Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57582
Gene Symbol: KCNT1
KCNT1 		0.300 Biomarker disease CTD_human Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy. 23086396 2012
Entrez Id: 57282
Gene Symbol: SLC4A10
SLC4A10 		0.300 Biomarker disease CTD_human Disruption of sodium bicarbonate transporter SLC4A10 in a patient with complex partial epilepsy and mental retardation. 18413482 2008
Entrez Id: 1137
Gene Symbol: CHRNA4
CHRNA4 		0.300 Biomarker disease CTD_human Nicotine-induced dystonic arousal complex in a mouse line harboring a human autosomal-dominant nocturnal frontal lobe epilepsy mutation. 17881519 2007
Entrez Id: 1137
Gene Symbol: CHRNA4
CHRNA4 		0.300 Biomarker disease CTD_human Mice lacking neuronal nicotinic acetylcholine receptor beta4-subunit and mice lacking both alpha5- and beta4-subunits are highly resistant to nicotine-induced seizures. 14996991 2004
Entrez Id: 1141
Gene Symbol: CHRNB2
CHRNB2 		0.300 Biomarker disease CTD_human Mice lacking neuronal nicotinic acetylcholine receptor beta4-subunit and mice lacking both alpha5- and beta4-subunits are highly resistant to nicotine-induced seizures. 14996991 2004
Entrez Id: 1137
Gene Symbol: CHRNA4
CHRNA4 		0.300 Biomarker disease CTD_human A new Chrna4 mutation with low penetrance in nocturnal frontal lobe epilepsy. 12823585 2003