opsin 1, short wave sensitive

Preferred Label : opsin 1, short wave sensitive;

Approved symbol HGNC : OPN1SW;

Name synonyms HGNC : tritan; blue-sensitive opsin; color blindness;

Alias symbols HGNC : BOP; CBT;

Chromosome HGNC : 7q32.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000128617;

Details

Origin ID

HGNC:1012;

UMLS CUI

C1412770;

Automatic exact mappings (from CISMeF team)
- 3,4-didehydroretinal binding [GO term]
- Blindness color [MedDRA LLT]
- Color Blindness [NCIt concept]
- Color blindness [MedDRA LLT]
- Color blindness [LOINC component]
- Color blindness (disorder) [SNOMED CT concept]
- Color vision deficiencies [ICD-10 Sub-category]
- Dyschromatopsia [HPO term]
- Opsin 1, short-wave-sensitive [OMIM gene]
- UV-A, blue light phototransduction [GO term]
- color blindness [MeSH concept]
- color blindness [DO Concept]
- color blindness [MedlinePlus Topic]
- color vision defects [MeSH Descriptor]
- opsin 1, short wave sensitive [ORDO Gene]
- photoreceptor activity [GO term]
- retinal binding [GO term]
OMIM gene
- Opsin 1, short-wave-sensitive [OMIM gene]
Orphanet gene
- opsin 1, short wave sensitive [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Opsin 1, short-wave-sensitive [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients