Primary Antiphospholipid Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0409980
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Genes

29 genes associated with the disease Primary Antiphospholipid Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ANXA5 annexin A5
APOH apolipoprotein H (beta-2-glycoprotein I)
CFH complement factor H
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HMGB1 high mobility group box 1
IFNA1 interferon, alpha 1
IFNA13 interferon, alpha 13
IFNL1 interferon, lambda 1
IL10 interleukin 10
IL17A interleukin 17A
IL23A interleukin 23, alpha subunit p19
IL37 interleukin 37
IRF5 interferon regulatory factor 5
KLK3 kallikrein-related peptidase 3
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
P2RX7 purinergic receptor P2X, ligand gated ion channel, 7
PROC protein C (inactivator of coagulation factors Va and VIIIa)
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
RBM45 RNA binding motif protein 45
S100A10 S100 calcium binding protein A10
SH2B2 SH2B adaptor protein 2
SKAP2 src kinase associated phosphoprotein 2
STING1 stimulator of interferon response cGAMP interactor 1
TNF tumor necrosis factor