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]

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
View/Edit HumanView/Edit Mouse

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), icatibant, leuprolide, and morphine.[7]

See also

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References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000183695Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000074109Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Dong X, Han S, Zylka MJ, Simon MI, Anderson DJ (September 2001). "A diverse family of GPCRs expressed in specific subsets of nociceptive sensory neurons". Cell. 106 (5): 619–632. doi:10.1016/S0092-8674(01)00483-4. PMID 11551509.
  6. ^ "Entrez Gene: MRGPRX2 MAS-related GPR, member X2".
  7. ^ a b Akin C, Elhosni M, Khokar DS (2023). "Mast Cells and Mast Cell disorders". In Rich RR, Fleisher TA, Schroeder HW, Weyand CM, Corry DB, Puck J (eds.). Clinical immunology: principles and practice. Elsevier. p. 563. ISBN 978-0-7020-8165-1.

Further reading

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