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RNASEH2A, ribonuclease H2 subunit A

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RNASEH2A, ribonuclease H2 subunit A

  • The protein encoded by this gene is a component of the heterotrimeric type II ribonuclease H enzyme (RNAseH2). RNAseH2 is the major source of ribonuclease H activity in mammalian cells and endonucleolytically cleaves ribonucleotides. It is predicted to remove Okazaki fragment RNA primers during lagging strand DNA synthesis and to excise single ribonucleotides from DNA-DNA duplexes. Mutations in this gene cause Aicardi-Goutieres Syndrome (AGS), a an autosomal recessive neurological disorder characterized by progressive microcephaly and psychomotor retardation, intracranial calcifications, elevated levels of interferon-alpha and white blood cells in the cerebrospinal fluid.[provided by RefSeq, Aug 2009]

  • Gene Synonyms (AGS4, JUNB, RNASEHI, RNHIA, RNHL, THSD8, ribonuclease H2 subunit A, RNase H(35), RNase H2 subunit A, RNase HI large subunit, aicardi-Goutieres syndrome 4 protein, ribonuclease H2, large subunit, ribonuclease HI large subunit, ribonuclease HI subunit A,)
  • NCBI Gene ID: 10535
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>O75792
  • 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.

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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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