Seroatlas · Human Serome Atlas

GSTM1

Glutathione S-transferase Mu 1

Also known as: GST1, GSTM1_HUMAN, H-B, MU

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
P09488
Gene
GSTM1
Ensembl
ENSG00000134184
Chromosome
1
Canonical length
218 aa
Protein class
Cancer-related genes, Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
Subcellular location
Microtubules,Cytokinetic bridge,Primary cilium,Primary cilium tip,Primary cilium transition zone,Cytosol
Quaternary structure
Homodimer

OverviewNCBI Gene

Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S-transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S-transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are organized in a gene cluster on chromosome 1p13.3 and are known to be highly polymorphic. These genetic variations can change an individual's susceptibility to carcinogens and toxins as well as affect the toxicity and efficacy of certain drugs. Null mutations of this class mu gene have been linked with an increase in a number of cancers, likely due to an increased susceptibility to environmental toxins and carcinogens. Multiple protein isoforms are encoded by transcript variants of this gene. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

218 residues, UniProt reviewed canonical sequence.

>P09488|GSTM1
     1  MPMILGYWDI RGLAHAIRLL LEYTDSSYEE KKYTMGDAPD YDRSQWLNEK FKLGLDFPNL
    61  PYLIDGAHKI TQSNAILCYI ARKHNLCGET EEEKIRVDIL ENQTMDNHMQ LGMICYNPEF
   121  EKLKPKYLEE LPEKLKLYSE FLGKRPWFAG NKITFVDFLV YDVLDLHRIF EPKCLDAFPN
   181  LKDFISRFEG LEKISAYMKS SRFLPRPVFS KMAVWGNK

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against GSTM1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.

Antibody reachability
Intracellular
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.26
Highest tissue expression
570 nTPM

Expression across tissuesHPA

Tissue

  • liver: 570 nTPM
  • ovary: 168 nTPM
  • adrenal gland: 152 nTPM
  • esophagus: 145 nTPM
  • choroid plexus: 136 nTPM
  • vagina: 135 nTPM

Single-cell type

  • urothelial cells: 13 nCPM
  • basal keratinocytes: 7.5 nCPM
  • kupffer cells: 7.2 nCPM
  • hepatic stellate cells: 6.5 nCPM
  • suprabasal keratinocytes: 5.6 nCPM
  • medullary thymic epithelial cells: 4.8 nCPM

Immune cell

  • myeloid DC: 78 nTPM
  • plasmacytoid DC: 41 nTPM
  • intermediate monocyte: 39 nTPM
  • T-reg: 39 nTPM
  • naive CD4 T-cell: 33 nTPM
  • naive B-cell: 33 nTPM

Brain region

  • cerebral cortex: 13 nTPM
  • choroid plexus: 12 nTPM
  • basal ganglia: 11 nTPM
  • thalamus: 11 nTPM
  • midbrain: 11 nTPM
  • amygdala: 10 nTPM

Genetic constraint and essentialitygnomAD · DepMap

Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.

gnomAD LOEUF (loss-of-function intolerance)
1.01
gnomAD pLI
0
gnomAD missense Z
1.52
DepMap mean gene effect
0.07
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads GSTM1 as an antibody target. Whether an autoantibody or antibody against GSTM1 could matter depends on whether native GSTM1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

GSTM1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.

Annotation status

The present source text does not explicitly label GSTM1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/GSTM1. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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