GSTM5

glutathione S-transferase mu 5

Summary

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. Diversification of these genes has occurred in regions encoding substrate-binding domains, as well as in tissue expression patterns, to accommodate an increasing number of foreign compounds. [provided by RefSeq, Jul 2008]

Known Variants25 total

rsidPosition (GRCh37)AllelesClassClinVar
rs3666311:110,252,472A/G——
rs37544461:110,253,241A/Cdownstream gene variant—
rs12920961:110,253,380A/T——
rs284617551:110,254,456A/G——
rs287431051:110,254,513C/T——
rs127313841:110,254,520G/Tdownstream gene variant—
rs7614186601:110,255,243G/A—uncertain significance
rs7651389411:110,255,779T/G—uncertain significance
rs7582629421:110,255,784G/C—uncertain significance
rs1448398851:110,256,162C/G—benign
rs8906089061:110,256,301A/G—uncertain significance
rs5543800381:110,256,342A/G—uncertain significance
rs14440324051:110,257,638A/C—uncertain significance
rs1404990991:110,257,641C/T—benign
rs11577718691:110,257,645C/T—uncertain significance
rs7817170421:110,257,659G/A—uncertain significance
rs7677648561:110,257,798G/A—uncertain significance
rs789556791:110,257,814G/C—benign
rs3763131971:110,257,825C/T—uncertain significance
rs25246046131:110,257,832A/C—likely benign
rs1504175851:110,257,854C/T—likely benign
rs37684901:110,259,016G/Tintron variant—
rs1996639291:110,259,966A/T—uncertain significance
rs7519551051:110,259,995C/G—uncertain significance
rs1131300581:110,260,040A/G—benign

Gene information from NCBI Gene. Variant classifications from ClinVar.