Endocarditis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A heart disease involving non-infectious inflammation of the endocardium (inner layer of the heart).|Inflammation of the inner lining of the heart (ENDOCARDIUM), the continuous membrane lining the four chambers and HEART VALVES. It is often caused by microorganisms including bacteria, viruses, fungi, and rickettsiae. Left untreated, endocarditis can damage heart valves and become life-threatening.|Inflammation of the endocardium. (Experimental Factor Ontology, EFO_0000465)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D004696
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Genes

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

Symbol Name Standardized Value
IL10 interleukin 10 1.26794
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) 1.23392
VEGFA vascular endothelial growth factor A 1.19999
MPO myeloperoxidase 1.18652
SLC22A6 solute carrier family 22 (organic anion transporter), member 6 1.13211
CES2 carboxylesterase 2 1.12117
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1 1.11911
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9 1.11431
CAT catalase 1.09611
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.06952
FAS Fas cell surface death receptor 1.04427
CD74 CD74 molecule, major histocompatibility complex, class II invariant chain 1.01174