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Symbol
Name
ID

Ppargc1a
peroxisome proliferative activated receptor, gamma, coactivator 1 alpha
MGI:1342774

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Abnormality of eye movement	Diplopia	Color vision defect
Disease(s) Associated with PPARGC1A	Abnormality of eye movement	Diplopia	Color vision defect
Huntington's disease
Parkinson's disease

Mouse Phenotypes		abnormal choriocapillaris morphology	abnormal choroid vasculature morphology	short photoreceptor inner segment	short photoreceptor outer segment	retina photoreceptor degeneration	abnormal retina pigment epithelium morphology	retina macular degeneration	abnormal Bruch membrane morphology
Availability	Mouse Genotype
	Ppargc1a^tm1Brsp/Ppargc1a⁺

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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