Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: BCAP29 ENSPTRG00000019580

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Description

B cell receptor associated protein 29 [Source:VGNC Symbol;Acc:VGNC:14457]

Location

Chromosome 7: 111,853,124-111,896,615 forward strand.

Pan_tro_3.0:CM000321.4

About this gene

This gene has 2 transcripts (splice variants), 247 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000108368.1	BCAP29-202	993	330aa	ENSPTRP00000069124.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RWQ2	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,
ENSPTRT00000055240.4	BCAP29-201	6312	241aa	ENSPTRP00000047699.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8QXZ9 A0A6D2WGI2	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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