Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: BCR ENSBTAG00000020566

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Description

BCR activator of RhoGEF and GTPase [Source:VGNC Symbol;Acc:VGNC:56808]

Location

Primary_assembly 17: 71,710,381-71,795,479 reverse strand.

ARS-UCD2.0:CM008184.2

About this gene

This gene has 1 transcript (splice variant), 266 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000071096.2	BCR-201	5052	1283aa	ENSBTAP00000065181.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M4M7	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,

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Summary

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