abnormality of vitamin k metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Vitamin K is a fat-soluble vitamin with a role in promoting the coagulation cascade. (Human Phenotype Ontology, HP_0100831)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100831
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Genes

3 genes associated with the abnormality of vitamin k metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BAAT bile acid CoA:amino acid N-acyltransferase
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
TJP2 tight junction protein 2