Seroatlas · Human Serome Atlas

GSTM3

Glutathione S-transferase Mu 3

Also known as: GST5, GSTM3_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
P21266
Gene
GSTM3
Ensembl
ENSG00000134202
Chromosome
1
Canonical length
225 aa
Protein class
Cancer-related genes, Enzymes, Metabolic 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. Mutations of this class mu gene have been linked with a slight increase in a number of cancers, likely due to exposure with environmental toxins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008]

Canonical amino-acid sequenceUniProt

225 residues, UniProt reviewed canonical sequence.

>P21266|GSTM3
     1  MSCESSMVLG YWDIRGLAHA IRLLLEFTDT SYEEKRYTCG EAPDYDRSQW LDVKFKLDLD
    61  FPNLPYLLDG KNKITQSNAI LRYIARKHNM CGETEEEKIR VDIIENQVMD FRTQLIRLCY
   121  SSDHEKLKPQ YLEELPGQLK QFSMFLGKFS WFAGEKLTFV DFLTYDILDQ NRIFDPKCLD
   181  EFPNLKAFMC RFEALEKIAA YLQSDQFCKM PINNKMAQWG NKPVC

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against GSTM3 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)
0.27
Highest tissue expression
93 nTPM

Expression across tissuesHPA

Tissue

  • choroid plexus: 93 nTPM
  • epididymis: 66 nTPM
  • kidney: 52 nTPM
  • testis: 43 nTPM
  • ovary: 36 nTPM
  • seminal vesicle: 36 nTPM

Single-cell type

  • late spermatids: 6,018 nCPM
  • late primary spermatocytes: 3,269 nCPM
  • early spermatids: 1,991 nCPM
  • erythrocyte progenitors: 870 nCPM
  • epididymal principal cells: 866 nCPM
  • mast cells: 718 nCPM

Immune cell

  • naive CD4 T-cell: 2.4 nTPM
  • naive CD8 T-cell: 1.2 nTPM
  • memory CD4 T-cell: 0.9 nTPM
  • eosinophil: 0.6 nTPM
  • gdT-cell: 0.5 nTPM
  • memory CD8 T-cell: 0.5 nTPM

Brain region

  • choroid plexus: 69 nTPM
  • hypothalamus: 28 nTPM
  • basal ganglia: 27 nTPM
  • white matter: 26 nTPM
  • cerebral cortex: 25 nTPM
  • spinal cord: 24 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)
1.17
gnomAD pLI
0
gnomAD missense Z
0.94
DepMap mean gene effect
-0.23
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

InteractionsUniProt · HPA

Protein binding partners of GSTM3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads GSTM3 as an antibody target. Whether an autoantibody or antibody against GSTM3 could matter depends on whether native GSTM3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

GSTM3 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 GSTM3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/GSTM3. 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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