KCNQ1 wt Allele

Cancer Terms -> Gene -> Ion Channel Protein Gene -> KCNQ1 Gene -> KCNQ1 wt Allele

KCNQ1 wt Allele Definition

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.

KCNQ1 wt Allele Synonyms

KCNQ1 wt Allele, ATFB1, FLJ26167, JLNS1, KCNA8, KCNA9, KVLQT1, Kv1.9, Kv7.1, LQT, LQT1, Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 wt Allele, RWS, SQT2, WRS

Terms in KCNQ1 wt Allele category

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