About   Help   FAQ
Symbol
Name
ID
Fkrp
fukutin related protein
MGI:2447586
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Megalocornea
Corneal opacity
Cataract
Buphthalmos
Peters anomaly
Retinal atrophy
Retinal detachment
Retinal dysplasia
Optic nerve hypoplasia
Microphthalmia
Coloboma
Myopia
Blindness
Glaucoma
Disease(s) Associated with FKRP
congenital muscular dystrophy-dystroglycanopathy type A1
congenital muscular dystrophy-dystroglycanopathy type A5

Mouse Phenotypes
abnormal retinal 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 retinal ganglion layer morphology
abnormal retinal inner nuclear layer morphology
thin retinal inner nuclear layer
thin retinal 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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
08/06/2019
MGI 6.14
The Jackson Laboratory