Potassium channel, inwardly rectifying, subfamily j, member 5

Preferred Label : Potassium channel, inwardly rectifying, subfamily j, member 5;

Symbol : KCNJ5;

CISMeF acronym : KCNJ5;

Type : Gene;

Alternative titles and symbols : Cardiac inward rectifier; G protein-activated inwardly rectifying potassium channel 4; Inwardly rectifying potassium channel kir3.4; CIR; GIRK4; KATP1;

Ensembl ID : ENSG00000120457;

Prefixed ID : *600734;

Détails

Origin ID

600734;

UMLS CUI

C1416587;

Automatic exact mappings (from CISMeF team)
- G Protein-Activated Inward Rectifier Potassium Channel 4 [NCIt concept]
- KCNJ5 Gene [NCIt concept]
- KCNJ5 wt Allele [NCIt concept]
- potassium inwardly rectifying channel subfamily J member 5 [ORDO Gene]
- potassium inwardly rectifying channel subfamily J member 5 [HGNC gene]
HGNC gene
- potassium inwardly rectifying channel subfamily J member 5 [HGNC gene]
NCIt concept(s)
- G Protein-Activated Inward Rectifier Potassium Channel 4 [NCIt concept]
- KCNJ5 Gene [NCIt concept]
- KCNJ5 wt Allele [NCIt concept]
ORDO concept(s)
- potassium inwardly rectifying channel subfamily J member 5 [ORDO Gene]
Phenotypes related
- Hyperaldosteronism, familial, type III [OMIM Phenotype]
- Long qt syndrome 13 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KCNJ5 Gene [NCIt concept]
- potassium inwardly rectifying channel subfamily J member 5 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients