arterial thrombosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The formation of a blood clot inside an artery. (Human Phenotype Ontology, HP_0004420)
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22 genes associated with the arterial thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
C4A complement component 4A (Rodgers blood group)
CALR calreticulin
CBS cystathionine-beta-synthase
HLA-B major histocompatibility complex, class I, B
IL10 interleukin 10
IL12RB2 interleukin 12 receptor, beta 2
IL23R interleukin 23 receptor
JAK2 Janus kinase 2
MEFV Mediterranean fever
MPL MPL proto-oncogene, thrombopoietin receptor
MYH7 myosin, heavy chain 7, cardiac muscle, beta
NOD2 nucleotide-binding oligomerization domain containing 2
PROS1 protein S (alpha)
PTEN phosphatase and tensin homolog
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SH2B3 SH2B adaptor protein 3
STAT4 signal transducer and activator of transcription 4
TET2 tet methylcytosine dioxygenase 2
THPO thrombopoietin
TLR4 toll-like receptor 4
TP53 tumor protein p53