of the mouse pink-eyed dilution gene (oca2, 611409.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse pink-eyed dilution gene (oca2, 611409.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2067. en:caused by mutation in the homolog of the rat nexilin gene (nexn, 613121.0004) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the rat nexilin gene (nexn, 613121.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2068. en:caused by mutation in the homolog of the s. cerevisiae alg13 gene (alg13, 300776.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae alg13 gene (alg13, 300776.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2069. en:caused by mutation in the homolog of the s. cerevisiae alg6 gene (alg6, 604566.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae alg6 gene (alg6, 604566.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2070. en:caused by mutation in the homolog of the yeast dna replication helicase 2 gene (dna2, 601810.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the yeast dna replication helicase 2 gene (dna2, 601810.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2071. en:caused by mutation in the human homolog of the drosophila 'patched' gene 2 (ptch2, 603673.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the human homolog of the drosophila 'patched' gene 2 (ptch2, 603673.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2072. en:caused by mutation in the hypocretin gene (hcrt, 602358.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hypocretin gene (hcrt, 602358.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2073. en:caused by mutation in the inhibitor of kappa light polypeptide gene enhancer in b cells, kinase of, beta gene (ikbkb, 603258.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inhibitor of kappa light polypeptide gene enhancer in b cells, kinase of, beta gene (ikbkb, 603258.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2074. en:caused by mutation in the insulin gene (ins, 176730.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the insulin gene (ins, 176730.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2075. en:caused by mutation in the insulin receptor gene (insr, 147670.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the insulin receptor gene (insr, 147670.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2076. en:caused by mutation in the integrin alpha-7 gene (itga7, 600536.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the integrin alpha-7 gene (itga7, 600536.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2077. en:caused by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interferon regulatory factor 6 gene (irf6, 607199.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2078. en:caused by mutation in the ionotrophic glutamate receptor, n-methyl-d-aspartate, subunit 2b gene (grin2b, 138252.0010) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ionotrophic glutamate receptor, n-methyl-d-aspartate, subunit 2b gene (grin2b, 138252.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2079. en:caused by mutation in the ionotropic n-methyl-d-aspartate glutamate receptor subunit 2a gene (grin2a, 138253.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ionotropic n-methyl-d-aspartate glutamate receptor subunit 2a gene (grin2a, 138253.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2080. en:caused by mutation in the kcnq1-overlapping transcript 1 gene (kcnq1ot1, 604115.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kcnq1-overlapping transcript 1 gene (kcnq1ot1, 604115.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2081. en:caused by mutation in the kelch-like 3 gene (klhl3, 605775.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kelch-like 3 gene (klhl3, 605775.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2082. en:caused by mutation in the kelch-like 41 gene (klhl41, 607701.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kelch-like 41 gene (klhl41, 607701.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2083. en:caused by mutation in the kiaa0196 gene (kiaa0196, 610657.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kiaa0196 gene (kiaa0196, 610657.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2084. en:caused by mutation in the kinesin family member 1b gene (kif1b, 605995.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 1b gene (kif1b, 605995.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2085. en:caused by mutation in the kinesin family member 5c gene (kif5c, 604593.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 5c gene (kif5c, 604593.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2086. en:caused by mutation in the kinesin-5a gene (kif5a, 602821.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin-5a gene (kif5a, 602821.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2087. en:caused by mutation in the kiss1 receptor gene (kiss1r, 604161.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kiss1 receptor gene (kiss1r, 604161.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2088. en:caused by mutation in the latent transforming growth factor beta binding protein 2 gene (ltbp2, 602091.0005) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the latent transforming growth factor beta binding protein 2 gene (ltbp2, 602091.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2089. en:caused by mutation in the lem domain-containing-3 gene (lemd3, 607844.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lem domain-containing-3 gene (lemd3, 607844.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2090. en:caused by mutation in the leucine-rich repeat, immunoglobulin-like, and transmembrane domains-containing protein-3 gene (lrit3, 615004.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucine-rich repeat, immunoglobulin-like, and transmembrane domains-containing protein-3 gene (lrit3, 615004.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2091. en:caused by mutation in the lipin 1 gene (lpin1, 605518.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lipin 1 gene (lpin1, 605518.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2092. en:caused by mutation in the lymphocyte-specific protein-tyrosine kinase gene (lck, 153390.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lymphocyte-specific protein-tyrosine kinase gene (lck, 153390.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2093. en:caused by mutation in the lysophosphatidic acid receptor 6 gene (p2ry5, 609239.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lysophosphatidic acid receptor 6 gene (p2ry5, 609239.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2094. en:caused by mutation in the lysyl-trna synthetase gene (kars, 601421.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lysyl-trna synthetase gene (kars, 601421.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2095. en:caused by mutation in the matrix metalloproteinase-13 gene (mmp13, 600108.0001). --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the matrix metalloproteinase-13 gene (mmp13, 600108.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2096. en:caused by mutation in the mesenchyme homeobox 1 gene (meox1, 600147.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mesenchyme homeobox 1 gene (meox1, 600147.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2097. en:caused by mutation in the microfibrillar-associated protein-5 gene (mfap5, 601103.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the microfibrillar-associated protein-5 gene (mfap5, 601103.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2098. en:caused by mutation in the midline 2 gene (mid2, 300204.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the midline 2 gene (mid2, 300204.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2099. en:caused by mutation in the mitochondrial poly(a) polymerase gene (mtpap, 613669.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial poly(a) polymerase gene (mtpap, 613669.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2100. en:caused by mutation in the mitochondrial ribosomal protein l44 gene (mrpl44, 611849.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial ribosomal protein l44 gene (mrpl44, 611849.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2101. en:caused by mutation in the mitochondrial trna (leucine)-1 gene (mttl1, 590050.0011) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial trna (leucine)-1 gene (mttl1, 590050.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2102. en:caused by mutation in the mitochondrial trna lysine 1 gene (mttl1, 590050.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial trna lysine 1 gene (mttl1, 590050.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2103. en:caused by mutation in the mitochondrial trna-leucine 1 gene (mttl1, 590050.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial trna-leucine 1 gene (mttl1, 590050.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2104. en:caused by mutation in the mitochondrial-encoded atp synthase 6 gene (mtatp6, 516060.0005) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial-encoded atp synthase 6 gene (mtatp6, 516060.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2105. en:caused by mutation in the mothers against decapentaplegic, drosophila, homolog of, 6 gene (smad6, 602931.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mothers against decapentaplegic, drosophila, homolog of, 6 gene (smad6, 602931.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2106. en:caused by mutation in the multiple epidermal growth factor-like domains-8 gene (megf8, 604267.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the multiple epidermal growth factor-like domains-8 gene (megf8, 604267.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2107. en:caused by mutation in the muscle phosphofructokinase gene (pfkm, 610681.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the muscle phosphofructokinase gene (pfkm, 610681.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2108. en:caused by mutation in the muscle-specific phosphorylase kinase subunit a1 gene (phka1, 311870.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the muscle-specific phosphorylase kinase subunit a1 gene (phka1, 311870.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2109. en:caused by mutation in the myc-induced mitochondrial protein gene (mmtn, 609653.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myc-induced mitochondrial protein gene (mmtn, 609653.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2110. en:caused by mutation in the myeloid/lymphoid or mixed lineage leukemia 2 gene (mll2, 602113.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myeloid/lymphoid or mixed lineage leukemia 2 gene (mll2, 602113.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2111. en:caused by mutation in the myocilin gene (myoc, 601652.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myocilin gene (myoc, 601652.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2112. en:caused by mutation in the myosin viia gene (myo7a, 276903.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin viia gene (myo7a, 276903.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2113. en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0022) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0022) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2114. en:caused by mutation in the myosin, heavy polypeptide-8 gene (myh8, 160741.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin, heavy polypeptide-8 gene (myh8, 160741.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2115. en:caused by mutation in the myotubularin gene (mtm1, 300415.0001). --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myotubularin gene (mtm1, 300415.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2116. en:caused by mutation in the n-acylsphingosine amidohydrolase 1 gene (asah1, 613468.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the n-acylsphingosine amidohydrolase 1 gene (asah1, 613468.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2117. en:caused by mutation in the n-acylsphingosine amidohydrolase 1 gene (asah1, 613468.0006) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the n-acylsphingosine amidohydrolase 1 gene (asah1, 613468.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2118. en:caused by mutation in the nadh dehydrogenase (ubiquinone) flavoprotein 1 gene (ndufv1, 161015.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) flavoprotein 1 gene (ndufv1, 161015.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2119. en:caused by mutation in the nadh dehydrogenase, subunit 3 gene (mtnd3, 516002.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase, subunit 3 gene (mtnd3, 516002.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2120. en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 beta subcomplex 3 gene (ndufb3, 603839.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 beta subcomplex 3 gene (ndufb3, 603839.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2121. en:caused by mutation in the nata catalytic subunit of n-alpha-acetyltransferase-10 gene (naa10, 300013.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nata catalytic subunit of n-alpha-acetyltransferase-10 gene (naa10, 300013.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2122. en:caused by mutation in the neurofibromin gene (nf1, 613113.0033) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neurofibromin gene (nf1, 613113.0033) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2123. en:caused by mutation in the neutrophil cytosolic factor-2 gene, p67-phox (ncf2, 608515.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neutrophil cytosolic factor-2 gene, p67-phox (ncf2, 608515.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2124. en:caused by mutation in the nuclear factor kappa-beta, subunit 2 gene (nfkb2, 164012.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear factor kappa-beta, subunit 2 gene (nfkb2, 164012.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2125. en:caused by mutation in the nucleolar protein family a, member 3 gene (nola3, 606471.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nucleolar protein family a, member 3 gene (nola3, 606471.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2126. en:caused by mutation in the occludin gene (ocln, 602876.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the occludin gene (ocln, 602876.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2127. en:caused by mutation in the ofd1 gene (ofd1, 300170.0011) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ofd1 gene (ofd1, 300170.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2128. en:caused by mutation in the ornithine aminotransferase gene (oat, 258870.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ornithine aminotransferase gene (oat, 258870.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2129. en:caused by mutation in the paired-related homeobox gene 1 (prrx1, 167420.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the paired-related homeobox gene 1 (prrx1, 167420.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2130. en:caused by mutation in the pantothenate kinase-2 gene (pank2, 607157.0011) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pantothenate kinase-2 gene (pank2, 607157.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2131. en:caused by mutation in the peptidase d gene (pepd, 613230.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peptidase d gene (pepd, 613230.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2132. en:caused by mutation in the peroxisome biogenesis factor-14 gene (pex14, 601791.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor-14 gene (pex14, 601791.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2133. en:caused by mutation in the phosphodiesterase 6d, cgmp-specific, rod, delta gene (pde6d, 602676.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphodiesterase 6d, cgmp-specific, rod, delta gene (pde6d, 602676.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2134. en:caused by mutation in the phosphodiesterase 6h, cgmp-specific, cone, gamma gene (pde6h, 601190.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphodiesterase 6h, cgmp-specific, cone, gamma gene (pde6h, 601190.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2135. en:caused by mutation in the phosphoglycerate dehydrogenase gene (phgdh, 606879.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoglycerate dehydrogenase gene (phgdh, 606879.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2136. en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2137. en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2138. en:caused by mutation in the platelet-derived growth factor receptor, beta, gene (pdgfrb, 173410.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the platelet-derived growth factor receptor, beta, gene (pdgfrb, 173410.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2139. en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 5 gene (plekhg5, 611101.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pleckstrin homology domain-containing protein, family g, member 5 gene (plekhg5, 611101.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2140. en:caused by mutation in the plectin 1 gene (plec1, 601282.0010) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the plectin 1 gene (plec1, 601282.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2141. en:caused by mutation in the polo-like kinase 4 gene (plk4, 605031.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polo-like kinase 4 gene (plk4, 605031.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2142. en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 10 gene (kcnj10, 602208.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 10 gene (kcnj10, 602208.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2143. en:caused by mutation in the potassium channel, subfamily t, member 1 gene (kcnt1, 608167.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium channel, subfamily t, member 1 gene (kcnt1, 608167.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2144. en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 192500.0013) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 192500.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2145. en:caused by mutation in the presenilin 2 gene (psen2, 600759.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the presenilin 2 gene (psen2, 600759.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2146. en:caused by mutation in the prolactin receptor gene (prlr, 176761.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prolactin receptor gene (prlr, 176761.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2147. en:caused by mutation in the prominin-1 gene (prom1, 604365.0013) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prominin-1 gene (prom1, 604365.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2148. en:caused by mutation in the protein kinase, interferon-inducible double-stranded rna-dependent activator gene (prkra, 603424.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein kinase, interferon-inducible double-stranded rna-dependent activator gene (prkra, 603424.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2149. en:caused by mutation in the pyrin gene (mefv, 608107.0018) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pyrin gene (mefv, 608107.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2150. en:caused by mutation in the r-type arachidonate 12-lipoxygenase gene (alox12b, 603741.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the r-type arachidonate 12-lipoxygenase gene (alox12b, 603741.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2151. en:caused by mutation in the ras-associated protein rab39b gene (rab39b, 300774.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ras-associated protein rab39b gene (rab39b, 300774.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2152. en:caused by mutation in the receptor expression-enhancing protein 2 gene (reep2, 609347.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the receptor expression-enhancing protein 2 gene (reep2, 609347.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2153. en:caused by mutation in the ribosomal protein l15 gene (rpl15, 604174.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribosomal protein l15 gene (rpl15, 604174.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2154. en:caused by mutation in the rotatin gene (rttn, 610436.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rotatin gene (rttn, 610436.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2155. en:caused by mutation in the ryanodine receptor-1 gene (ryr1, 180901.0025) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ryanodine receptor-1 gene (ryr1, 180901.0025) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2156. en:caused by mutation in the s. cerevisiae homolog of the trna splicing endonuclease 2 gene (tsen2, 608753.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the s. cerevisiae homolog of the trna splicing endonuclease 2 gene (tsen2, 608753.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2157. en:caused by mutation in the sodium channel, nonvoltage-gated 1, alpha gene (scnn1a, 600228.0006) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sodium channel, nonvoltage-gated 1, alpha gene (scnn1a, 600228.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2158. en:caused by mutation in the solute carrier family 20 (phosphate transporter), member 2 gene (slc20a, 158378.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 20 (phosphate transporter), member 2 gene (slc20a, 158378.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2159. en:caused by mutation in the solute carrier family 26, member 4 gene (slc26a4, 605646.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 26, member 4 gene (slc26a4, 605646.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2160. en:caused by mutation in the solute carrier family 29 (nucleoside transporter), member 3 gene (slc29a3, 612373.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 29 (nucleoside transporter), member 3 gene (slc29a3, 612373.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2161. en:caused by mutation in the solute carrier family 33 (acetyl-coa transporter), member 1 gene (slc33a1, 603690.0001). --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 33 (acetyl-coa transporter), member 1 gene (slc33a1, 603690.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2162. en:caused by mutation in the solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene (slc7a9, 604144.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 7 (cationic amino acid transporter, y+ system), member 9 gene (slc7a9, 604144.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2163. en:caused by mutation in the sry-box 17 gene (sox17, 610928.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sry-box 17 gene (sox17, 610928.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2164. en:caused by mutation in the sry-box 18 gene (sox18, 601618.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sry-box 18 gene (sox18, 601618.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2165. en:caused by mutation in the stip1 homologous and u box-containing protein 1 gene (stub1, 607207.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the stip1 homologous and u box-containing protein 1 gene (stub1, 607207.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2166. en:caused by mutation in the t-cell immune regulator 1 gene (tcirg1, 604592.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the t-cell immune regulator 1 gene (tcirg1, 604592.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2167. en:caused by mutation in the tar dna-binding protein (tardbp, 605078.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tar dna-binding protein (tardbp, 605078.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2168. en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0014) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2169. en:caused by mutation in the telomerase reverse transcriptase gene (tert, 187270.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the telomerase reverse transcriptase gene (tert, 187270.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2170. en:caused by mutation in the titin gene (ttn, 188840.0004) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the titin gene (ttn, 188840.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2171. en:caused by mutation in the trafficking protein particle complex, subunit 11 gene (trappc11, 614138.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the trafficking protein particle complex, subunit 11 gene (trappc11, 614138.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2172. en:caused by mutation in the transforming growth factor, beta receptor i, 53kd gene (tgfbr1, 190181.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transforming growth factor, beta receptor i, 53kd gene (tgfbr1, 190181.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2173. en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0001). --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2174. en:caused by mutation in the transmembrane channel-like protein 1 gene (tmc1, 606706.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane channel-like protein 1 gene (tmc1, 606706.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2175. en:caused by mutation in the transmembrane protein 173 gene (tmem173, 612374.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 173 gene (tmem173, 612374.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2176. en:caused by mutation in the transmembrane protein 216 gene (tmem216, 613277.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 216 gene (tmem216, 613277.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2177. en:caused by mutation in the transmembrane protein 237 (tmem237, 614423.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 237 (tmem237, 614423.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2178. en:caused by mutation in the transporter, atp-binding cassette, major histocompatibility complex, 2 gene (tap2, 170261.0004) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transporter, atp-binding cassette, major histocompatibility complex, 2 gene (tap2, 170261.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2179. en:caused by mutation in the tripeptidyl peptidase 1 gene (tpp1, 607998.0004) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tripeptidyl peptidase 1 gene (tpp1, 607998.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2180. en:caused by mutation in the trk-fused gene (tfg, 602498.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the trk-fused gene (tfg, 602498.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2181. en:caused by mutation in the troponin t1 gene (tnnt1, 191041.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the troponin t1 gene (tnnt1, 191041.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2182. en:caused by mutation in the tubulin, gamma-1 gene (tubg1, 191135.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin, gamma-1 gene (tubg1, 191135.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2183. en:caused by mutation in the type 2 bone morphogenetic protein receptor gene (bmpr2, 600799.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the type 2 bone morphogenetic protein receptor gene (bmpr2, 600799.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2184. en:caused by mutation in the tyrosine hydroxylase gene (th, 191290.0001). --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tyrosine hydroxylase gene (th, 191290.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2185. en:caused by mutation in the ubiquinol-cytochrome c reductase-protein complex iii subunit vii gene (uqcrq, 612080.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquinol-cytochrome c reductase-protein complex iii subunit vii gene (uqcrq, 612080.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2186. en:caused by mutation in the vacuolar protein sorting 13a gene (vps13a, 605978.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the vacuolar protein sorting 13a gene (vps13a, 605978.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2187. en:caused by mutation in the very long-chain acyl-coa dehydrogenase gene (acavld, 609575.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the very long-chain acyl-coa dehydrogenase gene (acavld, 609575.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2188. en:caused by mutation in the voltage-gated, type ii sodium channel, alpha subunit (scn2a, 182390.0008) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated, type ii sodium channel, alpha subunit (scn2a, 182390.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2189. en:caused by mutation in the von hippel-lindau gene (vhl, 608537.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the von hippel-lindau gene (vhl, 608537.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2190. en:caused by mutation in the vps33b-interacting protein, apical-basolateral polarity regulator gene (vipar, 613401.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the vps33b-interacting protein, apical-basolateral polarity regulator gene (vipar, 613401.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2191. en:caused by mutation in the was gene (was, 300392.0012) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the was gene (was, 300392.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2192. en:caused by mutation in the wd repeat-containing planar cell polarity effector gene (wdpcp, 613580.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing planar cell polarity effector gene (wdpcp, 613580.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2193. en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0003) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein-19 gene (wdr19, 608151.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2194. en:caused by mutation in the wnk lysine deficient protein kinase 4 gene (wnk4, 601844.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wnk lysine deficient protein kinase 4 gene (wnk4, 601844.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2195. en:caused by mutation in the zinc finger protein 335 gene (znf335, 610827.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger protein 335 gene (znf335, 610827.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2196. en:caused by mutations in the 25-hydroxyvitamin d3-1-alpha-hydroxylase gene (cyp27b1, 609506.0001). --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the 25-hydroxyvitamin d3-1-alpha-hydroxylase gene (cyp27b1, 609506.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2197. en:caused by mutations in the chemokine (c-x-c motif) receptor 4 gene (cxcr4, 162643.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the chemokine (c-x-c motif) receptor 4 gene (cxcr4, 162643.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2198. en:caused by mutations in the cystic fibrosis transmembrane conductance regulator gene (cftr, 602421.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cystic fibrosis transmembrane conductance regulator gene (cftr, 602421.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2199. en:caused by mutations in the gap junction protein, beta-6 gene (gjb6, 604418.0002) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the gap junction protein, beta-6 gene (gjb6, 604418.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2200. en:caused by mutations in the glycosylceramidase gene (galc, 606890.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the glycosylceramidase gene (galc, 606890.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2201. en:caused by mutations in the keratin 6b gene (krt6b, 148042.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the keratin 6b gene (krt6b, 148042.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2202. en:caused by mutations in the lecithin:cholesterol acyltransferase gene (lcat, 606967.0001). --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the lecithin:cholesterol acyltransferase gene (lcat, 606967.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2203. en:caused by mutations in the neuroblastoma-derived v-myc avian myelocytomatosis viral-related oncogene (mycn, 164840.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the neuroblastoma-derived v-myc avian myelocytomatosis viral-related oncogene (mycn, 164840.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2204. en:caused by mutations in the prion protein gene (prnp, 176640.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the prion protein gene (prnp, 176640.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2205. en:caused by mutations in the properdin p factor gene (pfc, 300383.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the properdin p factor gene (pfc, 300383.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2206. en:caused by mutations in the recombinase activating gene 1 (rag1, 179615.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the recombinase activating gene 1 (rag1, 179615.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2207. en:caused by mutations in the survival of motor neuron 1 gene (smn1, 600354.0011) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the survival of motor neuron 1 gene (smn1, 600354.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2208. en:caused by mutations in the titin immunoglobulin domain protein gene (ttid, 604103.0002). --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the titin immunoglobulin domain protein gene (ttid, 604103.0002). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2209. en:caused by mutations in the triggering receptor expressed on myeloid cells-2 gene (trem2, 605086.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the triggering receptor expressed on myeloid cells-2 gene (trem2, 605086.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2210. en:caused by mutations in the tropomyosin 2 gene (tpm2, 190990.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the tropomyosin 2 gene (tpm2, 190990.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2211. en:caused by mutations in the uridine diphosphate glycosyltransferase 1 gene (ugt1a1, 191740.0010) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the uridine diphosphate glycosyltransferase 1 gene (ugt1a1, 191740.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2212. en:caused by mutations in the zinc finger transcription factor trps1 gene (trps1, 604386.0007) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the zinc finger transcription factor trps1 gene (trps1, 604386.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2213. en:caused by somatic mosaic mutation in the guanine nucleotide-binding protein q gene (gnaq, 600998.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mosaic mutation in the guanine nucleotide-binding protein q gene (gnaq, 600998.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2214. en:caused by somatic mutation in the v-akt murine thymoma viral oncogene homolog 1 gene (akt1, 164730.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the v-akt murine thymoma viral oncogene homolog 1 gene (akt1, 164730.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2215. en:contiguous duplication of 2.2mb on chromosome 17q23.1-q23.2 --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous duplication of 2.2mb on chromosome 17q23.1-q23.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2216. en:contiguous gene syndrome caused by deletion of 91.3kb on chromosome 11p11.2 involving the creb3l1 (616215) and dgkz (601441) genes --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by deletion of 91.3kb on chromosome 11p11.2 involving the creb3l1 (616215) and dgkz (601441) genes | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2217. en:contiguous gene syndrome caused by deletion on chromosome 22q11.2 --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by deletion on chromosome 22q11.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2218. en:contiguous gene syndrome caused by microdeletion (600-800kb) of chromosome 17q21.31 encompassing genes crhr1 (122561), mapt (157140), sth (607067), imp5 (608284), and kansl1 (612452) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by microdeletion (600-800kb) of chromosome 17q21.31 encompassing genes crhr1 (122561), mapt (157140), sth (607067), imp5 (608284), and kansl1 (612452) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2219. en:due to hemizygous deletion of 4p16.3 --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:due to hemizygous deletion of 4p16.3 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2220. en:susceptibility conferred by 9-snp haplotype in malic enzyme 2 (me2, 154270.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by 9-snp haplotype in malic enzyme 2 (me2, 154270.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2221. en:susceptibility conferred by duplication of the homolog of the mouse t brachyury gene (t, 601397) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by duplication of the homolog of the mouse t brachyury gene (t, 601397) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2222. en:susceptibility conferred by mutation in the complement component 3 gene (c3, 120700.0005) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the complement component 3 gene (c3, 120700.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2223. en:susceptibility conferred by mutation in the major histocompatibility complex, class i, b gene (hla-b, 142830.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the major histocompatibility complex, class i, b gene (hla-b, 142830.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2224. en:susceptibility to sle caused by mutation in the tumor necrosis factor ligand superfamily, member 6 gene (tnfsf6, 134638.0001) --- r_associated #0: 25 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility to sle caused by mutation in the tumor necrosis factor ligand superfamily, member 6 gene (tnfsf6, 134638.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=25
