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NDUFAF3, NADH:ubiquinone oxidoreductase complex assembly factor 3

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NDUFAF3, NADH:ubiquinone oxidoreductase complex assembly factor 3

  • This gene encodes a mitochondrial complex I assembly protein that interacts with complex I subunits. Mutations in this gene cause mitochondrial complex I deficiency, a fatal neonatal disorder of the oxidative phosphorylation system. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2009]

  • Gene Synonyms (NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 3, NADH dehydrogenase (ubiquinone) complex I, assembly factor 3, nuclear protein E3-3, 2P1, C3orf60, E3-3, MC1DN18,)
  • NCBI Gene ID: 25915
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A4FU71
    UNIPROT ID#>>Q9BU61
    UNIPROT ID#>>Q9Y3Z0
  • 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.

NADH:ubiquinone oxidoreductase complex assembly factor 3 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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