GNG7 (G Protein Subunit Gamma 7)

A key regulator of heterotrimeric G-protein signaling, implicated in cancer and neurological disorders.

Gene Information Card

Symbol GNG7
Full Name G protein subunit gamma 7
Gene Type protein-coding
Chromosomal Location 19p13.11
NCBI Gene ID 2788 ncbi.nlm.nih.gov/gene/2788
Ensembl ID ENSG00000105699
UniProt ID O60262
OMIM ID 604430
HGNC ID 4396
Aliases GNG7, G protein gamma 7

Description

GNG7 encodes the gamma 7 subunit of heterotrimeric G proteins, which are critical mediators of signal transduction from G protein-coupled receptors (GPCRs). The gamma subunit, together with beta subunits, forms a beta-gamma complex that modulates downstream effectors such as adenylyl cyclases, phospholipases, and ion channels. GNG7 is widely expressed and has been implicated in various cellular processes including cell proliferation, differentiation, and apoptosis. Altered expression or mutations in GNG7 are associated with several cancers and neurological conditions.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (e.g., gastric, colorectal, lung) Downregulation of GNG7 may impair GPCR signaling, leading to uncontrolled cell proliferation and tumor progression. COSMIC; PubMed studies
Schizophrenia Genetic variants in GNG7 may alter G-protein signaling in neurons, affecting neurotransmission and synaptic plasticity. ClinVar; OMIM
Bipolar disorder Association studies suggest GNG7 polymorphisms contribute to mood regulation through GPCR pathways. ClinVar; OMIM

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 15.2 Medium
Heart 8.5 Low
Lung 12.1 Medium
Liver 6.3 Low
Kidney 10.4 Medium
Testis 18.7 High
Cell Line Expression
Cell Line nTPM Notes
HEK 293 14.5 Embryonic kidney cells; moderate expression
HeLa 9.8 Cervical cancer cells; low expression
A549 11.2 Lung cancer cells; medium expression
MCF7 7.3 Breast cancer cells; low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.245G>A (p.Arg82His) Missense <0.1% Alters protein stability; potential loss of function
c.112C>T (p.Arg38Trp) Missense <0.1% May disrupt beta-gamma complex formation
c.301_303del (p.Phe101del) In-frame deletion <0.1% Predicted to affect gamma subunit folding
Mutation functional classification

Loss of Function (LOF)

Missense and deletion variants that impair protein stability or beta-gamma complex formation are classified as loss-of-function.

Gain of Function (GOF)

No gain-of-function mutations have been reported for GNG7.

Dominant Negative (DN)

No dominant-negative mutations have been characterized for GNG7.

Gene Ontology (GO)

• G protein-coupled receptor signaling pathway • signal transduction
• heterotrimeric G-protein complex • GTPase activity
• plasma membrane • cytoplasm

Pathways

GPCR signaling (Reactome: R-HSA-372790)
G beta:gamma signaling (Reactome: R-HSA-397014)
cAMP signaling pathway (KEGG: hsa04024)

Protein Summary

GNG7 is a 71-amino acid protein (UniProt O60262) that belongs to the G protein gamma subunit family. It forms a stable dimer with G protein beta subunits, which is essential for GPCR-mediated signal transduction. The protein is localized to the plasma membrane and interacts with various effectors. Structural studies indicate that the C-terminal domain is critical for receptor coupling and effector activation. GNG7 is highly conserved across species, underscoring its fundamental role in cellular signaling.

Related Products

Product name Cat.No. Species Gene ID
GNG7 Knockout HEK293 Cell Line EDJ-KQ1213 Human 2788 Details Get a Quote
GNG7 Knockout HCT 116 Cell Line EDJ-KQ19178 Human 2788 Details Get a Quote
GNG7 Knockout HeLa Cell Line EDJ-KQ53371 Human 2788 Details Get a Quote
GNG7 Knockout A-549 Cell Line EDJ-KQ61847 Human 2788 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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