Potassium channel, calcium-activated, intermediate/small conductance, subfamily n, member 2

Preferred Label : Potassium channel, calcium-activated, intermediate/small conductance, subfamily n, member 2;

Symbol : KCNN2;

CISMeF acronym : KCNN2;

Type : Gene;

Alternative titles and symbols : SK2;

Ensembl ID : ENSG00000080709;

Prefixed ID : *605879;

Details

Origin ID

605879;

UMLS CUI

C1416609;

Automatic exact mappings (from CISMeF team)
- SPHK2 wt Allele [NCIt concept]
- potassium calcium-activated channel subfamily N member 2 [HGNC gene]
HGNC gene
- potassium calcium-activated channel subfamily N member 2 [HGNC gene]
Phenotypes related
- Dystonia 34, myoclonic [OMIM Phenotype]
- Neurodevelopmental disorder with or without variable movement or behavioral abnormalities [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- potassium calcium-activated channel subfamily N member 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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