  2225. en:a contiguous gene syndrome caused by deletion (1.5mb - 3.0mb) of 22q11.2 --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome caused by deletion (1.5mb - 3.0mb) of 22q11.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2226. en:a contiguous gene syndrome caused by deletion of chromosome 16q22 including the cbfb gene (121360) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome caused by deletion of chromosome 16q22 including the cbfb gene (121360) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2227. en:a mutation in the homeobox d13 gene (hoxd13, 142989.0012) has been identified in 1 patient. --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a mutation in the homeobox d13 gene (hoxd13, 142989.0012) has been identified in 1 patient. | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2228. en:cause by mutation in the xylosyltransferase-1 gene (xylt1, 608124.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:cause by mutation in the xylosyltransferase-1 gene (xylt1, 608124.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2229. en:caused by a 1.37mb deletion on 4q21 encompassing 5 genes --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a 1.37mb deletion on 4q21 encompassing 5 genes | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2230. en:caused by a trinucleotide repeat expansion (cag)n in the ataxin 8 gene (atxn8, 613289.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a trinucleotide repeat expansion (cag)n in the ataxin 8 gene (atxn8, 613289.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2231. en:caused by chromosomal mosaicism --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by chromosomal mosaicism | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2232. en:caused by contiguous gene duplication of imprinted region of 11p15.5 --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by contiguous gene duplication of imprinted region of 11p15.5 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2233. en:caused by deletion of 539.77kb (grch37 chr8 77226464-77766239) on chromosome 8q21.11 --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion of 539.77kb (grch37 chr8 77226464-77766239) on chromosome 8q21.11 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2234. en:caused by deletion of multiple genes in the mitochondrial dna --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion of multiple genes in the mitochondrial dna | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2235. en:caused by duplication of 0.25 to 1.08 mb on chromosome 5p13 --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of 0.25 to 1.08 mb on chromosome 5p13 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2236. en:caused by duplication of 0.9 - 1.2 mb on 8q22.1 --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of 0.9 - 1.2 mb on 8q22.1 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2237. en:caused by fusion of rad51b (602948) and hmgic (600698) genes --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by fusion of rad51b (602948) and hmgic (600698) genes | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2238. en:caused by mutation in chromosome 6 open reading frame 221 gene (c6orf221, 611687.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in chromosome 6 open reading frame 221 gene (c6orf221, 611687.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2239. en:caused by mutation in myosin, heavy chain 9, non-muscle gene (myh9, 160775.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in myosin, heavy chain 9, non-muscle gene (myh9, 160775.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2240. en:caused by mutation in phosphorylase kinase, beta subunit (phkb, 172490.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in phosphorylase kinase, beta subunit (phkb, 172490.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2241. en:caused by mutation in the 3-beta-hydroxy-delta-5-c27-steroid oxidoreductase gene (hsd3b7, 607764.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 3-beta-hydroxy-delta-5-c27-steroid oxidoreductase gene (hsd3b7, 607764.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2242. en:caused by mutation in the 43-kd receptor-association protein of the synapse, gene (rapsn, 601592.0013) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 43-kd receptor-association protein of the synapse, gene (rapsn, 601592.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2243. en:caused by mutation in the 57-kd centrosomal protein gene (cep57, 607951.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 57-kd centrosomal protein gene (cep57, 607951.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2244. en:caused by mutation in the 6-@pyruvoyl-tetrahydropterin synthase gene pts, (612719.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 6-@pyruvoyl-tetrahydropterin synthase gene pts, (612719.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2245. en:caused by mutation in the 68-kd transforming growth factor-beta-induced gene (tgfbi, 601692.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 68-kd transforming growth factor-beta-induced gene (tgfbi, 601692.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2246. en:caused by mutation in the acetylglucosaminyltransferase-like protein (large, 603590.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the acetylglucosaminyltransferase-like protein (large, 603590.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2247. en:caused by mutation in the acid beta-glucosidase gene (gba, 606463.0004) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the acid beta-glucosidase gene (gba, 606463.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2248. en:caused by mutation in the adaptor-related protein complex 3, beta-1 subunit gene (ap3b1, 603401.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adaptor-related protein complex 3, beta-1 subunit gene (ap3b1, 603401.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2249. en:caused by mutation in the aicar formyltransferase/imp cyclohydrolase gene (atic, 601731.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aicar formyltransferase/imp cyclohydrolase gene (atic, 601731.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2250. en:caused by mutation in the alpha subunit of the 3-methylcrotonyl-coa carboxylase gene (mccc1, 609010.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha subunit of the 3-methylcrotonyl-coa carboxylase gene (mccc1, 609010.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2251. en:caused by mutation in the alpha subunit of the type v voltage-gated sodium channel gene (scn5a, 600163.0034) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha subunit of the type v voltage-gated sodium channel gene (scn5a, 600163.0034) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2252. en:caused by mutation in the alpha-1a calcium channel subunit gene (cacna1a, 601011.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1a calcium channel subunit gene (cacna1a, 601011.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2253. en:caused by mutation in the alpha-3 laminin gene (lama3, 600805.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-3 laminin gene (lama3, 600805.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2254. en:caused by mutation in the alpha-5 gap junction protein gene (gja5, 121013.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-5 gap junction protein gene (gja5, 121013.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2255. en:caused by mutation in the alpha-a-crystallin gene (cryaa, 123580.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-a-crystallin gene (cryaa, 123580.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2256. en:caused by mutation in the alpha-actin-1 gene (acta1, 102610.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-actin-1 gene (acta1, 102610.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2257. en:caused by mutation in the alpha-aminoadipic semialdehyde synthase gene (aass, 605113.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-aminoadipic semialdehyde synthase gene (aass, 605113.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2258. en:caused by mutation in the alpha-b crystallin gene (cryab, 123590.0005) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-b crystallin gene (cryab, 123590.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2259. en:caused by mutation in the alpha-synuclein gene (snca, 163890.0004) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-synuclein gene (snca, 163890.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2260. en:caused by mutation in the angiopoietin-like-3 gene (angptl3, 604774.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the angiopoietin-like-3 gene (angptl3, 604774.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2261. en:caused by mutation in the angiotensin ii receptor type 1 gene (agtr1, 106165.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the angiotensin ii receptor type 1 gene (agtr1, 106165.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2262. en:caused by mutation in the ankyrin 1 gene (ank1, 182900.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ankyrin 1 gene (ank1, 182900.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2263. en:caused by mutation in the anoctamin 5 gene (ano5, 608662.0004) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the anoctamin 5 gene (ano5, 608662.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2264. en:caused by mutation in the aprataxin gene (aptx, 606350.0001). --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aprataxin gene (aptx, 606350.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2265. en:caused by mutation in the aspartyl-trna synthetase gene (dars, 603084.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aspartyl-trna synthetase gene (dars, 603084.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2266. en:caused by mutation in the atp synthase 6 gene (mtatp6, 516060.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp synthase 6 gene (mtatp6, 516060.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2267. en:caused by mutation in the barttin gene (bsnd, 606412.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the barttin gene (bsnd, 606412.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2268. en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bcs1, s. cerevisiae, homolog-like gene (bcs1l, 603647.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2269. en:caused by mutation in the beta acid glucosidase 2 gene (gba2, 609471.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta acid glucosidase 2 gene (gba2, 609471.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2270. en:caused by mutation in the beta cardiac myosin heavy chain gene (myh7, 160760.0028) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta cardiac myosin heavy chain gene (myh7, 160760.0028) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2271. en:caused by mutation in the calcium channel, voltage-dependent, l type, alpha 1d subunit gene (cacna1d, 114206.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calcium channel, voltage-dependent, l type, alpha 1d subunit gene (cacna1d, 114206.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2272. en:caused by mutation in the calcium- and integrin-binding protein 2 gene (cib2, 605564.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calcium- and integrin-binding protein 2 gene (cib2, 605564.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2273. en:caused by mutation in the camp-specific phosphodiesterase 4d gene (pde4d, 600129.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the camp-specific phosphodiesterase 4d gene (pde4d, 600129.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2274. en:caused by mutation in the carbamoylphosphate synthetase i gene (cps1, 608307.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carbamoylphosphate synthetase i gene (cps1, 608307.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2275. en:caused by mutation in the carbohydrate sulfotransferase 8 gene (chst8, 610190.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carbohydrate sulfotransferase 8 gene (chst8, 610190.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2276. en:caused by mutation in the carbonic anhydrase va gene (ca5a, 114761.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carbonic anhydrase va gene (ca5a, 114761.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2277. en:caused by mutation in the cardiac troponin-t2 gene (tnnt2, 191045.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cardiac troponin-t2 gene (tnnt2, 191045.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2278. en:caused by mutation in the cathepsin d gene (ctsd, 116840.0001). --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cathepsin d gene (ctsd, 116840.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2279. en:caused by mutation in the chmp family, member 2b gene (chmp2b, 609512.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chmp family, member 2b gene (chmp2b, 609512.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2280. en:caused by mutation in the cholinergic receptor, nicotinic, alpha polypeptide-1 gene (chrna1, 100690.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, alpha polypeptide-1 gene (chrna1, 100690.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2281. en:caused by mutation in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2282. en:caused by mutation in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0004) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2283. en:caused by mutation in the cholinergic receptor, nicotinic, gamma polypeptide gene (chrng, 100730.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, gamma polypeptide gene (chrng, 100730.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2284. en:caused by mutation in the chromatin-modifying protein 2b (chmp2b, 609512.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromatin-modifying protein 2b (chmp2b, 609512.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2285. en:caused by mutation in the coiled-coil domain-containing protein 65 (ccdc65, 611088.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil domain-containing protein 65 (ccdc65, 611088.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2286. en:caused by mutation in the coiled-coil domain-containing protein 88c (ccdc88c, 611204.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil domain-containing protein 88c (ccdc88c, 611204.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2287. en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2288. en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0007) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2289. en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0045) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0045) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2290. en:caused by mutation in the collagen iii, alpha-1 polypeptide gene (col3a1, 120180.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen iii, alpha-1 polypeptide gene (col3a1, 120180.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2291. en:caused by mutation in the collagen vi, alpha-3 polypeptide gene (col6a3, 120250.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen vi, alpha-3 polypeptide gene (col6a3, 120250.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2292. en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0004) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2293. en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0005) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2294. en:caused by mutation in the complex i, subunit nd5 gene (mtnd5, 516005.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complex i, subunit nd5 gene (mtnd5, 516005.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2295. en:caused by mutation in the complex i, subunit nd6 gene (mtnd6, 516006.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complex i, subunit nd6 gene (mtnd6, 516006.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2296. en:caused by mutation in the connexin 43 gene (gja1, 121014.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the connexin 43 gene (gja1, 121014.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2297. en:caused by mutation in the cyclic nucleotide-gated channel, alpha-3 gene (cnga3, 600053.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclic nucleotide-gated channel, alpha-3 gene (cnga3, 600053.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2298. en:caused by mutation in the cyclin-dependent kinase-like 5 gene (cdkl5, 300203.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclin-dependent kinase-like 5 gene (cdkl5, 300203.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2299. en:caused by mutation in the cytoskeleton-associated protein 2-like gene (ckap2l, 616174.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytoskeleton-associated protein 2-like gene (ckap2l, 616174.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2300. en:caused by mutation in the ddb1- and cul4-associated factor 8 gene (dcaf8, 615820.0001). --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ddb1- and cul4-associated factor 8 gene (dcaf8, 615820.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2301. en:caused by mutation in the desmocollin 2 gene (dsc2, 125645.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the desmocollin 2 gene (dsc2, 125645.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2302. en:caused by mutation in the dimethylglycine dehydrogenase gene (dmgdh, 605849.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dimethylglycine dehydrogenase gene (dmgdh, 605849.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2303. en:caused by mutation in the disintegrin and metalloproteinase domain 17 gene (adam17, 603639.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the disintegrin and metalloproteinase domain 17 gene (adam17, 603639.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2304. en:caused by mutation in the dna ligase-4 gene (lig4, 601837.0007) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna ligase-4 gene (lig4, 601837.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2305. en:caused by mutation in the dna polymerase gamma-2 gene (polg2, 604983.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna polymerase gamma-2 gene (polg2, 604983.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2306. en:caused by mutation in the ectodysplasin anhidrotic receptor gene (edar, 604095.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ectodysplasin anhidrotic receptor gene (edar, 604095.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2307. en:caused by mutation in the elongation factor tu gtp-binding domain-containing 2 gene (eftud2, 603892.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the elongation factor tu gtp-binding domain-containing 2 gene (eftud2, 603892.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2308. en:caused by mutation in the endothelin-converting enzyme-like 1 gene (ecel1, 605896.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endothelin-converting enzyme-like 1 gene (ecel1, 605896.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2309. en:caused by mutation in the eyes absent-1 gene (eya1, 601653.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eyes absent-1 gene (eya1, 601653.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2310. en:caused by mutation in the fad-dependent oxidoreductase domain-containing protein 1 gene (foxred1, 613622.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fad-dependent oxidoreductase domain-containing protein 1 gene (foxred1, 613622.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2311. en:caused by mutation in the family with sequence similarity 111, member a gene (fam111a, 615292.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the family with sequence similarity 111, member a gene (fam111a, 615292.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2312. en:caused by mutation in the fatty acid 2-hydroxylase gene (fa2h, 611026.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fatty acid 2-hydroxylase gene (fa2h, 611026.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2313. en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0050) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0050) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2314. en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0012) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2315. en:caused by mutation in the filamin c gene (flnc, 102565.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the filamin c gene (flnc, 102565.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2316. en:caused by mutation in the fk506-binding protein 10 gene (fkbp10, 607063.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fk506-binding protein 10 gene (fkbp10, 607063.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2317. en:caused by mutation in the forkhead box p2 gene (foxp2, 605317.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead box p2 gene (foxp2, 605317.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2318. en:caused by mutation in the fukutin gene (fktn, 607440.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fukutin gene (fktn, 607440.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2319. en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0016) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fukutin-related protein gene (fkrp, 606596.0016) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2320. en:caused by mutation in the fumarate hydratase gene (fh, 136850.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fumarate hydratase gene (fh, 136850.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2321. en:caused by mutation in the fyve, rhogef, and ph domain-containing protein-4 gene (fgd4, 611104.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fyve, rhogef, and ph domain-containing protein-4 gene (fgd4, 611104.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2322. en:caused by mutation in the g protein signaling modulator 2 gene (gpsm2, 609245.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the g protein signaling modulator 2 gene (gpsm2, 609245.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2323. en:caused by mutation in the gap junction, alpha-3, 46kd protein gene (gja3, 121015.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gap junction, alpha-3, 46kd protein gene (gja3, 121015.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2324. en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0005) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2325. en:caused by mutation in the gene encoding growth/differentiation factor-g (gdf6, 601147.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding growth/differentiation factor-g (gdf6, 601147.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2326. en:caused by mutation in the gene encoding member a9 of the basic helix-loop-helix family (bhlha9, 615416.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding member a9 of the basic helix-loop-helix family (bhlha9, 615416.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2327. en:caused by mutation in the gigaxonin gene (gan, 605379.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gigaxonin gene (gan, 605379.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2328. en:caused by mutation in the glucokinase gene (gck, 138079.0011) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glucokinase gene (gck, 138079.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2329. en:caused by mutation in the glutaredoxin, cysteine-rich, 2 gene (grxcr2, 615762.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutaredoxin, cysteine-rich, 2 gene (grxcr2, 615762.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2330. en:caused by mutation in the glycoprotein ib, platelet, alpha polypeptide gene (gp1ba, 606672.0006) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycoprotein ib, platelet, alpha polypeptide gene (gp1ba, 606672.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2331. en:caused by mutation in the growth/differentiation factor 6 gene (gdf6, 601147.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the growth/differentiation factor 6 gene (gdf6, 601147.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2332. en:caused by mutation in the heat-shock 27-kd protein 1 gene (hspb1, 602195.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heat-shock 27-kd protein 1 gene (hspb1, 602195.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2333. en:caused by mutation in the hepatocyte cell adhesion molecule gene (hepacam, 611642.0006) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hepatocyte cell adhesion molecule gene (hepacam, 611642.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2334. en:caused by mutation in the hereditary hemochromatosis gene (hfe, 613609.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hereditary hemochromatosis gene (hfe, 613609.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2335. en:caused by mutation in the histone deacetylase 4 gene (hdac4, 605314.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the histone deacetylase 4 gene (hdac4, 605314.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2336. en:caused by mutation in the homeobox a2 gene (hoxa2, 604685.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeobox a2 gene (hoxa2, 604685.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2337. en:caused by mutation in the homolog 2 of drosophila enhancer of zeste (ezh2, 601573.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog 2 of drosophila enhancer of zeste (ezh2, 601573.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2338. en:caused by mutation in the homolog of drosophila odz-3 gene (odz3, 610083.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of drosophila odz-3 gene (odz3, 610083.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2339. en:caused by mutation in the homolog of s. cerevisiae mediator of rna polymerase ii transcription, subunit 12 gene (med12, 300188.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of s. cerevisiae mediator of rna polymerase ii transcription, subunit 12 gene (med12, 300188.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2340. en:caused by mutation in the homolog of the drosophila aristaless homeobox gene (arix, 602753.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila aristaless homeobox gene (arix, 602753.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2341. en:caused by mutation in the homolog of the drosophila crumbs 2 gene (crb2, 609720.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila crumbs 2 gene (crb2, 609720.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2342. en:caused by mutation in the homolog of the drosophila notch 2 gene (notch2, 600275.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila notch 2 gene (notch2, 600275.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2343. en:caused by mutation in the homolog of the drosophila notch, 3, gene (notch3, 600276.0012) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila notch, 3, gene (notch3, 600276.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2344. en:caused by mutation in the homolog of the e. coli atp-dependent protease clpap, proteolytic subunit gene (clpp, 601119.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the e. coli atp-dependent protease clpap, proteolytic subunit gene (clpp, 601119.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2345. en:caused by mutation in the homolog of the e. coli bola, 3 gene (bola3, 613183.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the e. coli bola, 3 gene (bola3, 613183.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2346. en:caused by mutation in the homolog of the e. coli mutl 1 gene (mlh1, 120436.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the e. coli mutl 1 gene (mlh1, 120436.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2347. en:caused by mutation in the homolog of the e. coli mutl 1 gene (mlh1, 120436.0006) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the e. coli mutl 1 gene (mlh1, 120436.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2348. en:caused by mutation in the homolog of the e. coli muts 2 gene (msh2, 609309.0014) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the e. coli muts 2 gene (msh2, 609309.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2349. en:caused by mutation in the homolog of the mouse seizure threshold 2 gene (szt2, 615463.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse seizure threshold 2 gene (szt2, 615463.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2350. en:caused by mutation in the homolog of the mouse tubby gene (tub, 601197.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse tubby gene (tub, 601197.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2351. en:caused by mutation in the homolog of the s. cerevisiae postmeiotic segregation increased 2 gene (pms2, 600259.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae postmeiotic segregation increased 2 gene (pms2, 600259.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2352. en:caused by mutation in the homolog of the s. cerevisiae rad51a gene (rad51a, 179617.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae rad51a gene (rad51a, 179617.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2353. en:caused by mutation in the homolog of the s. pombe rad21 gene (rad21, 606462.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. pombe rad21 gene (rad21, 606462.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2354. en:caused by mutation in the homolog of yeast dna replication helicase-2 gene (dna2, 601810.0004) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of yeast dna replication helicase-2 gene (dna2, 601810.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2355. en:caused by mutation in the hsn2 isoform of the protein kinase, lysine-deficient 1 gene (wnk1, 605232.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hsn2 isoform of the protein kinase, lysine-deficient 1 gene (wnk1, 605232.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2356. en:caused by mutation in the iduronate-2-sulfatase gene (ids, 309900.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the iduronate-2-sulfatase gene (ids, 309900.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2357. en:caused by mutation in the inositol polyphosphate-5-phosphatase, 72-kd gene (inpp5e, 613037.0001). --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inositol polyphosphate-5-phosphatase, 72-kd gene (inpp5e, 613037.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2358. en:caused by mutation in the integrin-alpha-6 gene (itga6, 147556.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the integrin-alpha-6 gene (itga6, 147556.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2359. en:caused by mutation in the intrinsic factor-vitamin b12 receptor gene (cubn, 602997.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the intrinsic factor-vitamin b12 receptor gene (cubn, 602997.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2360. en:caused by mutation in the jumonji, at-rich interactive domain 1c gene gene (jarid1c, 314690.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the jumonji, at-rich interactive domain 1c gene gene (jarid1c, 314690.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2361. en:caused by mutation in the kelch-like 7 gene (klhl7, 611119.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kelch-like 7 gene (klhl7, 611119.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2362. en:caused by mutation in the keratin 1 gene (krt1, 139350.0004) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 1 gene (krt1, 139350.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2363. en:caused by mutation in the keratin 14 gene (krt14, 148066.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 14 gene (krt14, 148066.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2364. en:caused by mutation in the keratin 83 gene (krt83, 602765.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 83 gene (krt83, 602765.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2365. en:caused by mutation in the keratin 9 gene (krt9, 607606.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 9 gene (krt9, 607606.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2366. en:caused by mutation in the kinesin family member 14 gene (kif14, 611279.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 14 gene (kif14, 611279.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2367. en:caused by mutation in the kinesin family member 1c gene (kif1c, 603060.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 1c gene (kif1c, 603060.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2368. en:caused by mutation in the kit ligand gene (kitlg, 184745.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kit ligand gene (kitlg, 184745.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2369. en:caused by mutation in the lamin a/c gene (lmna, 150330.0047) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin a/c gene (lmna, 150330.0047) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2370. en:caused by mutation in the laminin gamma-2 gene (lamc2, 150292.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the laminin gamma-2 gene (lamc2, 150292.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2371. en:caused by mutation in the leiomodin 3 (lmod3, 616112.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leiomodin 3 (lmod3, 616112.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2372. en:caused by mutation in the leucine-rich repeat-containing protein 50 gene (lrrc50, 613190.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucine-rich repeat-containing protein 50 gene (lrrc50, 613190.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2373. en:caused by mutation in the leucine-rich repeats- and immunoglobulin-like domains-containing protein 2 gene (lrig2, 608869.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucine-rich repeats- and immunoglobulin-like domains-containing protein 2 gene (lrig2, 608869.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2374. en:caused by mutation in the lysosomal trafficking regulator gene (chs1, 606897.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lysosomal trafficking regulator gene (chs1, 606897.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2375. en:caused by mutation in the mads box transcription enhancer factor 2, polypeptide c gene (mef2c, 600662.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mads box transcription enhancer factor 2, polypeptide c gene (mef2c, 600662.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2376. en:caused by mutation in the matrilin 3 gene (matn3, 602109.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the matrilin 3 gene (matn3, 602109.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2377. en:caused by mutation in the medium-chain acyl-coa dehydrogenase (mcad) gene (acadm, 607008.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the medium-chain acyl-coa dehydrogenase (mcad) gene (acadm, 607008.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2378. en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the membrane-bound transcription factor protease, site 2 gene (mbtps2, 300294.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2379. en:caused by mutation in the methylthioadenosine phosphorylase gene (mtap, 156540.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methylthioadenosine phosphorylase gene (mtap, 156540.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2380. en:caused by mutation in the microphthalmia-associated transcription factor gene (mitf, 156845.0006) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the microphthalmia-associated transcription factor gene (mitf, 156845.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2381. en:caused by mutation in the microtubule-associated tau protein gene (mapt, 157140.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the microtubule-associated tau protein gene (mapt, 157140.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2382. en:caused by mutation in the mitochondrial acetoacetyl-coa thiolase gene (acat1, 607809.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial acetoacetyl-coa thiolase gene (acat1, 607809.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2383. en:caused by mutation in the mitochondrial complex i, subunit nd1 gene (mtnd1, 516000.0012) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial complex i, subunit nd1 gene (mtnd1, 516000.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2384. en:caused by mutation in the mitochondrial nad kinase 2 gene (nadk2, 615787.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial nad kinase 2 gene (nadk2, 615787.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2385. en:caused by mutation in the mitochondrial trna-lysine gene (mttk, 590060.0005) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial trna-lysine gene (mttk, 590060.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2386. en:caused by mutation in the mitogen-activated kinase kinase kinase 1 gene (map3k1, 600982.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitogen-activated kinase kinase kinase 1 gene (map3k1, 600982.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2387. en:caused by mutation in the monocarboxylate transporter 8 gene (mct8, 300095.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the monocarboxylate transporter 8 gene (mct8, 300095.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2388. en:caused by mutation in the myosin heavy chain 11 gene (myh11, 160745.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin heavy chain 11 gene (myh11, 160745.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2389. en:caused by mutation in the myosin viia gene (myo7a, 276903.0011) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin viia gene (myo7a, 276903.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2390. en:caused by mutation in the myotubularin-related protein-2 gene (mtmr2, 603557.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myotubularin-related protein-2 gene (mtmr2, 603557.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2391. en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex 9 gene (ndufa9, 603834.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex 9 gene (ndufa9, 603834.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2392. en:caused by mutation in the nephrocystin 3 gene (nphp3, 608002.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nephrocystin 3 gene (nphp3, 608002.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2393. en:caused by mutation in the nephrocystin 4 gene (nphp4, 607215.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nephrocystin 4 gene (nphp4, 607215.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2394. en:caused by mutation in the neuroblastoma-amplified sequence gene (nbas, 608025.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neuroblastoma-amplified sequence gene (nbas, 608025.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2395. en:caused by mutation in the neurofibromin gene (nf1, 162200.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neurofibromin gene (nf1, 162200.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2396. en:caused by mutation in the nipped-b-like gene (nipbl, 608667.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nipped-b-like gene (nipbl, 608667.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2397. en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nk2 homeobox-5 gene (nkx2-5, 600584.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2398. en:caused by mutation in the nlr family, caspase recruitment domain-containing 4 gene (nlrc4, 606831.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nlr family, caspase recruitment domain-containing 4 gene (nlrc4, 606831.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2399. en:caused by mutation in the nol1/nop2/sun domain family, member 2 gene nsun2 (610916.