Potassium channel, inwardly rectifying, subfamily j, member 11

Preferred Label : Potassium channel, inwardly rectifying, subfamily j, member 11;

Symbol : KCNJ11;

CISMeF acronym : KCNJ11;

Type : Gene;

Alternative titles and symbols : Potassium channel, inwardly rectifying, bir subunit; Beta-cell inward rectifier subunit; Inwardly rectifying potassium channel kir6.2; BIR;

Ensembl ID : ENSG00000187486;

Prefixed ID : *600937;

Details

Origin ID

600937;

UMLS CUI

C1416578;

Automatic exact mappings (from CISMeF team)
- Break-Induced Replication [NCIt concept]
- KCNJ11 gene [LOINC component]
- potassium inwardly rectifying channel subfamily J member 11 [ORDO Gene]
- potassium inwardly rectifying channel subfamily J member 11 [HGNC gene]
HGNC gene
- potassium inwardly rectifying channel subfamily J member 11 [HGNC gene]
NCIt concept(s)
- ATP-Sensitive Inward Rectifier Potassium Channel 11 [NCIt concept]
- KCNJ11 Gene [NCIt concept]
- KCNJ11 wt Allele [NCIt concept]
ORDO concept(s)
- potassium inwardly rectifying channel subfamily J member 11 [ORDO Gene]
Phenotypes related
- Diabetes mellitus, permanent neonatal, 2 [OMIM Phenotype]
- Diabetes mellitus, transient neonatal, 3 [OMIM Phenotype]
- Hyperinsulinemic hypoglycemia, familial, 2 [OMIM Phenotype]
- Maturity-onset diabetes of the young, type 13 [OMIM Phenotype]
- Type 2 diabetes mellitus [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KCNJ11 gene [LOINC component]
- potassium inwardly rectifying channel subfamily J member 11 [HGNC gene]

Keyword's position in hierarchy(ies) :

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