Potassium channel, inwardly rectifying, subfamily j, member 18

Preferred Label : Potassium channel, inwardly rectifying, subfamily j, member 18;

Symbol : KCNJ18;

CISMeF acronym : KCNJ18;

Type : Gene;

Alternative titles and symbols : KIR2.6;

Ensembl ID : ENSG00000260458;

Prefixed ID : *613236;

Details

Origin ID

613236;

UMLS CUI

C2750476;

Automatic exact mappings (from CISMeF team)
- potassium inwardly rectifying channel subfamily J member 18 [ORDO Gene]
- potassium inwardly rectifying channel subfamily J member 18 [HGNC gene]
HGNC gene
- potassium inwardly rectifying channel subfamily J member 18 [HGNC gene]
NCIt concept(s)
- Inward Rectifier Potassium Channel 18 [NCIt concept]
- KCNJ18 Gene [NCIt concept]
- KCNJ18 wt Allele [NCIt concept]
ORDO concept(s)
- potassium inwardly rectifying channel subfamily J member 18 [ORDO Gene]
Phenotypes related
- Thyrotoxic periodic paralysis, susceptibility to, 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- potassium inwardly rectifying channel subfamily J member 18 [HGNC gene]

Keyword's position in hierarchy(ies) :

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