| Human Disease |
Parkinson Disease, Mitochondrial OMIM ID: 556500 |
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| View all models | View ALL (2) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Slc6a3tm1(cre)Lrsn/Slc6a3+ Tfamtm1Lrsn/Tfamtm1Lrsn |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL | J:119515 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Th-Peo1*,-EGFP)2Gcor/0 |
involves: C57BL/6J | J:188914 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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