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  Domain Name: COG1428
Deoxynucleoside kinases [Nucleotide transport and metabolism]
No pairwise interactions found for the domain COG1428

Total Mutations Found: 29
Total Disease Mutations Found: 27
This domain occurred 4 times on human genes (10 proteins).



  LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
  MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)
  MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for COG1428









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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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