chest pain Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the chest. (Human Phenotype Ontology, HP_0100749)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100749
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Genes

24 genes associated with the chest pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APC adenomatous polyposis coli
CALR calreticulin
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
HLA-B major histocompatibility complex, class I, B
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
IL12B interleukin 12B
JAK2 Janus kinase 2
MEFV Mediterranean fever
MLX MLX, MAX dimerization protein
MPL MPL proto-oncogene, thrombopoietin receptor
MYH7 myosin, heavy chain 7, cardiac muscle, beta
PRTN3 proteinase 3
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SCN4A sodium channel, voltage gated, type IV alpha subunit
SH2B3 SH2B adaptor protein 3
TET2 tet methylcytosine dioxygenase 2
THPO thrombopoietin
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
TP53 tumor protein p53
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1