purpura Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000979
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Genes

17 genes associated with the purpura phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACP5 acid phosphatase 5, tartrate resistant
AIP aryl hydrocarbon receptor interacting protein
C2 complement component 2
C4A complement component 4A (Rodgers blood group)
CD81 CD81 molecule
CECR1 cat eye syndrome chromosome region, candidate 1
GBA glucosidase, beta, acid
GP1BA glycoprotein Ib (platelet), alpha polypeptide
GP1BB glycoprotein Ib (platelet), beta polypeptide
GP9 glycoprotein IX (platelet)
HOXA11 homeobox A11
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
PROC protein C (inactivator of coagulation factors Va and VIIIa)
PROS1 protein S (alpha)
TREX1 three prime repair exonuclease 1
WAS Wiskott-Aldrich syndrome