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Symbol
Name
ID

Opn1mw
opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan)
MGI:1097692

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Abnormality of macular pigmentation	Nystagmus	Pendular nystagmus	Myopia	Deuteranomaly	Protanomaly	Blue cone monochromacy	Photophobia	Visual impairment	Reduced visual acuity
Disease(s) Associated with OPN1LW	Abnormality of macular pigmentation	Nystagmus	Pendular nystagmus	Myopia	Deuteranomaly	Protanomaly	Blue cone monochromacy	Photophobia	Visual impairment	Reduced visual acuity
blue cone monochromacy
red color blindness
Disease(s) Associated with OPN1MW
blue cone monochromacy
red-green color blindness

Mouse Phenotypes		abnormal retina morphology	decreased b-wave amplitude
Availability	Mouse Genotype
	Opn1mw^{tm1a(EUCOMM)Wtsi}/Opn1mw^{tm1a(EUCOMM)Wtsi}

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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