potassium inwardly rectifying channel subfamily J member 18

Preferred Label : potassium inwardly rectifying channel subfamily J member 18;

Approved symbol HGNC : KCNJ18;

Alias symbols HGNC : KIR2.6; TTPP2;

Chromosome HGNC : 17p11.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000260458;

Details

Origin ID

HGNC:39080;

UMLS CUI

C2750476;

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

Keyword's position in hierarchy(ies) :

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