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Symbol
Name
ID

Rd3
retinal degeneration 3
MGI:1921273

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Keratoconus	Cataract	Abnormal optic disc morphology	Abnormality of macular pigmentation	Abnormality of retinal pigmentation	Abnormal electroretinogram	Nystagmus	Congenital blindness	Severely reduced visual acuity
Disease(s) Associated with RD3	Keratoconus	Cataract	Abnormal optic disc morphology	Abnormality of macular pigmentation	Abnormality of retinal pigmentation	Abnormal electroretinogram	Nystagmus	Congenital blindness	Severely reduced visual acuity
Leber congenital amaurosis
Leber congenital amaurosis 12

Mouse Phenotypes

absent retina rod cells

retina photoreceptor degeneration

increased cornea thickness

abnormal eye anterior chamber depth

abnormal retina morphology

abnormal retina inner nuclear layer morphology

abnormal retina outer nuclear layer morphology

thin retina outer nuclear layer

abnormal retina photoreceptor layer morphology

decreased total retina thickness

abnormal eye electrophysiology

Availability

Mouse Genotype

Rd3^em1(IMPC)Bay/Rd3^em1(IMPC)Bay

Rd3^rd3/Rd3^rd3

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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