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: BCAR1 ENSBTAG00000012002

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Description

BCAR1 scaffold protein, Cas family member [Source:VGNC Symbol;Acc:VGNC:26437]

Location

Primary_assembly 18: 2,573,411-2,608,699 reverse strand.

ARS-UCD2.0:CM008185.2

About this gene

This gene has 4 transcripts (splice variants), 201 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000072130.2	BCAR1-204	3032	866aa	ENSBTAP00000066068.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M7M1	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,
ENSBTAT00000073322.2	BCAR1-203	3293	846aa	ENSBTAP00000073626.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MQ07	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,
ENSBTAT00000072519.2	BCAR1-202	3136	861aa	ENSBTAP00000065321.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M4Z7	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,
ENSBTAT00000015922.6	BCAR1-201	2966	844aa	ENSBTAP00000015922.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MCH0	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,

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Summary

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