thrombocytopenia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A blood platelet disease characterized by low a platelet count in the blood. (Human Disease Ontology, DOID_1588)
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Genes

18 genes associated with the disease thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CYCS cytochrome c, somatic
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
FCGR3A Fc fragment of IgG, low affinity IIIa, receptor (CD16a)
GP1BA glycoprotein Ib (platelet), alpha polypeptide
GP1BB glycoprotein Ib (platelet), beta polypeptide
GP5 glycoprotein V (platelet)
GP9 glycoprotein IX (platelet)
HLA-DRB3 major histocompatibility complex, class II, DR beta 3
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MYH9 myosin, heavy chain 9, non-muscle
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)