Symbol Name ID |
Fkrp
fukutin related protein MGI:2447586 |
Darker colors indicate more annotations |
Human Phenotypes | Corneal opacity |
Cataract |
Retinal detachment |
Microphthalmia |
Coloboma |
Myopia |
Disease(s) Associated with FKRP | ||||||
congenital muscular dystrophy-dystroglycanopathy type A5 |
Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal Muller cell morphology |
abnormal optic disk morphology |
optic nerve hypoplasia |
corneal opacity |
abnormal eye size |
abnormal retina inner limiting membrane morphology |
abnormal retina ganglion layer morphology |
abnormal retina inner nuclear layer morphology |
thin retina inner nuclear layer |
thin retina outer nuclear layer |
abnormal vitreous body morphology |
vitreal fibroplasia |
increased a-wave amplitude |
abnormal b-wave amplitude |
abnormal cone electrophysiology |
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Availability | Mouse Genotype | ||||||||||||||||
Fkrptm1Itl/Fkrptm1Itl | |||||||||||||||||
Fkrptm1Scbr/Fkrptm1Scbr | |||||||||||||||||
Fkrptvrm53/Fkrptvrm53 |
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 04/16/2024 MGI 6.23 |
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