Coronary Occlusion Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D054059
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Genes

12 genes/proteins associated with the disease Coronary Occlusion from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa 1.27595
FOS FBJ murine osteosarcoma viral oncogene homolog 1.23296
FAS Fas cell surface death receptor 1.22884
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.18326
CRP C-reactive protein, pentraxin-related 1.17366
MAP2K1 mitogen-activated protein kinase kinase 1 1.17235
FGF2 fibroblast growth factor 2 (basic) 1.15695
PRKCE protein kinase C, epsilon 1.04904
MAOB monoamine oxidase B 1.04831
NPY neuropeptide Y 1.02634
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8) 1.02596
CAT catalase 1.01776