abnormality of the common coagulation pathway Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of blood coagulation, common pathway. (Human Phenotype Ontology, HP_0010990)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010990
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Genes

17 genes associated with the abnormality of the common coagulation pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANO6 anoctamin 6
F10 coagulation factor X
F13A1 coagulation factor XIII, A1 polypeptide
F13B coagulation factor XIII, B polypeptide
F5 coagulation factor V (proaccelerin, labile factor)
FGA fibrinogen alpha chain
FGB fibrinogen beta chain
FGG fibrinogen gamma chain
GGCX gamma-glutamyl carboxylase
LMAN1 lectin, mannose-binding, 1
MCFD2 multiple coagulation factor deficiency 2
PRF1 perforin 1 (pore forming protein)
PTPN11 protein tyrosine phosphatase, non-receptor type 11
STX11 syntaxin 11
UNC13D unc-13 homolog D (C. elegans)
VKORC1 vitamin K epoxide reductase complex, subunit 1
XIAP X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase