Gene Gene information from NCBI Gene database.
Entrez ID 117194
Gene name MAS related GPR family member X2
Gene symbol MRGPRX2
Synonyms (NCBI Gene)
MGRG3MRGX2
Chromosome 11
Chromosome location 11p15.1
miRNA miRNA information provided by mirtarbase database.
4
miRTarBase ID miRNA Experiments Reference
MIRT1158058 hsa-miR-489 CLIP-seq
MIRT2045226 hsa-miR-450b-5p CLIP-seq
MIRT2045227 hsa-miR-518a-5p CLIP-seq
MIRT2045228 hsa-miR-527 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IBA
GO:0004930 Function G protein-coupled receptor activity IDA 12915402, 22069323
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607228 17983 ENSG00000183695
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96LB1
Protein name Mas-related G-protein coupled receptor member X2
Protein function Mast cell-specific receptor for basic secretagogues, i.e. cationic amphiphilic drugs, as well as endo- or exogenous peptides, consisting of a basic head group and a hydrophobic core (PubMed:25517090). Recognizes and binds small molecules contain
PDB 7S8L , 7S8M , 7S8N , 7S8O , 7VDH , 7VDL , 7VDM , 7VUY , 7VUZ , 7VV0 , 7VV3 , 7VV4 , 7VV5 , 7VV6
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 47 279 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Mainly expressed in mast cells. Has a limited expression profile, both peripheral and within the central nervous system, with highest levels in dorsal root ganglion (PubMed:12915402). Detected in blood vessels, scattered lymphocytes, a
Sequence
Sequence length 330
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Anaphylaxis Associate 30072729, 34385999
★☆☆☆☆
Found in Text Mining only
Asthma Associate 33790895
★☆☆☆☆
Found in Text Mining only
Chronic Periodontitis Stimulate 28694291
★☆☆☆☆
Found in Text Mining only
Chronic Urticaria Associate 33790895, 34090787
★☆☆☆☆
Found in Text Mining only
Dermatitis Atopic Associate 33790895
★☆☆☆☆
Found in Text Mining only
Drug Hypersensitivity Associate 30072729, 34385999, 36726977
★☆☆☆☆
Found in Text Mining only
Eczema Associate 33429916
★☆☆☆☆
Found in Text Mining only
Inflammation Stimulate 28694291
★☆☆☆☆
Found in Text Mining only
Mastocytosis Associate 38022672
★☆☆☆☆
Found in Text Mining only
Mastocytosis Cutaneous Associate 35958589
★☆☆☆☆
Found in Text Mining only