About   Help   FAQ
Symbol
Name
ID
Myrf
myelin regulatory factor
MGI:2684944
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Abnormal choroid morphology
Optic disc drusen
Abnormality of retinal pigmentation
Microphthalmia
Bilateral microphthalmos
Strabismus
Hypermetropia
High hypermetropia
Reduced visual acuity
Glaucoma
Angle closure glaucoma
Disease(s) Associated with MYRF
nanophthalmos

Mouse Phenotypes
decreased retina cone cell number
short photoreceptor inner segment
short photoreceptor outer segment
abnormal optic nerve morphology
abnormal retina pigmentation
retina pigment epithelium atrophy
increased cornea thickness
thin retina outer nuclear layer
decreased total retina thickness
retina degeneration
abnormal cone electrophysiology
abnormal rod electrophysiology
Availability Mouse Genotype
Myrfem1(IMPC)Bay/Myrf+
Myrftm1Barr/Myrftm1Barr
Olig2tm2(TVA,cre)Rth/Olig2+  (conditional)
Myrftm1Barr/Myrftm1Barr
Tg(rx3-icre)1Mjam/0  (conditional)
Myrftm1Barr/Myrf+
Tg(rx3-icre)1Mjam/0  (conditional)
Myrftm1Barr/Myrftm1.1Barr
Tg(rx3-icre)1Mjam/0  (conditional)

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
04/30/2024
MGI 6.23
The Jackson Laboratory