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nol1/nop2/sun domain family, member 2 gene nsun2 (610916.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2400. en:caused by mutation in the nonimprinted gene in prader-willi syndrome/angelman syndrome chromosome region-1 (nipa1, 608145.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nonimprinted gene in prader-willi syndrome/angelman syndrome chromosome region-1 (nipa1, 608145.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2401. en:caused by mutation in the norrin gene (ndp, 300658.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the norrin gene (ndp, 300658.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2402. en:caused by mutation in the nucleolar protein-3 gene (nol3, 605235.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nucleolar protein-3 gene (nol3, 605235.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2403. en:caused by mutation in the peroxisome biogenesis factor 10 gene (pex10, 602859.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor 10 gene (pex10, 602859.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2404. en:caused by mutation in the peroxisome biogenesis factor-2 gene (pex2, 170993.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor-2 gene (pex2, 170993.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2405. en:caused by mutation in the peroxisome biogenesis factor-26 gene (pex26, 608666.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor-26 gene (pex26, 608666.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2406. en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0007) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatase and tensin homolog gene (pten, 601728.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2407. en:caused by mutation in the phosphatidylinositol 3-kinase, catalytic subunit delta gene (pik3cd, 602839.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol 3-kinase, catalytic subunit delta gene (pik3cd, 602839.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2408. en:caused by mutation in the phosphatidylinositol glycan, class l gene (pigl, 605947.0001). --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol glycan, class l gene (pigl, 605947.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2409. en:caused by mutation in the phosphatidylinositol polyphosphate 5-phosphatase gene (ocrl, 300535.0005) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol polyphosphate 5-phosphatase gene (ocrl, 300535.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2410. en:caused by mutation in the phosphomannomutase 2 gene (pmm2, 601785.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphomannomutase 2 gene (pmm2, 601785.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2411. en:caused by mutation in the phosphoribosylpyrophosphate synthetase 1 gene (prps1, 311850.0009) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoribosylpyrophosphate synthetase 1 gene (prps1, 311850.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2412. en:caused by mutation in the piezo-type mechanosensitive ion channel component 2 gene (piezo2, 613629.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the piezo-type mechanosensitive ion channel component 2 gene (piezo2, 613629.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2413. en:caused by mutation in the plastin 3 gene (pls3, 300131.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the plastin 3 gene (pls3, 300131.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2414. en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 2 gene (kcnj1, 600681.0014) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 2 gene (kcnj1, 600681.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2415. en:caused by mutation in the potassium channel, subfamily t, member 1 gene (kcnt1, 608167.0005) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium channel, subfamily t, member 1 gene (kcnt1, 608167.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2416. en:caused by mutation in the potassium channel, voltage-gated, shaker-related subfamily, member 5 gene (kcna5, 176267.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium channel, voltage-gated, shaker-related subfamily, member 5 gene (kcna5, 176267.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2417. en:caused by mutation in the potassium voltage-gated channel, isk-related subfamily, member 1 gene (kcne1, 176261.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, isk-related subfamily, member 1 gene (kcne1, 176261.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2418. en:caused by mutation in the presenilin-1 gene (psen1, 104311.0034) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the presenilin-1 gene (psen1, 104311.0034) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2419. en:caused by mutation in the prominin 1 gene (prom1, 604365.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prominin 1 gene (prom1, 604365.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2420. en:caused by mutation in the propionyl coenzyme a carboxylase, alpha polypeptide gene (pcca, 232000.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the propionyl coenzyme a carboxylase, alpha polypeptide gene (pcca, 232000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2421. en:caused by mutation in the protein kinase c substrate, 80-kd heavy chain gene (prkcsh, 177060.0001), or in the gene encoding the human homolog of s. cerevisiae sec63 (sec63, 608648.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein kinase c substrate, 80-kd heavy chain gene (prkcsh, 177060.0001), or in the gene encoding the human homolog of s. cerevisiae sec63 (sec63, 608648.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2422. en:caused by mutation in the protein kinase, amp-activated, noncatalytic, gamma-2 gene (prkag2, 602743.0007) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein kinase, amp-activated, noncatalytic, gamma-2 gene (prkag2, 602743.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2423. en:caused by mutation in the protein o-glucosyltransferase-1 gene (poglut1, 615618.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein o-glucosyltransferase-1 gene (poglut1, 615618.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2424. en:caused by mutation in the protein o-mannosyltransferase 2 gene (pomt2, 607439.0010) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein o-mannosyltransferase 2 gene (pomt2, 607439.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2425. en:caused by mutation in the protein tyrosine phosphatase, receptor type, c polypeptide gene (ptprc, 151460.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein tyrosine phosphatase, receptor type, c polypeptide gene (ptprc, 151460.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2426. en:caused by mutation in the protein-tyrosine phosphatase receptor-type, q gene (ptprq, 603317.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein-tyrosine phosphatase receptor-type, q gene (ptprq, 603317.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2427. en:caused by mutation in the pyridoxamine 5-prime-phosphate oxidase gene (pnpo, 603287.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pyridoxamine 5-prime-phosphate oxidase gene (pnpo, 603287.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2428. en:caused by mutation in the ras-associated protein rab33b gene (rab33b, 605950.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ras-associated protein rab33b gene (rab33b, 605950.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2429. en:caused by mutation in the red cell membrane band 3 gene (bnd3, 109270.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the red cell membrane band 3 gene (bnd3, 109270.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2430. en:caused by mutation in the regulatory factor x-associated protein gene (rfxap, 601861.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the regulatory factor x-associated protein gene (rfxap, 601861.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2431. en:caused by mutation in the ret protooncogene (ret, 164761.0013) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ret protooncogene (ret, 164761.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2432. en:caused by mutation in the reticulon 2 gene (rtn2, 603183.0001). --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the reticulon 2 gene (rtn2, 603183.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2433. en:caused by mutation in the rho gtpase-activating protein 31 gene (arhgap31, 610911.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rho gtpase-activating protein 31 gene (arhgap31, 610911.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2434. en:caused by mutation in the rpgrip1-like gene (rpgrip1l, 610937.0011) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rpgrip1-like gene (rpgrip1l, 610937.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2435. en:caused by mutation in the serologically defined colon cancer antigen 8 gene (sdccag8, 613524.0004) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the serologically defined colon cancer antigen 8 gene (sdccag8, 613524.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2436. en:caused by mutation in the serpin peptidase inhibitor, clade a, member 6 gene (serpina6, 122500.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the serpin peptidase inhibitor, clade a, member 6 gene (serpina6, 122500.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2437. en:caused by mutation in the sh3 domain-binding protein-2 gene (sh3bp2, 602104.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sh3 domain-binding protein-2 gene (sh3bp2, 602104.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2438. en:caused by mutation in the short chain acyl-coa dehydrogenase gene (acads, 606885.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the short chain acyl-coa dehydrogenase gene (acads, 606885.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2439. en:caused by mutation in the sigma nonopioid intracellular receptor 1 gene (sigmar1, 601978.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sigma nonopioid intracellular receptor 1 gene (sigmar1, 601978.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2440. en:caused by mutation in the skeletal muscle chloride channel-1 gene (clcn1, 118425.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the skeletal muscle chloride channel-1 gene (clcn1, 118425.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2441. en:caused by mutation in the slit- and ntrk-like family, member-6 gene (slitrk6, 609681.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the slit- and ntrk-like family, member-6 gene (slitrk6, 609681.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2442. en:caused by mutation in the slow-type myosin-binding protein-c gene (mybpc1, 160794.0003) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the slow-type myosin-binding protein-c gene (mybpc1, 160794.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2443. en:caused by mutation in the soluble guanylate cyclase 1, alpha 3 gene (gucy1a3, 139396.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the soluble guanylate cyclase 1, alpha 3 gene (gucy1a3, 139396.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2444. en:caused by mutation in the solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 gene (cact, 613698.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 gene (cact, 613698.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2445. en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, citrin), member 13 gene (slc25a13, 603859.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, citrin), member 13 gene (slc25a13, 603859.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2446. en:caused by mutation in the solute carrier family 52 (riboflavin transporter), member 3 gene (slc52a3, 613350.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 52 (riboflavin transporter), member 3 gene (slc52a3, 613350.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2447. en:caused by mutation in the solute carrier organic anion transporter family, member 2a1 gene (slco2a1, 601460.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier organic anion transporter family, member 2a1 gene (slco2a1, 601460.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2448. en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605291.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the stromal interaction molecule 1 gene (stim1, 605291.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2449. en:caused by mutation in the stt3, subunit of the oligosaccharyltransferase complex, s. cerevisiae, homolog of, b gene (stt3b, 608605.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the stt3, subunit of the oligosaccharyltransferase complex, s. cerevisiae, homolog of, b gene (stt3b, 608605.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2450. en:caused by mutation in the t7 gene 4-like protein with intramitochondrial nucleoid localization gene (c10orf2, 606075.0012) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the t7 gene 4-like protein with intramitochondrial nucleoid localization gene (c10orf2, 606075.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2451. en:caused by mutation in the tau tubulin kinase 2 gene (ttbk2, 611695.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tau tubulin kinase 2 gene (ttbk2, 611695.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2452. en:caused by mutation in the teashirt zinc finger homeobox-1 gene (tshz1, 614427.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the teashirt zinc finger homeobox-1 gene (tshz1, 614427.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2453. en:caused by mutation in the thiazide-sensitive na-cl cotransporter (slc12a3, 600968.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thiazide-sensitive na-cl cotransporter (slc12a3, 600968.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2454. en:caused by mutation in the thiopurine s-methyltransferase gene (tpmt, 187680.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thiopurine s-methyltransferase gene (tpmt, 187680.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2455. en:caused by mutation in the tho complex, subunit 6 gene (thoc6, 615403.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tho complex, subunit 6 gene (thoc6, 615403.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2456. en:caused by mutation in the thyroid transcription factor-1 gene (titf1, 600635.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thyroid transcription factor-1 gene (titf1, 600635.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2457. en:caused by mutation in the thyroid-stimulating hormone receptor gene (tshr, 603372.0005) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thyroid-stimulating hormone receptor gene (tshr, 603372.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2458. en:caused by mutation in the transcription factor-4 gene (tcf4, 602272.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transcription factor-4 gene (tcf4, 602272.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2459. en:caused by mutation in the transglutaminase 1 gene (tgm1, 190195.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transglutaminase 1 gene (tgm1, 190195.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2460. en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 3 gene (trpv3, 607066.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 3 gene (trpv3, 607066.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2461. en:caused by mutation in the transmembrane 43 gene (tmem43, 612048.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane 43 gene (tmem43, 612048.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2462. en:caused by mutation in the transmembrane protein 70 gene (tmem70, 612418.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 70 gene (tmem70, 612418.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2463. en:caused by mutation in the transportin 3 gene (tnpo3, 610032.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transportin 3 gene (tnpo3, 610032.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2464. en:caused by mutation in the tripartite motif-containing 37 gene (trim37, 605073.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tripartite motif-containing 37 gene (trim37, 605073.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2465. en:caused by mutation in the trna 5-methylaminomethyl-2-thiouridylate methyltransferase gene (trmu, 610230.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the trna 5-methylaminomethyl-2-thiouridylate methyltransferase gene (trmu, 610230.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2466. en:caused by mutation in the troponin i, fast-twitch skeletal muscle isoform, gene (tnni2, 191043.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the troponin i, fast-twitch skeletal muscle isoform, gene (tnni2, 191043.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2467. en:caused by mutation in the tubulin beta-1 gene (tubb1, 612901.0001). --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubulin beta-1 gene (tubb1, 612901.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2468. en:caused by mutation in the twist transcription factor gene (twist, 601622.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the twist transcription factor gene (twist, 601622.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2469. en:caused by mutation in the type iv voltage-gated sodium channel beta subunit gene (scn4b, 608256.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the type iv voltage-gated sodium channel beta subunit gene (scn4b, 608256.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2470. en:caused by mutation in the tyrosinase gene (tyr, 606933.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tyrosinase gene (tyr, 606933.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2471. en:caused by mutation in the udp-gal:beta-gal beta-1,3-galactosyltransferase polypeptide 6 gene (b3galt6, 615291.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the udp-gal:beta-gal beta-1,3-galactosyltransferase polypeptide 6 gene (b3galt6, 615291.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2472. en:caused by mutation in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0012) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2473. en:caused by mutation in the uroporphyrinogen decarboxylase gene (urod, 176100.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the uroporphyrinogen decarboxylase gene (urod, 176100.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2474. en:caused by mutation in the v-raf murine sarcoma viral oncogene homolog b1 gene (braf, 164757.0012) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-raf murine sarcoma viral oncogene homolog b1 gene (braf, 164757.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2475. en:caused by mutation in the voltage-gated potassium channel, shab-related subfamily, member 1 gene (kcnb1, 600397.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated potassium channel, shab-related subfamily, member 1 gene (kcnb1, 600397.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2476. en:caused by mutation in the wd repeat-containing protein 62 (wdr62, 613583.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein 62 (wdr62, 613583.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2477. en:caused by mutation in the wingless-type mmtv integration site family, member 7a gene (wnt7a, 601570.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wingless-type mmtv integration site family, member 7a gene (wnt7a, 601570.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2478. en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0002). --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0002). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2479. en:caused by mutation in the zinc finger and btb-domain containing 20 gene (zbtb20, 606025.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger and btb-domain containing 20 gene (zbtb20, 606025.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2480. en:caused by mutations in the acid lysosomal sphingomyelin phosphodiesterase-1 gene (smpd1, 607608.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the acid lysosomal sphingomyelin phosphodiesterase-1 gene (smpd1, 607608.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2481. en:caused by mutations in the alpha-l-fucosidase gene (fuca1, 230000.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the alpha-l-fucosidase gene (fuca1, 230000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2482. en:caused by mutations in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0005) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2483. en:caused by mutations in the cathepsin k gene (ctsk, 601105.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cathepsin k gene (ctsk, 601105.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2484. en:caused by mutations in the cystinosin gene (ctns, 219800.0009) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cystinosin gene (ctns, 219800.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2485. en:caused by mutations in the cytochrome p450, subfamily i, dioxin-inducible, polypeptide 1 gene (cyp1b1, 601771.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cytochrome p450, subfamily i, dioxin-inducible, polypeptide 1 gene (cyp1b1, 601771.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2486. en:caused by mutations in the delta-7-dehydrocholesterol reductase gene (dhcr7, 602858.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the delta-7-dehydrocholesterol reductase gene (dhcr7, 602858.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2487. en:caused by mutations in the emopamil-binding protein gene (ebp, 300205.0006) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the emopamil-binding protein gene (ebp, 300205.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2488. en:caused by mutations in the exostosin 2 gene (ext2, 133701.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the exostosin 2 gene (ext2, 133701.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2489. en:caused by mutations in the lamin b receptor gene (lbr, 600024.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the lamin b receptor gene (lbr, 600024.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2490. en:caused by mutations in the nlr family, pyrin-domain containing 12 gene (nlrp12, 609648.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the nlr family, pyrin-domain containing 12 gene (nlrp12, 609648.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2491. en:caused by mutations in the parkin gene (park2, 602544.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the parkin gene (park2, 602544.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2492. en:caused by mutations in the sry-box 9 gene (sox9, 114290.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the sry-box 9 gene (sox9, 114290.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2493. en:caused by mutations in the torsion dystonia-1 gene (dyt1, 605204.0001). --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the torsion dystonia-1 gene (dyt1, 605204.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2494. en:caused by mutations in the tumor protein p63 gene (tp63, 603273.0009) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the tumor protein p63 gene (tp63, 603273.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2495. en:caused by simultaneous mutation in the g protein-coupled receptor 98 gene (gpr98, 602851.0010) and the pdz domain-containing 7 gene (pdzd7, 612971.0002) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by simultaneous mutation in the g protein-coupled receptor 98 gene (gpr98, 602851.0010) and the pdz domain-containing 7 gene (pdzd7, 612971.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2496. en:caused by somatic mutation in the gnas gene (gnas1, 139320.0009) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the gnas gene (gnas1, 139320.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2497. en:contiguous gene deletion of at least 16mb encompassing 39 genes on 13q14 --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene deletion of at least 16mb encompassing 39 genes on 13q14 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2498. en:contiguous gene syndrome caused by deletion of chromosome xq21 including at least the rab escort protein 1 gene (chm, 300390) and the pou domain, class 3, transcription factor 4 gene (pou3f4, 300039) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by deletion of chromosome xq21 including at least the rab escort protein 1 gene (chm, 300390) and the pou domain, class 3, transcription factor 4 gene (pou3f4, 300039) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2499. en:mosaic trisomy 21, 2.4% --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:mosaic trisomy 21, 2.4% | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2500. en:susceptibility conferred by allele 2 of the dinucleotide repeat in the dopamine receptor drd5 gene (126453.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by allele 2 of the dinucleotide repeat in the dopamine receptor drd5 gene (126453.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2501. en:susceptibility conferred by mutation in the toll-like receptor-2 gene (tlr2, 603028.0001) --- r_associated #0: 24 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the toll-like receptor-2 gene (tlr2, 603028.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=24
  2502. en:a contiguous gene syndrome caused by deletion (160kb to 9mb) of 22q13.3 --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome caused by deletion (160kb to 9mb) of 22q13.3 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2503. en:a contiguous gene syndrome caused by deletion of the lissencephaly 1 gene (lis1, 601545) and the tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon isoform gene (ywhae, 605066) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome caused by deletion of the lissencephaly 1 gene (lis1, 601545) and the tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon isoform gene (ywhae, 605066) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2504. en:caused by a pentanucleotide repeat expansion (attct)n in the ataxin 10 gene (atxn10, 603516.0001). --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a pentanucleotide repeat expansion (attct)n in the ataxin 10 gene (atxn10, 603516.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2505. en:caused by contraction of a d4z4 repeat array at chromosome 4q35 --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by contraction of a d4z4 repeat array at chromosome 4q35 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2506. en:caused by deletion of mtdna --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion of mtdna | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2507. en:caused by duplication of 300kb (chr12:64,803,839-65,098,981 (grch37)) on 12q14 --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of 300kb (chr12:64,803,839-65,098,981 (grch37)) on 12q14 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2508. en:caused by duplication of 59kb on chromosome 2q35 --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplication of 59kb on chromosome 2q35 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2509. en:caused by hexanucleotide repeat expansion (ggcctg)n in the homolog of the s. cerevisiae nop56 gene (nop56, 614154.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by hexanucleotide repeat expansion (ggcctg)n in the homolog of the s. cerevisiae nop56 gene (nop56, 614154.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2510. en:caused by insertion of 8 extra octapeptide repeats in the prion protein gene (prnp, 176640.0020) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by insertion of 8 extra octapeptide repeats in the prion protein gene (prnp, 176640.0020) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2511. en:caused by mutation in glycoprotein 1b, platelet, alpha polypeptide (gp1ba, 606672.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in glycoprotein 1b, platelet, alpha polypeptide (gp1ba, 606672.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2512. en:caused by mutation in the 24-dehydrocholesterol reductase gene (dhcr24, 606418.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 24-dehydrocholesterol reductase gene (dhcr24, 606418.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2513. en:caused by mutation in the 290-kd centrosomal protein (cep290, 610142.0013) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 290-kd centrosomal protein (cep290, 610142.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2514. en:caused by mutation in the 300-kd e1a-binding protein gene (ep300, 602700.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 300-kd e1a-binding protein gene (ep300, 602700.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2515. en:caused by mutation in the 62-kd nucleoporin gene (nup62, 605815.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 62-kd nucleoporin gene (nup62, 605815.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2516. en:caused by mutation in the aarf domain-containing kinase 4 gene (adck4, 615567.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aarf domain-containing kinase 4 gene (adck4, 615567.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2517. en:caused by mutation in the actin-binding protein anillin gene (anln, 616027.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the actin-binding protein anillin gene (anln, 616027.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2518. en:caused by mutation in the adenosine monophosphate deaminase 1 gene (ampd1, 102770.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenosine monophosphate deaminase 1 gene (ampd1, 102770.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2519. en:caused by mutation in the adenosine monophosphate deaminase 2 gene (ampd2, 102771.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenosine monophosphate deaminase 2 gene (ampd2, 102771.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2520. en:caused by mutation in the adenylate cyclase 5 gene (adcy5, 600293.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenylate cyclase 5 gene (adcy5, 600293.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2521. en:caused by mutation in the adenylate kinase-1 gene (ak1, 103000.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenylate kinase-1 gene (ak1, 103000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2522. en:caused by mutation in the agrin gene (agrn, 103320.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the agrin gene (agrn, 103320.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2523. en:caused by mutation in the alpha-b-crystallin gene (cryab, 123590.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-b-crystallin gene (cryab, 123590.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2524. en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-l-iduronidase gene (idua, 252800.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2525. en:caused by mutation in the alpha-n-acetylgalactosaminidase gene (naga, 104170.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-n-acetylgalactosaminidase gene (naga, 104170.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2526. en:caused by mutation in the alsin gene (als2, 606352.0005) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alsin gene (als2, 606352.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2527. en:caused by mutation in the amnionless gene (amn, 605799.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the amnionless gene (amn, 605799.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2528. en:caused by mutation in the androgen receptor gene (ar, 313700.0008) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the androgen receptor gene (ar, 313700.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2529. en:caused by mutation in the angiotensin-converting enzyme gene (ace, 106180.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the angiotensin-converting enzyme gene (ace, 106180.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2530. en:caused by mutation in the angiotensinogen gene (agt, 106150.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the angiotensinogen gene (agt, 106150.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2531. en:caused by mutation in the antithrombin iii gene (at3, 107300.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the antithrombin iii gene (at3, 107300.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2532. en:caused by mutation in the artemis gene (artemis, 605988.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the artemis gene (artemis, 605988.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2533. en:caused by mutation in the aryl hydrocarbon receptor nuclear translocator-2 gene (arnt2, 606036.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aryl hydrocarbon receptor nuclear translocator-2 gene (arnt2, 606036.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2534. en:caused by mutation in the arylsulfatase e gene (arse, 300180.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the arylsulfatase e gene (arse, 300180.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2535. en:caused by mutation in the atp synthase, h+ transporting, mitochondrial f1 complex, alpha subunit 1 gene (atp5a1, 164360.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp synthase, h+ transporting, mitochondrial f1 complex, alpha subunit 1 gene (atp5a1, 164360.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2536. en:caused by mutation in the atp-binding cassette, subfamily a, member 1 gene (abca1, 600046.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily a, member 1 gene (abca1, 600046.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2537. en:caused by mutation in the atp-binding cassette, subfamily b, member 6 gene (abcb6, 605452.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily b, member 6 gene (abcb6, 605452.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2538. en:caused by mutation in the atpase family gene 3-like 2 gene (afg3l2, 604581.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase family gene 3-like 2 gene (afg3l2, 604581.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2539. en:caused by mutation in the atpase type 13a2 gene (atp13a2, 610513.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase type 13a2 gene (atp13a2, 610513.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2540. en:caused by mutation in the atpase, h+ transporting, lysosomal, v0 subunit a2 gene (atp6v0a2, 611716.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, h+ transporting, lysosomal, v0 subunit a2 gene (atp6v0a2, 611716.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2541. en:caused by mutation in the atpase, na+/k+ transporting, alpha-3 polypeptide (atp1a3, 182350.0014) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, na+/k+ transporting, alpha-3 polypeptide (atp1a3, 182350.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2542. en:caused by mutation in the bbs7 gene (bbs7, 607590.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bbs7 gene (bbs7, 607590.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2543. en:caused by mutation in the beta-3 gap junction protein gene (gjb3, 603324.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-3 gap junction protein gene (gjb3, 603324.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2544. en:caused by mutation in the blk nonreceptor tyrosine kinase gene (blk, 191305.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the blk nonreceptor tyrosine kinase gene (blk, 191305.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2545. en:caused by mutation in the bone morphogenetic protein 4 (bmp4, 112262.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bone morphogenetic protein 4 (bmp4, 112262.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2546. en:caused by mutation in the calsequestrin 1 gene (casq1, 114250.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calsequestrin 1 gene (casq1, 114250.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2547. en:caused by mutation in the camp-dependent protein kinase, regulatory, type i, alpha gene (prkar1a, 188830.0009) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the camp-dependent protein kinase, regulatory, type i, alpha gene (prkar1a, 188830.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2548. en:caused by mutation in the carboxypeptidase a6 gene (cpa6, 609562.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carboxypeptidase a6 gene (cpa6, 609562.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2549. en:caused by mutation in the cardiac troponin i gene (tnni3, 191044.0009) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cardiac troponin i gene (tnni3, 191044.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2550. en:caused by mutation in the cd36 antigen gene (cd36, 173510.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd36 antigen gene (cd36, 173510.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2551. en:caused by mutation in the cd96 gene (cd96, 606037.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd96 gene (cd96, 606037.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2552. en:caused by mutation in the cell death-inducing dffa-like effector c gene (cidec, 612120.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cell death-inducing dffa-like effector c gene (cidec, 612120.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2553. en:caused by mutation in the chloride channel-2 gene (clcn2, 600570.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chloride channel-2 gene (clcn2, 600570.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2554. en:caused by mutation in the cholinergic receptor, nicotinic, beta-1 subunit (chrnb1, 100710.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, beta-1 subunit (chrnb1, 100710.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2555. en:caused by mutation in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0005) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, delta polypeptide gene (chrnd, 100720.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2556. en:caused by mutation in the chromosome 12 open reading frame 65 gene (c12orf65, 613541.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 12 open reading frame 65 gene (c12orf65, 613541.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2557. en:caused by mutation in the claudin 19 (cldn19, 610036.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the claudin 19 (cldn19, 610036.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2558. en:caused by mutation in the cln5 gene (cln5, 608102.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cln5 gene (cln5, 608102.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2559. en:caused by mutation in the coagulation factor x gene (f10, 613872.0001). --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coagulation factor x gene (f10, 613872.