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Symbol
Name
ID
Fkrp
fukutin related protein
MGI:2447586
Phenotype annotations related to vision/eye
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
Availability Mouse Genotype
Fkrptm1Itl/Fkrptm1Itl
Fkrptm1Scbr/Fkrptm1Scbr
Fkrptvrm53/Fkrptvrm53

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
04/16/2024
MGI 6.23
The Jackson Laboratory