Left Ventricular Systolic Dysfunction Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1277187
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Genes

41 genes associated with the disease Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADRB1 adrenoceptor beta 1
AGER advanced glycosylation end product-specific receptor
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
AMPD1 adenosine monophosphate deaminase 1
APOE apolipoprotein E
ATP7B ATPase, Cu++ transporting, beta polypeptide
BGLAP bone gamma-carboxyglutamate (gla) protein
CAT catalase
CCL3 chemokine (C-C motif) ligand 3
CCL4 chemokine (C-C motif) ligand 4
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
CRP C-reactive protein, pentraxin-related
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DMD dystrophin
DPP4 dipeptidyl-peptidase 4
FGF21 fibroblast growth factor 21
GH1 growth hormone 1
GSR glutathione reductase
HLA-G major histocompatibility complex, class I, G
IL1B interleukin 1, beta
IL1RN interleukin 1 receptor antagonist
IL33 interleukin 33
IL6 interleukin 6
INS insulin
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
LGALS3 lectin, galactoside-binding, soluble, 3
LMNA lamin A/C
LPA lipoprotein, Lp(a)
MAPKAPK5 mitogen-activated protein kinase-activated protein kinase 5
MYBPC3 myosin binding protein C, cardiac
NR3C2 nuclear receptor subfamily 3, group C, member 2
POMT2 protein-O-mannosyltransferase 2
PPP1R2P9 protein phosphatase 1, regulatory (inhibitor) subunit 2 pseudogene 9
REN renin
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
SULT1E1 sulfotransferase family 1E, estrogen-preferring, member 1
SYNM synemin, intermediate filament protein
TNF tumor necrosis factor
TNNI3 troponin I type 3 (cardiac)