Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2646
Gene Symbol: GCKR
GCKR
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926

2019

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. 29632382

2018

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. 30054458

2018

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. 28869590

2017

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. 22885922

2012

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.490 GeneticVariation GWASCAT A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia. 27599772

2017

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.490 GeneticVariation GWASCAT Through GWAS, we identified common variants in APOA5, GCKR, LPL and APOB associated with HTG. 20657596

2010

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.200 GeneticVariation GWASCAT Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. 31511532

2019

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.200 GeneticVariation GWASCAT Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers. 29385134

2018

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.200 GeneticVariation GWASCAT Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean population. 30382898

2018

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.200 GeneticVariation GWASCAT New Common and Rare Variants Influencing Metabolic Syndrome and Its Individual Components in a Korean Population. 29632305

2018

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.200 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.200 GeneticVariation GWASCAT Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits. 22399527

2012

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.200 GeneticVariation GWASCAT A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0011847
Disease: Diabetes
Diabetes
0.180 GeneticVariation GWASCAT Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. 31511532

2019

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0011847
Disease: Diabetes
Diabetes
0.180 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.120 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.110 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528

2019

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.110 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.110 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443

2018

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.110 GeneticVariation GWASCAT GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes. 27899376

2017

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.110 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908

2017

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.110 GeneticVariation GWASCAT Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes. 25646370

2016

Entrez Id: 2646
Gene Symbol: GCKR
GCKR
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.110 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016