Symbol Name ID |
Vldlr
very low density lipoprotein receptor MGI:98935 |
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 |
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Availability | Mouse Genotype | ||||||||||||||||||||
Vldlrm1Btlr/Vldlrm1Btlr | |||||||||||||||||||||
Vldlrm2Btlr/Vldlrm2Btlr | |||||||||||||||||||||
Vldlrrnv4/Vldlrrnv4 | |||||||||||||||||||||
Vldlrtm1Her/Vldlrtm1Her | |||||||||||||||||||||
Vldlrtm1Lex/Vldlrtm1Lex | |||||||||||||||||||||
Vldlrm1Btlr/Vldlrtm1Her |
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 |
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