Human (GRCh38.p14)
Description

G protein-coupled receptor 89B [Source:HGNC Symbol;Acc:HGNC:13840]

Gene Synonyms

GPR89, GPR89C, SH120

Location

Chromosome 1: 147,928,393-147,993,592 forward strand.

GRCh38:CM000663.2

About this gene

This gene has 8 transcripts (splice variants), 201 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000314163.12GPR89B-2012160455aaENSP00000358233.4
 
Protein coding
CCDS930P0CG08 X5D7G6 NM_016334.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000468618.6GPR89B-203750216aaENSP00000475253.1
 
Protein coding
U3KPV2 -TSL:3CDS 3' incomplete
ENST00000488165.5GPR89B-2051954124aaENSP00000480882.1
 
Nonsense mediated decay
--TSL:1
ENST00000491975.5GPR89B-208683128aaENSP00000480018.1
 
Nonsense mediated decay
A0A087WW82 -TSL:5CDS 5' incomplete
ENST00000461786.5GPR89B-20257493aaENSP00000480007.1
 
Nonsense mediated decay
A0A087WW78 -TSL:3CDS 5' incomplete
ENST00000488603.5GPR89B-2062701No protein-
 
Retained intron
--TSL:2
ENST00000478307.5GPR89B-2042633No protein-
 
Retained intron
--TSL:2
ENST00000490955.1GPR89B-2071906No protein-
 
Retained intron
--TSL:2