mortality/aging
|
• reduced lifespan compared to wild-type controls
• however lifespan is similar to transgenic mice wild-type for Cnr1
|
nervous system
|
• increase in the density of ubiquitin positive aggregates in the striatum compared to transgenic mice wild-type for Cnr1
|
behavior/neurological
|
• reduced latency to fall and an increased number of falls in a rotarod assay
• motor performance is worse than in transgenic mice wild-type for Cnr1
|
growth/size/body
|
• fail to gain weight after 16 weeks of age
|
|
• fail to gain weight after 16 weeks of age
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
| Huntington's disease | DOID:12858 |
OMIM:143100 |
J:172874 | |


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