RNASEH2A
Sign in to saveAlso known as AGS4, JUNB, RNASEHI, RNHIA, RNHL, ribonuclease H2 subunit A, THSD8
Ribonuclease H2 subunit A, also known as RNase H2 subunit A, is an enzyme that in humans is encoded by the RNASEH2A gene.
Gene data
RNASEH2A- Name
- ribonuclease H2 subunit A
- Type
- protein-coding
- Aliases
- AGS4, RNASEHI, RNHIA, RNHL
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].
via MyGene.info
Gene · Ensembl
ribonuclease H2 subunit A
- Symbol
- RNASEH2A
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 19:12,806,505-12,813,644
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Image
- 3puf highlight subunit A.png
Show 5 more facts
- HomoloGene ID
- 4664
- exact match
- identifiers.org/ncbigene/10535
- genomic end
- 12813640
- genomic start
- 12806584
- cytogenetic location
- 19p13.13
via Wikidata · CC0
~1 min read
Article
5 sectionsContents
- Function
- Clinical significance
- References
- Further reading
- External links
Ribonuclease H2 subunit A, also known as RNase H2 subunit A, is an enzyme that in humans is encoded by the RNASEH2A gene.
== Function ==