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

Configure this page

Share this page

Bookmark this page

.

Gene: ANXA13 ENSBTAG00000005585

.

Description

annexin A13 [Source:UniProtKB Gene Name;Acc:F1N2Q7]

Location

Primary_assembly 14: 16,167,589-16,200,592 forward strand.

ARS-UCD2.0:CM008181.2

About this gene

This gene has 3 transcripts (splice variants), 282 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000118871.2	ANXA13-202	1657	352aa	ENSBTAP00000103259.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9U0R7	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,
ENSBTAT00000112694.2	ANXA13-203	1597	300aa	ENSBTAP00000078052.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RZG9	-
ENSBTAT00000007336.8	ANXA13-201	1353	336aa	ENSBTAP00000007336.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N2Q7	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

.

Summary

.

.