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  Domain Name: Cadherin
Cadherin domain.
No pairwise interactions found for the domain Cadherin

Total Mutations Found: 224
Total Disease Mutations Found: 36
This domain occurred 71 times on human genes (118 proteins).



  ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  CARDIOMYOPATHY, DILATED, 1BB, SUSCEPTIBILITY TO, INCLUDED
  DEAFNESS, AUTOSOMAL RECESSIVE 12
  DEAFNESS, AUTOSOMAL RECESSIVE 23
  ENDOMETRIAL CARCINOMA, SOMATIC
  EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9
  GASTRIC CANCER, HEREDITARY DIFFUSE
  GASTRIC CANCER, HEREDITARY DIFFUSE, INCLUDED
  HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
  HYPOTRICHOSIS 6
  HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY
  MENTAL RETARDATION, AUTOSOMAL DOMINANT 3
  PALMOPLANTAR KERATODERMA I, STRIATE
  RENAL AGENESIS
  USHER SYNDROME, TYPE ID
  USHER SYNDROME, TYPE IF
  VAN MALDERGEM SYNDROME 2


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Cadherin








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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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