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Symbol
Name
ID
Lrit3
leucine-rich repeat, immunoglobulin-like and transmembrane domains 3
MGI:2685267
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Congenital stationary night blindness
Strabismus
Myopia
Disease(s) Associated with LRIT3
congenital stationary night blindness 1F

Mouse Phenotypes
abnormal retinal neuronal layer morphology
thin retinal inner nuclear layer
increased a wave implicit time
increased b wave implicit time
increased a wave amplitude
decreased b wave amplitude
abnormal cone electrophysiology
abnormal rod electrophysiology
abnormal vision
Availability Mouse Genotype
Lrit3tm1Lex/Lrit3tm1Lex
Lrit3tvrm257/Lrit3tvrm257

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
08/04/2020
MGI 6.15
The Jackson Laboratory