KCNQ1 wt Allele

Human KCNQ1 wild-type allele is located in the vicinity of 11p15.5 and is approximately 404 kb in length. This allele, which encodes potassium voltage-gated channel subfamily KQT member 1 protein, plays a role in the regulation of both cardiac repolarization and potassium transport. Mutations in the gene are associated with hereditary long QT syndrome, Romano-Ward syndrome, Jervell and Lange-Nielsen syndrome and familial atrial fibrillation. (NCI Thesaurus)

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KCNQ1 Gene

This gene is involved in both potassium transport and cardiac repolarization.

KCNMA1 wt Allele

Human KCNMA1 wild-type allele is located in the vicinity of 10q22.3 and is approximately 769 kb in length. This allele, which encodes…

KCNMA1 Gene

This gene plays a role in potassium transport.

KCNK18 wt Allele

Human KCNK18 wild-type allele is located in the vicinity of 10q25.3 and is approximately 13 kb in length. This allele, which encodes…

KCNK18 Gene

This gene is involved in ion transport.

KCNJ5 wt Allele

Human KCNJ5 wild-type allele is located in the vicinity of 11q24 and is approximately 27 kb in length. This allele, which encodes…