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2560. en:caused by mutation in the cochlin gene (coch, 603196.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cochlin gene (coch, 603196.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2561. en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2562. en:caused by mutation in the collagen v, alpha-1 polypeptide gene (col5a1, 120215.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen v, alpha-1 polypeptide gene (col5a1, 120215.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2563. en:caused by mutation in the collagen vi, alpha-2 polypeptide gene (col6a2, 120240.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen vi, alpha-2 polypeptide gene (col6a2, 120240.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2564. en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0008) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2565. en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2566. en:caused by mutation in the collagenic tail of endplate acetylcholinesterase gene (colq, 603033.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagenic tail of endplate acetylcholinesterase gene (colq, 603033.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2567. en:caused by mutation in the complement component 1, q subcomponent, a chain gene (c1qa, 120550.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement component 1, q subcomponent, a chain gene (c1qa, 120550.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2568. en:caused by mutation in the complement component 5 gene (c5, 120900.0006) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement component 5 gene (c5, 120900.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2569. en:caused by mutation in the complex i, subunit nd1 gene (mtnd1, 516000.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complex i, subunit nd1 gene (mtnd1, 516000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2570. en:caused by mutation in the component of oligomeric golgi complex 6 gene (cog6, 606977.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the component of oligomeric golgi complex 6 gene (cog6, 606977.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2571. en:caused by mutation in the corneodesmosin gene (cdsn, 602593.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the corneodesmosin gene (cdsn, 602593.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2572. en:caused by mutation in the cyclin m4 gene (cnnm4, 607805.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclin m4 gene (cnnm4, 607805.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2573. en:caused by mutation in the cytochrome c oxidase iii gene (mtco3, 516050.0005) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase iii gene (mtco3, 516050.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2574. en:caused by mutation in the cytochrome c oxidase subunit x gene (cox10, 602125.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase subunit x gene (cox10, 602125.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2575. en:caused by mutation in the cytochrome c oxidase, subunit 15 gene (cox15, 603646.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome c oxidase, subunit 15 gene (cox15, 603646.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2576. en:caused by mutation in the cytochrome p450 subfamily xib, polypeptide 2 gene (cyp11b2, 124080.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450 subfamily xib, polypeptide 2 gene (cyp11b2, 124080.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2577. en:caused by mutation in the cytochrome p450, family 2, subfamily u, polypeptide 1 gene (cyp2u1, 610670.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450, family 2, subfamily u, polypeptide 1 gene (cyp2u1, 610670.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2578. en:caused by mutation in the cytochrome p450, family 7, subfamily b, polypeptide 1 gene (cyp7b1, 603711.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450, family 7, subfamily b, polypeptide 1 gene (cyp7b1, 603711.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2579. en:caused by mutation in the cytochrome p450, subfamily iic (mephenytoin 4'-hydroxylase) gene (cyp2c, 124020.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450, subfamily iic (mephenytoin 4'-hydroxylase) gene (cyp2c, 124020.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2580. en:caused by mutation in the cytochrome p450, subfamily xib, polypeptide 2 gene (cyp11b2, 124080.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450, subfamily xib, polypeptide 2 gene (cyp11b2, 124080.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2581. en:caused by mutation in the decorin gene (dcn, 125255.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the decorin gene (dcn, 125255.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2582. en:caused by mutation in the desmocollin 3 gene (dsc3, 600271.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the desmocollin 3 gene (dsc3, 600271.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2583. en:caused by mutation in the dfna5 gene (608798.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dfna5 gene (608798.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2584. en:caused by mutation in the diacylglycerol kinase, epsilon, 64-kd gene (dgke, 601440.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the diacylglycerol kinase, epsilon, 64-kd gene (dgke, 601440.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2585. en:caused by mutation in the dihydrolipoamide dehydrogenase gene (dld, 238331.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dihydrolipoamide dehydrogenase gene (dld, 238331.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2586. en:caused by mutation in the discoidin domain receptor family, member 2 gene (ddr2, 191311.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the discoidin domain receptor family, member 2 gene (ddr2, 191311.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2587. en:caused by mutation in the dna helicase, recq-like, type 4 gene (recql4, 603780.0012) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna helicase, recq-like, type 4 gene (recql4, 603780.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2588. en:caused by mutation in the dna polymerase-gamma gene (polg, 174763.0006) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna polymerase-gamma gene (polg, 174763.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2589. en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 2 gene (dnajb2, 604139.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dnaj/hsp40 homolog, subfamily b, member 2 gene (dnajb2, 604139.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2590. en:caused by mutation in the dopa decarboxylase gene (ddc, 107930.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dopa decarboxylase gene (ddc, 107930.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2591. en:caused by mutation in the dual-specificity phosphatase-6 gene (dusp6, 602748.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dual-specificity phosphatase-6 gene (dusp6, 602748.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2592. en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0013) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2593. en:caused by mutation in the dystonin gene (dst, 113810.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dystonin gene (dst, 113810.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2594. en:caused by mutation in the dystrophin gene (dmd, 300377.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dystrophin gene (dmd, 300377.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2595. en:caused by mutation in the dystrophin gene (dmd, 300377.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dystrophin gene (dmd, 300377.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2596. en:caused by mutation in the ef-hand domain (c-terminal)-containing 1 gene efhc1, (608815.0006) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ef-hand domain (c-terminal)-containing 1 gene efhc1, (608815.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2597. en:caused by mutation in the egf domain-specific o-linked n-acetylglucosamine transferase gene (eogt, 614789.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the egf domain-specific o-linked n-acetylglucosamine transferase gene (eogt, 614789.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2598. en:caused by mutation in the elongation of very long chain fatty acids-like 5 gene (elovl5, 611805.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the elongation of very long chain fatty acids-like 5 gene (elovl5, 611805.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2599. en:caused by mutation in the endoglin gene (eng, 131195.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endoglin gene (eng, 131195.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2600. en:caused by mutation in the endoplasmic reticulum membrane-associated rna degradation protein gene (ermard, 615532.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endoplasmic reticulum membrane-associated rna degradation protein gene (ermard, 615532.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2601. en:caused by mutation in the endothelin 3 (edn3, 131242.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endothelin 3 (edn3, 131242.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2602. en:caused by mutation in the endothelin 3 gene (edn3, 131242.0004) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endothelin 3 gene (edn3, 131242.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2603. en:caused by mutation in the endothelin-1 gene (edn1, 131240.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endothelin-1 gene (edn1, 131240.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2604. en:caused by mutation in the epithelial cellular adhesion molecule gene (epcam, 185535.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the epithelial cellular adhesion molecule gene (epcam, 185535.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2605. en:caused by mutation in the excision-repair cross-complementing group 8 gene (ercc8, 609412.0006) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the excision-repair cross-complementing group 8 gene (ercc8, 609412.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2606. en:caused by mutation in the excision-repair, complementing defective, in chinese hamster, number 5 gene (ercc5, 133530.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the excision-repair, complementing defective, in chinese hamster, number 5 gene (ercc5, 133530.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2607. en:caused by mutation in the ferm domain-containing 7 gene (frmd7, 300628.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ferm domain-containing 7 gene (frmd7, 300628.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2608. en:caused by mutation in the ferritin light chain gene (ftl, 134790.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ferritin light chain gene (ftl, 134790.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2609. en:caused by mutation in the fms-like tyrosine kinase-4 gene (flt4, 136352.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fms-like tyrosine kinase-4 gene (flt4, 136352.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2610. en:caused by mutation in the forkhead box c1 gene (foxc1, 601090.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead box c1 gene (foxc1, 601090.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2611. en:caused by mutation in the forkhead box e3 gene (foxe3, 601094.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead box e3 gene (foxe3, 601094.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2612. en:caused by mutation in the fructose-1,6-bisphosphatase gene (fbp1, 611570.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fructose-1,6-bisphosphatase gene (fbp1, 611570.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2613. en:caused by mutation in the fumarate hydratase gene (fh, 136850.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fumarate hydratase gene (fh, 136850.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2614. en:caused by mutation in the gamma subunit of the nonvoltage-gated sodium channel 1 gene (scnn1g, 600761.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma subunit of the nonvoltage-gated sodium channel 1 gene (scnn1g, 600761.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2615. en:caused by mutation in the gamma-2 laminin gene (lamc2, 150292.0006) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma-2 laminin gene (lamc2, 150292.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2616. en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606589.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ganglioside-induced differentiation-associated protein-1 gene (gdap1, 606589.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2617. en:caused by mutation in the gli-kruppel family member 2 gene (gli2, 165230.0008) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gli-kruppel family member 2 gene (gli2, 165230.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2618. en:caused by mutation in the glial cell line-derived neurotrophic factor gene (gdnf, 600837.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glial cell line-derived neurotrophic factor gene (gdnf, 600837.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2619. en:caused by mutation in the glioma-inactivated leucine-rich 1 gene (lgi1, 604619.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glioma-inactivated leucine-rich 1 gene (lgi1, 604619.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2620. en:caused by mutation in the glycerol kinase gene (gk, 300474) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycerol kinase gene (gk, 300474) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2621. en:caused by mutation in the glycosyltransferase-like domain-containing protein 2 gene (gtdc2, 614828.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycosyltransferase-like domain-containing protein 2 gene (gtdc2, 614828.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2622. en:caused by mutation in the glypican 3 gene (gpc3, 300037.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glypican 3 gene (gpc3, 300037.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2623. en:caused by mutation in the gnas complex locus, antisense transcript (gnasas, 610540.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gnas complex locus, antisense transcript (gnasas, 610540.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2624. en:caused by mutation in the granulin gene (grn, 138945.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the granulin gene (grn, 138945.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2625. en:caused by mutation in the granulocyte colony-stimulating factor-3 receptor gene (csf3r, 138971.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the granulocyte colony-stimulating factor-3 receptor gene (csf3r, 138971.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2626. en:caused by mutation in the h19 gene (h19, 103290.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the h19 gene (h19, 103290.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2627. en:caused by mutation in the heat repeat-containing protein-2 gene (heatr2, 614864.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heat repeat-containing protein-2 gene (heatr2, 614864.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2628. en:caused by mutation in the heat-shock transcription factor 4 (hsf4, 602438.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the heat-shock transcription factor 4 (hsf4, 602438.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2629. en:caused by mutation in the histidine ammonia lyase gene (hal, 609457.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the histidine ammonia lyase gene (hal, 609457.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2630. en:caused by mutation in the histone deacetylase 6 gene (hdac6, 300272.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the histone deacetylase 6 gene (hdac6, 300272.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2631. en:caused by mutation in the homeo box c13 gene (hoxc13, 142976.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeo box c13 gene (hoxc13, 142976.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2632. en:caused by mutation in the homeobox (h6 family) 1 gene (hmx1, 142992.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeobox (h6 family) 1 gene (hmx1, 142992.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2633. en:caused by mutation in the homolog a of s. cerevisiae trna methyltransferase 10 gene (trmt10a, 616013.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog a of s. cerevisiae trna methyltransferase 10 gene (trmt10a, 616013.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2634. en:caused by mutation in the homolog of chlamydomonas poc1 centriolar protein a gene (poc1a, 614783.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of chlamydomonas poc1 centriolar protein a gene (poc1a, 614783.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2635. en:caused by mutation in the homolog of mouse peripherin 2 (prph2, 179605.0009) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of mouse peripherin 2 (prph2, 179605.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2636. en:caused by mutation in the homolog of s. cerevisiae atp-dependent dna helicase hfm1 gene (hfm1, 615684.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of s. cerevisiae atp-dependent dna helicase hfm1 gene (hfm1, 615684.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2637. en:caused by mutation in the homolog of the a. nidulans nude 1 gene (nde1, 609449.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the a. nidulans nude 1 gene (nde1, 609449.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2638. en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 122 gene (ift122, 606045.0001). --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 122 gene (ift122, 606045.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2639. en:caused by mutation in the homolog of the drosophila dachsous 1 gene (dchs1, 603057.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila dachsous 1 gene (dchs1, 603057.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2640. en:caused by mutation in the homolog of the drosophila lines 1 gene (lins1, 610350.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila lines 1 gene (lins1, 610350.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2641. en:caused by mutation in the homolog of the mouse peripherin 2 gene (prph2, 179605.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse peripherin 2 gene (prph2, 179605.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2642. en:caused by mutation in the homolog of the s. cerevisiae iba57 gene (iba57, 615316.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae iba57 gene (iba57, 615316.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2643. en:caused by mutation in the homolog of the s. cerevisiae vacuolar protein sorting 53 gene (vps53, 615850.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae vacuolar protein sorting 53 gene (vps53, 615850.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2644. en:caused by mutation in the host cell factor c1 gene (hcfc1, 300019.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the host cell factor c1 gene (hcfc1, 300019.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2645. en:caused by mutation in the hyls1 gene (hyls1, 610693.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hyls1 gene (hyls1, 610693.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2646. en:caused by mutation in the immunoglobulin-like domain-containing receptor 1 gene (ildr1, 609739.0001). --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the immunoglobulin-like domain-containing receptor 1 gene (ildr1, 609739.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2647. en:caused by mutation in the insulin receptor gene (insr, 147670.0012) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the insulin receptor gene (insr, 147670.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2648. en:caused by mutation in the insulin receptor gene (insr, 147670.0037) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the insulin receptor gene (insr, 147670.0037) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2649. en:caused by mutation in the jagged 1 gene (jag1, 601920.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the jagged 1 gene (jag1, 601920.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2650. en:caused by mutation in the junction plakoglobin gene (jup, 173325.0002). --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the junction plakoglobin gene (jup, 173325.0002). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2651. en:caused by mutation in the junctional adhesion molecule 3 gene (jam3, 606871.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the junctional adhesion molecule 3 gene (jam3, 606871.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2652. en:caused by mutation in the keratin 16 gene (krt16, 148068.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 16 gene (krt16, 148068.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2653. en:caused by mutation in the keratin 5 gene (krt5, 148040.0018) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 5 gene (krt5, 148040.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2654. en:caused by mutation in the keratin-14 gene (krt14, 148066.0004). --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin-14 gene (krt14, 148066.0004). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2655. en:caused by mutation in the keratin-14 gene (krt14, 148066.0015) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin-14 gene (krt14, 148066.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2656. en:caused by mutation in the kiaa0196 gene (kiaa0196, 610657.0004) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kiaa0196 gene (kiaa0196, 610657.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2657. en:caused by mutation in the kiaa0415 gene (kiaa0415, 613653.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kiaa0415 gene (kiaa0415, 613653.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2658. en:caused by mutation in the lamin a/c gene (lmna, 150330.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin a/c gene (lmna, 150330.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2659. en:caused by mutation in the lamin b receptor gene (lbr, 600024.0007) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin b receptor gene (lbr, 600024.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2660. en:caused by mutation in the leucine zipper transcription factor-like 1 gene (lztfl1, 606568.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucine zipper transcription factor-like 1 gene (lztfl1, 606568.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2661. en:caused by mutation in the leucine- and proline-enriched proteoglycan 1 gene (lepre1, 610339.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucine- and proline-enriched proteoglycan 1 gene (lepre1, 610339.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2662. en:caused by mutation in the leucine-rich repeat-containing protein 6 gene (lrrc6, 614930.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the leucine-rich repeat-containing protein 6 gene (lrrc6, 614930.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2663. en:caused by mutation in the light polypeptide neurofilament protein gene (nefl, 162280.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the light polypeptide neurofilament protein gene (nefl, 162280.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2664. en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0009) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the low density lipoprotein receptor-related protein 4 gene (lrp4, 604270.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2665. en:caused by mutation in the malonyl-coa decarboxylase gene (mlycd, 606761.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the malonyl-coa decarboxylase gene (mlycd, 606761.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2666. en:caused by mutation in the melanocortin-2 receptor gene (mc2r, 607397.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the melanocortin-2 receptor gene (mc2r, 607397.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2667. en:caused by mutation in the methyl-cpg-binding protein 2 gene (mecp2, 300005.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methyl-cpg-binding protein 2 gene (mecp2, 300005.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2668. en:caused by mutation in the microphthalmia-associated transcription factor gene (mitf, 156845.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the microphthalmia-associated transcription factor gene (mitf, 156845.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2669. en:caused by mutation in the microtubule-associated protein tau gene (mapt, 157140.0019) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the microtubule-associated protein tau gene (mapt, 157140.0019) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2670. en:caused by mutation in the mitochondrial arginyl-trna synthetase gene (rars2, 611524.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial arginyl-trna synthetase gene (rars2, 611524.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2671. en:caused by mutation in the mitochondrial complex i, subunit nd3 gene (mtnd3, 516002.0004) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial complex i, subunit nd3 gene (mtnd3, 516002.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2672. en:caused by mutation in the mitochondrial transfer rna serine 2 gene (mtts2, 590085.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial transfer rna serine 2 gene (mtts2, 590085.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2673. en:caused by mutation in the mitogen-activated protein kinase kinase 1 gene (map2k2, 601263.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitogen-activated protein kinase kinase 1 gene (map2k2, 601263.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2674. en:caused by mutation in the myelin-oligodendrocyte glycoprotein (mog, 159465.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myelin-oligodendrocyte glycoprotein (mog, 159465.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2675. en:caused by mutation in the myeloproliferative leukemia virus oncogene (mpl, 159530.0009) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myeloproliferative leukemia virus oncogene (mpl, 159530.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2676. en:caused by mutation in the myosin va gene (myo5a, 160777) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin va gene (myo5a, 160777) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2677. en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2678. en:caused by mutation in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0006) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2679. en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, alpha/beta subunits gene (gnptab, 607840.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, alpha/beta subunits gene (gnptab, 607840.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2680. en:caused by mutation in the nadh dehydrogenase (ubiquinone) 1 alpha subcomplex, 1 gene (ndufa1, 300078.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) 1 alpha subcomplex, 1 gene (ndufa1, 300078.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2681. en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex, assembly factor 3 gene (ndufaf3, 612911.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh-dehydrogenase 1 alpha subcomplex, assembly factor 3 gene (ndufaf3, 612911.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2682. en:caused by mutation in the nephrocystin gene (nphp1, 607100.0005) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nephrocystin gene (nphp1, 607100.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2683. en:caused by mutation in the neuraminidase 1 gene (neu1, 608272.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neuraminidase 1 gene (neu1, 608272.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2684. en:caused by mutation in the neutrophil-expressed elastase gene (elane, 130130.0006) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neutrophil-expressed elastase gene (elane, 130130.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2685. en:caused by mutation in the nicotinamide nucleotide adenylyltransferase-1 gene (nmnat1, 608700.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nicotinamide nucleotide adenylyltransferase-1 gene (nmnat1, 608700.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2686. en:caused by mutation in the nuclear receptor subfamily 0, group b, member 1 gene (nr0b1, 300473.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear receptor subfamily 0, group b, member 1 gene (nr0b1, 300473.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2687. en:caused by mutation in the o-phosphoserine trna-selenocysteine trna synthase gene (sepsecs, 613009.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the o-phosphoserine trna-selenocysteine trna synthase gene (sepsecs, 613009.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2688. en:caused by mutation in the opa1 gene (opa1, 605290.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the opa1 gene (opa1, 605290.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2689. en:caused by mutation in the otoancorin gene (otoa, 607038.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the otoancorin gene (otoa, 607038.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2690. en:caused by mutation in the paired box gene 2 gene (pax2, 167409.0013) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the paired box gene 2 gene (pax2, 167409.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2691. en:caused by mutation in the perilipin-1 gene (plin1, 170290.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the perilipin-1 gene (plin1, 170290.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2692. en:caused by mutation in the phosphatidylinositol glycan, class n gene (pign, 606097.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol glycan, class n gene (pign, 606097.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2693. en:caused by mutation in the phosphodiesterase 11a gene (pde11a, 604961.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphodiesterase 11a gene (pde11a, 604961.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2694. en:caused by mutation in the phosphodiesterase-6c, cgmp-specific, cone, alpha prime gene (pde6c, 600827.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphodiesterase-6c, cgmp-specific, cone, alpha prime gene (pde6c, 600827.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2695. en:caused by mutation in the phospholamban gene (pln, 172405.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phospholamban gene (pln, 172405.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2696. en:caused by mutation in the phospholipase c, beta-4 gene (plcb4, 600810.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phospholipase c, beta-4 gene (plcb4, 600810.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2697. en:caused by mutation in the phytanoyl-coa hydroxylase gene (phyh, 602026.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phytanoyl-coa hydroxylase gene (phyh, 602026.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2698. en:caused by mutation in the plakoglobin gene (jup, 173325.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the plakoglobin gene (jup, 173325.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2699. en:caused by mutation in the plakophilin-2 gene (602861.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the plakophilin-2 gene (602861.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2700. en:caused by mutation in the platelet glycoprotein ib, beta polypeptide, gene (gp1bb, 138720.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the platelet glycoprotein ib, beta polypeptide, gene (gp1bb, 138720.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2701. en:caused by mutation in the platelet glycoprotein ix gene (gp9, 173515.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the platelet glycoprotein ix gene (gp9, 173515.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2702. en:caused by mutation in the plectin gene (plec1, 601282.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the plectin gene (plec1, 601282.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2703. en:caused by mutation in the polycystin 1 gene (pkd1, 601313.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polycystin 1 gene (pkd1, 601313.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2704. en:caused by mutation in the polycystin 2 gene (pkd2, 173910.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polycystin 2 gene (pkd2, 173910.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2705. en:caused by mutation in the potassium voltage-gated channel, shal-related subfamily, member 3 gene (kcnd3, 605411.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, shal-related subfamily, member 3 gene (kcnd3, 605411.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2706. en:caused by mutation in the potassium voltage-gated channel, subfamily h, member 2 gene or human ether-a-go-go related gene (kcnh2, 152427.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, subfamily h, member 2 gene or human ether-a-go-go related gene (kcnh2, 152427.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2707. en:caused by mutation in the pou domain, class 1, transcription factor 1 gene (pou1f1, 173110.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pou domain, class 1, transcription factor 1 gene (pou1f1, 173110.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2708. en:caused by mutation in the prickle-like 1 gene (prickle1, 608500.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prickle-like 1 gene (prickle1, 608500.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2709. en:caused by mutation in the prosaposin gene (psap, 176801.0005) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prosaposin gene (psap, 176801.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2710. en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase gene (pomgnt1, 606822.0014) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein o-mannose beta-1,2-n-acetylglucosaminyltransferase gene (pomgnt1, 606822.0014) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2711. en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0005) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2712. en:caused by mutation in the ras-associated protein rab39b (300774.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ras-associated protein rab39b (300774.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2713. en:caused by mutation in the recombination-activating gene 1 (rag1, 179615.0018) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the recombination-activating gene 1 (rag1, 179615.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2714. en:caused by mutation in the regulator of telomere elongation helicase 1 gene (rtel1, 608833.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the regulator of telomere elongation helicase 1 gene (rtel1, 608833.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2715. en:caused by mutation in the ribosomal protein l21 gene (rpl12, 603636.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribosomal protein l21 gene (rpl12, 603636.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2716. en:caused by mutation in the sal-like 2 gene (sall2, 602219.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sal-like 2 gene (sall2, 602219.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2717. en:caused by mutation in the set-binding factor-2 gene (sbf2, 607697.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the set-binding factor-2 gene (sbf2, 607697.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2718. en:caused by mutation in the sh3 domain and tetratricopeptide repeat domain 2 gene (sh3tc2, 608206.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sh3 domain and tetratricopeptide repeat domain 2 gene (sh3tc2, 608206.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2719. en:caused by mutation in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0025) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0025) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2720. en:caused by mutation in the solute carrier family 19, folate transporter, member 3 gene (slc19a3, 606152.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 19, folate transporter, member 3 gene (slc19a3, 606152.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2721. en:caused by mutation in the solute carrier family 22 (organic cation transporter), member 5 gene (slc22a5, 603377.0001). --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 22 (organic cation transporter), member 5 gene (slc22a5, 603377.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2722. en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, ornithine transporter), member 15 gene (slc25a15, 603861.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, ornithine transporter), member 15 gene (slc25a15, 603861.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2723. en:caused by mutation in the solute carrier family 30 (zinc transporter), member 10 gene (slc30a10, 611146.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 30 (zinc transporter), member 10 gene (slc30a10, 611146.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2724. en:caused by mutation in the solute carrier family 34 (sodium/phosphate cotransporter), member 2 gene (slc34a2, 604217.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 34 (sodium/phosphate cotransporter), member 2 gene (slc34a2, 604217.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2725. en:caused by mutation in the solute carrier family 34, member 3 gene (609826.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 34, member 3 gene (609826.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2726. en:caused by mutation in the solute carrier family 35 (udp-n-acetylglucosamine transporter), member 3 gene (slc35a3, 605632.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 35 (udp-n-acetylglucosamine transporter), member 3 gene (slc35a3, 605632.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2727. en:caused by mutation in the solute carrier family 38 (amino acid transporter), member 8 gene (slc38a8, 615585.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 38 (amino acid transporter), member 8 gene (slc38a8, 615585.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2728. en:caused by mutation in the spartin gene (spg20, 607111.