Idiopathic Epilepsy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group neurological (Genetic Association Database)
External Link https://www.disgenet.org/browser/0/1/0/C0391957
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Genes

28 genes associated with the disease Idiopathic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAM23 ADAM metallopeptidase domain 23
BRD2 bromodomain containing 2
CASR calcium-sensing receptor
CHRNA4 cholinergic receptor, nicotinic, alpha 4 (neuronal)
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
CLCN1 chloride channel, voltage-sensitive 1
CLCN2 chloride channel, voltage-sensitive 2
EFHC1 EF-hand domain (C-terminal) containing 1
ENO2 enolase 2 (gamma, neuronal)
EPO erythropoietin
GABRG3 gamma-aminobutyric acid (GABA) A receptor, gamma 3
HCN1 hyperpolarization activated cyclic nucleotide gated potassium channel 1
IL1B interleukin 1, beta
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
LGI1 leucine-rich, glioma inactivated 1
RARRES2 retinoic acid receptor responder (tazarotene induced) 2
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1
RBFOX3 RNA binding protein, fox-1 homolog (C. elegans) 3
SCN1A sodium channel, voltage gated, type I alpha subunit
SCN2B sodium channel, voltage gated, type II beta subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SYN1 synapsin I
SYN2 synapsin II
SYNGAP1 synaptic Ras GTPase activating protein 1
TRIM39 tripartite motif containing 39
VCP valosin containing protein