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CHD7, chromodomain helicase DNA binding protein 7

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CHD7, chromodomain helicase DNA binding protein 7

  • This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]

  • Gene Synonyms (CRG, HH5, IS3, KAL5, chromodomain-helicase-DNA-binding protein 7, ATP-dependent helicase CHD7, CHARGE association, chromodomain helicase DNA binding protein 7 isoform CRA_e,)
  • NCBI Gene ID: 55636
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q6ZWF9
    UNIPROT ID#>>Q9P2D1
  • 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.

chromodomain helicase DNA binding protein 7 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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