Description

dorsal root ganglia homeobox [Source:HGNC Symbol;Acc:HGNC:21536]

Synonyms

DRG11, PRRXL1

Location
INSDC coordinates

chromosome:GRCh38:CM000672.2:49364181:49396016:1

About this gene

This gene has 2 transcripts (splice variants), 63 orthologues, 14 paralogues, is a member of 1 Ensembl protein family and is associated with 53 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
DRGX-001ENST000003741392738263aaENSP00000363254
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS44388A6NNA5 -TSL:2

Transcript Support Level 2, when transcripts are supported by multiple ESTs or by an mRNA flagged as suspect.

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.

DRGX-201ENST00000434016955263aaENSP00000401653
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS44388A6NNA5 NM_001276451
NP_001263380
TSL:5

Transcript Support Level 5, for transcripts that are not supported at all by either an mRNA or an EST.

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