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Gene Symbol |
GSTM3 |
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Aliases |
GST5, GSTB, GSTM3-3, GTM3 |
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Entrez Gene ID |
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Gene Name |
Glutathione S-transferase mu 3 |
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Chromosomal Location |
1p13.3 |
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HGNC ID |
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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. 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]
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e!Ensembl
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Protein Information |
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Protein Name |
Glutathione S-transferase Mu 3, GST class-mu 3, S-(hydroxyalkyl)glutathione lyase M3, brain GST, brain type mu-glutathione S-transferase, epididymis secretory sperm binding protein, glutathione S-alkyltransferase M3, glutathione S-aralkyltransferase M3, glutathione S-aryltransferase M3, glutathione S-transferase M3 (brain), glutathione S-transferase mu 3 (brain), glutathione S-transferase, Mu-3, hGSTM3-3 |
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Function |
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. May govern uptake and detoxification of both endogenous compounds and xenobiotics at the testis and brain blood barriers. |
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UniProt |
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PDB |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000405330 |
P03372 |
P03372 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Digestive System Diseases |
Hepatitis |
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Liver Diseases |
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Endocrine System Diseases |
PCOS |
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Neoplasms |
Colorectal Cancer |
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Prostate cancer |
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Skin and Connective Tissue Diseases |
Chloracne |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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Proapolipoprotein Apo-A1, annexin V,PRDX2,triosephosphate isomerase, peroxiredoxin 2 isoform a, actin and adipocyte plasma membrane-associated protein |
Visceral adiposity |
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Presence of oligo-ovulation, clinical and/or biochemical hyperandrogenism, and exclusion of hyperprolactinemia, non-classic congenital adrenal hyperplasia and androgen-secreting tumors |
Related
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This preliminary study revealed differences in expression of proteins that may be involved in lipid and glucose metabolism, oxidative stress processes and adipocyte differentiation; they include proapolipoprotein Apo-A1, annexin V, glutathione S-transferase M3 (GSTM3), triosephosphate isomerase, peroxiredoxin 2 isoform a, actin and adipocyte plasma membrane-associated protein. |
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DHEAS, SHBG, 2-h plasma glucose,malondialdehyde (MDA), protein carbonyl (PC), reduced glutathione (GSH), carotene, vitamin A, C, E and the enzyme activities of catalase |
Oxidative stress,Insulin resistance and Hyperglycemia |
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Related
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Oxidative stress characterized by increased oxidants and decreased antioxidant levels which are independent of IR may be involved in the pathogenesis of PCOS in young non-obese women. |
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