KCNT1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human KCNT1 wild-type allele is located in the vicinity of 9q34.3 and is approximately 93 kb in length. This allele, which encodes potassium channel subfamily T member 1 protein, is involved in ion conductance and developmental signaling. Mutation of the gene is associated with developmental and epileptic encephalopathy 14 and nocturnal frontal lobe epilepsy 5.

**Synonyms:** - DEE14 - EIEE14 - ENFL5 - KCa4.1 - KIAA1422 - Potassium Channel, Sodium Activated Subfamily T, Member 1 Gene - Potassium Channel, Subfamily T, Member 1 Gene - Potassium Sodium-Activated Channel Subfamily T Member 1 wt Allele - SLACK - Sequence Like A Calcium-Activated K+ Channel Gene - Slo2.2 - bA100C15.2