Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2677
Gene Symbol: GGCX
GGCX
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders 		0.320 GeneticVariation BEFREE Here we report the identification and characterization of novel GGCX mutations in a patient with both severe cerebral bleeding disorder and comorbid Keutel syndrome, a nonbleeding malady caused by functional defects of matrix γ-carboxyglutamate protein (MGP). 26758921

2016
Entrez Id: 2677
Gene Symbol: GGCX
GGCX
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders 		0.320 Biomarker CTD_human Familial deficiency of vitamin K-dependent clotting factors. 19141161

2008
Entrez Id: 2677
Gene Symbol: GGCX
GGCX
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders 		0.320 GeneticVariation BEFREE Patients with mutation L394R in gamma-glutamyl carboxylase have a severe bleeding disorder because of decreased biological activities of all vitamin K-dependent coagulation proteins. 10934213

2000