Potassium channel, voltage-gated, subfamily V, member 2

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

Symbol : KCNV2;

CISMeF acronym : KCNV2;

Type : Gene;

Alternative titles and symbols : KV8.2;

Ensembl ID : ENSG00000168263;

Prefixed ID : *607604;

Details

Origin ID

607604;

UMLS CUI

C1426343;

Automatic exact mappings (from CISMeF team)
- potassium voltage-gated channel modifier subfamily V member 2 [ORDO Gene]
- potassium voltage-gated channel modifier subfamily V member 2 [HGNC gene]
HGNC gene
- potassium voltage-gated channel modifier subfamily V member 2 [HGNC gene]
NCIt concept(s)
- KCNV2 Gene [NCIt concept]
- KCNV2 wt Allele [NCIt concept]
- Potassium Voltage-Gated Channel Subfamily V Member 2 [NCIt concept]
ORDO concept(s)
- potassium voltage-gated channel modifier subfamily V member 2 [ORDO Gene]
Phenotypes related
- Retinal cone dystrophy 3b [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- potassium voltage-gated channel modifier subfamily V member 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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