About Help FAQ

Symbol
Name
ID

Myrf
myelin regulatory factor
MGI:2684944

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Stroke
Disease(s) Associated with MYRF	Stroke
cerebral infarction

Mouse Phenotypes		nervous system phenotype	seizures	abnormal oligodendrocyte morphology	decreased retina cone cell number	short photoreceptor inner segment	short photoreceptor outer segment	abnormal optic nerve morphology	abnormal spinal cord morphology	abnormal myelination
Availability	Mouse Genotype	nervous system phenotype	seizures	abnormal oligodendrocyte morphology	decreased retina cone cell number	short photoreceptor inner segment	short photoreceptor outer segment	abnormal optic nerve morphology	abnormal spinal cord morphology	abnormal myelination
	Myrf^tm1Barr/Myrf^tm1Barr Olig2^{tm2(TVA,cre)Rth}/Olig2⁺ (conditional)	*
	Myrf^tm1Barr/Myrf^tm1Barr Cnp^tm1(cre)Kan/Cnp⁺ (conditional)
	Myrf^tm1Barr/Myrf^tm1Barr 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 04/23/2024 MGI 6.23