Symbol Name ID |
Lrat
lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) MGI:1891259 |
Darker colors indicate more annotations |
Human Phenotypes | Photophobia |
Intellectual disability |
Hyperreflexia |
Falls |
Disease(s) Associated with LRAT | ||||
Leber congenital amaurosis 14 | ||||
retinitis pigmentosa |
Mouse Phenotypes | abnormal retina photoreceptor morphology |
short photoreceptor outer segment |
abnormal retina cone cell outer segment morphology |
retina cone cell degeneration |
retina rod cell degeneration |
retina photoreceptor degeneration |
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Availability | Mouse Genotype | ||||||
Lrattm1.1Bok/Lrattm1.1Bok | |||||||
Lrattm1Kpal/Lrattm1Kpal | |||||||
Lrattm1Bok/Lrattm1Bok Tg(Tyrp1-cre)1Ipc/? (conditional) |
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 04/23/2024 MGI 6.23 |
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