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  Domain Name: TGF_beta
Transforming growth factor beta like domain.
No pairwise interactions found for the domain TGF_beta

Total Mutations Found: 27
Total Disease Mutations Found: 25
This domain occurred 28 times on human genes (45 proteins).



  BRACHYDACTYLY, TYPE A1, C
  BRACHYDACTYLY, TYPE A2, INCLUDED
  BRACHYDACTYLY, TYPE C
  CHONDRODYSPLASIA, GREBE TYPE
  DOUBLE-OUTLET RIGHT VENTRICLE
  FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY
  HETEROTAXY, VISCERAL, 5, AUTOSOMAL
  HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
  LEFT-RIGHT AXIS MALFORMATIONS
  LOEYS-DIETZ SYNDROME, TYPE 4
  MULTIPLE SYNOSTOSES SYNDROME 2
  MULTIPLE SYNOSTOSES SYNDROME 2, INCLUDED
  OROFACIAL CLEFT 11
  RIENHOFF SYNDROME (1 FAMILY)
  SYMPHALANGISM, PROXIMAL, 1B


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for TGF_beta








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Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.

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