Potassium channel, inwardly rectifying, subfamily j, member 1

Preferred Label : Potassium channel, inwardly rectifying, subfamily j, member 1;

Symbol : KCNJ1;

CISMeF acronym : KCNJ1;

Type : Gene;

Alternative titles and symbols : Renal outer-medullary potassium channel; ROMK; ROMK1; KIR1.1;

Ensembl ID : ENSG00000151704;

Prefixed ID : *600359;

Details

Origin ID

600359;

UMLS CUI

C1416576;

Automatic exact mappings (from CISMeF team)
- potassium inwardly rectifying channel subfamily J member 1 [ORDO Gene]
- potassium inwardly rectifying channel subfamily J member 1 [HGNC gene]
HGNC gene
- potassium inwardly rectifying channel subfamily J member 1 [HGNC gene]
ORDO concept(s)
- potassium inwardly rectifying channel subfamily J member 1 [ORDO Gene]
Phenotypes related
- Bartter syndrome, type 2, antenatal [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- potassium inwardly rectifying channel subfamily J member 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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