RGS20: Regulator of G Protein Signaling 20

A key modulator of G protein-coupled receptor signaling with implications in cancer and neurological disorders.

Gene Information Card

Symbol RGS20
Full Name Regulator of G Protein Signaling 20
Gene Type Protein coding
Chromosomal Location 8q11.23
NCBI Gene ID 8601 ncbi.nlm.nih.gov/gene/8601
Ensembl ID ENSG00000147509
UniProt ID O76082
OMIM ID 607193
HGNC ID 14601
Aliases RGSZ1, RGS-20, ZGAP1

Description

RGS20 (Regulator of G Protein Signaling 20) encodes a member of the RGS (regulator of G protein signaling) family. The protein acts as a GTPase-activating protein (GAP) for G alpha subunits, accelerating the termination of G protein-coupled receptor (GPCR) signaling. RGS20 is highly expressed in brain and is implicated in modulating opioid, dopamine, and other neurotransmitter pathways. Altered expression or mutations have been linked to certain cancers and neurological conditions.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer RGS20 overexpression may enhance GPCR signaling promoting cell proliferation and migration. COSMIC; PMID: 25691885
Lung cancer RGS20 upregulation associated with poor prognosis; potential role in metastasis. COSMIC; PMID: 28723891
Ovarian cancer RGS20 expression correlates with tumor grade and chemoresistance. COSMIC; PMID: 27381368
Neuropathic pain RGS20 modulates mu-opioid receptor signaling, affecting pain sensitivity. ClinVar; PMID: 20018946

Expression Profile

Tissue Expression
Tissue nTPM level
Brain (cerebral cortex) 12.5 Medium
Cerebellum 15.3 Medium
Pituitary gland 8.7 Low
Testis 6.2 Low
Adrenal gland 5.1 Low
Cell Line Expression
Cell Line nTPM Notes
SH-SY5Y (neuroblastoma) 10.4 Neuronal model
MCF7 (breast cancer) 7.8 ER+ breast cancer line
A549 (lung cancer) 9.1 Lung adenocarcinoma
HEK293 (embryonic kidney) 4.3 Low endogenous expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.511C>T (p.Arg171Trp) Missense <0.1% Altered GAP activity; reported in COSMIC
c.763G>A (p.Glu255Lys) Missense <0.1% Unknown functional effect
c.1009_1011del (p.Lys337del) In-frame deletion <0.1% Reported in cancer samples
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in major databases.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported.

Dominant Negative (DN)

No confirmed dominant-negative mutations reported.

Gene Ontology (GO)

• GTPase activator activity • G protein-coupled receptor signaling pathway
• negative regulation of signal transduction • cytoplasm
• plasma membrane

Pathways

GPCR downstream signaling
Opioid signaling
G alpha (i) signaling events

Protein Summary

RGS20 is a 241-amino acid protein containing an RGS domain that binds to activated G alpha subunits (particularly Gi/o family) and accelerates GTP hydrolysis, thereby terminating GPCR signaling. It is predominantly expressed in the brain and plays roles in modulating neurotransmission, pain perception, and cell proliferation. Post-translational modifications include palmitoylation, which influences membrane localization.

Related Products

Product name Cat.No. Species Gene ID
RGS20 Knockout HEK293 Cell Line EDJ-KQ6297 Human 8601 Details Get a Quote
RGS20 Knockout A-549 Cell Line EDJ-KQ30199 Human 8601 Details Get a Quote
RGS20 Knockout HCT 116 Cell Line EDJ-KQ30200 Human 8601 Details Get a Quote
RGS20 Knockout HeLa Cell Line EDJ-KQ28887 Human 8601 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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