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This gene encodes a mitochondrial inner membrane protein that is implicated in the metabolism of reactive oxygen species. Mutations in this gene have been associated with the hepatocerebral form of mitochondrial DNA depletion syndrome.
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Protein Aliases: h-MPV; hMPV; Mitochondrial inner membrane protein Mpv17; Mpv-17; MpV17 mitochondrial inner membrane protein; Mpv17 protein; Mpv17, human homolog of glomerulosclerosis and nephrotic syndrome; OTTHUMP00000122591; Protein Mpv17
Gene Aliases: MPV17; MTDPS6; SYM1; Tg.Mpv17
UniProt ID: (Human) P39210, (Mouse) P19258
Entrez Gene ID: (Human) 4358, (Mouse) 17527
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