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  Domain Name: C2
C2 domain.
No pairwise interactions found for the domain C2

Total Mutations Found: 124
Total Disease Mutations Found: 56
This domain occurred 103 times on human genes (190 proteins).



  COACH SYNDROME
  CONE-ROD DYSTROPHY 13
  CONE-ROD DYSTROPHY 7
  HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2
  LIMB-GIRDLE MUSCULAR DYSTROPHY 2B (LGMD2B)
  MECKEL SYNDROME, TYPE 5
  MIYOSHI MUSCULAR DYSTROPHY 1 (MMD1)
  MIYOSHI MYOPATHY
  MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
  SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for C2









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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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