Description

neuropeptides B/W receptor 2 [Source:HGNC Symbol;Acc:HGNC:4530]

Synonyms

GPR8

Location

Chromosome 20: 64,105,820-64,107,171 reverse strand.

View alleles of this gene on alternate assemblies

INSDC coordinates

chromosome:GRCh38:CM000682.2:64105820:64107171:1

About this gene

This gene has 1 transcript (splice variant), 1 gene allele, 41 orthologues, 16 paralogues, is a member of 1 Ensembl protein family and is associated with 72 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
NPBWR2-001ENST000003697681352333aaENSP00000358783
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS13557P48146 NM_005286
NP_005277
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