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MPV17, mitochondrial inner membrane protein MPV17

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MPV17, mitochondrial inner membrane protein MPV17

  • 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 (MDDS). [provided by RefSeq, Jul 2008]

  • Gene Synonyms (CMT2EE, MTDPS6, SYM1, protein Mpv17, MPV17, mitochondrial inner membrane protein, MpV17 mitochondrial inner membrane protein, Mpv17, human homolog of glomerulosclerosis and nephrotic syndrome,)
  • NCBI Gene ID: 4358
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>P39210
    UNIPROT ID#>>A0A0S2Z3Z9
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

mitochondrial inner membrane protein MPV17 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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