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Symbol Name ID |
Lca5
Leber congenital amaurosis 5 (human) MGI:1923032 |
| Darker colors indicate more annotations |
| Human Phenotypes | Undetectable electroretinogram |
Nystagmus |
Hypermetropia |
High hypermetropia |
Visual impairment |
Visual loss |
| Disease(s) Associated with LCA5 | ||||||
| Leber congenital amaurosis 5 |
| Mouse Phenotypes | short photoreceptor inner segment |
abnormal photoreceptor outer segment morphology |
short photoreceptor outer segment |
disorganized photoreceptor outer segment |
abnormal retina pigmentation |
abnormal retina photoreceptor layer morphology |
abnormal eye physiology |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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| Availability | Mouse Genotype | |||||||||
| Lca5Gt(AG0283)Wtsi/Lca5Gt(AG0283)Wtsi | ||||||||||
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 04/16/2024 MGI 6.23 |
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