Description

BarH-like homeobox 1 [Source:HGNC Symbol;Acc:HGNC:953]

INSDC coordinates

chromosome:GRCh38:CM000671.2:132582185:132590266:1

About this gene

This gene has 2 transcripts (splice variants), 58 orthologues, 11 paralogues, is a member of 1 Ensembl protein family and is associated with 51 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
BARHL1-001ENST000002636102341327aaENSP00000263610
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS6950Q9BZE3 NM_020064
NP_064448
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

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.

BARHL1-201ENST000005420901197327aaENSP00000444704
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS6950Q9BZE3 -TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

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