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

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Gene: BCR ENSSSCG00000010052

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Description

BCR activator of RhoGEF and GTPase [Source:HGNC Symbol;Acc:HGNC:1014]

Location

Primary_assembly 14: 49,208,762-49,322,103 forward strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 2 transcripts (splice variants), 274 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000056015.3	BCR-201	6187	1265aa	ENSSSCP00000043635.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AIC4 A0A8D1F7Q0	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,
ENSSSCT00000040754.3	BCR-202	6055	1221aa	ENSSSCP00000048886.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AY63 A0A8D1FA00	-

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Summary

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