Potassium channel, voltage-gated, kqt-like subfamily, member 1

Preferred Label : Potassium channel, voltage-gated, kqt-like subfamily, member 1;

Symbol : KCNQ1;

CISMeF acronym : KCNQ1;

Type : Gene;

Alternative titles and symbols : Potassium channel, voltage-gated, shaker-related subfamily, member 9; KVLQT1; KCNA9; KCNA8;

Ensembl ID : ENSG00000053918;

Prefixed ID : *607542;

Détails

Origin ID

607542;

UMLS CUI

C1416612;

Automatic exact mappings (from CISMeF team)
- KCNQ1 Gene [NCIt concept]
- KCNQ1 gene [LOINC component]
- KCNQ1 wt Allele [NCIt concept]
- Potassium Voltage-Gated Channel Subfamily KQT Member 1 [NCIt concept]
- potassium voltage-gated channel subfamily Q member 1 [ORDO Gene]
- potassium voltage-gated channel subfamily Q member 1 [HGNC gene]
HGNC gene
- potassium voltage-gated channel subfamily Q member 1 [HGNC gene]
NCIt concept(s)
- KCNQ1 Gene [NCIt concept]
- KCNQ1 wt Allele [NCIt concept]
- Potassium Voltage-Gated Channel Subfamily KQT Member 1 [NCIt concept]
ORDO concept(s)
- potassium voltage-gated channel subfamily Q member 1 [ORDO Gene]
Phenotypes related
- Atrial fibrillation, familial, 3 [OMIM Phenotype]
- Jervell and lange-nielsen syndrome 1 [OMIM Phenotype]
- Long qt syndrome 1 [OMIM Phenotype]
- Short qt syndrome 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KCNQ1 Gene [NCIt concept]
- KCNQ1 gene [LOINC component]
- potassium voltage-gated channel subfamily Q member 1 [HGNC gene]

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