Preferred Label : KCNE1 wt Allele;
NCIt synonyms : Minimal Potassium Ion Channel Gene; Long QT Syndrome 5 Gene; Potassium Voltage-Gated Channel, Isk-Related Family, Member 1 Gene; Minimal Potassium Channel Gene; IsK; Potassium Voltage-Gated Channel Subfamily E Regulatory Subunit 1 wt Allele; JLNS; Cardiac Delayed Rectifier Potassium Channel Protein Gene; LQT2/5; Potassium Voltage-Gated Channel, Isk-Related Subfamily, Member 1 Gene; JLNS2; Voltage Gated Potassiun Channel Accessory Subunit Gene; Jervell and Lange-Nielsen Syndrome 2 Gene; Potassium Channel, Voltage-Gated, Isk-Related, Subfamily, Member 1 Gene; Potassium Channel, Voltage Gated Subfamily E Regulatory Beta Subunit 1 Gene; MinK; LQT5;
NCIt definition : Human KCNE1 wild-type allele is located in the vicinity of 21q22.12 and is approximately
66 kb in length. This allele, which encodes potassium voltage-gated channel subfamily
E member 1 protein, plays a role in mediating the slow deactivation of the delayed
rectifying potassium channel. Mutation of the gene is associated with Jervell and
Lange-Nielsen syndrome 2 and long QT syndrome 5.;
NCI Metathesaurus CUI : CL1921900;
GenBank Accession Number : L28168;
Origin ID : C202628;
UMLS CUI : C5891012;
OMIM relation
- Semantic type(s)
- gene_found_in_organism
- gene_plays_role_in_process
