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XRCC4, X-ray repair cross complementing 4

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XRCC4, X-ray repair cross complementing 4

  • The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternate transcript variants such as NM_022406 are unlikely to be expressed in some individuals due to a polymorphism (rs1805377) in the last splice acceptor site. [provided by RefSeq, Oct 2019]

  • Gene Synonyms (DNA repair protein XRCC4, X-ray repair complementing defective repair in Chinese hamster cells 4, SSMED,)
  • NCBI Gene ID: 7518
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A024RAP0
    UNIPROT ID#>>A0A024RAL0
    UNIPROT ID#>>Q7Z763
    UNIPROT ID#>>A0A024RAQ8
    UNIPROT ID#>>Q13426
  • 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.

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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