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

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Gene: BHLHA15 ENSBTAG00000046010

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Description

basic helix-loop-helix family member a15 [Source:VGNC Symbol;Acc:VGNC:26482]

Location

Primary_assembly 25: 37,789,599-37,798,384 reverse strand.

ARS-UCD2.0:CM008192.2

About this gene

This gene has 2 transcripts (splice variants), 174 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000108670.1	BHLHA15-202	4701	187aa	ENSBTAP00000087032.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G5E6I7	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,
ENSBTAT00000062953.3	BHLHA15-201	1490	187aa	ENSBTAP00000055623.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G5E6I7	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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