opn1sw opsin 1 (cone pigments), short-wave-sensitive
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
|Human (4 sources): Abnormal light-adapted electroretinogram, Color vision defect, Dyschromatopsia, Tritanomaly|
|Mouse (3 sources): abnormal cone electrophysiology, disorganized photoreceptor outer segment, vision/eye phenotype|
View all ortholog results at Monarch