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  Domain Name: IGv
Immunoglobulin V-Type.
No pairwise interactions found for the domain IGv

Total Mutations Found: 63
Total Disease Mutations Found: 26
This domain occurred 92 times on human genes (298 proteins).



  AND CATARACTS
  CD8 DEFICIENCY, FAMILIAL
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, INCLUDED
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B, WITH FOCALLY FOLDED MYELIN SHEATHS
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 2I
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 2J
  DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
  HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,
  NEUROPATHY, CONGENITAL HYPOMYELINATING, AUTOSOMAL DOMINANT
  RADIN BLOOD GROUP ANTIGEN
  SCIANNA BLOOD GROUP SYSTEM, SC:-1,2
  SCIANNA BLOOD GROUP SYSTEM, STAR ANTIGEN
  SPONDYLOEPIMETAPHYSEAL DYSPLASIA AGGRECAN TYPE (SEMD-ACAN)


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for IGv








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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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