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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Paralogues
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RNASEH2A ENSG00000104889

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Description

ribonuclease H2, subunit A [Source:HGNC Symbol;Acc:18518]

Gene Synonyms

AGS4, JUNB, RNASEHI, RNHIA, RNHL

Location

Chromosome 19: 12,917,394-12,924,452 forward strand.

GRCh37:CM000681.1

About this gene

This gene has 4 transcripts (splice variants) and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000221486.4	RNASEH2A-001	1165	299aa	ENSP00000221486.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS12282	O75792	NM_006397.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000593017.1	RNASEH2A-002	1487	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-
ENST00000590121.1	RNASEH2A-003	859	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-
ENST00000590279.1	RNASEH2A-004	696	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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