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: Itgav ENSRNOG00000004912

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Description

integrin subunit alpha V [Source:RGD Symbol;Acc:1310613]

Gene Synonyms

Cd51

Location

Primary_assembly 3: 89,245,095-89,333,511 forward strand.

GRCr8:CM070393.1

About this gene

This gene has 2 transcripts (splice variants), 242 orthologues, 17 paralogues and is associated with 19 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000006961.9	Itgav-201	7247	1043aa	ENSRNOP00000006961.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LZX9	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,
ENSRNOT00000088549.3	Itgav-202	7139	1007aa	ENSRNOP00000069681.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JVZ6	-

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data