GPR89B

Protein GPR89 is a protein that in humans is encoded by the GPR89B gene.^[5][6]

GPR89B
Identifiers
Aliases	GPR89B, GPHR, GPR89, GPR89C, SH120, UNQ192, G protein-coupled receptor 89B
External IDs	OMIM: 612806; MGI: 1914799; HomoloGene: 9475; GeneCards: GPR89B; OMA:GPR89B - orthologs
Gene location (Human) Chr. Chromosome 1 (human)[1] Band 1q21.2 Start 147,928,393 bp[1] End 147,993,592 bp[1]
Gene location (Mouse) Chr. Chromosome 3 (mouse)[2] Band 3|3 F2.1 Start 96,775,597 bp[2] End 96,812,662 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in testicle duodenum corpus callosum Achilles tendon human kidney body of pancreas granulocyte cerebellar cortex cerebellar hemisphere right lobe of liver Top expressed in spermatocyte lacrimal gland jejunum otic vesicle ileum saccule intestinal epithelium interventricular septum epithelium of small intestine right lobe of liver More reference expression data BioGPS n/a
Gene ontology Molecular function voltage-gated anion channel activity signal transducer activity voltage-gated ion channel activity Cellular component integral component of membrane Golgi cisterna membrane Golgi-associated vesicle membrane Golgi membrane Golgi apparatus membrane Biological process protein transport positive regulation of I-kappaB kinase/NF-kappaB signaling regulation of ion transmembrane transport ion transport intracellular pH reduction signal transduction regulation of anion transmembrane transport transport ion transmembrane transport inorganic anion transport Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 51463 67549 Ensembl ENSG00000188092 ENSMUSG00000028096 UniProt P0CG08 Q8BS95 RefSeq (mRNA) NM_001097616 NM_001350180 NM_001350181 NM_001350182 NM_001350183 NM_001350184 NM_016334 NM_026229 RefSeq (protein) NP_001091081 NP_001091082 NP_001337109 NP_001337110 NP_001337111 NP_001337112 NP_001337113 NP_057418 NP_001337109 NP_001337110 NP_001337111 NP_001337112 NP_001337113 NP_057418 NP_001091081 NP_001091082 NP_080505 Location (UCSC) Chr 1: 147.93 – 147.99 Mb Chr 3: 96.78 – 96.81 Mb PubMed search [3] [4]
Wikidata
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Related gene problems

• 1q21.1 deletion syndrome
• 1q21.1 duplication syndrome