potassium inwardly rectifying channel subfamily J member 13

Preferred Label : potassium inwardly rectifying channel subfamily J member 13;

Approved symbol HGNC : KCNJ13;

Alias symbols HGNC : Kir7.1; LCA16; Kir1.4;

Chromosome HGNC : 2q37.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000115474;

Details

Origin ID

HGNC:6259;

UMLS CUI

C1416580;

Automatic exact mappings (from CISMeF team)
- Leber congenital amaurosis 16 [OMIM Phenotype]
- Potassium channel, inwardly rectifying, subfamily j, member 13 [OMIM gene]
OMIM gene
- Potassium channel, inwardly rectifying, subfamily j, member 13 [OMIM gene]
Orphanet gene
- potassium inwardly rectifying channel subfamily J member 13 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Potassium channel, inwardly rectifying, subfamily j, member 13 [OMIM gene]

Keyword's position in hierarchy(ies) :

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