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Symbol
Name
ID

Unc119
unc-119 lipid binding chaperone
MGI:1328357

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Abnormality of retinal pigmentation	Color vision defect	Nyctalopia	Photophobia	Visual impairment
Disease(s) Associated with UNC119
cone-rod dystrophy

Mouse Phenotypes		abnormal retina pigment epithelium morphology	abnormal retina morphology	thin retina outer nuclear layer	increased susceptibility to age-related retinal degeneration	decreased total retina thickness	abnormal eye electrophysiology
Availability	Mouse Genotype	abnormal retina pigment epithelium morphology	abnormal retina morphology	thin retina outer nuclear layer		decreased total retina thickness	abnormal eye electrophysiology
	Unc119^tm1Gina/Unc119^tm1Gina
	Unc119^tm1Gina/Unc119⁺

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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