Gene: KCNT1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57582
Gene Symbol: KCNT1
KCNT1 		0.310 GeneticVariation disease BEFREE After extensive workup, seizure panel testing revealed KCNT1 gene mutation, which is associated with nocturnal frontal lobe epilepsy and epilepsy of infancy with migrating focal seizures. 31653631 2019
Entrez Id: 57582
Gene Symbol: KCNT1
KCNT1 		0.310 Biomarker disease CTD_human Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy. 23086396 2012