| Human Disease |
Parkinson Disease 8, Autosomal Dominant; PARK8 OMIM ID: 607060 |
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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 |
| Tg(Lrrk2*G2019S)2Yue/0 |
involves: C3H * C57BL/6 * C57BL/6J | J:157931 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(LRRK2*R1441G)135Cjli/0 |
FVB-Tg(LRRK2*R1441G)135Cjli | J:149135 | 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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