Potassium channel, inwardly rectifying, subfamily j, member 10

Preferred Label : Potassium channel, inwardly rectifying, subfamily j, member 10;

Symbol : KCNJ10;

CISMeF acronym : KCNJ10;

Type : Gene;

Alternative titles and symbols : Glial inwardly rectifying potassium channel kir4.1;

Ensembl ID : ENSG00000177807;

Prefixed ID : *602208;

Détails

Origin ID

602208;

UMLS CUI

C1416577;

Automatic exact mappings (from CISMeF team)
- potassium inwardly rectifying channel subfamily J member 10 [HGNC gene]
- potassium inwardly rectifying channel subfamily J member 10 [ORDO Gene]
HGNC gene
- potassium inwardly rectifying channel subfamily J member 10 [HGNC gene]
ORDO concept(s)
- potassium inwardly rectifying channel subfamily J member 10 [ORDO Gene]
Phenotypes related
- Deafness, autosomal recessive 4, with enlarged vestibular aqueduct [OMIM Phenotype]
- Seizures, sensorineural deafness, ataxia, impaired intellectual development, and electrolyte imbalance [OMIM Phenotype]
See also inter- (CISMeF)
- Kcnj10 Channel [MeSH Descriptor]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- potassium inwardly rectifying channel subfamily J member 10 [HGNC gene]

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