Skip Navigation Links Home » Resources » Gene Detail

CHCHD10, coiled-coil-helix-coiled-coil-helix domain containing 10

Matching ORF Clones

    No catalog ORF clones available (link to the custom ORF request form)

Request a Custom Clone

Don't see what you need?

Request My Custom Clone »
  • Gene Overview
  • Interaction Network
  • Sequence Verification

CHCHD10, coiled-coil-helix-coiled-coil-helix domain containing 10

  • This gene encodes a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. Mutations in this gene cause frontotemporal dementia and/or amyotrophic lateral sclerosis-2. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7 and 19. [provided by RefSeq, Aug 2014]

  • Gene Synonyms (C22orf16, FTDALS2, IMMD, MIX17A, N27C7-4, SMAJ, coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial, MIX17 homolog A,)
  • NCBI Gene ID: 400916
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>B5MBW9
    UNIPROT ID#>>Q8WYQ3
  • 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.

coiled-coil-helix-coiled-coil-helix domain containing 10 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.

It appears that you have Javascript disabled. Our website requires Javascript to function correctly. For the best browsing experience, please enable Javascript.