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GeneE
2 sources retrieved Β· Most recent: April 2026 Β· Index updated 15 days ago
β“˜GeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
MRGPRG
MAS related GPR family member G
Chromosome 11 Β· 11p15.4
NCBI Gene: 386746Ensembl: ENSG00000182170.3HGNC: HGNC:24829UniProt: Q86SM5
4PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Receptor
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
G protein-coupled receptor activityG protein-coupled receptor signaling pathwayplasma membraneadenylate cyclase-modulating G protein-coupled receptor signaling pathwayfamilial hemolytic anemianeurodegenerative diseaseaneurysmhemolytic anemia
✦AI Summary

Based on limited published evidence, MRGPRG is an orphan G protein-coupled receptor localized to the plasma membrane with predicted involvement in nociceptor function and pain modulation. The gene exhibits tissue-restricted distribution, including expression in skin 1. DNA methylation studies identified MRGPRG as a target of prenatal nutritional perturbations during early gestation, suggesting potential roles in developmental programming 2. However, unlike related family member MRGPRX2, MRGPRG does not respond to histamine-releasing agents in functional assays 1, indicating distinct physiological functions within the MRGPR family.

Sources cited
1
MRGPRG is expressed in limited tissues including skin and does not respond to histamine-releasing agents, unlike MRGPRX2
PMID: 32999394
2
MRGPRG is associated with DNA methylation changes following prenatal famine exposure during early gestation, linking it to developmental and metabolic processes
PMID: 25944819
⚠Limited data available β€” This gene has 2 indexed publications. Summary and analysis may be incomplete.
Disease Associationsβ“˜20
familial hemolytic anemiaOpen Targets
0.30Weak
neurodegenerative diseaseOpen Targets
0.24Weak
aneurysmOpen Targets
0.12Weak
hemolytic anemiaOpen Targets
0.11Weak
migraine disorderOpen Targets
0.07Suggestive
Griscelli diseaseOpen Targets
0.07Suggestive
Griscelli disease type 3Open Targets
0.06Suggestive
Griscelli syndrome type 3Open Targets
0.06Suggestive
congenital anomaly of cardiovascular systemOpen Targets
0.05Suggestive
uncombable hair syndromeOpen Targets
0.05Suggestive
oculocutaneous albinism type 3Open Targets
0.05Suggestive
Griscelli disease type 1Open Targets
0.04Suggestive
Griscelli syndrome type 1Open Targets
0.04Suggestive
Microcephaly - albinism - digital anomaliesOpen Targets
0.04Suggestive
microcephaly-albinism-digital anomalies syndromeOpen Targets
0.04Suggestive
Tietz syndromeOpen Targets
0.04Suggestive
Tietze syndromeOpen Targets
0.04Suggestive
ermine phenotypeOpen Targets
0.04Suggestive
isolated familial wooly hair disorderOpen Targets
0.04Suggestive
Woolly hairOpen Targets
0.04Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar β†—
Related Genes
NPFFProtein interaction72%MRGPRX3Shared pathway50%GNAZShared pathway50%MRGPRX4Shared pathway33%PTH2RShared pathway33%CNR1Shared pathway25%
Tissue Expression6 tissues
Heart
0%
Lung
0%
Bone Marrow
0%
Ovary
0%
Liver
0%
Brain
0%
Gene Interaction Network
Click a node to explore
MRGPRGNPFFMRGPRX3GNAZMRGPRX4PTH2RCNR1
PROTEIN STRUCTURE
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AlphaFoldAI-predicted Β· UniProt Q86SM5
View on AlphaFold β†—
RankingsWhere MRGPRG stands among ~20K protein-coding genes
  • #18,617of 20,598
    Most Researched4
Genes detectedMRGPRG
Sources retrieved2 papers
Response timeβ€”
πŸ“„ Sources
2
1
Identification of the dog orthologue of human MAS-related G protein coupled receptor X2 (MRGPRX2) essential for drug-induced pseudo-allergic reactions.
PMID: 32999394
Sci Rep Β· 2020
1.00
2
Early gestation as the critical time-window for changes in the prenatal environment to affect the adult human blood methylome.
PMID: 25944819
Int J Epidemiol Β· 2015
0.50