Seizures Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Seizures are an intermittent abnormality of the central nervous system due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements. The term epilepsy is used to describe chronic, recurrent seizures. (Human Phenotype Ontology, HP_0001250)
External Link https://www.disgenet.org/browser/0/1/0/C1843140
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Genes

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

Symbol Name
CHRNA2 cholinergic receptor, nicotinic, alpha 2 (neuronal)
DIAPH1 diaphanous-related formin 1
EXT2 exostosin glycosyltransferase 2
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
MT-ATP6 ATP synthase F0 subunit 6
PRRT2 proline-rich transmembrane protein 2
SCN2A sodium channel, voltage gated, type II alpha subunit
SCN8A sodium channel, voltage gated, type VIII alpha subunit