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  Domain Name: MgtA
Cation transport ATPase [Inorganic ion transport and metabolism]
No pairwise interactions found for the domain MgtA

Total Mutations Found: 266
Total Disease Mutations Found: 129
This domain occurred 31 times on human genes (74 proteins).



  ALTERNATING HEMIPLEGIA OF CHILDHOOD 1
  ALTERNATING HEMIPLEGIA OF CHILDHOOD 2
  BRODY MYOPATHY
  BRODY MYOPATHY (BRM)
  CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 4 (CMARQ4)
  CEROID LIPOFUSCINOSIS, NEURONAL, 12 (1 FAMILY)
  CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1
  CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1
  CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1
  CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1, INCLUDED
  CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 1 (PFIC1)
  DEAFNESS, AUTOSOMAL RECESSIVE 12, MODIFIER OF
  DYSTONIA 12
  HAILEY-HAILEY DISEASE
  KUFOR-RAKEB SYNDROME
  MENKES DISEASE
  MIGRAINE, FAMILIAL BASILAR
  MIGRAINE, FAMILIAL HEMIPLEGIC, 2
  OCCIPITAL HORN SYNDROME
  SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3
  WILSON DISEASE


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for MgtA























































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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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