About   Help   FAQ
Symbol
Name
ID
Plp1
proteolipid protein (myelin) 1
MGI:97623
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Optic atrophy
Abnormality of visual evoked potentials
Nystagmus
Rotary nystagmus
Visual impairment
Disease(s) Associated with PLP1
hereditary spastic paraplegia 2
Pelizaeus-Merzbacher disease

Mouse Phenotypes
abnormal optic nerve morphology
delayed eyelid opening
Availability Mouse Genotype
Plp1tm3Wst/Plp1tm3Wst
Tg(Plp)72Kan/Tg(Plp)72Kan
Plp1jp/Y

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
10/08/2019
MGI 6.14
The Jackson Laboratory