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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	Vertical supranuclear gaze palsy	Nystagmus	Rotary nystagmus	Visual impairment
Disease(s) Associated with PLP1	Optic atrophy	Abnormality of visual evoked potentials	Vertical supranuclear gaze palsy	Nystagmus	Rotary nystagmus	Visual impairment
hereditary spastic paraplegia 2
Pelizaeus-Merzbacher disease

Mouse Phenotypes		abnormal optic nerve morphology	delayed eyelid opening
Availability	Mouse Genotype	abnormal optic nerve morphology	delayed eyelid opening
	Plp1^tm3Wst/Plp1^tm3Wst
	Tg(Plp)72Kan/Tg(Plp)72Kan
	Plp1^jp/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)
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