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

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Gene: Anxa2 ENSRNOG00000010362

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Description

annexin A2 [Source:RGD Symbol;Acc:621170]

Gene Synonyms

ANX2, PAP-IV, p36

Location

Primary_assembly 8: 78,986,242-79,022,631 forward strand.

GRCr8:CM070398.1

About this gene

This gene has 1 transcript (splice variant), 314 orthologues, 12 paralogues and is associated with 29 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000096961.2	Anxa2-201	1782	339aa	ENSRNOP00000094972.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ANV9 A6KEW0 Q07936	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Summary

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