GSTO2: Glutathione S-Transferase Omega 2

A member of the omega class glutathione S-transferase family involved in cellular detoxification and redox homeostasis.

Gene Information Card

Symbol GSTO2
Full Name Glutathione S-Transferase Omega 2
Gene Type Protein coding
Chromosomal Location 10q25.1
NCBI Gene ID 119391 ncbi.nlm.nih.gov/gene/119391
Ensembl ID ENSG00000165637
UniProt ID Q9H4Y5
OMIM ID 612314
HGNC ID 16818
Aliases GSTO2-1, GSTO2-2, MGC10798

Description

GSTO2 (Glutathione S-Transferase Omega 2) is a protein-coding gene that encodes a member of the omega class of glutathione S-transferases. The enzyme catalyzes the conjugation of reduced glutathione to a variety of electrophilic compounds, playing a role in cellular detoxification, oxidative stress response, and modulation of calcium release from ryanodine receptors. GSTO2 is expressed in multiple tissues and has been implicated in cancer susceptibility, neurodegenerative diseases, and inflammatory conditions.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (various types) Altered GSTO2 expression may affect detoxification of carcinogens and oxidative stress response, influencing tumor progression and drug resistance. COSMIC; NCBI Gene; ClinVar
Alzheimer's disease GSTO2 polymorphisms may modulate oxidative stress and calcium signaling, contributing to neurodegeneration. NCBI Gene; OMIM
Parkinson's disease Variants in GSTO2 have been associated with altered risk, possibly through impaired detoxification of neurotoxins. NCBI Gene; OMIM
Asthma GSTO2 expression changes may influence inflammatory responses and oxidative stress in airway epithelium. NCBI Gene

Expression Profile

Tissue Expression
Tissue nTPM level
Liver 12.5 Medium
Kidney 8.3 Medium
Lung 6.1 Low
Brain 4.2 Low
Heart 3.8 Low
Testis 15.7 High
Cell Line Expression
Cell Line nTPM Notes
HepG2 14.2 Hepatocellular carcinoma cell line
A549 7.8 Lung adenocarcinoma cell line
HEK293 5.3 Embryonic kidney cells
SH-SY5Y 4.1 Neuroblastoma cell line
MCF7 6.9 Breast cancer cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.424A>G (p.Asn142Asp) Missense 0.5% (gnomAD) May alter enzyme activity; associated with altered risk in Parkinson's disease
c.1A>G (p.Met1Val) Missense (start loss) 0.1% (gnomAD) Likely loss of function; potential impact on protein expression
c.155C>T (p.Pro52Leu) Missense 0.2% (gnomAD) Unknown functional effect; rare variant
c.313G>A (p.Gly105Ser) Missense 0.3% (gnomAD) May affect substrate binding; reported in COSMIC
Mutation functional classification

Loss of Function (LOF)

Start loss variant (p.Met1Val) and nonsense variants are predicted to result in loss of enzyme activity.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in GSTO2.

Dominant Negative (DN)

No evidence of dominant-negative effects for GSTO2 mutations.

Pathways

• Glutathione metabolism (Reactome: R-HSA-156590)
• Phase II conjugation (Reactome: R-HSA-156580)
• Detoxification of Reactive Oxygen Species (Reactome: R-HSA-3299685)

Protein Summary

GSTO2 is a 243-amino acid protein belonging to the omega class glutathione S-transferases. It functions as a homodimer, catalyzing the conjugation of glutathione to electrophilic substrates, and also exhibits thioltransferase and dehydroascorbate reductase activities. The protein is involved in cellular detoxification, redox regulation, and modulation of ryanodine receptor-mediated calcium signaling. GSTO2 is widely expressed, with highest levels in testis, liver, and kidney. Structural studies reveal a conserved GSH-binding site and a C-terminal domain that contributes to substrate specificity.

Related Products

Product name Cat.No. Species Gene ID
GSTO2 Knockout HEK293 Cell Line EDJ-KQ7639 Human 119391 Details Get a Quote
GSTO2 Knockout A-549 Cell Line EDJ-KQ32996 Human 119391 Details Get a Quote
GSTO2 Knockout HCT 116 Cell Line EDJ-KQ32997 Human 119391 Details Get a Quote
GSTO2 Knockout HeLa Cell Line EDJ-KQ32998 Human 119391 Details Get a Quote
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