Potassium channel, voltage-gated, kqt-like subfamily, member 2

Preferred Label : Potassium channel, voltage-gated, kqt-like subfamily, member 2;

Symbol : KCNQ2;

CISMeF acronym : KCNQ2;

Type : Gene;

Alternative titles and symbols : Potassium channel, voltage-gated, subfamily q, member 2;

Ensembl ID : ENSG00000075043;

Prefixed ID : *602235;

Details

Origin ID

602235;

UMLS CUI

C1416614;

Automatic exact mappings (from CISMeF team)
- KCNQ2 gene [LOINC component]
- potassium voltage-gated channel subfamily Q member 2 [ORDO Gene]
- potassium voltage-gated channel subfamily Q member 2 [HGNC gene]
HGNC gene
- potassium voltage-gated channel subfamily Q member 2 [HGNC gene]
NCIt concept(s)
- KCNQ2 Gene [NCIt concept]
- KCNQ2 wt Allele [NCIt concept]
- Potassium Voltage-Gated Channel Subfamily KQT Member 2 [NCIt concept]
ORDO concept(s)
- potassium voltage-gated channel subfamily Q member 2 [ORDO Gene]
Phenotypes related
- Developmental and epileptic encephalopathy 7 [OMIM Phenotype]
- Seizures, benign familial neonatal, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KCNQ2 Gene [NCIt concept]
- KCNQ2 gene [LOINC component]
- potassium voltage-gated channel subfamily Q member 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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