Wolff-Parkinson-White Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A disorder of the cardiac conduction system of the heart characterized by ventricular preexcitation due to the presence of an abnormal accessory atrioventricular electrical conduction pathway. (Human Phenotype Ontology, HP_0001716)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D014927
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6 genes/proteins associated with the disease Wolff-Parkinson-White Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit 2.88009
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4 1.507
SLC22A1 solute carrier family 22 (organic cation transporter), member 1 1.28765
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2 1.15122
CASP7 caspase 7, apoptosis-related cysteine peptidase 1.08372
ADRB1 adrenoceptor beta 1 1.04465