GPBAR1
G-protein coupled bile acid receptor 1
Also known as: BG37, GPBAR_HUMAN, GPCR, GPCR19, GPR131, M-BAR, MGC40597, TGR5
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TDU6
- Gene
- GPBAR1
- Ensembl
- ENSG00000179921
- Chromosome
- 2
- Canonical length
- 330 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins, Transporters
OverviewNCBI Gene
This gene encodes a member of the G protein-coupled receptor (GPCR) superfamily. This enzyme functions as a cell surface receptor for bile acids. Treatment of cells expressing this GPCR with bile acids induces the production of intracellular cAMP, activation of a MAP kinase signaling pathway, and internalization of the receptor. The receptor is implicated in the suppression of macrophage functions and regulation of energy homeostasis by bile acids. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
330 residues, UniProt reviewed canonical sequence.
>Q8TDU6|GPBAR1
1 MTPNSTGEVP SPIPKGALGL SLALASLIIT ANLLLALGIA WDRRLRSPPA GCFFLSLLLA
61 GLLTGLALPT LPGLWNQSRR GYWSCLLVYL APNFSFLSLL ANLLLVHGER YMAVLRPLQP
121 PGSIRLALLL TWAGPLLFAS LPALGWNHWT PGANCSSQAI FPAPYLYLEV YGLLLPAVGA
181 AAFLSVRVLA TAHRQLQDIC RLERAVCRDE PSALARALTW RQARAQAGAM LLFGLCWGPY
241 VATLLLSVLA YEQRPPLGPG TLLSLLSLGS ASAAAVPVAM GLGDQRYTAP WRAAAQRCLQ
301 GLWGRASRDS PGPSIAYHPS SQSSVDLDLNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPBAR1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 7
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 30 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 30 nTPM
- breast: 17 nTPM
- gallbladder: 16 nTPM
- smooth muscle: 9.5 nTPM
- spleen: 7.1 nTPM
- kidney: 6.7 nTPM
Single-cell type
- decidual stromal cells: 169 nCPM
- kupffer cells: 61 nCPM
- neuroendocrine cells: 45 nCPM
- monocytes: 31 nCPM
- hofbauer cells: 23 nCPM
- endometrial stromal cells: 12 nCPM
Immune cell
- intermediate monocyte: 713 nTPM
- non-classical monocyte: 699 nTPM
- classical monocyte: 289 nTPM
- total PBMC: 156 nTPM
- myeloid DC: 140 nTPM
- neutrophil: 6.5 nTPM
Brain region
- cerebral cortex: 1.8 nTPM
- cerebellum: 1.2 nTPM
- thalamus: 1.2 nTPM
- choroid plexus: 0.9 nTPM
- basal ganglia: 0.8 nTPM
- hippocampal formation: 0.8 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.95
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.1
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adenylate cyclase-activating G protein-coupled bile acid receptor signaling pathway
- cellular response to bile acid
- energy homeostasis
- positive regulation of ERK1 and ERK2 cascade
- regulation of bicellular tight junction assembly
- positive regulation of cholangiocyte proliferation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GPBAR1 as an antibody target. Whether an autoantibody or antibody against GPBAR1 could matter depends on whether native GPBAR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPBAR1 is annotated at the cell surface, where native GPBAR1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label GPBAR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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