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  Domain Name: BCS1_N
BCS1 N terminal. This domain is found at the N terminal of the mitochondrial ATPase BSC1. It encodes the import and intramitochondrial sorting for the protein.
No pairwise interactions found for the domain BCS1_N

Total Mutations Found: 10
Total Disease Mutations Found: 10
This domain occurred 1 times on human genes (1 proteins).



  BJORNSTAD SYNDROME
  BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
  GRACILE SYNDROME
  LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX III DEFICIENCY
  MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
  MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1,


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for BCS1_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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