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the spartin gene (spg20, 607111.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2729. en:caused by mutation in the spatacsin gene (spg11, 610844.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the spatacsin gene (spg11, 610844.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2730. en:caused by mutation in the sperm-associated antigen 1 gene (spag1, 603395.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sperm-associated antigen 1 gene (spag1, 603395.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2731. en:caused by mutation in the sry-box-10 gene (sox10, 602229.0005) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sry-box-10 gene (sox10, 602229.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2732. en:caused by mutation in the succinate dehydrogenase complex assembly factor-2 gene (sdhaf2, 613019.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the succinate dehydrogenase complex assembly factor-2 gene (sdhaf2, 613019.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2733. en:caused by mutation in the succinate dehydrogenase complex, subunit a, flavoprotein gene (sdha, 614165.0005) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the succinate dehydrogenase complex, subunit a, flavoprotein gene (sdha, 614165.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2734. en:caused by mutation in the succinate-coa ligase adp-forming beta-subunit gene (sucla2, 603921.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the succinate-coa ligase adp-forming beta-subunit gene (sucla2, 603921.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2735. en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the survival of motor neuron 1 gene (smn1, 600354.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2736. en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily b, member 1 gene (smarcb1, 601607.0005) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the swi/snf-related, matrix-associated, actin-dependent regulator of chromatin, subfamily b, member 1 gene (smarcb1, 601607.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2737. en:caused by mutation in the syntaxin 11 gene (stx11, 605014.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the syntaxin 11 gene (stx11, 605014.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2738. en:caused by mutation in the system b(0) neutral amino acid transporter-1 gene (slc6a19, 608893.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the system b(0) neutral amino acid transporter-1 gene (slc6a19, 608893.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2739. en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0012) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2740. en:caused by mutation in the tdp-glucose 4,6-dehydratase gene (tgds, 616146.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tdp-glucose 4,6-dehydratase gene (tgds, 616146.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2741. en:caused by mutation in the thap domain-containing protein 1 gene (thap1, 609520.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thap domain-containing protein 1 gene (thap1, 609520.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2742. en:caused by mutation in the thrombospondin-type laminin g domain and ear repeats gene (tspear, 612920.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thrombospondin-type laminin g domain and ear repeats gene (tspear, 612920.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2743. en:caused by mutation in the tia1 cytotoxic granule-associated rna-binding protein gene (tia1, 603518.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tia1 cytotoxic granule-associated rna-binding protein gene (tia1, 603518.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2744. en:caused by mutation in the tight junction protein 2 gene (tjp2, 607709.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tight junction protein 2 gene (tjp2, 607709.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2745. en:caused by mutation in the transcription factor sp7 gene gene (sp7, 606633.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transcription factor sp7 gene gene (sp7, 606633.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2746. en:caused by mutation in the transient receptor potential cation channel, subfamily m, member 4 gene (trpm4, 606936.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transient receptor potential cation channel, subfamily m, member 4 gene (trpm4, 606936.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2747. en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0008) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2748. en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0018) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 67 gene (tmem67, 609884.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2749. en:caused by mutation in the tripartite motif-containing protein 32 gene (trim32, 602290.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tripartite motif-containing protein 32 gene (trim32, 602290.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2750. en:caused by mutation in the troponin t3, fast skeletal muscle gene (tnnt3, 600692.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the troponin t3, fast skeletal muscle gene (tnnt3, 600692.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2751. en:caused by mutation in the tumor necrosis factor receptor superfamily, member 11a gene (tnfrsf11a, 603499.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tumor necrosis factor receptor superfamily, member 11a gene (tnfrsf11a, 603499.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2752. en:caused by mutation in the type iv collagen alpha-2 gene (col4a2, 120090.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the type iv collagen alpha-2 gene (col4a2, 120090.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2753. en:caused by mutation in the ubiquilin 2 gene (ubqln2, 300264.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquilin 2 gene (ubqln2, 300264.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2754. en:caused by mutation in the ubiquitin-specific protease 9, x chromosome gene (usp9x, 300072.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquitin-specific protease 9, x chromosome gene (usp9x, 300072.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2755. en:caused by mutation in the ventral anterior homeobox-1 gene (vax1, 604924.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ventral anterior homeobox-1 gene (vax1, 604924.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2756. en:caused by mutation in the vesicle-associated membrane protein-associated protein b gene (vapb, 605704.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the vesicle-associated membrane protein-associated protein b gene (vapb, 605704.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2757. en:caused by mutation in the voltage-gated potassium channel, subfamily h, member 1 gene (kcnh1, 603305.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated potassium channel, subfamily h, member 1 gene (kcnh1, 603305.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2758. en:caused by mutation in the wd repeat-containing protein 11 gene (wdr11, 606417.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein 11 gene (wdr11, 606417.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2759. en:caused by mutation in the wingless-type mmtv integration site family, member 10a gene (wnt10a, 606268.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wingless-type mmtv integration site family, member 10a gene (wnt10a, 606268.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2760. en:caused by mutation in the x-prolyl aminopeptidase 3 gene (xpnpep3, 613553.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the x-prolyl aminopeptidase 3 gene (xpnpep3, 613553.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2761. en:caused by mutation in tumor protein p53 (tp53, 191170.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in tumor protein p53 (tp53, 191170.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2762. en:caused by mutations in the 17-beta-hydroxysteroid dehydrogenase iv gene (hsd17b4, 601860.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the 17-beta-hydroxysteroid dehydrogenase iv gene (hsd17b4, 601860.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2763. en:caused by mutations in the apolipoprotein lp(a) gene (lpa, 152200.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the apolipoprotein lp(a) gene (lpa, 152200.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2764. en:caused by mutations in the beta-glucuronidase gene (gusb, 611499.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the beta-glucuronidase gene (gusb, 611499.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2765. en:caused by mutations in the cln8 gene (cln8, 607837.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cln8 gene (cln8, 607837.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2766. en:caused by mutations in the follicle-stimulating hormone receptor gene (fshr, 136435.0008) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the follicle-stimulating hormone receptor gene (fshr, 136435.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2767. en:caused by mutations in the gli-kruppel family member 3 gene (gli3, 165240.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the gli-kruppel family member 3 gene (gli3, 165240.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2768. en:caused by mutations in the glial fibrillary acidic protein gene (gfap, 137780.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the glial fibrillary acidic protein gene (gfap, 137780.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2769. en:caused by mutations in the hamartin gene (tsc1, 605284.0007) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the hamartin gene (tsc1, 605284.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2770. en:caused by mutations in the heat-shock 22-kd protein 8 gene (hspb8, 608014.0003) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the heat-shock 22-kd protein 8 gene (hspb8, 608014.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2771. en:caused by mutations in the hexosaminidase a, alpha polypeptide gene (hexa, 272800.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the hexosaminidase a, alpha polypeptide gene (hexa, 272800.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2772. en:caused by mutations in the homolog of the drosophila notch 3 gene (notch3, 600276.0001). --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the homolog of the drosophila notch 3 gene (notch3, 600276.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2773. en:caused by mutations in the interleukin-2 receptor, gamma chain, gene (il2rg, 308380.0008) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the interleukin-2 receptor, gamma chain, gene (il2rg, 308380.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2774. en:caused by mutations in the kindlin 1 gene (kind1, 607900.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the kindlin 1 gene (kind1, 607900.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2775. en:caused by mutations in the mannosephosphate isomerase gene (mpi, 154550.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the mannosephosphate isomerase gene (mpi, 154550.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2776. en:caused by mutations in the mitochondrial atp synthase 6 gene (mtatp6, 516060.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the mitochondrial atp synthase 6 gene (mtatp6, 516060.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2777. en:caused by mutations in the mitochondrial rna-processing endoribonuclease gene (rmrp, 157660.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the mitochondrial rna-processing endoribonuclease gene (rmrp, 157660.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2778. en:caused by mutations in the n-acetyl-alpha-d-glucosaminidase gene (naglu, 609701.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the n-acetyl-alpha-d-glucosaminidase gene (naglu, 609701.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2779. en:caused by mutations in the senataxin gene (setx, 608465.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the senataxin gene (setx, 608465.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2780. en:caused by mutations in the synaptosomal-associated protein 29kd gene (snap29, 604202.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the synaptosomal-associated protein 29kd gene (snap29, 604202.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2781. en:caused by mutations in the vitamin d 25-hydroxylase gene (cyp2r1, 608713.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the vitamin d 25-hydroxylase gene (cyp2r1, 608713.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2782. en:caused by mutations in treacle gene (tcof1, 154500.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in treacle gene (tcof1, 154500.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2783. en:caused by palindrome-mediated interchromosomal insertions on chromosome xq27.1 --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by palindrome-mediated interchromosomal insertions on chromosome xq27.1 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2784. en:caused by somatic mosaic mutation in the neuroblastoma ras viral (v-ras) oncogene homolog gene (nras, 164790.0002) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mosaic mutation in the neuroblastoma ras viral (v-ras) oncogene homolog gene (nras, 164790.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2785. en:caused by trinucleotide repeat expansion (cag)n in the ataxin-3 gene (mjd, 607047.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by trinucleotide repeat expansion (cag)n in the ataxin-3 gene (mjd, 607047.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2786. en:contiguous gene syndrome caused by 4.3-mb triplication of chromosome 4q32.1-q32.2 --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by 4.3-mb triplication of chromosome 4q32.1-q32.2 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2787. en:contiguous gene syndrome caused by deletion (minimum 1.3mb) of chromosome 6pter-p24 --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by deletion (minimum 1.3mb) of chromosome 6pter-p24 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2788. en:contiguous gene syndrome caused by deletion of 3.2mb deletion on 8q22.1 --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by deletion of 3.2mb deletion on 8q22.1 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2789. en:features other than acd/mpv are variably present --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:features other than acd/mpv are variably present | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2790. en:susceptibility conferred by mutation in the homolog of the mouse aristaless-like 4 gene (alx4, 605420.0009) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the homolog of the mouse aristaless-like 4 gene (alx4, 605420.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2791. en:susceptibility conferred by mutation in the homolog of the s. pombe checkpoint kinase 2 gene (chek2, 604373.0007) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the homolog of the s. pombe checkpoint kinase 2 gene (chek2, 604373.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2792. en:susceptibility conferred by mutation in the major histocompatibility complex, class ii, dr beta-1 gene (hla-dr1b, 142857.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the major histocompatibility complex, class ii, dr beta-1 gene (hla-dr1b, 142857.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2793. en:susceptibility conferred by mutation in the neuroligin-3 gene (nlgn3, 300336.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the neuroligin-3 gene (nlgn3, 300336.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2794. en:susceptibility conferred by mutation in the semaphorin 3a gene (sema3a, 603961.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the semaphorin 3a gene (sema3a, 603961.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2795. en:susceptibility conferred by mutations in the protein tyrosine phosphatase, receptor type, c polypeptide gene (ptprc, 151460.0001) --- r_associated #0: 23 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutations in the protein tyrosine phosphatase, receptor type, c polypeptide gene (ptprc, 151460.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=23
  2796. en:a contiguous gene syndrome caused by deletion of the stereocilin gene (strc, 606440) and the sperm-associated cation channel-2 gene (catsper2, 607249) gene --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene syndrome caused by deletion of the stereocilin gene (strc, 606440) and the sperm-associated cation channel-2 gene (catsper2, 607249) gene | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2797. en:associated with mutation in the neuroligin-4 gene (nlgn4, 300427.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:associated with mutation in the neuroligin-4 gene (nlgn4, 300427.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2798. en:caused by a 2.5- to 3.8-kb insertion containing pentanucleotide expansion repeats including (tggaa)n within an intron of the brain-expressed, associated with nedd4 gene (bean, 612051.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a 2.5- to 3.8-kb insertion containing pentanucleotide expansion repeats including (tggaa)n within an intron of the brain-expressed, associated with nedd4 gene (bean, 612051.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2799. en:caused by a trinucleotide repeat expansion (gcg)n in the poly(a)-binding protein-2 gene (pabpn1, 602279.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a trinucleotide repeat expansion (gcg)n in the poly(a)-binding protein-2 gene (pabpn1, 602279.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2800. en:caused by complex genomic rearrangement resulting in misexpression of the paired-like homeodomain transcription factor-1 gene (pitx1, 602149) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by complex genomic rearrangement resulting in misexpression of the paired-like homeodomain transcription factor-1 gene (pitx1, 602149) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2801. en:caused by deletion in the nephrocystin gene (nphp1, 607100.0005) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion in the nephrocystin gene (nphp1, 607100.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2802. en:caused by deletion of 3.7mb on chromosome 6q13-q14 --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by deletion of 3.7mb on chromosome 6q13-q14 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2803. en:caused by disruption of the calmodulin-binding transcription activator 1 gene (camta1, 611501.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by disruption of the calmodulin-binding transcription activator 1 gene (camta1, 611501.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2804. en:caused by expanded cag trinucleotide repeats in the ataxin-1 gene (atx1, 601556.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by expanded cag trinucleotide repeats in the ataxin-1 gene (atx1, 601556.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2805. en:caused by fusion of the cytochrome p450, subfamily xib, polypeptide 1 gene (cyp11b1, 610613) and the cytochrome p450, subfamily xib, polypeptide 2 gene (cyp11b2, 124080) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by fusion of the cytochrome p450, subfamily xib, polypeptide 1 gene (cyp11b1, 610613) and the cytochrome p450, subfamily xib, polypeptide 2 gene (cyp11b2, 124080) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2806. en:caused by microdeletions of 11p13 --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by microdeletions of 11p13 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2807. en:caused by mutation in aldo-keto reductase family 1, member c2 gene (akr1c2, 600450.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in aldo-keto reductase family 1, member c2 gene (akr1c2, 600450.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2808. en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0005) and the gap junction protein, beta-6 gene (gjb6, 604418.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in both the gap junction protein, beta-2 gene (gjb2, 121011.0005) and the gap junction protein, beta-6 gene (gjb6, 604418.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2809. en:caused by mutation in cytochrome p450, family 24, subfamily a, polypeptide-1 gene (cyp24a1, 126065.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in cytochrome p450, family 24, subfamily a, polypeptide-1 gene (cyp24a1, 126065.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2810. en:caused by mutation in lactase (lct, 603202.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in lactase (lct, 603202.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2811. en:caused by mutation in leprecan-like-1 gene (leprel1, 610341.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in leprecan-like-1 gene (leprel1, 610341.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2812. en:caused by mutation in origin recognition complex, subunit 6, gene (orc6, 607213.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in origin recognition complex, subunit 6, gene (orc6, 607213.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2813. en:caused by mutation in paired box gene-1 (pax1, 167411.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in paired box gene-1 (pax1, 167411.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2814. en:caused by mutation in the 3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2 gene (papss2, 603005.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2 gene (papss2, 603005.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2815. en:caused by mutation in the 4-hydroxyphenylpyruvate dioxygenase gene (hpd, 609695.0005) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 4-hydroxyphenylpyruvate dioxygenase gene (hpd, 609695.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2816. en:caused by mutation in the abhydrolase domain-containing protein 12 gene (abhd12, 613599.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the abhydrolase domain-containing protein 12 gene (abhd12, 613599.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2817. en:caused by mutation in the acid phosphatase 5, tartrate resistant gene (acp5, 171640.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the acid phosphatase 5, tartrate resistant gene (acp5, 171640.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2818. en:caused by mutation in the acylglycerol kinase gene (agk, 610345.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the acylglycerol kinase gene (agk, 610345.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2819. en:caused by mutation in the adamts-like 4 gene (adamtsl4, 610113.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adamts-like 4 gene (adamtsl4, 610113.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2820. en:caused by mutation in the adaptin, beta-3a gene (adtb3a, 603401.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adaptin, beta-3a gene (adtb3a, 603401.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2821. en:caused by mutation in the adaptor-related protein complex 4, mu-1 subunit gene (ap4m1, 602296.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adaptor-related protein complex 4, mu-1 subunit gene (ap4m1, 602296.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2822. en:caused by mutation in the adenylate kinase-2 gene (ak2, 103020.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adenylate kinase-2 gene (ak2, 103020.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2823. en:caused by mutation in the adp ribosylation factor-like 2-binding protein gene (arl2bp, 615407.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adp ribosylation factor-like 2-binding protein gene (arl2bp, 615407.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2824. en:caused by mutation in the alanyl-trna synthetase 2 gene (aars2, 612035.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alanyl-trna synthetase 2 gene (aars2, 612035.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2825. en:caused by mutation in the alpha subunit of succinate-coenzyme a ligase (suclg1, 611224.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha subunit of succinate-coenzyme a ligase (suclg1, 611224.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2826. en:caused by mutation in the alpha-1 subunit of the glycine receptor gene (glra1, 138491.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-1 subunit of the glycine receptor gene (glra1, 138491.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2827. en:caused by mutation in the alpha-3 catenin gene (ctnna3, 607667.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-3 catenin gene (ctnna3, 607667.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2828. en:caused by mutation in the alpha-sarcoglycan gene (sgca, 600119.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-sarcoglycan gene (sgca, 600119.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2829. en:caused by mutation in the ankyrin 3 gene (ank3, 600465.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ankyrin 3 gene (ank3, 600465.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2830. en:caused by mutation in the ankyrin repeat domain-containing protein 11 gene (ankrd11, 611192.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ankyrin repeat domain-containing protein 11 gene (ankrd11, 611192.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2831. en:caused by mutation in the annexin a5 gene (anxa5, 131230.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the annexin a5 gene (anxa5, 131230.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2832. en:caused by mutation in the apolipoprotein a-i gene (apoa1, 107680.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the apolipoprotein a-i gene (apoa1, 107680.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2833. en:caused by mutation in the armadillo repeat-containing protein 4 gene (armc4, 615408.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the armadillo repeat-containing protein 4 gene (armc4, 615408.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2834. en:caused by mutation in the aryl hydrocarbon receptor-interacting protein gene (aip, 605555.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aryl hydrocarbon receptor-interacting protein gene (aip, 605555.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2835. en:caused by mutation in the atp synthase f1 complex assembly factor-2 gene (atpaf2, 608918.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp synthase f1 complex assembly factor-2 gene (atpaf2, 608918.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2836. en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0002) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily b, member 4 gene (abcb4, 171060.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2837. en:caused by mutation in the atp-binding cassette, subfamily g, member 5 gene (abcg5, 605459.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily g, member 5 gene (abcg5, 605459.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2838. en:caused by mutation in the atpase, ca++ transporting, slow-twitch, cardiac muscle-2 gene (atp2a2, 108740) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, ca++ transporting, slow-twitch, cardiac muscle-2 gene (atp2a2, 108740) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2839. en:caused by mutation in the atpase, h+ transporting, lysosomal, v0 subunit a2 gene (atp6v0a2, 611716.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, h+ transporting, lysosomal, v0 subunit a2 gene (atp6v0a2, 611716.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2840. en:caused by mutation in the atr-x gene (atrx, 300032.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atr-x gene (atrx, 300032.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2841. en:caused by mutation in the aurora kinase c gene (aurkc, 603495.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aurora kinase c gene (aurkc, 603495.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2842. en:caused by mutation in the beta choline kinase gene (chkb, 612395.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta choline kinase gene (chkb, 612395.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2843. en:caused by mutation in the beta subunit of the hydroxyacyl-coa dehydrogenase/3-ketoacyl-coa thiolase/enoyl-coa hydratase (hadhb, 143450.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta subunit of the hydroxyacyl-coa dehydrogenase/3-ketoacyl-coa thiolase/enoyl-coa hydratase (hadhb, 143450.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2844. en:caused by mutation in the beta-1,3-glucuronyltransferase 3 gene (b3gat3, 606374.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1,3-glucuronyltransferase 3 gene (b3gat3, 606374.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2845. en:caused by mutation in the beta-1,3-n-acetylglucosaminyltransferase gene (b3gnt1, 605581.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1,3-n-acetylglucosaminyltransferase gene (b3gnt1, 605581.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2846. en:caused by mutation in the beta-1,4-n-acetylgalactosaminyltransferase 1 gene (b4galnt1, 601873.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1,4-n-acetylgalactosaminyltransferase 1 gene (b4galnt1, 601873.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2847. en:caused by mutation in the c. elegans homolog of the ectopic p-granules autophagy protein 5 gene (epg5, 615068.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the c. elegans homolog of the ectopic p-granules autophagy protein 5 gene (epg5, 615068.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2848. en:caused by mutation in the c1 esterase inhibitor gene (c1nh, 106100.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the c1 esterase inhibitor gene (c1nh, 106100.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2849. en:caused by mutation in the c20orf7 gene (c20orf7, 612360.0002) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the c20orf7 gene (c20orf7, 612360.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2850. en:caused by mutation in the cadherin 3 gene (cdh3, 114021.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cadherin 3 gene (cdh3, 114021.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2851. en:caused by mutation in the cadherin-related family, member 1 gene (cdhr1, 609502.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cadherin-related family, member 1 gene (cdhr1, 609502.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2852. en:caused by mutation in the calcium/calmodulin-dependent serine protein kinase gene (cask, 300172.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calcium/calmodulin-dependent serine protein kinase gene (cask, 300172.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2853. en:caused by mutation in the calmodulin-1 gene (calm1, 114180.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calmodulin-1 gene (calm1, 114180.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2854. en:caused by mutation in the calmodulin-1 gene (calm1, 114180.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the calmodulin-1 gene (calm1, 114180.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2855. en:caused by mutation in the carcinoembryonic antigen-related cell adhesion molecule-16 gene (ceacam16, 614591.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carcinoembryonic antigen-related cell adhesion molecule-16 gene (ceacam16, 614591.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2856. en:caused by mutation in the cardiac troponin t2 gene (tnnt2, 191045.0011) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cardiac troponin t2 gene (tnnt2, 191045.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2857. en:caused by mutation in the cardiotrophin-like cytokine gene (clcf1, 607672.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cardiotrophin-like cytokine gene (clcf1, 607672.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2858. en:caused by mutation in the cat eye syndrome chromosome region, candidate 1 gene (cecr1, 607575.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cat eye syndrome chromosome region, candidate 1 gene (cecr1, 607575.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2859. en:caused by mutation in the caveolin-3 gene (cav3, 601253.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the caveolin-3 gene (cav3, 601253.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2860. en:caused by mutation in the cd81 antigen gene (cd81, 186845.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd81 antigen gene (cd81, 186845.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2861. en:caused by mutation in the cereblon gene (crbn, 609262.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cereblon gene (crbn, 609262.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2862. en:caused by mutation in the cgmp-dependent regulatory protein kinase, type 1 gene (prkg1, 176894.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cgmp-dependent regulatory protein kinase, type 1 gene (prkg1, 176894.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2863. en:caused by mutation in the chaperonin-containing t-complex peptide-1 subunit 5 gene (cct5, 610150.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chaperonin-containing t-complex peptide-1 subunit 5 gene (cct5, 610150.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2864. en:caused by mutation in the chromodomain helicase dna-binding protein 2 gene (chd2, 602119.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromodomain helicase dna-binding protein 2 gene (chd2, 602119.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2865. en:caused by mutation in the chromosome 10 open reading frame 11 gene (c10orf11, 614537.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chromosome 10 open reading frame 11 gene (c10orf11, 614537.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2866. en:caused by mutation in the cln2 gene (cln2, 607998.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cln2 gene (cln2, 607998.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2867. en:caused by mutation in the cln6 gene (606725.0011). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cln6 gene (606725.0011). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2868. en:caused by mutation in the cln6 gene (cln6, 606725.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cln6 gene (cln6, 606725.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2869. en:caused by mutation in the coagulation factor ix gene (f9, 300746.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coagulation factor ix gene (f9, 300746.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2870. en:caused by mutation in the coiled-coil domain-containing protein 114 gene (ccdc114, 615038.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil domain-containing protein 114 gene (ccdc114, 615038.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2871. en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0026) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0026) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2872. en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0029) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0029) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2873. en:caused by mutation in the collagen ix, alpha-1 polypeptide gene (col9a1, 120210.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ix, alpha-1 polypeptide gene (col9a1, 120210.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2874. en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2875. en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0002). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen type vii, alpha-1 gene (col7a1, 120120.0002). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2876. en:caused by mutation in the collagen vi, alpha-1 polypeptide gene (col6a1, 120220.0007) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen vi, alpha-1 polypeptide gene (col6a1, 120220.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2877. en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen xi, alpha-1 polypeptide gene (col11a1, 120280.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2878. en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0012) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen xi, alpha-2 polypeptide gene (col11a2, 120290.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2879. en:caused by mutation in the collagen, type iv, alpha-5 gene (col4a5, 303630.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type iv, alpha-5 gene (col4a5, 303630.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2880. en:caused by mutation in the complement component 1, q subcomponent, b chain gene (c1qb, 120570.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement component 1, q subcomponent, b chain gene (c1qb, 120570.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2881. en:caused by mutation in the complement component 1, q subcomponent, c chain gene (c1qc, 120575.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement component 1, q subcomponent, c chain gene (c1qc, 120575.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2882. en:caused by mutation in the complex i, subunit nd3 gene (mtnd3, 516002.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complex i, subunit nd3 gene (mtnd3, 516002.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2883. en:caused by mutation in the component of oligomeric golgi complex 4 gene (cog4, 606976.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the component of oligomeric golgi complex 4 gene (cog4, 606976.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2884. en:caused by mutation in the cyclin-dependent kinase inhibitor 1c gene (cdkn1c, 600856.0007) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cyclin-dependent kinase inhibitor 1c gene (cdkn1c, 600856.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2885. en:caused by mutation in the cystatin b gene (cstb, 601145.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cystatin b gene (cstb, 601145.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2886. en:caused by mutation in the cytochrome p450 oxidoreductase gene (por, 124015.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450 oxidoreductase gene (por, 124015.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2887. en:caused by mutation in the cytokine-like factor 1 gene (crlf1, 604237.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytokine-like factor 1 gene (crlf1, 604237.