Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: hnrnpa0b ENSDARG00000036162

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Description

heterogeneous nuclear ribonucleoprotein A0b [Source:ZFIN;Acc:ZDB-GENE-030131-6154]

Gene Synonyms

fi36h08, hnrnpa0, hnrpa0, wu:fa16d06, wu:fi36h08, zgc:77280

Location

Chromosome 14: 38,845,674-38,848,166 forward strand.

GRCz11:CM002898.2

About this gene

This gene has 3 transcripts (splice variants), 368 orthologues and 46 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000129958.3	hnrnpa0b-202	2493	314aa	ENSDARP00000108805.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QTL9	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,
ENSDART00000052512.5	hnrnpa0b-201	1293	314aa	ENSDARP00000052511.4	Nonsense mediated decay	F1QTL9	-
ENSDART00000144599.2	hnrnpa0b-203	745	155aa	ENSDARP00000124839.1	Nonsense mediated decay	F8W265	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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