Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2645
Gene Symbol: GCK
GCK
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.200 GeneticVariation LHGDN Permanent neonatal diabetes mellitus caused by a novel homozygous (T168A) glucokinase (GCK) mutation: initial response to oral sulphonylurea therapy. 18571549

2008
Entrez Id: 2645
Gene Symbol: GCK
GCK
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.200 GeneticVariation LHGDN Four novel mutations, including the first gross deletion in TCF1, identified in HNF-4alpha, GCK and TCF1 in patients with MODY in Israel. 17937063

2007