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2888. en:caused by mutation in the cytotoxic t lymphocyte-associated 4 gene (ctla4, 123890.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytotoxic t lymphocyte-associated 4 gene (ctla4, 123890.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2889. en:caused by mutation in the deleted in colorectal carcinoma gene (dcc, 120470.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the deleted in colorectal carcinoma gene (dcc, 120470.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2890. en:caused by mutation in the desmoplakin gene (dsp, 125647.0015) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the desmoplakin gene (dsp, 125647.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2891. en:caused by mutation in the diacylglycerol o-acyltransferase 1 gene (dgat1, 604900.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the diacylglycerol o-acyltransferase 1 gene (dgat1, 604900.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2892. en:caused by mutation in the direct iap-binding protein with low pi (diablo, 605219.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the direct iap-binding protein with low pi (diablo, 605219.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2893. en:caused by mutation in the disintegrin-like and metalloproteinase with thrombospondin type 1 motif 18 gene (adamts18, 607512.0002) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the disintegrin-like and metalloproteinase with thrombospondin type 1 motif 18 gene (adamts18, 607512.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2894. en:caused by mutation in the dna methyltransferase 1 gene (dnmt1, 126375.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna methyltransferase 1 gene (dnmt1, 126375.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2895. en:caused by mutation in the dolichyl-diphosphooligosaccharide-protein glycosyltransferase gene (ddost, 602202.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dolichyl-diphosphooligosaccharide-protein glycosyltransferase gene (ddost, 602202.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2896. en:caused by mutation in the downstream of tyrosine kinase 7 gene (dok7, 610285.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the downstream of tyrosine kinase 7 gene (dok7, 610285.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2897. en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dynamin-2 gene (dnm2, 602378.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2898. en:caused by mutation in the dyskerin gene (dkc1, 300126.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dyskerin gene (dkc1, 300126.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2899. en:caused by mutation in the ectodysplasin a gene (ed1, 300451.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ectodysplasin a gene (ed1, 300451.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2900. en:caused by mutation in the emerin gene (emd, 300384.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the emerin gene (emd, 300384.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2901. en:caused by mutation in the ercc6-like 2 gene (ercc6l2, 615667.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ercc6-like 2 gene (ercc6l2, 615667.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2902. en:caused by mutation in the eukaryotic translation initiation factor 2-alpha kinase 3 (eif2ak3, 604032.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation initiation factor 2-alpha kinase 3 (eif2ak3, 604032.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2903. en:caused by mutation in the eukaryotic translation initiation factor 2-alpha kinase 4 gene (eif2ak4, 609280.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the eukaryotic translation initiation factor 2-alpha kinase 4 gene (eif2ak4, 609280.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2904. en:caused by mutation in the ferritin heavy chain-1 gene (fth1, 134770.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ferritin heavy chain-1 gene (fth1, 134770.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2905. en:caused by mutation in the fibroblast growth factor 23 gene (fgf23, 605380.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor 23 gene (fgf23, 605380.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2906. en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0010) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-2 gene (fgfr2, 176943.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2907. en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2908. en:caused by mutation in the g protein-coupled receptor 56 gene (gpr56, 604110.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the g protein-coupled receptor 56 gene (gpr56, 604110.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2909. en:caused by mutation in the g-protein, alpha-stimulating 1 gene (gnas1, 139320.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the g-protein, alpha-stimulating 1 gene (gnas1, 139320.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2910. en:caused by mutation in the gaip c-terminus-interacting protein 3 (gipc3, 608792.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gaip c-terminus-interacting protein 3 (gipc3, 608792.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2911. en:caused by mutation in the gamma-c-crystallin (crygc, 123680.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma-c-crystallin (crygc, 123680.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2912. en:caused by mutation in the gap junction protein, gamma-2 gene (gjc2, 608803.0009) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gap junction protein, gamma-2 gene (gjc2, 608803.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2913. en:caused by mutation in the gastric intrinsic factor gene (gif, 609342.0001). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gastric intrinsic factor gene (gif, 609342.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2914. en:caused by mutation in the gata-binding protein 1 gene (gata1, 305371.0006) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein 1 gene (gata1, 305371.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2915. en:caused by mutation in the gata-binding protein-3 gene (gata3, 131320.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein-3 gene (gata3, 131320.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2916. en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gata-binding protein-6 gene (gata6, 601656.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2917. en:caused by mutation in the glutamate receptor, ionotropic, ampa, 3 gene (gria3, 305915.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glutamate receptor, ionotropic, ampa, 3 gene (gria3, 305915.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2918. en:caused by mutation in the glycine cleavage system h protein gene (gcsh, 238330.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glycine cleavage system h protein gene (gcsh, 238330.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2919. en:caused by mutation in the granulocyte-macrophage colony-stimulating factor receptor, beta (csf2rb, 138981.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the granulocyte-macrophage colony-stimulating factor receptor, beta (csf2rb, 138981.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2920. en:caused by mutation in the guanine nucleotide-binding protein, alpha-activating activity polypeptide o gene (gnao1, 139311.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the guanine nucleotide-binding protein, alpha-activating activity polypeptide o gene (gnao1, 139311.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2921. en:caused by mutation in the hect domain and rcc1-like domain 2 (herc2, 605837.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hect domain and rcc1-like domain 2 (herc2, 605837.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2922. en:caused by mutation in the homeo box-a11 gene (hoxa11, 142958.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeo box-a11 gene (hoxa11, 142958.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2923. en:caused by mutation in the homogentisate 1,2-dioxygenase gene (hgd, 607474.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homogentisate 1,2-dioxygenase gene (hgd, 607474.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2924. en:caused by mutation in the homolog of drosophila frizzled-6 gene (fzd6, 603409.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of drosophila frizzled-6 gene (fzd6, 603409.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2925. en:caused by mutation in the homolog of s. cerevisiae rad51 gene (rad51, 179617.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of s. cerevisiae rad51 gene (rad51, 179617.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2926. en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 27 gene (ift27, 615870.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport 27 gene (ift27, 615870.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2927. en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport-43 gene (itf43, 614068.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the chlamydomonas intraflagellar transport-43 gene (itf43, 614068.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2928. en:caused by mutation in the homolog of the drosophila muscle segment homeo box (msx1, 142983.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila muscle segment homeo box (msx1, 142983.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2929. en:caused by mutation in the homolog of the drosophila rogdi gene (rogdi, 614574.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila rogdi gene (rogdi, 614574.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2930. en:caused by mutation in the homolog of the mouse aristaless-like 4 gene (alx4, 605420.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the mouse aristaless-like 4 gene (alx4, 605420.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2931. en:caused by mutation in the homolog of the s. cerevisiae bms1 ribosome assembly protein gene (bms1, 611448.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae bms1 ribosome assembly protein gene (bms1, 611448.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2932. en:caused by mutation in the homolog of the s. cerevisiae fig4 gene (fig4, 609390.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae fig4 gene (fig4, 609390.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2933. en:caused by mutation in the homolog of the s. cerevisiae mediator of rna polymerase ii transcription, subunit 12 (med12, 300188.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae mediator of rna polymerase ii transcription, subunit 12 (med12, 300188.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2934. en:caused by mutation in the homolog of the s. cerevisiae sco1 gene (sco1, 603644.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae sco1 gene (sco1, 603644.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2935. en:caused by mutation in the human homolog of the mouse noggin gene (nog, 602991.0012) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the human homolog of the mouse noggin gene (nog, 602991.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2936. en:caused by mutation in the human homolog of the mouse progressive ankylosis gene (ankh, 605145.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the human homolog of the mouse progressive ankylosis gene (ankh, 605145.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2937. en:caused by mutation in the hypoxanthine phosphoribosyltransferase gene (hprt1, 308000.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hypoxanthine phosphoribosyltransferase gene (hprt1, 308000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2938. en:caused by mutation in the hypoxanthine phosphoribosyltransferase gene (hprt1, 308000.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hypoxanthine phosphoribosyltransferase gene (hprt1, 308000.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2939. en:caused by mutation in the immunoglobulin mu binding protein 2 gene (ighmbp2, 600502.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the immunoglobulin mu binding protein 2 gene (ighmbp2, 600502.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2940. en:caused by mutation in the immunoglobulin superfamily member-3 gene (igsf3, 603491.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the immunoglobulin superfamily member-3 gene (igsf3, 603491.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2941. en:caused by mutation in the inhibitor of kappa light polypeptide gene enhancer in b cells, kinase complex-associated protein gene (ikbkap, 603722.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inhibitor of kappa light polypeptide gene enhancer in b cells, kinase complex-associated protein gene (ikbkap, 603722.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2942. en:caused by mutation in the inositol polyphosphate phosphatase-like 1 gene (inppl1, 600829.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inositol polyphosphate phosphatase-like 1 gene (inppl1, 600829.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2943. en:caused by mutation in the integrin-beta-4 gene (itgb4, 147557.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the integrin-beta-4 gene (itgb4, 147557.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2944. en:caused by mutation in the intestinal cell kinase gene (ick, 612325.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the intestinal cell kinase gene (ick, 612325.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2945. en:caused by mutation in the iodotyrosine deiodinase gene (iyd, 612025.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the iodotyrosine deiodinase gene (iyd, 612025.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2946. en:caused by mutation in the isg15 ubiquitin-like modifier gene (isg15, 146571.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the isg15 ubiquitin-like modifier gene (isg15, 146571.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2947. en:caused by mutation in the kat8 regulatory nsl complex subunit 1 gene (kansl1, 612452.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kat8 regulatory nsl complex subunit 1 gene (kansl1, 612452.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2948. en:caused by mutation in the katanin, p80 subunit, b1 gene (katnb1, 602703.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the katanin, p80 subunit, b1 gene (katnb1, 602703.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2949. en:caused by mutation in the keratin 14 gene (krt14, 148066.0002) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 14 gene (krt14, 148066.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2950. en:caused by mutation in the keratin-14 gene (krt14, 148066.0016) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin-14 gene (krt14, 148066.0016) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2951. en:caused by mutation in the keratin-5 gene (krt5, 148040.0009) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin-5 gene (krt5, 148040.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2952. en:caused by mutation in the kiaa0226 gene (kiaa0226, 613516.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kiaa0226 gene (kiaa0226, 613516.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2953. en:caused by mutation in the kinesin family member 4a gene (kif4a, 300521.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 4a gene (kif4a, 300521.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2954. en:caused by mutation in the kinesin family member 7 gene (kif7, 611254.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kinesin family member 7 gene (kif7, 611254.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2955. en:caused by mutation in the krupple-like factor 1 gene (klf1, 600599.0006) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the krupple-like factor 1 gene (klf1, 600599.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2956. en:caused by mutation in the lamin a/c gene (lmna, 150330.0030) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin a/c gene (lmna, 150330.0030) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2957. en:caused by mutation in the laminin alpha-2 chain gene (lama2, 156225.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the laminin alpha-2 chain gene (lama2, 156225.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2958. en:caused by mutation in the latent transforming growth factor-beta-binding protein 2 gene (ltbp2, 602091.0012) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the latent transforming growth factor-beta-binding protein 2 gene (ltbp2, 602091.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2959. en:caused by mutation in the lim domain-binding 3 gene (ldb3, 605906.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lim domain-binding 3 gene (ldb3, 605906.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2960. en:caused by mutation in the low density lipoprotein receptor-related protein-5 gene (lrp5, 603506.0020) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the low density lipoprotein receptor-related protein-5 gene (lrp5, 603506.0020) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2961. en:caused by mutation in the low-density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0013) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the low-density lipoprotein receptor-related protein 5 gene (lrp5, 603506.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2962. en:caused by mutation in the lysine (k)-specific demethylase-6a gene (kdm6a, 300128.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lysine (k)-specific demethylase-6a gene (kdm6a, 300128.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2963. en:caused by mutation in the lysyl-trna synthetase gene (lars, 601421.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lysyl-trna synthetase gene (lars, 601421.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2964. en:caused by mutation in the m-phase specific plk1 interacting protein (mplkip, 609188.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the m-phase specific plk1 interacting protein (mplkip, 609188.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2965. en:caused by mutation in the magnesium-dependent protein phosphatase 2c gene (ppm2c, 605993.0001). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the magnesium-dependent protein phosphatase 2c gene (ppm2c, 605993.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2966. en:caused by mutation in the mediator complex subunit 17 gene (med17, 603810.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mediator complex subunit 17 gene (med17, 603810.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2967. en:caused by mutation in the minichromosome maintenance deficient domain containing-1 gene (mcmdc1, 610098.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the minichromosome maintenance deficient domain containing-1 gene (mcmdc1, 610098.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2968. en:caused by mutation in the mitochondrial complex i, subunit nd5 gene (mtnd5, 516005.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial complex i, subunit nd5 gene (mtnd5, 516005.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2969. en:caused by mutation in the mitochondrial transfer rna histidine gene (mtth, 590040.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial transfer rna histidine gene (mtth, 590040.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2970. en:caused by mutation in the mitochondrial trna (valine) gene (mttv, 590105.0002) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial trna (valine) gene (mttv, 590105.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2971. en:caused by mutation in the mks1 gene (mks1, 609883.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mks1 gene (mks1, 609883.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2972. en:caused by mutation in the mothers against decapentaplegic, drosophila, homolog of, 3 gene (smad3, 603109.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mothers against decapentaplegic, drosophila, homolog of, 3 gene (smad3, 603109.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2973. en:caused by mutation in the myelin protein zero gene (mpz, 159440.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myelin protein zero gene (mpz, 159440.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2974. en:caused by mutation in the myotilin gene (ttid, 604103.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myotilin gene (ttid, 604103.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2975. en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 4 gene (ndufs4, 602694.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 4 gene (ndufs4, 602694.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2976. en:caused by mutation in the nadh dehydrogenase, subunit 5 gene (mtnd5, 516005.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase, subunit 5 gene (mtnd5, 516005.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2977. en:caused by mutation in the nephrocystin 3 gene (nphp3, 608002.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nephrocystin 3 gene (nphp3, 608002.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2978. en:caused by mutation in the neuronal nicotinic cholinergic receptor, alpha polypeptide 4 gene (chrna4, 118504.0002) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neuronal nicotinic cholinergic receptor, alpha polypeptide 4 gene (chrna4, 118504.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2979. en:caused by mutation in the neutrophil cytosolic factor 4 gene (ncf4, 601488.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neutrophil cytosolic factor 4 gene (ncf4, 601488.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2980. en:caused by mutation in the never in mitosis gene a-related kinase 1 gene (nek1, 604588.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the never in mitosis gene a-related kinase 1 gene (nek1, 604588.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2981. en:caused by mutation in the never in mitosis gene a-related kinase 8 gene (nek8, 609799.0002) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the never in mitosis gene a-related kinase 8 gene (nek8, 609799.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2982. en:caused by mutation in the nonerythrocytic beta 2 spectrin gene (sptbn2, 604985.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nonerythrocytic beta 2 spectrin gene (sptbn2, 604985.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2983. en:caused by mutation in the nuclear receptor subfamily 2, group f, member 1 gene (nr2f1, 132890.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear receptor subfamily 2, group f, member 1 gene (nr2f1, 132890.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2984. en:caused by mutation in the nuclear receptor subfamily 2, group f, member 2 gene (nr2f2, 107773.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear receptor subfamily 2, group f, member 2 gene (nr2f2, 107773.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2985. en:caused by mutation in the nucleolar protein family a, member 2 gene (nola2, 606470.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nucleolar protein family a, member 2 gene (nola2, 606470.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2986. en:caused by mutation in the otogelin gene (otog, 064487.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the otogelin gene (otog, 064487.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2987. en:caused by mutation in the paired box 3 gene (pax3, 606597.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the paired box 3 gene (pax3, 606597.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2988. en:caused by mutation in the palmitoyl-protein thioesterase 1 gene (ppt1, 600722.0001). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the palmitoyl-protein thioesterase 1 gene (ppt1, 600722.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2989. en:caused by mutation in the perforin 1 gene (prf1, 170280.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the perforin 1 gene (prf1, 170280.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2990. en:caused by mutation in the peroxisome biogenesis factor 7 gene (pex7, 601757.0007) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor 7 gene (pex7, 601757.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2991. en:caused by mutation in the phosphatidylinositol glycan, class o gene (pigo, 614730.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol glycan, class o gene (pigo, 614730.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2992. en:caused by mutation in the phosphoglycerate mutase 2 gene (pgam2, 612931.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoglycerate mutase 2 gene (pgam2, 612931.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2993. en:caused by mutation in the plasminogen gene (plg, 173350.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the plasminogen gene (plg, 173350.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2994. en:caused by mutation in the plectin 1 gene (plec1, 601282.0006) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the plectin 1 gene (plec1, 601282.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2995. en:caused by mutation in the post-gpi attachment to proteins 3 gene (pgap3, 611801.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the post-gpi attachment to proteins 3 gene (pgap3, 611801.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2996. en:caused by mutation in the presenilin-1 gene (psen1, 104311.0023) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the presenilin-1 gene (psen1, 104311.0023) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2997. en:caused by mutation in the proliferating cell nuclear antigen gene (pcna, 176740.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the proliferating cell nuclear antigen gene (pcna, 176740.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2998. en:caused by mutation in the proline dehydrogenase gene (prodh, 606810.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the proline dehydrogenase gene (prodh, 606810.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  2999. en:caused by mutation in the proline-rich transmembrane protein 2 gene (prrt2, 614386.0001). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the proline-rich transmembrane protein 2 gene (prrt2, 614386.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3000. en:caused by mutation in the proprotein convertase 1 gene (pc1, 162150.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the proprotein convertase 1 gene (pc1, 162150.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3001. en:caused by mutation in the protein c gene (proc, 612283.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein c gene (proc, 612283.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3002. en:caused by mutation in the protein kinase, amp-activated, noncatalytic, gamma-2 gene (prkag2, 602743.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein kinase, amp-activated, noncatalytic, gamma-2 gene (prkag2, 602743.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3003. en:caused by mutation in the protein tyrosine phosphatase, nonreceptor-type, 11 gene (ptpn11, 176876.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein tyrosine phosphatase, nonreceptor-type, 11 gene (ptpn11, 176876.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3004. en:caused by mutation in the protein-tyrosine phosphatase, receptor-type, o gene (ptpro, 600579.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein-tyrosine phosphatase, receptor-type, o gene (ptpro, 600579.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3005. en:caused by mutation in the proteolipid protein 1 gene (plp1, 300401.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the proteolipid protein 1 gene (plp1, 300401.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3006. en:caused by mutation in the psmc3-interacting protein gene (psmc3ip, 608665.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the psmc3-interacting protein gene (psmc3ip, 608665.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3007. en:caused by mutation in the pten-induced putative kinase-1 gene (pink1, 608309.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pten-induced putative kinase-1 gene (pink1, 608309.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3008. en:caused by mutation in the pulmonary-associated surfactant protein b gene (sftpb, 178640.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pulmonary-associated surfactant protein b gene (sftpb, 178640.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3009. en:caused by mutation in the ras-associated protein rab23 gene (rab23, 606144.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ras-associated protein rab23 gene (rab23, 606144.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3010. en:caused by mutation in the ras-associated protein rab7 (602298.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ras-associated protein rab7 (602298.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3011. en:caused by mutation in the ras-associated protein-28 gene (rab28, 612994.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ras-associated protein-28 gene (rab28, 612994.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3012. en:caused by mutation in the recombination-activating gene 2 (rag2, 179616.0009) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the recombination-activating gene 2 (rag2, 179616.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3013. en:caused by mutation in the retinol-binding protein-3 gene (rbp3, 180920.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the retinol-binding protein-3 gene (rbp3, 180920.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3014. en:caused by mutation in the ribonuclease h2, subunit a gene (rnaseh2a, 606034.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ribonuclease h2, subunit a gene (rnaseh2a, 606034.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3015. en:caused by mutation in the ring finger protein 170 gene (rnf170, 614649.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ring finger protein 170 gene (rnf170, 614649.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3016. en:caused by mutation in the rna polymerase i and transcript release factor gene (ptrf, 603198.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rna polymerase i and transcript release factor gene (ptrf, 603198.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3017. en:caused by mutation in the rna polymerase iii, subunit a gene (polr3a, 614258.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rna polymerase iii, subunit a gene (polr3a, 614258.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3018. en:caused by mutation in the rp9 gene (rp9, 607331.0002) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rp9 gene (rp9, 607331.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3019. en:caused by mutation in the sal-like 4 gene (sall4, 607343.0013) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sal-like 4 gene (sall4, 607343.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3020. en:caused by mutation in the scaffold protein containing ankyrin repeats and sam domain gene (sans, 607696.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the scaffold protein containing ankyrin repeats and sam domain gene (sans, 607696.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3021. en:caused by mutation in the seipin gene (bscl2, 606158.0013) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the seipin gene (bscl2, 606158.0013) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3022. en:caused by mutation in the seipin gene (bscl2, 606158.0017) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the seipin gene (bscl2, 606158.0017) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3023. en:caused by mutation in the selenoprotein n, 1 gene (sepn1, 606210.0008) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the selenoprotein n, 1 gene (sepn1, 606210.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3024. en:caused by mutation in the senataxin gene (setx, 608465.00006) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the senataxin gene (setx, 608465.00006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3025. en:caused by mutation in the set domain-containing protein 5 gene (setd5, 615743.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the set domain-containing protein 5 gene (setd5, 615743.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3026. en:caused by mutation in the set-binding protein-1 gene (setbp1, 611060.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the set-binding protein-1 gene (setbp1, 611060.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3027. en:caused by mutation in the short stature homeo box gene (shox, 312865.0002) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the short stature homeo box gene (shox, 312865.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3028. en:caused by mutation in the short stature homeo box gene (shox, 312865.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the short stature homeo box gene (shox, 312865.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3029. en:caused by mutation in the six-transmembrane epithelial antigen of prostate 3 gene (steap3, 609671.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the six-transmembrane epithelial antigen of prostate 3 gene (steap3, 609671.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3030. en:caused by mutation in the skeletal muscle chloride channel-1 gene (clcn1, 118425.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the skeletal muscle chloride channel-1 gene (clcn1, 118425.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3031. en:caused by mutation in the skeletal muscle receptor tyrosine kinase gene (musk, 601296.0001). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the skeletal muscle receptor tyrosine kinase gene (musk, 601296.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3032. en:caused by mutation in the small integral membrane protein 1 gene (smim1, 615242.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the small integral membrane protein 1 gene (smim1, 615242.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3033. en:caused by mutation in the small nuclear ribonucleoprotein polypeptide e gene (snrpe, 128160.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the small nuclear ribonucleoprotein polypeptide e gene (snrpe, 128160.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3034. en:caused by mutation in the solute carrier 22 (urate transporter), member 12 gene (slc22a12, 607096.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier 22 (urate transporter), member 12 gene (slc22a12, 607096.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3035. en:caused by mutation in the solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene (slc13a5, 608305.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 13 (sodium-dependent citrate transporter), member 5 gene (slc13a5, 608305.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3036. en:caused by mutation in the solute carrier family 16 (monocarboxylic acid transporter), member 1 (slc16a1, 600682.0005) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 16 (monocarboxylic acid transporter), member 1 (slc16a1, 600682.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3037. en:caused by mutation in the solute carrier family 19 (thiamine transporter), member 2 gene (slc19a2, 603941.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 19 (thiamine transporter), member 2 gene (slc19a2, 603941.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3038. en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene (slc25a4, 103220.0005) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4 gene (slc25a4, 103220.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3039. en:caused by mutation in the solute carrier family 25, member 38 gene (slc25a38, 610819.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25, member 38 gene (slc25a38, 610819.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3040. en:caused by mutation in the solute carrier family 5 (choline transporter), member 7 gene (slc5a7, 608761.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 5 (choline transporter), member 7 gene (slc5a7, 608761.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3041. en:caused by mutation in the solute carrier family 52 (riboflavin transporter), member 2 gene (slc52a2, 607882.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 52 (riboflavin transporter), member 2 gene (slc52a2, 607882.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3042. en:caused by mutation in the solute carrier family 6 (dopamine neurotransmitter transporter), member 3 gene (slc6a3, 126455.0002) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 6 (dopamine neurotransmitter transporter), member 3 gene (slc6a3, 126455.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3043. en:caused by mutation in the solute carrier family 7, member 14 gene (slc7a14, 615720.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 7, member 14 gene (slc7a14, 615720.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3044. en:caused by mutation in the son of sevenless, drosophila, homolog 1 gene (sos1, 182530.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the son of sevenless, drosophila, homolog 1 gene (sos1, 182530.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3045. en:caused by mutation in the sperm antigen with calponin homology and coiled-coil domains 1-like gene (specc1l, 614140.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sperm antigen with calponin homology and coiled-coil domains 1-like gene (specc1l, 614140.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3046. en:caused by mutation in the splicing factor 3b, subunit 4 gene (sf3b4, 605593.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the splicing factor 3b, subunit 4 gene (sf3b4, 605593.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3047. en:caused by mutation in the sulfatase-modifying factor 1 gene (sumf1, 607939.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sulfatase-modifying factor 1 gene (sumf1, 607939.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3048. en:caused by mutation in the syntaxin 16 gene (stx16, 603666.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the syntaxin 16 gene (stx16, 603666.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3049. en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tbc1 domain family, member 24 gene (tbc1d24, 613577.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3050. en:caused by mutation in the telomerase reverse transcriptase gene (tert, 187270.0007) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the telomerase reverse transcriptase gene (tert, 187270.