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Symbol
Name
ID

Opn1sw
opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)
MGI:99438

Phenotype annotations related to vision/eye

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Abnormal light-adapted electroretinogram	Color vision defect	Dyschromatopsia	Tritanomaly
Disease(s) Associated with OPN1SW
blue color blindness

Mouse Phenotypes		vision/eye phenotype	disorganized photoreceptor outer segment	abnormal cone electrophysiology
Availability	Mouse Genotype	vision/eye phenotype	disorganized photoreceptor outer segment	abnormal cone electrophysiology
	Opn1sw^tm1.1Pugh/Opn1sw^tm1.1Pugh	*
	Opn1sw^tm1Pugh/Opn1sw^tm1Pugh	*

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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