Gene: Bhlha9 ENSRNOG00000022232

Description

basic helix-loop-helix family, member a9 [Source:RGD Symbol;Acc:1311234]

Gene Synonyms

LOC363656, RGD1311234

Location

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant), 188 orthologues, 13 paralogues and is associated with 4 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000032934.4	Bhlha9-201	1122	230aa	ENSRNOP00000037513.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZY30	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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