| Human Disease |
Parkinson Disease, Late-Onset; PD OMIM ID: 168600 |
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| Synonyms | Park | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| View all models | View ALL (8) 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 |
| Adh7tm1Gdu/Adh7tm1Gdu |
B6.129-Adh7tm1Gdu | J:167234 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Atg7tm1Tchi/Atg7tm1Tchi En1tm2(cre)Wrst/En1+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj | J:192452 | View |
| Atg7tm1Tchi/Atg7tm1Tchi Slc6a3tm1(cre)Xz/Slc6a3+ |
involves: 129S1/Sv * C57BL/6NCrlj * CBA/JNCrlj | J:192452 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Gt(ROSA)26Sortm1.1(CAG-COX8A/Dendra2)Dcc/Gt(ROSA)26Sor+ Mfn2tm3Dcc/Mfn2tm3Dcc Slc6a3tm1.1(cre)Bkmn/Slc6a3+ |
involves: 129 * 129S6/SvEvTac * C57BL/6J * SJL/J | J:188347 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(CAG-SNCA*)1.1Ccs/? |
involves: C57BL/6 | J:168847 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Th-SNCA*)1.2Ccs/? |
involves: C57BL/6 | J:168847 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(GFAP-tTA)#Hyms/0 Tg(tetO-HMOX1)#Hyms/0 |
involves: FVB | J:190573 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Slc6a3tm2(tTA)Xz/Slc6a3+ Tg(tetO-COX8A/PstI*)1Ctm/0 |
involves: 129X1/SvJ * C57BL/6 * C57BL/6J * SJL | J:178139 | 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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