RPGR interacting protein 1

Preferred Label : RPGR interacting protein 1;

Approved symbol HGNC : RPGRIP1;

Alias symbols HGNC : CORD13; RGI1; LCA6;

Chromosome HGNC : 14q11.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000092200;

Details

Origin ID

HGNC:13436;

UMLS CUI

C1421991;

Automatic exact mappings (from CISMeF team)
- Leber congenital amaurosis 6 [OMIM Phenotype]
- RPGR interacting protein 1 [ORDO Gene]
- Retinitis pigmentosa gtpase regulator-interacting protein [OMIM gene]
OMIM gene
- Retinitis pigmentosa gtpase regulator-interacting protein [OMIM gene]
Orphanet gene
- RPGR interacting protein 1 [ORDO Gene]
See also inter- (CISMeF)
- Cone-rod dystrophy 13 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RPGRIP1 gene [LOINC component]
- Retinitis pigmentosa gtpase regulator-interacting protein [OMIM gene]

Keyword's position in hierarchy(ies) :

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