Description

basic helix-loop-helix family, member a9 [Source:HGNC Symbol;Acc:HGNC:35126]

Synonyms

bHLHa9, BHLHF42

Location
INSDC coordinates

chromosome:GRCh38:CM000679.2:1270559:1271460:1

About this gene

This gene has 1 transcript (splice variant), 33 orthologues, is a member of 1 Ensembl protein family and is associated with 2 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
BHLHA9-001ENST00000391429902235aaENSP00000375248
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS45560Q7RTU4 NM_001164405
NP_001157877
TSL:NA

Transcript Support Level Not Analysed. Pseudogenes, single exon transcripts, HLA, T-cell receptor and Ig transcripts are not analysed and therefore not given any of the TSL categories.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays