purpura Gene Set
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
|
