Description

trace amine associated receptor 2 [Source:HGNC Symbol;Acc:HGNC:4514]

Synonyms

GPR58

INSDC coordinates

chromosome:GRCh38:CM000668.2:132617022:132624275:1

About this gene

This gene has 2 transcripts (splice variants), 81 orthologues, 13 paralogues, is a member of 1 Ensembl protein family and is associated with 80 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
TAAR2-001ENST000002751911157306aaENSP00000275191
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS5157Q9P1P5 NM_014626
NP_055441
TSL:NA

TSL:NA:The transcript was not analyzed for one of the following reasons:

  • Pseudogene annotation, including transcribed pseudogenes
  • Human leukocyte antigen (HLA) transcript
  • Immunoglobin gene transcript
  • T-cell receptor transcript
  • Single-exon transcript (will be included in a future version)

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 PI3APPRIS candidate principal isoform (earliest CCDS)
Glossary entry for APPRIS
APPRIS website
TAAR2-002ENST000003679311056351aaENSP00000356908
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS34541Q9P1P5 NM_001033080
NP_001028252
TSL:1

TSL1: All splice junctions of the transcript 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 ALT2APPRIS candidate principal isoform that appears to be conserved in fewer than three tested non-primate species
Glossary entry for APPRIS
APPRIS website

Gene-based displays