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: hnrnpabb ENSDARG00000099865

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Description

heterogeneous nuclear ribonucleoprotein A/Bb [Source:ZFIN;Acc:ZDB-GENE-040426-2516]

Gene Synonyms

fd36h02, sqd-likeB, wu:fd36h02, zgc:77052

Location

Chromosome 21: 3,166,519-3,175,724 forward strand.

GRCz11:CM002905.2

About this gene

This gene has 2 transcripts (splice variants), 227 orthologues and 46 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000168163.2	hnrnpabb-202	3606	309aa	ENSDARP00000133355.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6NYA1	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,
ENSDART00000160585.2	hnrnpabb-201	1648	309aa	ENSDARP00000137921.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6NYA1	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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