MRGPRE
Mas-related G-protein coupled receptor member E
Also known as: GPR167, mrgE, MRGRE_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86SM8
- Gene
- MRGPRE
- Ensembl
- ENSG00000184350
- Chromosome
- 11
- Canonical length
- 312 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins
OverviewNCBI Gene
Predicted to enable G protein-coupled receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
312 residues, UniProt reviewed canonical sequence.
>Q86SM8|MRGPRE
1 MMEPREAGQH VGAANGAQED VAFNLIILSL TEGLGLGGLL GNGAVLWLLS SNVYRNPFAI
61 YLLDVACADL IFLGCHMVAI VPDLLQGRLD FPGFVQTSLA TLRFFCYIVG LSLLAAVSVE
121 QCLAALFPAW YSCRRPRHLT TCVCALTWAL CLLLHLLLSG ACTQFFGEPS RHLCRTLWLV
181 AAVLLALLCC TMCGASLMLL LRVERGPQRP PPRGFPGLIL LTVLLFLFCG LPFGIYWLSR
241 NLLWYIPHYF YHFSFLMAAV HCAAKPVVYF CLGSAQGRRL PLRLVLQRAL GDEAELGAVR
301 ETSRRGLVDI AALocalizationUniProt · AlphaFold · HPA
Whether an antibody against MRGPRE 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)
- 0.31
- Highest tissue expression
- 1.4 nTPM
Expression across tissuesHPA
Tissue
- cervix: 1.4 nTPM
- hypothalamus: 1.4 nTPM
- midbrain: 1.1 nTPM
- spinal cord: 0.9 nTPM
- endometrium: 0.8 nTPM
- vagina: 0.8 nTPM
Single-cell type
- pancreatic islet cells: 2.2 nCPM
- salivary duct cells: 1 nCPM
- breast myoepithelial cells: 0.9 nCPM
- brain excitatory neurons: 0.8 nCPM
- fibroblasts: 0.8 nCPM
- other brain neurons: 0.8 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- pons: 58 nTPM
- medulla oblongata: 31 nTPM
- hypothalamus: 14 nTPM
- cerebellum: 8.5 nTPM
- spinal cord: 7.1 nTPM
- midbrain: 5 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 missense Z
- -0.24
- 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
- adenylate cyclase-activating G protein-coupled bile acid receptor signaling pathway
- adenylate cyclase-activating G protein-coupled receptor signaling pathway
- cell surface receptor signaling pathway
- G protein-coupled receptor signaling pathway
- intracellular glucose homeostasis
- positive regulation of insulin secretion involved in cellular response to glucose stimulus
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- G protein-coupled receptor, rhodopsin-like
- GPCR, rhodopsin-like, 7TM
- Mas-related G protein-coupled receptor family
- 7 transmembrane receptor (rhodopsin family)
- Mas-related G protein-coupled receptor E
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MRGPRE as an antibody target. Whether an autoantibody or antibody against MRGPRE could matter depends on whether native MRGPRE is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MRGPRE is annotated at the cell surface, where native MRGPRE 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 MRGPRE as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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