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Symbol
Name
ID
Vldlr
very low density lipoprotein receptor
MGI:98935
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Cataract
Strabismus
Gaze-evoked nystagmus
Disease(s) Associated with VLDLR
cerebellar ataxia, mental retardation and dysequlibrium syndrome

Mouse Phenotypes
choroidal neovascularization
abnormal retina vasculature morphology
abnormal retina blood vessel pattern
retina neovascularization
decreased retina photoreceptor cell number
abnormal retina photoreceptor morphology
retina photoreceptor degeneration
abnormal retina pigment epithelium morphology
abnormal retina pigmentation
abnormal ocular fundus morphology
abnormal retina morphology
abnormal retina neuronal layer morphology
disorganized retina inner nuclear layer
abnormal retina outer nuclear layer morphology
thin retina outer nuclear layer
retina outer nuclear layer degeneration
decreased total retina thickness
eye lesions
abnormal cone electrophysiology
abnormal rod electrophysiology
Availability Mouse Genotype
Vldlrm1Btlr/Vldlrm1Btlr
Vldlrm2Btlr/Vldlrm2Btlr
Vldlrrnv4/Vldlrrnv4
Vldlrtm1Her/Vldlrtm1Her
Vldlrtm1Lex/Vldlrtm1Lex
Vldlrm1Btlr/Vldlrtm1Her

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
04/09/2024
MGI 6.23
The Jackson Laboratory