MRGPRD (Mas-Related G Protein-Coupled Receptor D)

A sensory neuron-enriched GPCR implicated in itch, pain, and potential therapeutic targeting

Gene Information Card

Symbol MRGPRD
Full Name MAS-related GPR, member D
Gene Type protein-coding
Chromosomal Location 11p15.1
NCBI Gene ID 259249 ncbi.nlm.nih.gov/gene/259249
Ensembl ID ENSG00000172985
UniProt ID Q8TDS7
OMIM ID 607240
HGNC ID 29698
Aliases MRGD, TGR7, GPR105

Description

MRGPRD encodes a G protein-coupled receptor (GPCR) that is predominantly expressed in a subset of dorsal root ganglion (DRG) neurons, specifically non-peptidergic nociceptors. It is activated by beta-alanine and is involved in the modulation of itch and pain signaling. MRGPRD has been implicated in the development of sensory neuron subtypes and is a potential target for analgesic and antipruritic therapies.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Not directly associated with a specific disease MRGPRD is primarily studied in the context of sensory neuron function; no germline disease-causing mutations have been reported in OMIM or ClinVar. No direct disease association; functional studies in animal models.

Expression Profile

Tissue Expression
Tissue nTPM level
Dorsal Root Ganglion Not available (nTPM not provided by GTEx) High expression in DRG neurons (RNA-seq and protein studies)
Skin Not available Low expression; mainly in nerve fibers
Spinal Cord Not available Low expression; in central terminals of DRG neurons
Cell Line Expression
Cell Line nTPM Notes
HEK293 (transfected) Not applicable Used for functional assays; not endogenous
DRG neurons (primary) Not applicable High endogenous expression in non-peptidergic neurons
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
No common variants reported SNV Not established No pathogenic variants in ClinVar; rare variants in population databases (e.g., gnomAD) but no clinical significance.
Mutation functional classification

Loss of Function (LOF)

No documented loss-of-function mutations in human disease; knockout mice show altered itch/pain behavior.

Gain of Function (GOF)

No documented gain-of-function mutations; constitutive activity may occur in vitro but not clinically relevant.

Dominant Negative (DN)

No evidence for dominant-negative effects.

Gene Ontology (GO)

• G protein-coupled receptor activity • signal transduction
• G protein-coupled receptor signaling pathway • plasma membrane
• response to beta-alanine • sensory perception of pain
• sensory perception of itch

Pathways

• GPCR downstream signaling (e.g.
• Gq/11-mediated calcium mobilization)
• Sensory neuron differentiation and function

Protein Summary

MRGPRD is a 7-transmembrane GPCR of the Mas-related gene family. It is selectively expressed in a subset of DRG neurons that are involved in nociception and pruriception. Activation by beta-alanine leads to intracellular calcium increase via Gq/11 proteins. MRGPRD is essential for the proper wiring of sensory neurons and has been shown to mediate histamine-independent itch. Its restricted expression pattern makes it an attractive target for peripheral analgesics.

Related Products

Product name Cat.No. Species Gene ID
MRGPRD Knockout HEK293 Cell Line EDJ-KQ7574 Human 116512 Details Get a Quote
MRGPRD Knockout HeLa Cell Line EDJ-KQ57993 Human 116512 Details Get a Quote
MRGPRD Knockout A-549 Cell Line EDJ-KQ66479 Human 116512 Details Get a Quote
MRGPRD Knockout HCT 116 Cell Line EDJ-KQ74902 Human 116512 Details Get a Quote
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