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Symbol
Name
ID
Lrat
lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase)
MGI:1891259
Phenotype annotations related to nervous system
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
Availability Mouse Genotype
Lrattm1.1Bok/Lrattm1.1Bok
Lrattm1Kpal/Lrattm1Kpal
Lrattm1Bok/Lrattm1Bok
Tg(Tyrp1-cre)1Ipc/?  (conditional)

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory