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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RNASEH1 ENSG00000171865

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Description

ribonuclease H1 [Source:HGNC Symbol;Acc:18466]

Gene Synonyms

H1RNA, RNH1

Location

Chromosome 2: 3,592,383-3,606,206 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 4 transcripts (splice variants), 1 paralogue and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000315212.3	RNASEH1-001	1887	286aa	ENSP00000313350.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS1647	B3KUD4 E5KN15 F8WD93 O60930	NM_002936.3	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000436842.1	RNASEH1-002	2120	43aa	ENSP00000404926.1	Nonsense mediated decay		F8WD93	-	-
ENST00000454734.1	RNASEH1-003	749	43aa	ENSP00000411646.1	Nonsense mediated decay		F8WBP0	-	-
ENST00000464986.1	RNASEH1-004	514	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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