Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0080178
Disease: Spina Bifida
Spina Bifida 		0.310 GeneticVariation BEFREE Genetic polymorphisms in the thioredoxin 2 (TXN2) gene and risk for spina bifida. 19165900

2009
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 GeneticVariation BEFREE The aim of our study was to investigate the relationship between genetic polymorphisms in the mitochondrial thioredoxin reductase 2 (TrxR2) and myocardial infarction (MI) in subjects with type 2 diabetes mellitus (T2DM) of Slovenian origin. 25703281

2015
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 GeneticVariation BEFREE Single nucleotide polymorphisms in the Trx2/TXNIP and TrxR2 genes of the mitochondrial thioredoxin antioxidant system and the risk of diabetic retinopathy in patients with Type 2 diabetes mellitus. 26763822

2016
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.010 GeneticVariation BEFREE Single nucleotide polymorphisms in the Trx2/TXNIP and TrxR2 genes of the mitochondrial thioredoxin antioxidant system and the risk of diabetic retinopathy in patients with Type 2 diabetes mellitus. 26763822

2016
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 GeneticVariation BEFREE The aim of our study was to investigate the relationship between genetic polymorphisms in the mitochondrial thioredoxin reductase 2 (TrxR2) and myocardial infarction (MI) in subjects with type 2 diabetes mellitus (T2DM) of Slovenian origin. 25703281

2015
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects 		0.010 GeneticVariation BEFREE We hypothesized that genetic variation in human TXN2 gene may alter the function of the encoded protein in a manner associated with an increased risk for neural tube defects (NTDs). 19165900

2009
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C4225200
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29 		0.500 Biomarker GENOMICS_ENGLAND Human thioredoxin 2 deficiency impairs mitochondrial redox homeostasis and causes early-onset neurodegeneration. 26626369

2016
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C4225200
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29 		0.500 Biomarker CTD_human

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C4225200
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29 		0.500 Biomarker GENOMICS_ENGLAND

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0080178
Disease: Spina Bifida
Spina Bifida 		0.310 Biomarker CTD_human Genetic polymorphisms in the thioredoxin 2 (TXN2) gene and risk for spina bifida. 19165900

2009
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0038219
Disease: Status Dysraphicus
Status Dysraphicus 		0.300 Biomarker CTD_human Genetic polymorphisms in the thioredoxin 2 (TXN2) gene and risk for spina bifida. 19165900

2009
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0266508
Disease: Rachischisis
Rachischisis 		0.300 Biomarker CTD_human Genetic polymorphisms in the thioredoxin 2 (TXN2) gene and risk for spina bifida. 19165900

2009
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental 		0.200 Biomarker RGD Effect of high glucose on gene expression in mesangial cells: upregulation of the thiol pathway is an adaptational response. 15039483

2004
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental 		0.200 Biomarker RGD [The change of thioredoxin system in myocardial tissue of type 2 diabetic rats undergoing myocardial injury]. 20571744

2010
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0027055
Disease: Myocardial Reperfusion Injury
Myocardial Reperfusion Injury 		0.200 Biomarker RGD Redox regulation of resveratrol-mediated switching of death signal into survival signal. 18045550

2008
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0035126
Disease: Reperfusion Injury
Reperfusion Injury 		0.200 Biomarker RGD The expression of thioredoxin-1/thioredoxin-2 and thioredoxin reductase-1/thioredoxin reductase-2 was significantly decreased in rats with ischemia/reperfusion injury, while it was increased by tetramethyl pyrazine administration. 19128823

2009
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0013421
Disease: Dystonia
Dystonia 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0029132
Disease: Disorder of the optic nerve
Disorder of the optic nerve 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker HPO