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RNASEH2C, ribonuclease H2 subunit C

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RNASEH2C, ribonuclease H2 subunit C

  • This gene encodes a ribonuclease H subunit that can cleave ribonucleotides from RNA:DNA duplexes. Mutations in this gene cause Aicardi-Goutieres syndrome-3, a disease that causes severe neurologic dysfunction. A pseudogene for this gene has been identified on chromosome Y, near the sex determining region Y (SRY) gene. [provided by RefSeq, Jul 2008]

  • Gene Synonyms (ribonuclease H2 subunit C, RNase H1 small subunit, RNase H2 subunit C, aicardi-Goutieres syndrome 3 protein, ribonuclease HI subunit C, AGS3, AYP1,)
  • NCBI Gene ID: 84153
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q8TDP1
    UNIPROT ID#>>A0A024R5B3
  • 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.

ribonuclease H2 subunit C 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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