Dyspnea, Paroxysmal Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0013405
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Genes

16 genes associated with the disease Dyspnea, Paroxysmal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTA2 actin, alpha 2, smooth muscle, aorta
ELN elastin
FBN1 fibrillin 1
FOXE3 forkhead box E3
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1
LOX lysyl oxidase
MAT2A methionine adenosyltransferase II, alpha
MFAP5 microfibrillar associated protein 5
MYH11 myosin, heavy chain 11, smooth muscle
MYLK myosin light chain kinase
PRKG1 protein kinase, cGMP-dependent, type I
SMAD3 SMAD family member 3
TGFB2 transforming growth factor, beta 2
TGFB3 transforming growth factor, beta 3
TGFBR1 transforming growth factor, beta receptor 1
TGFBR2 transforming growth factor, beta receptor II (70/80kDa)