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

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Gene: BCL2L10 ENSPTRG00000007083

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Description

BCL2 like 10 [Source:VGNC Symbol;Acc:VGNC:6459]

Location

Chromosome 15: 32,771,144-32,774,665 reverse strand.

Pan_tro_3.0:CM000329.3

About this gene

This gene has 1 transcript (splice variant), 129 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000013066.4	BCL2L10-201	1275	204aa	ENSPTRP00000012103.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2Y9E8 H2Q9G4	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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