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GENE INFORMATION

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Gene name

RNASEH2A (HGNC Symbol)

Synonyms

AGS4, RNASEHI, RNHIA, RNHL

Description

ribonuclease H2, subunit A (HGNC Symbol)

Entrez gene summary

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]

Chromosome

19 (Chromosome progress)

Cytoband

p13.2

Chromosome location (bp)

12917394 - 12924452

Ensembl

ENSG00000104889 (version 69.37)

Entrez gene

10535

UniProt

O75792

neXtProt

NX_O75792

Antibodypedia

RNASEH2A antibodies
 

PROTEIN VIEW

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RNASEH2A-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

RNASEH2A-001 ENSP00000221486
ENST00000221486
O75792
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