GSTM1, glutathione S-transferase mu 1, 2944

N. diseases: 627; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
0.010 GeneticVariation group BEFREE This protective effect mediated by the presence of GSTM1 was even more pronounced within the subset of therapy group B patients at highest clinical risk of treatment failure (B-ALL, disease stage IV, disease stage III with unresected abdominal tumor, and LDH activity > or = 500 U/L). 12091121 2002
CUI: C0271907
Disease: Acquired aplastic anemia
Acquired aplastic anemia
0.020 GeneticVariation disease BEFREE Increased frequencies of glutathione S-transferase (GSTM1 and GSTT1) gene deletions in Korean patients with acquired aplastic anemia. 11719393 2001
CUI: C0271907
Disease: Acquired aplastic anemia
Acquired aplastic anemia
0.020 GeneticVariation disease BEFREE We analyzed the impact of the polymorphisms in CYP4501A1 and GSTM1 and GSTT1 genes on the susceptibility and disease severity in 200 patients with AA and compared the frequency with the normal population. 16227674 2005
CUI: C3662490
Disease: Acquired sensorineural hearing loss
Acquired sensorineural hearing loss
0.010 GeneticVariation disease BEFREE Association of Glutathione s-transferase M1 and T1 gene polymorphisms with the susceptibility to acquired sensorineural hearing loss: a systematic review and meta-analysis. 30696891 2019
CUI: C0267026
Disease: Actinic cheilitis
Actinic cheilitis
0.010 GeneticVariation disease BEFREE A case-control study of 164 lung adenocarcinoma (AC) patients with 181 age- and gender-matched healthy controls was conducted in order to assess any associations between glutathione-S-transferase M1 (GSTM1), cytochrome P4501A1 (CYP1A1) and cytochrome P4502E1 (CYP2E1) polymorphisms and susceptibility to lung AC in Chinese. 12824892 2003
CUI: C0022602
Disease: Actinic keratosis
Actinic keratosis
0.020 Biomarker disease BEFREE To verify the possible association between the development of SK and the 'null' GSTM1 and/or T1 genotype. 19874347 2010
CUI: C0022602
Disease: Actinic keratosis
Actinic keratosis
0.020 GeneticVariation disease BEFREE The GSTM1 null genotype confers an increased risk for solar keratosis development in an Australian Caucasian population. 12485442 2002
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.020 Biomarker disease BEFREE The absence of GSTT1 and/or GSTM1 was an important risk factor for increasing the morbidity of SCA, especially in regard to acute chest syndrome. 23590899 2013
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.020 GeneticVariation disease BEFREE The GSTM1 null genotype was significantly associated with ACS and VOC (P = 0.03 and 0.01, respectively). 25880856 2015
CUI: C0267797
Disease: Acute hepatitis
Acute hepatitis
0.010 Biomarker disease BEFREE Patients with a history of anti-TB drug-induced acute hepatitis (cases with an increase to 3 times the upper limit of normal serum transaminases and symptoms of hepatitis) and patients with no evidence of anti-TB hepatic side effects (controls) were genotyped for NAT2, CYP2E1, GSTM1 and GSTT1 polymorphisms. 22012226 2011
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 Biomarker disease BEFREE When the OR used to determine statistical power was lowered to 1.2, 2 of the 4 noteworthy associations remained so: GSTM1 null with bladder cancer and acute leukemia. 18505952 2008
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 GeneticVariation disease BEFREE The results suggested that the GSTM1 null genotype and GSTT1null genotype, but not the GSTP1 polymorphism, might be a potential risk factors for acute leukemia. 24716937 2014
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 Biomarker disease BEFREE Role of CYP2D6, CYP1A1, CYP2E1, GSTT1, and GSTM1 genes in the susceptibility to acute leukemias. 16493615 2006
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 GeneticVariation disease BEFREE Deletion of GSTM1 and T1 genes as a risk factor for development of acute leukemia. 23725116 2013
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 GeneticVariation disease BEFREE This meta-analysis supports that GSTM1 null polymorphism is capable of causing childhood acute leukemia susceptibility. 24194954 2013
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 GeneticVariation disease BEFREE GSTM1-null genotype was associated with a lower risk of developing acute leukemia (P = 0.013; OR: 0.31; CI: 0.12-0.80), while GSTP1-GG variants displayed an increased risk (P = 0.01; OR: 3.9; CI: 1.85-8.2). 25799091 2015
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 GeneticVariation disease BEFREE Overall, the GSTM1 null genotype was significantly associated with increased risk of childhood acute leukemia in Chinese (fixed effect OR = 2.49; 95% CI, 1.84–3.37; P < 0.001). 24022662 2014
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 GeneticVariation disease BEFREE Individuals carrying null GSTTI and GSTM1 genotypes had a 1.52- and 1.78-fold increased risk of developing acute leukemia, respectively, compared to non-null genotype carriers (P < 0.05). 24854448 2014
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 GeneticVariation disease BEFREE Glutathione s-transferase polymorphisms (GSTM1, GSTP1 and GSTT1) and the risk of acute leukaemia: a systematic review and meta-analysis. 15862746 2005
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.100 GeneticVariation disease BEFREE This case-control study suggests a contribution of CYP2D6 and GSTM1 null variants in the development of acute leukaemia. 17581325 2007
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.100 GeneticVariation disease BEFREE When NAT2 slow acetylators were considered together with the other risk-elevating genotypes, GSTM1 null and CYP1A1*2A, the risk of ALL increased further, which showed that the combination of these genotypes is more predictive of risk then either of them independently. 10868688 2000
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.100 GeneticVariation disease BEFREE The odds ratios for both GSTM1 and GSTT1 deletions being associated with ALL was 2.78 (95% CI = 0.67-11.56). 15382273 2004
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.100 GeneticVariation disease BEFREE A combination between GSTM1 double-null genotype and rs1695 also showed an association with ALL (P=0.042). 27299594 2016
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.100 GeneticVariation disease BEFREE When combined with other GST genotypes, we found that the combination of GSTP1*B and GSTM1 null genotypes further increased the risk of ALL (OR = 2.1; 95% CI-1.3-3.4). 12439226 2002
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.100 GeneticVariation disease BEFREE In conclusion, our results suggest that the combined gene dose of GSTM1 and GSTT1 may influence outcome in childhood ALL. 22215096 2012