GRPR
Gastrin-releasing peptide receptor
Also known as: BB2, BB2R, BRS2, GRPR_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P30550
- Gene
- GRPR
- Ensembl
- ENSG00000126010
- Chromosome
- X
- Canonical length
- 384 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins
- Subcellular location
- Plasma membrane
OverviewNCBI Gene
Gastrin-releasing peptide (GRP) regulates numerous functions of the gastrointestinal and central nervous systems, including release of gastrointestinal hormones, smooth muscle cell contraction, and epithelial cell proliferation and is a potent mitogen for neoplastic tissues. The effects of GRP are mediated through the gastrin-releasing peptide receptor. This receptor is a glycosylated, 7-transmembrane G-protein coupled receptor that activates the phospholipase C signaling pathway. The receptor is aberrantly expressed in numerous cancers such as those of the lung, colon, and prostate. An individual with autism and multiple exostoses was found to have a balanced translocation between chromosome 8 and a chromosome X breakpoint located within the gastrin-releasing peptide receptor gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
384 residues, UniProt reviewed canonical sequence.
>P30550|GRPR
1 MALNDCFLLN LEVDHFMHCN ISSHSADLPV NDDWSHPGIL YVIPAVYGVI ILIGLIGNIT
61 LIKIFCTVKS MRNVPNLFIS SLALGDLLLL ITCAPVDASR YLADRWLFGR IGCKLIPFIQ
121 LTSVGVSVFT LTALSADRYK AIVRPMDIQA SHALMKICLK AAFIWIISML LAIPEAVFSD
181 LHPFHEESTN QTFISCAPYP HSNELHPKIH SMASFLVFYV IPLSIISVYY YFIAKNLIQS
241 AYNLPVEGNI HVKKQIESRK RLAKTVLVFV GLFAFCWLPN HVIYLYRSYH YSEVDTSMLH
301 FVTSICARLL AFTNSCVNPF ALYLLSKSFR KQFNTQLLCC QPGLIIRSHS TGRSTTCMTS
361 LKSTNPSVAT FSLINGNICH ERYVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GRPR 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)
- 0.36
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 19 nTPM
- epididymis: 1.8 nTPM
- breast: 1.7 nTPM
- stomach: 1.1 nTPM
- smooth muscle: 0.7 nTPM
- endometrium: 0.5 nTPM
Single-cell type
- oocytes: 14 nCPM
- pancreatic acinar cells: 11 nCPM
- retinal pigment epithelial cells: 4.3 nCPM
- neuroendocrine cells: 3.6 nCPM
- thyrotrophs: 3.4 nCPM
- brain inhibitory neurons: 3.1 nCPM
Immune cell
- intermediate monocyte: 0.3 nTPM
- non-classical monocyte: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- naive B-cell: 0.1 nTPM
- basophil: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- hypothalamus: 4.6 nTPM
- spinal cord: 3.6 nTPM
- cerebral cortex: 2.1 nTPM
- pons: 2 nTPM
- medulla oblongata: 1.8 nTPM
- hippocampal formation: 1.7 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about GRPR.
Disease | ImmuneIEDB
Conditions an epitope on GRPR was assayed in.
- melanoma T cell
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)
- 0.88
- gnomAD pLI
- 0.22
- gnomAD missense Z
- 0.72
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- G protein-coupled receptor signaling pathway
- learning or memory
- motor behavior
- phospholipase C-activating G protein-coupled receptor signaling pathway
- positive regulation of behavioral fear response
- positive regulation of respiratory gaseous exchange
- psychomotor behavior
- regulation of cell population proliferation
- response to external biotic stimulus
- social behavior
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- G protein-coupled receptor, rhodopsin-like
- Bombesin receptor-like
- GPCR, rhodopsin-like, 7TM
- 7 transmembrane receptor (rhodopsin family)
- Gastrin-releasing peptide receptor
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GRPR as an antibody target. Whether an autoantibody or antibody against GRPR could matter depends on whether native GRPR is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GRPR is annotated at the cell surface, where native GRPR 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 GRPR as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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