Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: itgb1b.2 ENSDARG00000022689

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Description

integrin, beta 1b.2 [Source:NCBI gene (formerly Entrezgene);Acc:405864]

Location

Chromosome 2: 43,638,983-43,653,328 reverse strand.

GRCz11:CM002886.2

About this gene

This gene has 2 transcripts (splice variants), 216 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000037808.9	itgb1b.2-201	2383	613aa	ENSDARP00000036611.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q19U09	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,
ENSDART00000148454.3	itgb1b.2-202	2133	613aa	ENSDARP00000124546.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q19U09	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,

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Summary

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