vision/eye
• shorter M-opsin positive OS
|
• shorter M-opsin positive OS
|
mortality/aging
• few survive longer than 30 days of age, presumably due to starvation as homozygotes are unable to feed themselves
|
growth/size/body
• smaller size is identifiable at 20 days of age
|
nervous system
• vestibulo-motor degeneration
|
• shorter M-opsin positive OS
|
• shorter M-opsin positive OS
|
chromatolysis
(
J:11718
)
• neurons in both the vestibular ganglion and nucleus have central chromatolysis
|
• dystrophic axons are concentrated in the ventral funiculus of the cervical segments of the spinal cord and are particularly numerous in ventro-medial aspects of the medulla dorsal to the pyramids and ventral to the medial lemniscus in the area of the vestibulospinal tract
• axons in the vestibular spinal tract and some axons projecting from the vestibular ganglion to the lateral vestibular nucleus are dystrophic
|
behavior/neurological
• unable to feed themselves leading to starvation
|
• when startled, jump sideways with legs splay out from the body
|
limb grasping
(
J:11718
)
• when picked up by tail, clasp hind legs and the entire body shakes violently
|
• tend to sit hunched over with rear feet and legs tucked in towards the body
|
integument
• ungroomed hair coat
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome | DOID:0050997 |
OMIM:PS224050 |
J:222308 |