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  Domain Name: CAMSAP_CH
CAMSAP CH domain. This domain is the N-terminal CH domain from the CAMSAP proteins.
No pairwise interactions found for the domain CAMSAP_CH

Total Mutations Found: 10
Total Disease Mutations Found: 6
This domain occurred 33 times on human genes (77 proteins).



  BLEEDING DISORDER, PLATELET-TYPE, 15
  FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1
  SPECTRIN KISSIMMEE
  SPHEROCYTOSIS, TYPE 2, AUTOSOMAL DOMINANT
  SPINOCEREBELLAR ATAXIA 5


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for CAMSAP_CH







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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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