MRGPRX2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Mas-related G-protein coupled receptor member X2 is a protein that in humans is encoded by the MRGPRX2 gene.[5][6] It is most abundant on cutaneous mast cells, sensory neurons, and keratinocytes.[7]

AliasesMRGPRX2, MGRG3, MRGX2, MAS related GPR family member X2
End19,060,717 bp[1]
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MRGPRX2
Identifiers
AliasesMRGPRX2, MGRG3, MRGX2, MAS related GPR family member X2
External IDsOMIM: 607228; MGI: 3588270; HomoloGene: 24986; GeneCards: MRGPRX2; OMA:MRGPRX2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001303615
NM_054030

NM_001034868

RefSeq (protein)

NP_001290544
NP_473371

NP_001030040

Location (UCSC)Chr 11: 19.05 – 19.06 MbChr 7: 48.13 – 48.15 Mb
PubMed search[3][4]
Wikidata
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Activation of MRGPRX2 on mast cells leads to IgE-independent type 1 hypersensitivity-like symptoms, also known as pseudoallergic reactions, although more rapid and brief. Medications identified to cause MRGPRX2 activation including neuromuscular blocking agents (NMBA) (except for succinylcholine), antibiotics like DNA gyrase inhibitor fluoroquinolones or cell wall synthesis inhibitor vancomycin (which caused Red Man syndrome[8]), icatibant, leuprolide, and morphine.[7]

See also

References

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