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  Domain Name: Dynamin_N
Dynamin family.
No pairwise interactions found for the domain Dynamin_N

Total Mutations Found: 48
Total Disease Mutations Found: 45
This domain occurred 15 times on human genes (46 proteins).



  ATAXIA, AND NEUROPATHY
  ATAXIA, AND NEUROPATHY, INCLUDED
  CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2
  CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2, AUTOSOMAL RECESSIVE
  CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2, INCLUDED
  HEREDITARY MOTOR AND SENSORY NEUROPATHY VI
  OPTIC ATROPHY 1
  OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY,


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Dynamin_N













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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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