potassium voltage-gated channel subfamily Q member 1

Preferred Label : potassium voltage-gated channel subfamily Q member 1;

Approved symbol HGNC : KCNQ1;

Name synonyms HGNC : Jervell and Lange-Nielsen syndrome 1;

Alias symbols HGNC : LQT1; KVLQT1; Kv7.1; JLNS1; KCNA8;

Chromosome HGNC : 11p15.5-p15.4;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000053918;

Details

Origin ID

HGNC:6294;

UMLS CUI

C1416612;

Automatic exact mappings (from CISMeF team)
- Jervell and lange-nielsen syndrome 1 [OMIM Phenotype]
- Jervell-Lange nielsen syndrome [MeSH Descriptor]
- Long qt syndrome 1 [OMIM Phenotype]
- Potassium channel, voltage-gated, kqt-like subfamily, member 1 [OMIM gene]
- potassium voltage-gated channel subfamily Q member 1 [ORDO Gene]
NCIt concept
- KCNQ1 Gene [NCIt concept]
OMIM gene
- Potassium channel, voltage-gated, kqt-like subfamily, member 1 [OMIM gene]
Orphanet gene
- potassium voltage-gated channel subfamily Q member 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KCNQ1 Gene [NCIt concept]
- KCNQ1 gene [LOINC component]
- Potassium channel, voltage-gated, kqt-like subfamily, member 1 [OMIM gene]

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