potassium voltage-gated channel subfamily E regulatory subunit 1

Preferred Label : potassium voltage-gated channel subfamily E regulatory subunit 1;

Approved symbol HGNC : KCNE1;

Name synonyms HGNC : Jervell and Lange-Nielsen syndrome 2; Long QT syndrome 5;

Alias symbols HGNC : IsK; LQT5; minK; JLNS2;

Chromosome HGNC : 21q22.12;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000180509;

Details

Origin ID

HGNC:6240;

UMLS CUI

C1416563;

Automatic exact mappings (from CISMeF team)
- Jervell and lange-nielsen syndrome 2 [OMIM Phenotype]
- Long QT Syndrome 5 [NCIt concept]
- Long qt syndrome 5 [OMIM Phenotype]
- Potassium channel, voltage-gated, isk-related subfamily, member 1 [OMIM gene]
- jervell and Lange-Nielsen syndrome 2 [MeSH concept]
- jervell and Lange-Nielsen syndrome 2 [MeSH Supplementary Concept]
- long QT syndrome 5 [DO Concept]
- long qt syndrome 5 [MeSH Supplementary Concept]
- long qt syndrome 5 [MeSH concept]
- potassium voltage-gated channel subfamily E regulatory subunit 1 [ORDO Gene]
NCIt concept
- KCNE1 Gene [NCIt concept]
OMIM gene
- Potassium channel, voltage-gated, isk-related subfamily, member 1 [OMIM gene]
Orphanet gene
- potassium voltage-gated channel subfamily E regulatory subunit 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Potassium channel, voltage-gated, isk-related subfamily, member 1 [OMIM gene]

Keyword's position in hierarchy(ies) :

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