Familial Epilepsies Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0391958
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Genes

15 genes associated with the disease Familial Epilepsies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAM22 ADAM metallopeptidase domain 22
ALDH7A1 aldehyde dehydrogenase 7 family, member A1
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CHRNA4 cholinergic receptor, nicotinic, alpha 4 (neuronal)
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
CLCN2 chloride channel, voltage-sensitive 2
FIG4 FIG4 phosphoinositide 5-phosphatase
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
LGI1 leucine-rich, glioma inactivated 1
PCDH19 protocadherin 19
PRRT2 proline-rich transmembrane protein 2
RORB RAR-related orphan receptor B
SCN1A sodium channel, voltage gated, type I alpha subunit
SCN1B sodium channel, voltage gated, type I beta subunit