TCF7L2, transcription factor 7 like 2, 6934

N. diseases: 257; N. variants: 70
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE Single nucleotide polymorphisms (SNPs) in the transcription factor 7-like 2 gene (TCF7L2) represent the strongest and most reproducible genetic associations with diabetes. 24128935 2013
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE In the DESIR cohort, a parental history of diabetes and the TCF7L2 at-risk variant were both associated with hypertension incidence at year 9, independently of waist circumference, BP, fasting glucose, insulin levels and HOMA-IR at inclusion (p = 0.02 for parental history, p = 0.006 for TCF7L2). 23942764 2013
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE Human genetic studies have revealed that the T minor allele of single nucleotide polymorphism rs7903146 in the transcription factor 7-like 2 (TCF7L2) gene is strongly associated with an increased risk of diabetes by 30%-40%. 25058603 2014
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE Analysis of TCF7L2 rs7903146 in normal controls and diabetics with or without nephropathy demonstrated that the 'T' allele is associated with both diabetes (p = 0.049) and DN (p = 0.024), but this association is not independent of T2DM. 25185853 2014
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE Linagliptin significantly improved hyperglycaemia in patients with type 2 diabetes both with and without the TCF7L2 gene diabetes risk alleles. 24906949 2014
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE Associations between TCF7L2 SNP and diabetic complications and diabetes-related factors were investigated. 24529562 2014
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE T2D-related variants HHEX rs7923837, TCF7L2 rs290481 and CDKAL1 rs7756992 increased cancer risk in patients with diabetes. 24468095 2014
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE The results indicated that the TCF7L2 rs11196172 polymorphism increases the risk of CRC independently, with no evidence of an interaction with diabetes or obesity. 27792933 2016
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE In addition, the TCF7L2 rs290487 TT genotype was associated with abdominal obesity and the GCG rs12104705 CC genotype was associated with both general obesity and abdominal obesity in case of new-onset diabetes. 27998387 2016
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE This study aimed to investigate the possible association between diabetes susceptibility gene transcription factor 7-like 2 (TCF7L2) and gestational diabetes mellitus (GDM) in a Chinese Han population. 27465520 2016
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 Biomarker disease BEFREE TCF7L2 Genotype and α-Cell Function in Humans Without Diabetes. 26525881 2016
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247 2016
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 AlteredExpression disease BEFREE TCF7L2 is a transcription factor in the canonical Wnt pathway, involved in multiple disorders, including diabetes, cancer and psychiatric conditions. 26934194 2016
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE Association between the rs7903146 Polymorphism in the TCF7L2 Gene and Parameters Derived with Continuous Glucose Monitoring in Individuals without Diabetes. 26914832 2016
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE The Role of TCF7L2 rs7903146 in Diabetes After Kidney Transplant: Results From a Single-Center Cohort and Meta-Analysis of the Literature. 26555947 2016
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE An interaction (p = 0.048) between TCF7L2 variants and coffee intake was apparent, with an inverse association between coffee and type 2 diabetes present among carriers of the diabetes risk allele (T) in rs12255372 (GG: HR 0.99 [95% CI 0.97, 1.02] per cup of coffee; GT: HR 0.96 [95% CI 0.93, 0.98]); and TT: HR 0.93 [95% CI 0.88, 0.98]). 27623947 2016
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 Biomarker disease BEFREE The Tcf7l2 gene encodes a key Wnt signalling pathway effector, and its human homologue TCF7L2 is a highly regarded diabetes risk gene. 28102847 2017
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE TCF7L2 rs7903146 C>T polymorphism is associated with diabetes in the general population but its independent impact on cardiovascular disease is debated. 28299838 2017
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE After adjusting for known confounding factors, we found a significant association between TCF7L2/rs122555372 and C-peptide (β = -0.76, P = .005) in patients with diabetes and between fasting glucose (β = 2.05, P = .039) and homeostatic model assessment of β-cell function (β = -32.14, P = .025) levels in individuals without diabetes. 28101933 2017
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 Biomarker disease BEFREE In this study, we discovered a previously unrecognized role for Tcf7l2, a transcription factor known as the canonical Wnt nuclear effector and diabetes risk-conferring gene, in establishing neuronal identity and circuits of the caudal forebrain. 28219675 2017
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE The aim of the study was to explore the correlation between rs7903146 and rs290487 polymorphisms in transcription factor 7-like 2 (TCF7L2) gene and diabetic nephropathy (DN) in Chinese Han population.Polymerase chain reaction-restriction fragment length polymorphism was used to determine genotypes of TCF7L2 polymorphisms in 90 patients with DN and 96 diabetes patients without DN. 30290587 2018
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 Biomarker disease BEFREE However, the mechanism(s) by which TCF7L2 predisposes to diabetes remain uncertain. 29993315 2018
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE Genetic variation in TCF7L2 rs7903146 and history of GDM negatively and independently impact on diabetes-associated metabolic traits. 30419301 2018
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 AlteredExpression disease BEFREE Our findings thus propose a potential cellular mechanism through which abnormal TCF7L2 activity predisposes individuals to diabetes and implicates abnormalities in the islet microenvironment in this disease. 29246974 2018
CUI: C0011847
Disease: Diabetes
Diabetes
0.200 GeneticVariation disease BEFREE Transcription factor 7-like 2 (TCF7L2), which previously known as TCF-4, is a major form of transcription factor involved in the downstream WNT signaling and exhibits the strongest association to diabetes susceptibility. 31312258 2019