Right Ventricular Failure Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Reduced ability of the right ventricle to perform its function (to receive blood from the right atrium and to eject blood into the pulmonary artery), often leading top pitting peripheral edema, ascites, and hepatomegaly. (Human Phenotype Ontology, HP_0001708)
External Link https://www.disgenet.org/browser/0/1/0/C2939447
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Genes

25 genes associated with the disease Right Ventricular Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADAMTS8 ADAM metallopeptidase with thrombospondin type 1 motif, 8
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
ATM ATM serine/threonine kinase
ATRX alpha thalassemia/mental retardation syndrome X-linked
BMPR2 bone morphogenetic protein receptor, type II (serine/threonine kinase)
CCR3 chemokine (C-C motif) receptor 3
CCR8 chemokine (C-C motif) receptor 8
CRP C-reactive protein, pentraxin-related
CXCR4 chemokine (C-X-C motif) receptor 4
DAXX death-domain associated protein
HTR2B 5-hydroxytryptamine (serotonin) receptor 2B, G protein-coupled
IGF1 insulin-like growth factor 1 (somatomedin C)
MAP4 microtubule-associated protein 4
MME membrane metallo-endopeptidase
MYH7 myosin, heavy chain 7, cardiac muscle, beta
POSTN periostin, osteoblast specific factor
PPARG peroxisome proliferator-activated receptor gamma
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SELENON selenoprotein N
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1
TNF tumor necrosis factor
TTN titin
WIPI1 WD repeat domain, phosphoinositide interacting 1