febrile seizures Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002373
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Genes

14 genes associated with the febrile seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADGRV1 adhesion G protein-coupled receptor V1
AUH AU RNA binding protein/enoyl-CoA hydratase
CHD2 chromodomain helicase DNA binding protein 2
CPA6 carboxypeptidase A6
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
HCN1 hyperpolarization activated cyclic nucleotide gated potassium channel 1
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
MBD5 methyl-CpG binding domain protein 5
SCN1A sodium channel, voltage gated, type I alpha subunit
SCN1B sodium channel, voltage gated, type I beta subunit
SCN9A sodium channel, voltage gated, type IX alpha subunit
TBC1D24 TBC1 domain family, member 24