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3051. en:caused by mutation in the tenascin xb gene (tnxb, 600985.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tenascin xb gene (tnxb, 600985.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3052. en:caused by mutation in the tetratricopeptide repeat domain 37 gene (ttc37, 614589.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tetratricopeptide repeat domain 37 gene (ttc37, 614589.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3053. en:caused by mutation in the thioredoxin domain-containing 3 gene (txndc3, 607421.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the thioredoxin domain-containing 3 gene (txndc3, 607421.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3054. en:caused by mutation in the transcobalamin ii gene (tcn2, 613441.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transcobalamin ii gene (tcn2, 613441.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3055. en:caused by mutation in the transmembrane and coiled-coil domains protein 1 gene (tmco1, 614123.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane and coiled-coil domains protein 1 gene (tmco1, 614123.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3056. en:caused by mutation in the transmembrane protease, serine 6 gene (tmprss6, 609862.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protease, serine 6 gene (tmprss6, 609862.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3057. en:caused by mutation in the transmembrane protein 165 gene (tmem165, 614726.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 165 gene (tmem165, 614726.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3058. en:caused by mutation in the transmembrane protein 70 (tmem70, 612418.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 70 (tmem70, 612418.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3059. en:caused by mutation in the tubby-like protein 1 gene (tulp1, 602280.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tubby-like protein 1 gene (tulp1, 602280.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3060. en:caused by mutation in the ubiquitin carboxyl-terminal esterase l1 gene (uchl1, 191342.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquitin carboxyl-terminal esterase l1 gene (uchl1, 191342.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3061. en:caused by mutation in the uridine monophosphate synthetase gene (umps, 613891.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the uridine monophosphate synthetase gene (umps, 613891.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3062. en:caused by mutation in the valosin-containing protein gene (vcp, 601023.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the valosin-containing protein gene (vcp, 601023.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3063. en:caused by mutation in the voltage-gated potassium channel, kqt-like subfamily, member 4 gene (kcnq4, 603537.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated potassium channel, kqt-like subfamily, member 4 gene (kcnq4, 603537.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3064. en:caused by mutation in the voltage-gated sodium channel, type i, beta subunit gene (scn1b, 600235.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated sodium channel, type i, beta subunit gene (scn1b, 600235.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3065. en:caused by mutation in the voltage-gated sodium channel, type viii, alpha subunit gene (scn8a, 600702.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated sodium channel, type viii, alpha subunit gene (scn8a, 600702.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3066. en:caused by mutation in the voltage-gated sodium channel, type xi, alpha subunit gene (scn11a, 604385.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated sodium channel, type xi, alpha subunit gene (scn11a, 604385.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3067. en:caused by mutation in the wilms tumor 1 gene (wt1, 607102.0003). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wilms tumor 1 gene (wt1, 607102.0003). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3068. en:caused by mutation in the xpc gene (xpc, 613208.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the xpc gene (xpc, 613208.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3069. en:caused by mutation in the zinc finger and btb domain containing 18 gene (zbtb18, 608433.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger and btb domain containing 18 gene (zbtb18, 608433.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3070. en:caused by mutation in the zinc finger fyve-domain containing protein-27 gene (zfyve27, 610243.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger fyve-domain containing protein-27 gene (zfyve27, 610243.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3071. en:caused by mutation of the dpy19-like 2 gene (dpy19l2, 613893.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation of the dpy19-like 2 gene (dpy19l2, 613893.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3072. en:caused by mutations in the bone morphogenetic protein receptor, type 1b gene (bmpr1b, 603248.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the bone morphogenetic protein receptor, type 1b gene (bmpr1b, 603248.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3073. en:caused by mutations in the ceruloplasmin gene (cp, 117700.0001). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the ceruloplasmin gene (cp, 117700.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3074. en:caused by mutations in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cholinergic receptor, nicotinic, epsilon polypeptide gene (chrne, 100725.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3075. en:caused by mutations in the deafness/dystonia-1 gene (timm8a, 300356.0001). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the deafness/dystonia-1 gene (timm8a, 300356.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3076. en:caused by mutations in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3077. en:caused by mutations in the filamin c gene (flnc, 102565.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the filamin c gene (flnc, 102565.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3078. en:caused by mutations in the glutamate dehydrogenase gene (glud1, 138130.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the glutamate dehydrogenase gene (glud1, 138130.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3079. en:caused by mutations in the nf-kappa-b essential modulator gene (ikbkg, 300248.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the nf-kappa-b essential modulator gene (ikbkg, 300248.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3080. en:caused by mutations in the ocrl1 gene (ocrl1, 300535.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the ocrl1 gene (ocrl1, 300535.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3081. en:caused by mutations in the parathyroid hormone receptor 1 gene (pthr1, 168468.0003) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the parathyroid hormone receptor 1 gene (pthr1, 168468.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3082. en:caused by mutations in the serine/threonine protein kinase 11 gene (stk11, 602216.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the serine/threonine protein kinase 11 gene (stk11, 602216.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3083. en:caused by mutations in the transforming growth factor, beta-induced, 68kd gene (tgfbi, 601692.0004) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the transforming growth factor, beta-induced, 68kd gene (tgfbi, 601692.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3084. en:caused by trinucleotide repeat expansion (cag)n in the drpla gene (drpla, 607462.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by trinucleotide repeat expansion (cag)n in the drpla gene (drpla, 607462.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3085. en:chromosome 15q26-qter deletion syndrome --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:chromosome 15q26-qter deletion syndrome | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3086. en:contiguous gene syndrome caused by mosaicism for tetrasomy of chromosome 12p --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by mosaicism for tetrasomy of chromosome 12p | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3087. en:due to mutation in the aspartylglucosaminidase gene (aga, 208400.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:due to mutation in the aspartylglucosaminidase gene (aga, 208400.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3088. en:due to mutation in the microsomal triglyceride transfer protein gene (mtp, 157147.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:due to mutation in the microsomal triglyceride transfer protein gene (mtp, 157147.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3089. en:linked to a locus at 7p15-p11.2. --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:linked to a locus at 7p15-p11.2. | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3090. en:linked to locus at 17q12-q21. --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:linked to locus at 17q12-q21. | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3091. en:mutation in the filamin b gene (flnb, 603381) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:mutation in the filamin b gene (flnb, 603381) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3092. en:susceptibility conferred by mutation in the lamin b2 gene (lmnb2, 150341.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the lamin b2 gene (lmnb2, 150341.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3093. en:susceptibility conferred by mutation in the paired box gene 4 (pax4, 167413.0022 ) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the paired box gene 4 (pax4, 167413.0022 ) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3094. en:susceptibility conferred by mutation in the platelet thromboxane a2 receptor gene (tbxa2r, 188070.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the platelet thromboxane a2 receptor gene (tbxa2r, 188070.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3095. en:susceptibility conferred by mutation in the thrombomodulin gene (thbd, 188040.0005) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the thrombomodulin gene (thbd, 188040.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3096. en:susceptibility conferred by mutation in the voltage-gated calcium channel beta-4 subunit gene (cacnb4, 601949.0001). --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the voltage-gated calcium channel beta-4 subunit gene (cacnb4, 601949.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3097. en:susceptibility conferred by somatic mutation in the sh2b adaptor protein 3 (sh2b3, 605093.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by somatic mutation in the sh2b adaptor protein 3 (sh2b3, 605093.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3098. en:susceptibility to sle caused by mutation in the receptor for fc fragment of igg, low affinity iia gene (fcgr2a, 146790.0001) --- r_associated #0: 22 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility to sle caused by mutation in the receptor for fc fragment of igg, low affinity iia gene (fcgr2a, 146790.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=22
  3099. en:a contiguous gene deletion syndrome caused by heterozygous deletion (582-738 kb) of 8q13 including the sulf1 (610012) and slco5a1 (613543) genes --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:a contiguous gene deletion syndrome caused by heterozygous deletion (582-738 kb) of 8q13 including the sulf1 (610012) and slco5a1 (613543) genes | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3100. en:associated with mutation in the met protooncogene (met, 164860.0008) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:associated with mutation in the met protooncogene (met, 164860.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3101. en:associated with mutation in the neuroligin-3 gene (nlgn3, 300336.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:associated with mutation in the neuroligin-3 gene (nlgn3, 300336.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3102. en:caused by a 1.35-mb deletion of chromosome 1q21 --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by a 1.35-mb deletion of chromosome 1q21 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3103. en:caused by an expanded hexanucleotide repeat (ggggcc)n in the chromosome 9 open reading frame 72 gene (c9orf72, 614260.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by an expanded hexanucleotide repeat (ggggcc)n in the chromosome 9 open reading frame 72 gene (c9orf72, 614260.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3104. en:caused by contiguous gene deletion on chromosome xp11.3, including the rp2 gene (312600) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by contiguous gene deletion on chromosome xp11.3, including the rp2 gene (312600) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3105. en:caused by duplications or deletions on xq26 involving the sry-box 3 gene (sox3, 313430) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by duplications or deletions on xq26 involving the sry-box 3 gene (sox3, 313430) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3106. en:caused by germline mutation in the armadillo repeat-containing protein 5 gene (armc5, 615549.0001) coupled with somatic mutation of the other armc5 allele in the adrenal tumors --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by germline mutation in the armadillo repeat-containing protein 5 gene (armc5, 615549.0001) coupled with somatic mutation of the other armc5 allele in the adrenal tumors | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3107. en:caused by microduplication of 3q29. --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by microduplication of 3q29. | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3108. en:caused by mutation in establishment of cohesion 1, s. cerevisiae, homolog of, 2 gene ( esco2, 609353.0004) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in establishment of cohesion 1, s. cerevisiae, homolog of, 2 gene ( esco2, 609353.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3109. en:caused by mutation in microrna 184 gene (mir184, 613146.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in microrna 184 gene (mir184, 613146.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3110. en:caused by mutation in the 152-kd centrosomal protein gene (cep152, 613529.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 152-kd centrosomal protein gene (cep152, 613529.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3111. en:caused by mutation in the 73-kd pdz-domain-containing protein (ush1c, 605242.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the 73-kd pdz-domain-containing protein (ush1c, 605242.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3112. en:caused by mutation in the adaptor-related protein complex 1, sigma-2 subunit gene (ap1s2, 300629.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adaptor-related protein complex 1, sigma-2 subunit gene (ap1s2, 300629.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3113. en:caused by mutation in the adaptor-related protein complex 4, beta-1 subunit gene (ap4b1, 607245.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adaptor-related protein complex 4, beta-1 subunit gene (ap4b1, 607245.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3114. en:caused by mutation in the adp-ribosylation factor-like 6 gene (arl6, 608845.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the adp-ribosylation factor-like 6 gene (arl6, 608845.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3115. en:caused by mutation in the aggrecan gene (acan, 155760.0003) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aggrecan gene (acan, 155760.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3116. en:caused by mutation in the alpha-tubulin 1a gene (tuba1a, 602529.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the alpha-tubulin 1a gene (tuba1a, 602529.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3117. en:caused by mutation in the aminomethyltransferase gene (amt, 238310.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aminomethyltransferase gene (amt, 238310.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3118. en:caused by mutation in the aquaporin-2 gene (aqp2, 107777.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aquaporin-2 gene (aqp2, 107777.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3119. en:caused by mutation in the argininosuccinate lyase gene (asl, 608310.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the argininosuccinate lyase gene (asl, 608310.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3120. en:caused by mutation in the argininosuccinate synthetase gene (ass, 603470.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the argininosuccinate synthetase gene (ass, 603470.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3121. en:caused by mutation in the aristaless-like 4, mouse, homolog of, gene (alx4, 605420.0008) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aristaless-like 4, mouse, homolog of, gene (alx4, 605420.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3122. en:caused by mutation in the aristaless-like homeobox 3 gene (alx3, 606014.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aristaless-like homeobox 3 gene (alx3, 606014.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3123. en:caused by mutation in the aspartate beta-hydroxylase gene (asph, 600582.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the aspartate beta-hydroxylase gene (asph, 600582.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3124. en:caused by mutation in the atp-binding cassette, subfamily a, member 12 gene (abca12, 607800.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily a, member 12 gene (abca12, 607800.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3125. en:caused by mutation in the atp-binding cassette, subfamily a, member 3 gene (abca3, 601615.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily a, member 3 gene (abca3, 601615.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3126. en:caused by mutation in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atp-binding cassette, subfamily c, member 6 gene (abcc6, 603234.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3127. en:caused by mutation in the atpase, h+ transporting, lysosomal, accessory protein-2 gene (atp6ap2, 300556.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the atpase, h+ transporting, lysosomal, accessory protein-2 gene (atp6ap2, 300556.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3128. en:caused by mutation in the au-specific rna-binding protein gene (auh, 600529.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the au-specific rna-binding protein gene (auh, 600529.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3129. en:caused by mutation in the avian myelocytomatosis viral (v-myc) oncogene homolog (myc, 190080.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the avian myelocytomatosis viral (v-myc) oncogene homolog (myc, 190080.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3130. en:caused by mutation in the b9 domain-containing protein 2 gene (b9d2, 611951.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the b9 domain-containing protein 2 gene (b9d2, 611951.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3131. en:caused by mutation in the bcl2-associated athanogene 3 gene (bag3, 603883.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the bcl2-associated athanogene 3 gene (bag3, 603883.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3132. en:caused by mutation in the beta-1,4-mannosyltransferase gene (alg1, 605907.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-1,4-mannosyltransferase gene (alg1, 605907.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3133. en:caused by mutation in the beta-3 laminin gene (lamb3, 150130.001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-3 laminin gene (lamb3, 150130.001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3134. en:caused by mutation in the beta-3 tubulin gene (tubb3, 602661.0006) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-3 tubulin gene (tubb3, 602661.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3135. en:caused by mutation in the beta-actin gene (actb, 102630.0001). --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the beta-actin gene (actb, 102630.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3136. en:caused by mutation in the carbohydrate sulfotransferase-14 gene (chst14, 608429.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carbohydrate sulfotransferase-14 gene (chst14, 608429.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3137. en:caused by mutation in the cardiac troponin i gene (tnni3, 191044.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cardiac troponin i gene (tnni3, 191044.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3138. en:caused by mutation in the carnitine palmitoyltransferase ia gene (cpt1a, 600528.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the carnitine palmitoyltransferase ia gene (cpt1a, 600528.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3139. en:caused by mutation in the caspase recruitment domain containing 9 (card9, 607212.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the caspase recruitment domain containing 9 (card9, 607212.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3140. en:caused by mutation in the cd3 antigen, epsilon subunit gene (cd3e, 186830.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cd3 antigen, epsilon subunit gene (cd3e, 186830.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3141. en:caused by mutation in the cdgsh iron sulfur domain protein 2 gene (cisd2, 611507.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cdgsh iron sulfur domain protein 2 gene (cisd2, 611507.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3142. en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0007) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the chloride channel 5 gene (clcn5, 300008.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3143. en:caused by mutation in the cholinergic receptor, nicotinic, gamma polypeptide gene (chrng, 100730.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cholinergic receptor, nicotinic, gamma polypeptide gene (chrng, 100730.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3144. en:caused by mutation in the coiled-coil and c2 domains-containing protein 2a gene (cc2d2a, 612013.0006) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil and c2 domains-containing protein 2a gene (cc2d2a, 612013.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3145. en:caused by mutation in the coiled-coil domain-containing protein 11 gene (ccdc11, 614759.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the coiled-coil domain-containing protein 11 gene (ccdc11, 614759.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3146. en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen i, alpha-1 polypeptide gene (col1a1, 120150.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3147. en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0005) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen i, alpha-2 polypeptide gene (col1a2, 120160.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3148. en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3149. en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0012) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3150. en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0030) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ii, alpha-1 polypeptide gene (col2a1, 120140.0030) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3151. en:caused by mutation in the collagen ix, alpha-3 polypeptide gene (col9a3, 120270.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen ix, alpha-3 polypeptide gene (col9a3, 120270.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3152. en:caused by mutation in the collagen v, alpha-2 polypeptide gene (col5a2, 120190.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen v, alpha-2 polypeptide gene (col5a2, 120190.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3153. en:caused by mutation in the collagen vi, alpha-2 gene (col6a2, 120240.0011) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen vi, alpha-2 gene (col6a2, 120240.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3154. en:caused by mutation in the collagen xviii, alpha-1 polypeptide gene (col18a1, 120328.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen xviii, alpha-1 polypeptide gene (col18a1, 120328.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3155. en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0007) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3156. en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0009) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a3, 120070.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3157. en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a4, 120131.0003) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type iv, alpha-3 gene (col4a4, 120131.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3158. en:caused by mutation in the collagen, type iv, alpha-4 gene (col4a4, 120131.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the collagen, type iv, alpha-4 gene (col4a4, 120131.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3159. en:caused by mutation in the complement component-8, alpha polypeptide gene (c8a, 120950.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complement component-8, alpha polypeptide gene (c8a, 120950.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3160. en:caused by mutation in the complex i, subunit nd2 gene (mtnd2, 516001.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the complex i, subunit nd2 gene (mtnd2, 516001.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3161. en:caused by mutation in the connexin 26 gene (gjb2, 121011.0020) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the connexin 26 gene (gjb2, 121011.0020) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3162. en:caused by mutation in the creb-binding protein gene (crebbp, 600140.0001). --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the creb-binding protein gene (crebbp, 600140.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3163. en:caused by mutation in the cullin 7 gene (cul7, 609577.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cullin 7 gene (cul7, 609577.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3164. en:caused by mutation in the cytochrome p450, family 4, subfamily f, polypeptide 22 gene (cyp4f22, 611495.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the cytochrome p450, family 4, subfamily f, polypeptide 22 gene (cyp4f22, 611495.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3165. en:caused by mutation in the dedicator of cytokinesis-6 gene (dock6, 614194.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dedicator of cytokinesis-6 gene (dock6, 614194.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3166. en:caused by mutation in the dehydrogenase e1 and transketolase domains-containing protein 1 gene (dhtkd1, 614984.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dehydrogenase e1 and transketolase domains-containing protein 1 gene (dhtkd1, 614984.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3167. en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0005) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dentin sialophosphoprotein gene (dspp, 125485.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3168. en:caused by mutation in the dis3 mitotic control, s. cerevisiae, homolog-like 2 gene (dis3l2, 614184.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dis3 mitotic control, s. cerevisiae, homolog-like 2 gene (dis3l2, 614184.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3169. en:caused by mutation in the dmx-like 2 gene (dmxl2, 612186.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dmx-like 2 gene (dmxl2, 612186.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3170. en:caused by mutation in the dna methyltransferase 1 gene (dnmt1, 126375.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna methyltransferase 1 gene (dnmt1, 126375.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3171. en:caused by mutation in the dna-activated protein kinase, catalytic subunit gene (prkdc, 600899.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dna-activated protein kinase, catalytic subunit gene (prkdc, 600899.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3172. en:caused by mutation in the dysferlin gene (dysf, 603009.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the dysferlin gene (dysf, 603009.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3173. en:caused by mutation in the e1-alpha subunit of the pyruvate dehydrogenase complex (pdha1, 300502.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the e1-alpha subunit of the pyruvate dehydrogenase complex (pdha1, 300502.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3174. en:caused by mutation in the early growth response-2 gene (egr2, 129010.0004) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the early growth response-2 gene (egr2, 129010.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3175. en:caused by mutation in the emopamil-binding protein gene (ebp, 300205.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the emopamil-binding protein gene (ebp, 300205.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3176. en:caused by mutation in the enamelin gene (enam, 606585.0003) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the enamelin gene (enam, 606585.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3177. en:caused by mutation in the endoplasmic reticulum lipid raft-associated protein 2 gene (erlin2, 611605.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endoplasmic reticulum lipid raft-associated protein 2 gene (erlin2, 611605.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3178. en:caused by mutation in the endothelin 1 gene (edn1, 131240.0004) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the endothelin 1 gene (edn1, 131240.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3179. en:caused by mutation in the enoyl-coenzyme a, hydratase/3-hydroxyacyl coenzyme a dehydrogenase gene (ehhadh, 607037.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the enoyl-coenzyme a, hydratase/3-hydroxyacyl coenzyme a dehydrogenase gene (ehhadh, 607037.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3180. en:caused by mutation in the excision-repair cross-complementing group 1 gene (ercc1, 126380.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the excision-repair cross-complementing group 1 gene (ercc1, 126380.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3181. en:caused by mutation in the f receptor-type protein-tyrosine phosphatase gene (ptprf, 179590.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the f receptor-type protein-tyrosine phosphatase gene (ptprf, 179590.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3182. en:caused by mutation in the faciogenital dysplasia gene (fgd1, 300546.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the faciogenital dysplasia gene (fgd1, 300546.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3183. en:caused by mutation in the factor xiii beta subunit (f13b, 134580.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the factor xiii beta subunit (f13b, 134580.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3184. en:caused by mutation in the family with sequence similarity 111, member b gene (fam111b, 615584.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the family with sequence similarity 111, member b gene (fam111b, 615584.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3185. en:caused by mutation in the fas antigen gene (fas, 134637.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fas antigen gene (fas, 134637.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3186. en:caused by mutation in the ferritin light-chain gene (ftl, 134790.0010) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ferritin light-chain gene (ftl, 134790.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3187. en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0015) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibrillin-1 gene (fbn1, 134797.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3188. en:caused by mutation in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0035) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor 2 gene (fgfr2, 176943.0035) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3189. en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0029) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor 3 gene (fgfr3, 134934.0029) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3190. en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3191. en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0005) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fibroblast growth factor receptor-3 gene (fgfr3, 134934.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3192. en:caused by mutation in the filamin a gene (300017.0009) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the filamin a gene (300017.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3193. en:caused by mutation in the filamin a gene (flna, 300017.0010) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the filamin a gene (flna, 300017.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3194. en:caused by mutation in the fk506-binding protein 10 gene (fkbp10, 607093.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fk506-binding protein 10 gene (fkbp10, 607093.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3195. en:caused by mutation in the flavoprotein subunit of succinate dehydrogenase complex gene (sdha, 600857.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the flavoprotein subunit of succinate dehydrogenase complex gene (sdha, 600857.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3196. en:caused by mutation in the forkhead box c2 gene (foxc2, 602402.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead box c2 gene (foxc2, 602402.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3197. en:caused by mutation in the forkhead box f1 gene (foxf1, 601089.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the forkhead box f1 gene (foxf1, 601089.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3198. en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0004). --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the four-and-a-half lim domains 1 gene (fhl1, 300163.0004). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3199. en:caused by mutation in the fras1-related extracellular matrix protein-1 gene (frem1, 608944.0008) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fras1-related extracellular matrix protein-1 gene (frem1, 608944.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3200. en:caused by mutation in the fused in sarcoma gene (fus, 137070.0007) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the fused in sarcoma gene (fus, 137070.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3201. en:caused by mutation in the g protein-coupled receptor-179 gene (gpr179, 614515.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the g protein-coupled receptor-179 gene (gpr179, 614515.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3202. en:caused by mutation in the gamma sarcoglycan gene (sgcg, 253700.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma sarcoglycan gene (sgcg, 253700.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3203. en:caused by mutation in the gamma-aminobutyric acid (gaba) a receptor, gamma-2 gene (gabrg2, 137164.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma-aminobutyric acid (gaba) a receptor, gamma-2 gene (gabrg2, 137164.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3204. en:caused by mutation in the gamma-aminobutyric acid (gaba) a receptor, gamma-2 gene (gabrg2, 137164.0003) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gamma-aminobutyric acid (gaba) a receptor, gamma-2 gene (gabrg2, 137164.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3205. en:caused by mutation in the gap junction protein, beta-2 gene (gjb2, 121011.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gap junction protein, beta-2 gene (gjb2, 121011.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3206. en:caused by mutation in the gap junction protein, gamma-2 gene (gjc2, 608803.0008) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gap junction protein, gamma-2 gene (gjc2, 608803.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3207. en:caused by mutation in the gdp-mannose pyrophosphorylase b gene (gmppb, 615320.0004) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gdp-mannose pyrophosphorylase b gene (gmppb, 615320.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3208. en:caused by mutation in the gene encoding the mapbp-interacting protein gene (mapbpip, 610389.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gene encoding the mapbp-interacting protein gene (mapbpip, 610389.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3209. en:caused by mutation in the glucokinase gene (gck, 138079.0009) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the glucokinase gene (gck, 138079.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3210. en:caused by mutation in the gnas complex locus gene (gnas, 139320.0031) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the gnas complex locus gene (gnas, 139320.0031) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3211. en:caused by mutation in the growth/differentiation factor-5 gene (gdf5, 601146.0020) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the growth/differentiation factor-5 gene (gdf5, 601146.0020) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3212. en:caused by mutation in the guanylate cyclase 2c gene (gucy2c, 601330.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the guanylate cyclase 2c gene (gucy2c, 601330.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3213. en:caused by mutation in the hemoglobin gamma a gene (hbg1, 142200.0026) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hemoglobin gamma a gene (hbg1, 142200.0026) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3214. en:caused by mutation in the holocytochrome c synthase gene (hccs, 300056.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the holocytochrome c synthase gene (hccs, 300056.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3215. en:caused by mutation in the homeobox d10 gene (hoxd10, 142984.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homeobox d10 gene (hoxd10, 142984.