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

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Gene: hnrnpa0l ENSDARG00000036161

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Description

heteroous nuclear ribonucleoprotein A0, like [Source:NCBI gene (formerly Entrezgene);Acc:321899]

Gene Synonyms

fb38a07, hnrpa0l, wu:fb38a07, wu:fb82e07

Location

Chromosome 14: 38,849,432-38,850,933 forward strand.

GRCz11:CM002898.2

About this gene

This gene has 1 transcript (splice variant), 367 orthologues and 46 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000052511.6	hnrnpa0l-201	1502	302aa	ENSDARP00000052510.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q7ZU48	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,

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Summary

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