Symbol Name ID |
Ppargc1a
peroxisome proliferative activated receptor, gamma, coactivator 1 alpha MGI:1342774 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of eye movement |
Diplopia |
Color vision defect |
Disease(s) Associated with PPARGC1A | |||
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 |
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Availability | Mouse Genotype | ||||||||
Ppargc1atm1Brsp/Ppargc1a+ |
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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last database update 04/16/2024 MGI 6.23 |
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