GSTM2 (glutathione S-transferase mu 2)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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2946 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Glutathione S-transferase mu 2 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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GSTM2 |
SynonymsGene synonyms aliases
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GST4, GSTM, GSTM2-2, GTHMUS |
ChromosomeChromosome number
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1 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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1p13.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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. [provided by RefSeq, Jul 2008] |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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GO ID |
Ontology |
Definition |
Evidence |
Reference |
GO:0004364 |
Function |
Glutathione transferase activity |
IBA |
21873635 |
GO:0004364 |
Function |
Glutathione transferase activity |
IDA |
2034681, 8373352, 16549767 |
GO:0004602 |
Function |
Glutathione peroxidase activity |
IDA |
16624487 |
GO:0005102 |
Function |
Signaling receptor binding |
IPI |
22406107 |
GO:0005504 |
Function |
Fatty acid binding |
IPI |
16624487 |
GO:0005515 |
Function |
Protein binding |
IPI |
24965446, 28514442, 32296183 |
GO:0005737 |
Component |
Cytoplasm |
IDA |
2034681, 8373352 |
GO:0005829 |
Component |
Cytosol |
IDA |
|
GO:0005829 |
Component |
Cytosol |
TAS |
|
GO:0006749 |
Process |
Glutathione metabolic process |
IBA |
21873635 |
GO:0006749 |
Process |
Glutathione metabolic process |
IDA |
2034681, 8373352, 16549767 |
GO:0010880 |
Process |
Regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum |
IDA |
17023043 |
GO:0010881 |
Process |
Regulation of cardiac muscle contraction by regulation of the release of sequestered calcium ion |
IC |
17023043, 22406107 |
GO:0014809 |
Process |
Regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion |
IC |
17023043 |
GO:0016529 |
Component |
Sarcoplasmic reticulum |
IDA |
22406107 |
GO:0018916 |
Process |
Nitrobenzene metabolic process |
IDA |
2034681, 8373352 |
GO:0019899 |
Function |
Enzyme binding |
IPI |
8373352 |
GO:0042178 |
Process |
Xenobiotic catabolic process |
IDA |
2034681, 8373352, 16549767 |
GO:0042803 |
Function |
Protein homodimerization activity |
IPI |
8373352 |
GO:0043295 |
Function |
Glutathione binding |
IDA |
2034681, 8373352 |
GO:0043651 |
Process |
Linoleic acid metabolic process |
IDA |
16624487 |
GO:0045171 |
Component |
Intercellular bridge |
IDA |
|
GO:0051122 |
Process |
Hepoxilin biosynthetic process |
IDA |
21046276 |
GO:0055119 |
Process |
Relaxation of cardiac muscle |
TAS |
21323602 |
GO:0060315 |
Process |
Negative regulation of ryanodine-sensitive calcium-release channel activity |
IDA |
17023043, 22406107 |
GO:0060316 |
Process |
Positive regulation of ryanodine-sensitive calcium-release channel activity |
IDA |
17023043 |
GO:0070062 |
Component |
Extracellular exosome |
HDA |
19056867, 23533145 |
GO:0070458 |
Process |
Cellular detoxification of nitrogen compound |
IDA |
2034681, 8373352 |
GO:0071313 |
Process |
Cellular response to caffeine |
IDA |
22406107 |
GO:0098869 |
Process |
Cellular oxidant detoxification |
IEA |
|
GO:1901687 |
Process |
Glutathione derivative biosynthetic process |
TAS |
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
P28161 |
Protein name |
Glutathione S-transferase Mu 2 (EC 2.5.1.18) (GST class-mu 2) (GSTM2-2) |
Protein function |
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. Participates in the formation of novel hepoxilin regioisomers (PubMed:21046276). |
PDB |
1HNA
,
1HNB
,
1HNC
,
1XW5
,
1YKC
,
2AB6
,
2C4J
,
2GTU
,
3GTU
,
3GUR
,
5HWL
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF02798 |
GST_N |
3 → 82 |
Glutathione S-transferase, N-terminal domain |
Domain |
PF00043 |
GST_C |
104 → 192 |
Glutathione S-transferase, C-terminal domain |
Domain |
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Sequence |
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Sequence length |
218 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Breast carcinoma |
Breast Carcinoma |
rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451, rs397507859, rs80359709, rs80359742, rs80359205, rs80357627, rs80357004, rs80357571, rs80357767, rs80357653, rs80358086, rs80357608, rs28897696, rs41293465, rs146650273, rs63751017, rs63750617, rs63750726, rs63750199, rs63749848, rs398122618, rs398122653, rs397509211, rs80357791, rs121912666, rs587778541, rs121908698, rs536907995, rs587781302, rs140342925, rs587781506, rs587782652, rs587782849, rs587783057, rs139770721, rs374950566, rs786202800, rs863224451, rs377153250, rs747727055, rs876658804, rs780001540, rs760815829, rs878854926, rs775248597, rs886040658, rs886040192, rs786203523, rs886040319, rs397508006, rs587782011, rs1060502772, rs1555461727, rs1553333072, rs1114167702, rs1257401983, rs886040950, rs1060502759, rs774684620, rs142947311, rs1555580883, rs748513310, rs376170600, rs863224499, rs1593909229, rs748453607, rs1294578913, rs1574737047, rs1593909960, rs2081922847, rs2082559544, rs2053694038 |
29059683 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs-1, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
22874804 |
Lung carcinoma |
Non-Small Cell Lung Carcinoma |
rs1805076, rs121909071, rs121913530, rs112445441, rs121913529, rs121913535, rs121913297, rs121913279, rs104886003, rs397516975, rs11554290, rs121913364, rs121913351, rs121913369, rs121913355, rs121912470, rs121913273, rs121913281, rs121913348, rs727503093, rs121913353, rs397516890, rs397516896, rs121913378, rs397516897, rs397516977, rs397516978, rs397516979, rs397516980, rs397516981, rs397516982, rs121913240, rs17851045, rs397517086, rs121913428, rs397517094, rs397517098, rs397517106, rs121913465, rs397517108, rs397517111, rs397517112, rs397517114, rs397517116, rs1554350366, rs397517127, rs397517200, rs397517202, rs121913283, rs121913370, rs121913357, rs727503106, rs121913238, rs727503108, rs397517040, rs397516976, rs1555618025, rs1057519729, rs-1, rs1584238193 |
19900515 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Degenerative diseases, central nervous system |
Degenerative Diseases, Central Nervous System, Degenerative Diseases, Spinal Cord |
|
15964507 |
Down syndrome |
Down Syndrome, Down Syndrome, Partial Trisomy 21 |
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11771762 |
Kidney failure |
Kidney Failure, Acute |
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20623750 |
Myocardial ischemia |
Myocardial Ischemia |
|
16214533 |
Neurodegenerative disorders |
Neurodegenerative Disorders |
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15964507 |
Acute kidney insufficiency |
Acute Kidney Insufficiency |
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20623750 |
Trisomy 21 |
Trisomy 21, Meiotic Nondisjunction, Trisomy 21, Mitotic Nondisjunction |
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11771762 |
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