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: ITGB2 ENSBTAG00000017060

.

Description

integrin subunit beta 2 [Source:VGNC Symbol;Acc:VGNC:30327]

Location

Primary_assembly 1: 144,759,562-144,788,699 reverse strand.

ARS-UCD2.0:CM008168.2

About this gene

This gene has 5 transcripts (splice variants), 107 orthologues, 8 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000081854.2	ITGB2-201	3027	881aa	ENSBTAP00000059292.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LQE4	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 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,
ENSBTAT00000076413.2	ITGB2-205	2796	769aa	ENSBTAP00000069668.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P32592	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,
ENSBTAT00000081335.2	ITGB2-204	2727	781aa	ENSBTAP00000062189.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N0H1	-
ENSBTAT00000022687.7	ITGB2-203	2724	780aa	ENSBTAP00000022687.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A452DIU0	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,
ENSBTAT00000128577.1	ITGB2-202	2697	771aa	ENSBTAP00000080071.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S814	-

.

Summary

.

.