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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	Retinal perforation	Electronegative electroretinogram	Strabismus	High myopia	Nyctalopia	Reduced visual acuity
Disease(s) Associated with LRIT3
congenital stationary night blindness 1F

Mouse Phenotypes		abnormal retina neuronal layer morphology	thin retina 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	abnormal retina neuronal layer morphology	thin retina 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
	Lrit3^tm1Lex/Lrit3^tm1Lex
	Lrit3^tvrm257/Lrit3^tvrm257

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23