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 		0.300 Biomarker disease CTD_human Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy. 23086396 2012