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: anxa2b ENSDARG00000053625

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Description

annexin A2b [Source:NCBI gene (formerly Entrezgene);Acc:799806]

Gene Synonyms

anx2b, wu:fb59b10, zgc:92492

Location

Chromosome 7: 29,518,396-29,534,001 reverse strand.

GRCz11:CM002891.2

About this gene

This gene has 3 transcripts (splice variants), 274 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000057289.7	anxa2b-201	1324	338aa	ENSDARP00000057288.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A8E5G1	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,
ENSDART00000124028.4	anxa2b-202	1297	338aa	ENSDARP00000110454.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A8E5G1	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,
ENSDART00000144465.2	anxa2b-203	313	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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