Vitamin K Deficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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5 genes associated with the Vitamin K Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
F7 coagulation factor VII (serum prothrombin conversion accelerator)
GGCX gamma-glutamyl carboxylase
VKORC1 vitamin K epoxide reductase complex, subunit 1