Symbol Name ID |
Unc119
unc-119 lipid binding chaperone MGI:1328357 |
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 | ||||||
Unc119tm1Gina/Unc119tm1Gina | |||||||
Unc119tm1Gina/Unc119+ |
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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last database update 08/02/2024 MGI 6.24 |
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