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3216. en:caused by mutation in the homolog of c. elegans unc119 gene (unc119, 604011.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of c. elegans unc119 gene (unc119, 604011.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3217. en:caused by mutation in the homolog of chlamydomonas dynein regulatory complex, subunit 1 gene (drc1, 615288.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of chlamydomonas dynein regulatory complex, subunit 1 gene (drc1, 615288.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3218. en:caused by mutation in the homolog of drosophila peroxidasin gene (pxdn, 605158.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of drosophila peroxidasin gene (pxdn, 605158.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3219. en:caused by mutation in the homolog of the drosophila hairy/enhancer of split 7 gene (hes7, 608059.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila hairy/enhancer of split 7 gene (hes7, 608059.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3220. en:caused by mutation in the homolog of the drosophila period 2 gene (per2, 603426.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila period 2 gene (per2, 603426.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3221. en:caused by mutation in the homolog of the drosophila sine oculis homeobox gene (six3, 603714.0001). --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila sine oculis homeobox gene (six3, 603714.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3222. en:caused by mutation in the homolog of the drosophila snail 2 gene (snai2, 602150.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the drosophila snail 2 gene (snai2, 602150.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3223. en:caused by mutation in the homolog of the s. cerevisiae precursor mrna-processing factor-6 gene (prpf6, 613979.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the s. cerevisiae precursor mrna-processing factor-6 gene (prpf6, 613979.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3224. en:caused by mutation in the homolog of the yeast cleavage and polyadenylation factor i subunit 1 gene (clp1, 608757.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the homolog of the yeast cleavage and polyadenylation factor i subunit 1 gene (clp1, 608757.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3225. en:caused by mutation in the hps4 gene (hps4, 606682) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the hps4 gene (hps4, 606682) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3226. en:caused by mutation in the htra serine peptidase 1 gene (htra1, 602194.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the htra serine peptidase 1 gene (htra1, 602194.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3227. en:caused by mutation in the human homolog of the iron-sulfur cluster scaffold gene (iscu, 611911.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the human homolog of the iron-sulfur cluster scaffold gene (iscu, 611911.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3228. en:caused by mutation in the il1 receptor accessory protein-like 1 gene (il1rapl, 300206.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the il1 receptor accessory protein-like 1 gene (il1rapl, 300206.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3229. en:caused by mutation in the inducible costimulator gene (icos, 605448.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the inducible costimulator gene (icos, 605448.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3230. en:caused by mutation in the interleukin 11 receptor alpha gene (il11ra, 600939.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interleukin 11 receptor alpha gene (il11ra, 600939.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3231. en:caused by mutation in the interleukin-36 receptor antagonist gene (il36rn, 605507.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the interleukin-36 receptor antagonist gene (il36rn, 605507.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3232. en:caused by mutation in the kelch-like 10 gene (klhl10, 608778.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the kelch-like 10 gene (klhl10, 608778.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3233. en:caused by mutation in the keratin 16 gene (krt16, 148067.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 16 gene (krt16, 148067.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3234. en:caused by mutation in the keratin 85 gene (krt85, 602767.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the keratin 85 gene (krt85, 602767.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3235. en:caused by mutation in the lamin a/c gene (lmna, 150330.0017) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin a/c gene (lmna, 150330.0017) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3236. en:caused by mutation in the lamin a/c gene (lmna, 150330.0045) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lamin a/c gene (lmna, 150330.0045) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3237. en:caused by mutation in the latent transforming growth factor-beta binding protein 4 gene (ltbp4, 604710.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the latent transforming growth factor-beta binding protein 4 gene (ltbp4, 604710.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3238. en:caused by mutation in the lim domain binding 3 gene (ldb3, 605906.0005) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the lim domain binding 3 gene (ldb3, 605906.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3239. en:caused by mutation in the liver glycogen phosphorylase gene (pygl, 613741.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the liver glycogen phosphorylase gene (pygl, 613741.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3240. en:caused by mutation in the mage-like 2 gene (magel2, 605283.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mage-like 2 gene (magel2, 605283.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3241. en:caused by mutation in the mannosidase, alpha, class 1b, member 1 gene (man1b1, 604346.0001). --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mannosidase, alpha, class 1b, member 1 gene (man1b1, 604346.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3242. en:caused by mutation in the member 5 solute carrier family 39 (zinc transporter) gene (slc39a5, 608730.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the member 5 solute carrier family 39 (zinc transporter) gene (slc39a5, 608730.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3243. en:caused by mutation in the membrane-type frizzled-related protein gene (mfrp, 606227.0005) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the membrane-type frizzled-related protein gene (mfrp, 606227.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3244. en:caused by mutation in the methionine synthase reductase gene (mtrr, 602568.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the methionine synthase reductase gene (mtrr, 602568.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3245. en:caused by mutation in the mitochondrial transfer rna leucine 1 gene (mttl1, 590050.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial transfer rna leucine 1 gene (mttl1, 590050.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3246. en:caused by mutation in the mitochondrial trna-glutamic acid gene (mtte, 590025.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mitochondrial trna-glutamic acid gene (mtte, 590025.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3247. en:caused by mutation in the mkks gene (mkks, 604896.0003) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the mkks gene (mkks, 604896.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3248. en:caused by mutation in the myofibrillogenesis regulator 1 gene (mr1, 609023.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myofibrillogenesis regulator 1 gene (mr1, 609023.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3249. en:caused by mutation in the myosin, heavy chain 14, nonmuscle gene (myh14, 608568.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin, heavy chain 14, nonmuscle gene (myh14, 608568.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3250. en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0029) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myosin, heavy polypeptide-7, cardiac muscle, beta gene (myh7, 160760.0029) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3251. en:caused by mutation in the myotilin gene (ttid, 604103.0006) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the myotilin gene (ttid, 604103.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3252. en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, alpha/beta subunits gene (gnptab, 607840.0003) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the n-acetylglucosamine-1-phosphotransferase, alpha/beta subunits gene (gnptab, 607840.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3253. en:caused by mutation in the n-glycanase 1 gene (ngly1, 610661.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the n-glycanase 1 gene (ngly1, 610661.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3254. en:caused by mutation in the nadh dehydrogenase (ubiquinone) 1 alpha subcomplex, 2 gene (ndufa2, 602137.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) 1 alpha subcomplex, 2 gene (ndufa2, 602137.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3255. en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 2 gene (ndufs2, 602985.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh dehydrogenase (ubiquinone) fe-s protein 2 gene (ndufs2, 602985.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3256. en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 12 gene (ndufa12, 614530.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nadh-ubiquinone oxidoreductase 1 alpha subcomplex, 12 gene (ndufa12, 614530.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3257. en:caused by mutation in the necap endocytosis-associated protein 1 gene (necap1, 611623.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the necap endocytosis-associated protein 1 gene (necap1, 611623.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3258. en:caused by mutation in the neurofibromin gene (nf1, 162200.0018) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the neurofibromin gene (nf1, 162200.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3259. en:caused by mutation in the nicastrin gene (ncstn, 605254.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nicastrin gene (ncstn, 605254.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3260. en:caused by mutation in the nonselective sodium leak channel gene (nalcn, 611549.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nonselective sodium leak channel gene (nalcn, 611549.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3261. en:caused by mutation in the nuclear receptor binding set domain protein 1 gene (nsd1, 606681.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nuclear receptor binding set domain protein 1 gene (nsd1, 606681.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3262. en:caused by mutation in the nucleotide-binding oligomerization domain protein 2 gene (nod2, 605956.0004). --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the nucleotide-binding oligomerization domain protein 2 gene (nod2, 605956.0004). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3263. en:caused by mutation in the olfactory receptor, family 2, subfamily j, member 3 gene (or2j3, 615016.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the olfactory receptor, family 2, subfamily j, member 3 gene (or2j3, 615016.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3264. en:caused by mutation in the opa1 gene (opa1, 605290.0011) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the opa1 gene (opa1, 605290.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3265. en:caused by mutation in the opa3 gene (606580.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the opa3 gene (606580.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3266. en:caused by mutation in the patatin-like phospholipase domain-containing protein 1 gene (pnpla1, 612121.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the patatin-like phospholipase domain-containing protein 1 gene (pnpla1, 612121.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3267. en:caused by mutation in the peroxisome biogenesis factor-3 gene (pex3, 603164.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the peroxisome biogenesis factor-3 gene (pex3, 603164.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3268. en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 1 gene (pik3r1, 171833.0007) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphatidylinositol 3-kinase, regulatory subunit 1 gene (pik3r1, 171833.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3269. en:caused by mutation in the phosphoglycerate kinase 1 gene (pgk1, 311800.0002). --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoglycerate kinase 1 gene (pgk1, 311800.0002). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3270. en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0009) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phospholipase a2, group vi gene (pla2g6, 603604.0009) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3271. en:caused by mutation in the phosphoribosylpyrophosphate synthetase i gene (prps1, 311850.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the phosphoribosylpyrophosphate synthetase i gene (prps1, 311850.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3272. en:caused by mutation in the piezo-type mechanosensitive ion channel component 2 gene (piezo2, 613629.0004) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the piezo-type mechanosensitive ion channel component 2 gene (piezo2, 613629.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3273. en:caused by mutation in the plasma membrane ca(2+)-transporting atpase 3 gene (atp2b3, 300014.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the plasma membrane ca(2+)-transporting atpase 3 gene (atp2b3, 300014.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3274. en:caused by mutation in the platelet-derived growth factor receptor alpha gene (pdgfra, 173490.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the platelet-derived growth factor receptor alpha gene (pdgfra, 173490.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3275. en:caused by mutation in the polyglutamine-binding protein-1 gene (pqbp1, 300463.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the polyglutamine-binding protein-1 gene (pqbp1, 300463.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3276. en:caused by mutation in the potassium channel tetramerisation domain containing 7 gene (kctd7, 611725.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium channel tetramerisation domain containing 7 gene (kctd7, 611725.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3277. en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 11 gene (kcnj11, 600937.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium channel, inwardly rectifying, subfamily j, member 11 gene (kcnj11, 600937.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3278. en:caused by mutation in the potassium channel, voltage-gated, subfamily v, member 2 gene (kcnv2, 607604.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium channel, voltage-gated, subfamily v, member 2 gene (kcnv2, 607604.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3279. en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 11 gene (kcnj11, 600937.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium inwardly-rectifying channel, subfamily j, member 11 gene (kcnj11, 600937.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3280. en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 192500.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 1 gene (kcnq1, 192500.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3281. en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 3 gene (kcnq3, 602232.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the potassium voltage-gated channel, kqt-like subfamily, member 3 gene (kcnq3, 602232.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3282. en:caused by mutation in the prolactin receptor gene (prlr, 176761.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prolactin receptor gene (prlr, 176761.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3283. en:caused by mutation in the prolyl hydroxylase domain-containing protein 2 gene (egln1, 606425.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the prolyl hydroxylase domain-containing protein 2 gene (egln1, 606425.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3284. en:caused by mutation in the protein o-fucosyltransferase-1 gene (pofut1, 607491.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein o-fucosyltransferase-1 gene (pofut1, 607491.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3285. en:caused by mutation in the protein-tyrosine phosphatase, nonreceptor-type, 11 (ptpn11, 176876.0005) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protein-tyrosine phosphatase, nonreceptor-type, 11 (ptpn11, 176876.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3286. en:caused by mutation in the proteolipid protein 1 gene (plp1, 300401.0012) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the proteolipid protein 1 gene (plp1, 300401.0012) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3287. en:caused by mutation in the protocadherin 15 gene (pcdh15, 605514.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the protocadherin 15 gene (pcdh15, 605514.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3288. en:caused by mutation in the pyruvate dehydrogenase kinase, isoenzyme 3 gene (pdk3, 300906.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the pyruvate dehydrogenase kinase, isoenzyme 3 gene (pdk3, 300906.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3289. en:caused by mutation in the rab3 gtpase-activating protein subunit 1 gene (rab3gap1, 602536.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rab3 gtpase-activating protein subunit 1 gene (rab3gap1, 602536.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3290. en:caused by mutation in the rb1 gene (rb1, 614041.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the rb1 gene (rb1, 614041.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3291. en:caused by mutation in the recq protein-like 3 gene (recql3, 604610.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the recq protein-like 3 gene (recql3, 604610.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3292. en:caused by mutation in the ric-like protein without caax motif 1 gene (rit1, 609591.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ric-like protein without caax motif 1 gene (rit1, 609591.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3293. en:caused by mutation in the romboid 5, drosophila, homolog of, 2 gene (rhbdf2, 614404.0001 ) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the romboid 5, drosophila, homolog of, 2 gene (rhbdf2, 614404.0001 ) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3294. en:caused by mutation in the sal-like 1 gene (sall1, 602218.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sal-like 1 gene (sall1, 602218.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3295. en:caused by mutation in the sbds gene (sbds, 607444.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sbds gene (sbds, 607444.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3296. en:caused by mutation in the scavenger receptor class b, member 2 gene (scarb2, 602257.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the scavenger receptor class b, member 2 gene (scarb2, 602257.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3297. en:caused by mutation in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sodium channel, voltage-gated, type v, alpha polypeptide gene (scn5a, 600163.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3298. en:caused by mutation in the sodium channel, voltage-gated, type v, alpha subunit gene (scn5a, 600163.0004) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sodium channel, voltage-gated, type v, alpha subunit gene (scn5a, 600163.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3299. en:caused by mutation in the sodium channel, voltage-gated, type v, alpha subunit gene (scn5a, 600163.0033) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the sodium channel, voltage-gated, type v, alpha subunit gene (scn5a, 600163.0033) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3300. en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, citrin), member 13 (slc25a13, 603859.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 25 (mitochondrial carrier, citrin), member 13 (slc25a13, 603859.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3301. en:caused by mutation in the solute carrier family 30 (zinc transporter), member 2 gene (slc30a2, 609617.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the solute carrier family 30 (zinc transporter), member 2 gene (slc30a2, 609617.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3302. en:caused by mutation in the spectrin, alpha, erythrocytic-1 gene (spta1, 182860.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the spectrin, alpha, erythrocytic-1 gene (spta1, 182860.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3303. en:caused by mutation in the succinate dehydrogenase complex subunit b gene (sdhb, 185470.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the succinate dehydrogenase complex subunit b gene (sdhb, 185470.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3304. en:caused by mutation in the suppression of tumorigenicity 14 gene (st14, 606797.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the suppression of tumorigenicity 14 gene (st14, 606797.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3305. en:caused by mutation in the taf4b rna polymerase ii, tata box-binding protein-associated factor, 105kd gene (taf4b, 601689.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the taf4b rna polymerase ii, tata box-binding protein-associated factor, 105kd gene (taf4b, 601689.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3306. en:caused by mutation in the tafazzin gene (taz, 300394.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tafazzin gene (taz, 300394.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3307. en:caused by mutation in the transformation gene erbb-3 (erbb3, 190151.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transformation gene erbb-3 (erbb3, 190151.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3308. en:caused by mutation in the transient receptor potential cation channel, subfamily m, member 6 gene (trpm6, 607009.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transient receptor potential cation channel, subfamily m, member 6 gene (trpm6, 607009.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3309. en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transient receptor potential cation channel, subfamily v, member 4 gene (trpv4, 605427.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3310. en:caused by mutation in the transmembrane protein 98 gene (tmem98, 615949.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the transmembrane protein 98 gene (tmem98, 615949.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3311. en:caused by mutation in the trk-fused gene (tfg, 602498.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the trk-fused gene (tfg, 602498.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3312. en:caused by mutation in the tropomyosin 3 gene (tpm3, 191030.0005) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tropomyosin 3 gene (tpm3, 191030.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3313. en:caused by mutation in the tumor necrosis factor receptor superfamily, member 13b gene (tnfrsf13b, 604907.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tumor necrosis factor receptor superfamily, member 13b gene (tnfrsf13b, 604907.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3314. en:caused by mutation in the tumor necrosis factor receptor superfamily, member 13c gene (tnfrsf13c, 606269.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tumor necrosis factor receptor superfamily, member 13c gene (tnfrsf13c, 606269.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3315. en:caused by mutation in the tumor necrosis factor receptor superfamily, member 7 gene (tnfrsf7, 186711.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tumor necrosis factor receptor superfamily, member 7 gene (tnfrsf7, 186711.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3316. en:caused by mutation in the tumor protein p63 gene (tp63, 603273.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tumor protein p63 gene (tp63, 603273.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3317. en:caused by mutation in the tyrosyl-trna synthetase 2 gene (yars2, 610957.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the tyrosyl-trna synthetase 2 gene (yars2, 610957.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3318. en:caused by mutation in the ubiquitin-like modifier-activating enzyme 1 gene (uba1, 314370.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ubiquitin-like modifier-activating enzyme 1 gene (uba1, 314370.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3319. en:caused by mutation in the ush3a gene (ush3a, 606397.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the ush3a gene (ush3a, 606397.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3320. en:caused by mutation in the v-ki-ras2 kirsten rat sarcoma viral oncogene homolog gene (kras, 190070.0005) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-ki-ras2 kirsten rat sarcoma viral oncogene homolog gene (kras, 190070.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3321. en:caused by mutation in the v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog gene (kit, 164920.0011) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the v-kit hardy-zuckerman 4 feline sarcoma viral oncogene homolog gene (kit, 164920.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3322. en:caused by mutation in the vaccinia-related kinase 1 gene (vrk1, 602168.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the vaccinia-related kinase 1 gene (vrk1, 602168.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3323. en:caused by mutation in the voltage-gated, type x, alpha subunit gene (scn10a, 604427.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the voltage-gated, type x, alpha subunit gene (scn10a, 604427.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3324. en:caused by mutation in the von willebrand factor gene (vwf, 613160.0028) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the von willebrand factor gene (vwf, 613160.0028) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3325. en:caused by mutation in the was gene (was, 300392.0004) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the was gene (was, 300392.0004) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3326. en:caused by mutation in the wd repeat-containing protein 72 gene (wdr72, 613214.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein 72 gene (wdr72, 613214.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3327. en:caused by mutation in the wd repeat-containing protein 81 gene (wdr81, 614218.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein 81 gene (wdr81, 614218.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3328. en:caused by mutation in the wd repeat-containing protein antisense to tp53 gene (wrap53, 612661.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd repeat-containing protein antisense to tp53 gene (wrap53, 612661.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3329. en:caused by mutation in the wd-repeat containing protein 34 gene (wdr34, 613363.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wd-repeat containing protein 34 gene (wdr34, 613363.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3330. en:caused by mutation in the wingless-type mmtv integration site family, member 1 gene (wnt1, 164820.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wingless-type mmtv integration site family, member 1 gene (wnt1, 164820.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3331. en:caused by mutation in the wingless-type mmtv integration site family, member 10a gene (wnt10a, 606268.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wingless-type mmtv integration site family, member 10a gene (wnt10a, 606268.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3332. en:caused by mutation in the wingless-type mmtv integration site family, member 4 gene (wnt4, 603490.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wingless-type mmtv integration site family, member 4 gene (wnt4, 603490.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3333. en:caused by mutation in the wingless-type mmtv integration site family, member 5a gene (wnt5a, 164975.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wingless-type mmtv integration site family, member 5a gene (wnt5a, 164975.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3334. en:caused by mutation in the wiskott-aldrich syndrome protein gene (wasp, 301000.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wiskott-aldrich syndrome protein gene (wasp, 301000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3335. en:caused by mutation in the wnk lysine deficient protein kinase 1 gene (wnk1, 605232.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the wnk lysine deficient protein kinase 1 gene (wnk1, 605232.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3336. en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0015) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the x-linked aristaless-related homeobox gene (arx, 300382.0015) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3337. en:caused by mutation in the yeast homolog, b, of the vacuolar protein sorting 33 gene (vps33b, 608552.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the yeast homolog, b, of the vacuolar protein sorting 33 gene (vps33b, 608552.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3338. en:caused by mutation in the zinc finger protein 469 gene (znf469, 612078.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger protein 469 gene (znf469, 612078.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3339. en:caused by mutation in the zinc finger protein 592 (znf592, 613624.0001). --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger protein 592 (znf592, 613624.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3340. en:caused by mutation in the zinc finger swim domain-containing protein 6 (zswim6, 615951.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger swim domain-containing protein 6 (zswim6, 615951.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3341. en:caused by mutation in the zinc finger- and btb domain-containing protein 16 gene (zbtb16, 176797.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zinc finger- and btb domain-containing protein 16 gene (zbtb16, 176797.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3342. en:caused by mutation in the zrs regulatory element located in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0018) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutation in the zrs regulatory element located in the homolog of the mouse limb region 1 gene (lmbr1, 605522.0018) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3343. en:caused by mutations in the alpha subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the alpha subunit of the type iv voltage-gated sodium channel gene (scn4a, 603967.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3344. en:caused by mutations in the alpha-3 subunit of the na+/k+-atpase gene (atp1a3, 182350.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the alpha-3 subunit of the na+/k+-atpase gene (atp1a3, 182350.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3345. en:caused by mutations in the cholinergic receptor, nicotinic, alpha polypeptide-1 gene (chrna1, 100690.0007) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the cholinergic receptor, nicotinic, alpha polypeptide-1 gene (chrna1, 100690.0007) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3346. en:caused by mutations in the claudin-1 gene (cldn1, 603718.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the claudin-1 gene (cldn1, 603718.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3347. en:caused by mutations in the distal-less homeo box-3 gene (dlx3, 600525.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the distal-less homeo box-3 gene (dlx3, 600525.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3348. en:caused by mutations in the helicase-2 gene (xh2, 300032.0011) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the helicase-2 gene (xh2, 300032.0011) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3349. en:caused by mutations in the homolog of drosophila muscle segment homeo box 1 gene (msx1, 142983.0003) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the homolog of drosophila muscle segment homeo box 1 gene (msx1, 142983.0003) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3350. en:caused by mutations in the homolog of the mouse ank gene (ankh, 605145.0006) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the homolog of the mouse ank gene (ankh, 605145.0006) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3351. en:caused by mutations in the leukemia inhibitory factor receptor gene (lifr, 151443.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the leukemia inhibitory factor receptor gene (lifr, 151443.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3352. en:caused by mutations in the lim/homeodomain protein lhx3 gene (lhx3, 600577.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the lim/homeodomain protein lhx3 gene (lhx3, 600577.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3353. en:caused by mutations in the matrilin 3 gene (matn3, 602109.0005) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the matrilin 3 gene (matn3, 602109.0005) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3354. en:caused by mutations in the midline 1 gene (mid1, 300000.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the midline 1 gene (mid1, 300000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3355. en:caused by mutations in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0010) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the myosin, heavy polypeptide-9, nonmuscle gene (myh9, 160775.0010) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3356. en:caused by mutations in the red cell pyruvate kinase gene (pkrl, 609712.0001). --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the red cell pyruvate kinase gene (pkrl, 609712.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3357. en:caused by mutations in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 606718.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the solute carrier family 26 (sulfate transporter), member 2 gene (slc26a2, 606718.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3358. en:caused by mutations in the swi/snf related, matrix associated, actin dependent regulator of chromatin, subfamily a-like gene (smarcal1, 606622.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the swi/snf related, matrix associated, actin dependent regulator of chromatin, subfamily a-like gene (smarcal1, 606622.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3359. en:caused by mutations in the transcription factor ap-2 beta gene (tfap2b, 601601.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the transcription factor ap-2 beta gene (tfap2b, 601601.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3360. en:caused by mutations in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase gene (gne, 603824.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3361. en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0001). --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by mutations in the wilms tumor 1 gene (wt1, 607102.0001). | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3362. en:caused by somatic mutation in the alpha-stimulatory subunit of the guanine nucleotide-binding protein gene (gnas1, 139320.0008) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the alpha-stimulatory subunit of the guanine nucleotide-binding protein gene (gnas1, 139320.0008) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3363. en:caused by somatic mutation in the neuroblastoma ras viral (v-ras) oncogene homolog gene (nras, 164790.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by somatic mutation in the neuroblastoma ras viral (v-ras) oncogene homolog gene (nras, 164790.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3364. en:caused by tandem duplication of the urinary plasminogen activator gene (plau, 191840.0002) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:caused by tandem duplication of the urinary plasminogen activator gene (plau, 191840.0002) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3365. en:contiguous gene syndrome associated with duplication (4.5 - 9.2mb) of chromosome xp11.22-p11.23 --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome associated with duplication (4.5 - 9.2mb) of chromosome xp11.22-p11.23 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3366. en:contiguous gene syndrome caused by deletion of 18p11.21-p11.1 --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:contiguous gene syndrome caused by deletion of 18p11.21-p11.1 | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3367. en:due to mutation in the retinol-binding protein 4 gene (rbp4, 180250.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:due to mutation in the retinol-binding protein 4 gene (rbp4, 180250.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3368. en:susceptibility conferred by mutation in the butyrophilin-like protein 2 gene (btnl2, 606000.0001) --- r_associated #0: 21 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:susceptibility conferred by mutation in the butyrophilin-like protein 2 gene (btnl2, 606000.0001) | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=21
  3369. chromosome --- r_associated #0: 20 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=chromosome | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=20
  3370. syndrome --- r_associated #0: 20 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=syndrome | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=20
  3371. en:chromosome --- r_associated #0: 5 --> en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370)
    n1=en:chromosome | n2=en:a contiguous gene deletion syndrome caused by deletion (5.8 mb) of chromosome 15q26-qter encompassing the igf1r gene (147370) | rel=r_associated | relid=0 | w=5
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Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr