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  Domain Name: Myosin_N
Myosin N-terminal SH3-like domain. This domain has an SH3-like fold. It is found at the N-terminus of many but not all myosins. The function of this domain is unknown.

Total Mutations Found: 37
Total Disease Mutations Found: 21
This domain occurred 13 times on human genes (24 proteins).



  ARTHROGRYPOSIS, DISTAL, 2B (DA2B)
  CARDIOMYOPATHY, DILATED 1EE (CMD1EE)
  CARDIOMYOPATHY, DILATED 1S (CMD1S)
  CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 1 (CMH1)
  CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 14 (CMH14)
  MAY-HEGGLIN ANOMALY (MHA)
  MYOPATHY, DISTAL, 1 (MPD1)
  SCAPULOPERONEAL MYOPATHY MYH7-RELATED (SPMM)
  SEBASTIAN SYNDROME (SBS)


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 Functional Features are displayed as orange boxes under the histograms. You can choose which features are displayed in the box below.



Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Myosin_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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