mortality/aging
|
• lifespan is on average 359 days
|
nervous system
|
• mutants exhibit extensive protein aggregates of the mutant protein in the gray matter of the spinal cord at 350 days of age
|
|
• mutants develop an amyotrophic lateral sclerosis-like phenotype by the age of 300-400 days, with an average onset of 336.3 days
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
| amyotrophic lateral sclerosis type 1 | DOID:0060193 |
OMIM:105400 |
J:109458 | |


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