Potassium channel, inwardly rectifying, subfamily j, member 2

Preferred Label : Potassium channel, inwardly rectifying, subfamily j, member 2;

Symbol : KCNJ2;

CISMeF acronym : KCNJ2;

Type : Gene;

Alternative titles and symbols : HHIRK1; IRK1; KIR2.1;

Ensembl ID : ENSG00000123700;

Prefixed ID : *600681;

Details

Origin ID

600681;

UMLS CUI

C1416584;

Automatic exact mappings (from CISMeF team)
- potassium inwardly rectifying channel subfamily J member 2 [ORDO Gene]
- potassium inwardly rectifying channel subfamily J member 2 [HGNC gene]
HGNC gene
- potassium inwardly rectifying channel subfamily J member 2 [HGNC gene]
NCIt concept(s)
- Inward Rectifier Potassium Channel 2 [NCIt concept]
- KCNJ2 Gene [NCIt concept]
- KCNJ2 wt Allele [NCIt concept]
ORDO concept(s)
- potassium inwardly rectifying channel subfamily J member 2 [ORDO Gene]
Phenotypes related
- Andersen cardiodysrhythmic periodic paralysis [OMIM Phenotype]
- Atrial fibrillation, familial, 9 [OMIM Phenotype]
- Short qt syndrome 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- potassium inwardly rectifying channel subfamily J member 2 [HGNC gene]

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