opsin 1, long wave sensitive

Preferred Label : opsin 1, long wave sensitive;

Approved symbol HGNC : OPN1LW;

Name synonyms HGNC : cone dystrophy 5 (X-linked);

Alias symbols HGNC : COD5;

Chromosome HGNC : Xq28;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000102076;

Details

Origin ID

HGNC:9936;

UMLS CUI

C1419325;

Automatic exact mappings (from CISMeF team)
- Blue cone monochromacy [OMIM Phenotype]
- Opsin 1, long-wave-sensitive [OMIM gene]
- opsin 1, long wave sensitive [ORDO Gene]
- opsin 1, medium wave sensitive [ORDO Gene]
OMIM gene
- Opsin 1, long-wave-sensitive [OMIM gene]
Orphanet gene
- opsin 1, long wave sensitive [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Opsin 1, long-wave-sensitive [OMIM gene]
- Partial color blindness, protan type [ORDO Disease]

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