Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease GWASCAT Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. 29358691 2018
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE Each of the ABCC8 gene mutation carrier family members were diagnosed with diabetes as follows: the grandfather with type 2 diabetes at 35 years of age, the aunt with slowly-progressive insulin-dependent diabetes at 18 years of age, the mother with ketosis-onset insulin-dependent diabetes at 14 years of age, the sister with impaired glucose tolerance at 9 years of age, and the proband with transient neonatal diabetes at birth. 30068891 2018
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE This study revealed significantly (p < 0.05) higher prevalence of the T allele of the ABCC8 gene in T2D patients (33.1%) compared to ND patients (28.0%). 29751826 2018
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease BEFREE Long used to target K<sub>ATP</sub> (Sur1-Kir6.2) channels for the treatment of diabetes mellitus type 2, glyburide was recently repurposed to target Sur1-transient receptor potential melastatin 4 (Trpm4) channels in acute central nervous system injury. 30147301 2018
Diabetes Mellitus, Non-Insulin-Dependent
0.700 AlteredExpression disease BEFREE Altered expression of Notch2 and ABCC8 genes may play a role in the pathogenesis of T2DM. 28794851 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE KCNJ11, ABCC8 and TCF7L2 polymorphisms and the response to sulfonylurea treatment in patients with type 2 diabetes: a bioinformatics assessment. 28587604 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE It has been hypothesized that the p.E23K (KCNJ11) mutation in the 11p15.1 region may play an important role in the development of T2DM.In 2009, Hamming et al. found that the p.1369A (ABCC8) variant may be a causal factor in the disease; therefore, in this study we performed a meta-analysis to evaluate the association between these single nucleotide polymorphisms (SNPs), including our original data on the Siberian population (1384 T2DM and 414 controls). 25955821 2015
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE Of note, the first two T2D-associated loci (PPARG and KCNJ11/ABCC8) encode known targets of antidiabetes medications. 25368101 2015
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE ABCC8 R1420H Loss-of-Function Variant in a Southwest American Indian Community: Association With Increased Birth Weight and Doubled Risk of Type 2 Diabetes. 26246406 2015
Diabetes Mellitus, Non-Insulin-Dependent
0.700 AlteredExpression disease BEFREE The aim of this study was to evaluate significance of kidney MRP8 expression in patients with obesity- or type 2 diabetes-associated kidney diseases. 24558454 2014
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE CYP2C9, KCNJ11 and ABCC8 polymorphisms and the response to sulphonylurea treatment in type 2 diabetes patients. 24442125 2014
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease BEFREE Among these proteins involved in ion homeostasis, the ischemia-induced, nonselective cation conductance formed by the SUR1-TRPM4 protein complex appears to play a prominent role and is potently inhibited by glibenclamide, an FDA-approved drug commonly used in patients with Type 2 diabetes. 24380477 2014
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE The present case-control study undertaken in the population of Punjab, evaluates the association of +45T>G polymorphism in AdipoQ gene; and Exon16-3C>T as well as Exon18C>T polymorphisms in ABCC8 gene with T2D. 23764562 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE Our meta-analysis demonstrated that KCNJ11 and ABCC8 polymorphisms are associated with risk for type 2 diabetes in the global population. 24065655 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE The C49620T ABCC8 polymorphism is associated with anthropometric risk factors for type 2 diabetes among ADPKD patients, with a protective effect of the TT genotype, but without influence on pancreatic β-cell secretory function or insulin sensitivity. 22466262 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE Gain-of-function ABCC8/sulfonylurea (SU) receptor 1 mutations cause neonatal diabetes mellitus (NDM) or late-onset diabetes in adult relatives. 22210575 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE The common ATP-sensitive potassium (KATP) channel variants E23K and S1369A, found in the KCNJ11 and ABCC8 genes, respectively, form a haplotype that is associated with an increased risk for type 2 diabetes. 22209866 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE We aimed to investigate the allele profiles and the risk alleles of the ABCC8 and KCNJ11 genes and to highlight the associations with the disease in patients in Konya region of Turkey where T2DM is common. 22704848 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE Although rare monogenic activating mutations in these genes cause overt neonatal diabetes, the common variants E23K (KCNJ11) and S1369A (ABCC8) form a tightly heritable haplotype that is associated with an increased susceptibility to type 2 diabetes (T2D) risk. 22187380 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease BEFREE A non-mutagenic SNP on nucleotide position 333 (Pro69Pro) added another exonic splicing enhancer sequence detected by ASF/SF2, reduced relative abundance of SUR1Δ2 and slightly protected from non-insulin dependent diabetes in homozygotic individuals. 21671119 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease CTD_human The common ATP-sensitive potassium (KATP) channel variants E23K and S1369A, found in the KCNJ11 and ABCC8 genes, respectively, form a haplotype that is associated with an increased risk for type 2 diabetes. 22209866 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE Variants in USF1, ABCC8, ISL1 and KCNJ11 showed nominal association, while haplotypes in these genes were significantly associated. rs3812704 upstream of NEUROG3 significantly increased risk for type 2 diabetes in normal-weight/lean subjects (OR=1.68 (95%CI 1.25-2.24), P=4.9 × 10(-4)). 21814221 2011
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE Whether or not the patients with heterozygous ABCC8 mutations submitted to conservative treatment may spontaneously develop type 2 diabetes in the long run, is a controversial issue. 20042013 2010
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease BEFREE Metabolic control in type 2 diabetes is associated with sulfonylurea receptor-1 (SUR-1) but not with KCNJ11 polymorphisms. 19766903 2009
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE The KCNJ11 E23K and ABCC8 exon 31 variants contribute to susceptibility to T2D diabetes, glucose intolerance and altered insulin secretion in a Russian population. 18758683 2009