febrile seizures Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Febrile seizures are convulsions induced by a fever in infants or small children and are generally characterized by loss of consciousness and tonic-clonic movements. Most febrile seizures last a minute or two. (Human Phenotype Ontology, HP_0002373)
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Genes

8 genes associated with the disease febrile seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
CNR1	cannabinoid receptor 1 (brain)
GABRG2	gamma-aminobutyric acid (GABA) A receptor, gamma 2
GJA1	gap junction protein, alpha 1, 43kDa
IL1B	interleukin 1, beta
SCN2A	sodium channel, voltage gated, type II alpha subunit
SLC4A3	solute carrier family 4 (anion exchanger), member 3
SLC9A1	solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
SLC9A3	solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3