GCK, glucokinase, 2645

N. diseases: 210; N. variants: 182
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE A case-control study and meta-analysis confirm glucokinase regulatory gene rs780094 is a risk factor for gestational diabetes mellitus. 29410004 2018
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE Our screening criteria allowed for the identification of glucokinase-deficient patients who were diagnosed with gestational diabetes, and these mutations in the GCK gene were not common in Chinese women with gestational diabetes. 28371533 2018
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE In the case of the GCK rs1799884 polymorphism, there was a predominance of the T allele in women with GDM; however, this association reached only borderline statistical significance (p=0.08). 28359772 2017
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE Due to the relationship between GCKRP and GCK, polymorphisms in GCKR are also candidates for genetic association with GDM. 27554451 2017
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE The NSC will refer 6.1% of GDM cases for GCK testing, with more Asian/Indian women referred despite lower disease prevalence. 26109503 2016
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE The association between the glucokinase (GCK)-30G > A polymorphism and GDM susceptibility was assessed using genetic models. 25633883 2015
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE To prospectively determine the prevalence of maturity onset diabetes of the young (MODY) due to glucokinase (GCK) mutations in an American population of women with recent onset diabetes mellitus and gestational diabetes. 25012807 2015
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 Biomarker phenotype BEFREE GCK monogenic diabetes and gestational diabetes: possible diagnosis on clinical grounds. 26043405 2015
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE The aim of this meta-analysis is to provide a relatively comprehensive picture of the association of the GCK -30G>A polymorphism with GDM and T2DM risk. 24520939 2014
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 Biomarker phenotype BEFREE The 0.1% of the population with glucokinase monogenic diabetes can be recognized by clinical characteristics in pregnancy: the Atlantic Diabetes in Pregnancy cohort. 24550216 2014
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE The minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (rs5219" genes_norm="3767">E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (rs1801278" genes_norm="3667">Gly972Arg, IRS1) were significantly associated with a higher risk of GDM. 23690305 2013
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE These polymorphisms were in or near the following genes: TCF7L2 (rs7903146), MTNR1B (rs10830963), IGF2BP2 (rs4402960), KCNJ11 (rs5219), CDKAL1 (rs7754840), KCNQ1 (rs2237892 and rs2237895) and GCK (rs4607517); while no association was found for PPARG with GDM risk. 23029294 2012
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE We report two women with gestational diabetes mellitus resulting from GCK mutations with hyperglycemia sufficient to merit treatment. 22773699 2012
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE Heterozygous mutations in glucokinase (GCK) are associated with mild fasting hyperglycemia and gestational diabetes mellitus while homozygous or compound heterozygous GCK mutations result in permanent neonatal diabetes mellitus. 21978167 2012
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE Maturity Onset Diabetes of the Young (MODY) due to glucokinase mutations may account for as much as 5% of GDM patients. 22145702 2012
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE A sample of 200 pregnant women classified as healthy (control, N = 100) or with gestational diabetes (N = 100) was analyzed for mutations in the GCK gene. 22653590 2012
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype LHGDN In summary, our results suggest that, because of high costs and time-consuming methods of genetic studies, the investigations of glucokinase gene mutations should be concentrated in women with gestational diabetes without clinical and biochemical features of insulin resistance, but with family history of diabetes in two generations. 18159847 2007
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype LHGDN GCK and HNF1alpha mutations and polymorphisms in Polish women with gestational diabetes. 16963153 2007
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 Biomarker phenotype BEFREE In addition, common variants in several candidate genes (e.g. potassium inwardly rectifying channel subfamily J, member 11 [KCNJ11], Glucokinase [GCK], Hepatocyte nuclear factor-1alpha [HNF1A] etc.) have been demonstrated to increase the risk of GDM. 17346148 2007
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE The -30G-->A polymorphism of the beta-cell-specific promoter of GCK and the I27L polymorphism of HNF1A seem to increase the risk of GDM in Scandinavian women. 16752173 2006
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 Biomarker phenotype BEFREE Direct sequencing of NEUROD1 was performed in (i) 73 probands with clinical MODY without mutations in hepatocyte nuclear factor (HNF)-4alpha (MODY1), glucokinase (MODY2) and hepatocyte nuclear factor (HNF)-1alpha (MODY3), and (ii) 51 subjects diagnosed with gestational diabetes. 16026366 2005
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE Influence of maternal and fetal glucokinase mutations in gestational diabetes. 11483936 2001
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE Phenotypic selection of subjects with gestational diabetes greatly increases the likelihood of detecting a mutation in the glucokinase gene as previous studies have suggested a prevalence of 2.5% (range 0-6%). 10753050 2000
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE We have screened the glucokinase gene by the polymerase chain reaction (PCR) and denaturing gradient gel electrophoresis (DGGE) in fifteen subjects with clinical characteristics of MODY and one parent with NIDDM, impaired glucose tolerance or gestational diabetes. 10694920 1998
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.200 GeneticVariation phenotype BEFREE In summary, in a cohort of 35 British Caucasian women with gestational diabetes neither missense nor nonsense glucokinase mutations were found. 9088772 1997