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

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Gene: rnaseh2b ENSDARG00000005128

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Description

ribonuclease H2, subunit B [Source:ZFIN;Acc:ZDB-GENE-040426-1090]

Gene Synonyms

zgc:56602

Location

Chromosome 9: 29,671,553-29,679,172 forward strand.

GRCz11:CM002893.2

About this gene

This gene has 3 transcripts (splice variants) and 223 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000015377.7	rnaseh2b-201	1042	306aa	ENSDARP00000006173.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QN47	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, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSDART00000145042.3	rnaseh2b-203	520	82aa	ENSDARP00000121023.1	Nonsense mediated decay	F1R3U5	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000123160.3	rnaseh2b-202	531	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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