" /> KCND3 wt Allele - CISMeF





Preferred Label : KCND3 wt Allele;

NCIt synonyms : Sha1-Related Potassium Channel Kv4.3 Gene; Potassium Ionic Channel Kv4.3 Gene; KV4.3; SCA22; Spinocerebellar Ataxia 19 Gene; Potassium Voltage-Gated Channel, Shal-Related Subfamily, Member 3 Gene; BRGDA9; KCND3L; Potassium Channel, Voltage Gated Shal Related Subfamily D, Member 3 Gene; KCND3S; KSHIVB; Potassium Voltage-Gated Channel, Shal-Related Subfamily D, Member 3 Gene; SCA19; Potassium Voltage-Gated Channel Long Gene; Spinocerebellar Ataxia 22 Gene; Potassium Voltage-Gated Channel Subfamily D Member 3 wt Allele;

NCIt definition : Human KCND3 wild-type allele is located in the vicinity of 1p13.2 and is approximately 219 kb in length. This allele, which encodes potassium voltage-gated channel subfamily D member 3 protein, is involved in regulation of the outward potassium current in excitable cells. Mutation of the gene is associated with Brugada syndrome 9 and spinocerebellar ataxia 19 (SCA19, SCA22).;

GenBank Accession Number : AF048713;

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19/05/2024


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