About   Help   FAQ
Symbol
Name
ID
Mfrp
membrane frizzled-related protein
MGI:2385957
Phenotype annotations related to vision/eye
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Cystoid macular edema
Abnormal retinal vascular morphology
Attenuation of retinal blood vessels
Keratoconus
Cataract
Posterior subcapsular cataract
Abnormal choroid morphology
Optic atrophy
Optic disc drusen
Optic disc pallor
Foveoschisis
Abnormality of retinal pigmentation
Bone spicule pigmentation of the retina
Retinal degeneration
Retinal pigment epithelial atrophy
Scleral thickening
Microphthalmia
Bilateral microphthalmos
Abnormal electroretinogram
Abnormal light- and dark-adapted electroretinogram
Strabismus
Nystagmus
Ophthalmoplegia
Hypermetropia
High hypermetropia
Nyctalopia
Progressive night blindness
Photophobia
Photopsia
Visual impairment
Reduced visual acuity
Blindness
Peripheral visual field loss
Glaucoma
Angle closure glaucoma
Disease(s) Associated with MFRP
isolated microphthalmia 5
nanophthalmos
retinitis pigmentosa

Mouse Phenotypes
vision/eye phenotype
abnormal photoreceptor outer segment morphology
disorganized photoreceptor outer segment
retina photoreceptor degeneration
abnormal retina pigment epithelium morphology
abnormal ocular fundus morphology
abnormal retina morphology
thin retina outer nuclear layer
retina degeneration
retina spots
abnormal electroretinogram waveform feature
decreased a-wave amplitude
decreased b-wave amplitude
abnormal rod electrophysiology
Availability Mouse Genotype
Mfrprd6-2J/Mfrprd6-2J
Mfrprd6/Mfrprd6 *
Mfrprdx/Mfrprdx *

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, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory