RGS10: Regulator of G Protein Signaling 10

A key modulator of G protein-coupled receptor signaling with roles in immune regulation, neuronal function, and cancer

Gene Information Card

Symbol RGS10
Full Name Regulator of G Protein Signaling 10
Gene Type Protein coding
Chromosomal Location 10q26.11
NCBI Gene ID 6001 ncbi.nlm.nih.gov/gene/6001
Ensembl ID ENSG00000148935
UniProt ID O43665
OMIM ID 602857
HGNC ID 9994
Aliases RGS10, dJ1068F16.3, RGS10A, RGS10B

Description

RGS10 (Regulator of G Protein Signaling 10) is a member of the regulator of G protein signaling (RGS) family. It accelerates the GTPase activity of G protein alpha subunits, thereby terminating G protein-coupled receptor (GPCR) signaling. RGS10 is expressed in multiple tissues, with highest levels in the brain, immune cells, and heart. It plays critical roles in modulating neurotransmission, immune responses, and cell proliferation. Dysregulation of RGS10 has been implicated in cancer, neurodegenerative diseases, and inflammatory disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Ovarian cancer RGS10 downregulation promotes chemoresistance and tumor progression via sustained GPCR signaling PMID: 22926525; COSMIC
Breast cancer Reduced RGS10 expression correlates with poor prognosis and increased metastasis PMID: 25609832
Parkinson's disease RGS10 loss in microglia leads to neuroinflammation and dopaminergic neuron death PMID: 22692725
Multiple sclerosis RGS10 deficiency exacerbates neuroinflammation in experimental autoimmune encephalomyelitis PMID: 23966870
Cardiac hypertrophy RGS10 modulates Gq signaling; altered expression linked to hypertrophic responses PMID: 17690171

Expression Profile

Tissue Expression
Tissue nTPM level
Brain (cerebral cortex) 12.5 Medium
Heart 9.8 Medium
Lung 6.2 Low
Liver 3.1 Low
Spleen 15.3 High
Whole blood 18.7 High
Cell Line Expression
Cell Line nTPM Notes
HEK293 14.2 High expression
HeLa 8.5 Medium expression
K562 20.1 Very high expression
SH-SY5Y 11.3 Medium expression
THP-1 22.6 Very high expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G (p.Met1?) Missense <0.1% Likely loss of start codon; predicted loss of function
c.124C>T (p.Arg42Cys) Missense <0.1% Reduced GTPase accelerating activity
c.301G>A (p.Glu101Lys) Missense <0.1% Unknown functional effect
c.424_425insA Frameshift <0.1% Premature truncation; loss of function
Mutation functional classification

Loss of Function (LOF)

Frameshift and start-loss mutations (e.g., c.424_425insA, c.1A>G) are predicted to cause loss of RGS10 protein function, impairing GPCR signal termination.

Gain of Function (GOF)

No gain-of-function mutations have been reported in RGS10.

Dominant Negative (DN)

No dominant-negative mutations have been characterized for RGS10.

Pathways

G alpha (i) signaling events (Reactome: R-HSA-418594)
G alpha (q) signaling events (Reactome: R-HSA-416476)
GPCR downstream signaling (Reactome: R-HSA-388396)

Protein Summary

RGS10 is a 181-amino acid protein (20 kDa) belonging to the RGS family. It contains a conserved RGS domain that binds to activated Gα subunits and accelerates GTP hydrolysis, thereby switching off GPCR signaling. RGS10 is predominantly cytosolic but can translocate to the plasma membrane upon receptor activation. It is highly expressed in immune cells (especially microglia and macrophages) and neurons, where it regulates cytokine production, cell migration, and survival. Post-translational modifications include phosphorylation and palmitoylation, which modulate its stability and localization.

Related Products

Product name Cat.No. Species Gene ID
RGS10 Knockout HEK293 Cell Line EDJ-KQ4910 Human 6001 Details Get a Quote
RGS10 Knockout A-549 Cell Line EDJ-KQ29003 Human 6001 Details Get a Quote
RGS10 Knockout HCT 116 Cell Line EDJ-KQ29005 Human 6001 Details Get a Quote
RGS10 Knockout HeLa Cell Line EDJ-KQ29006 Human 6001 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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