behavior/neurological
• motor coordination and behavioral phenotypes are less severe when compared to phenotypes observed in mice carrying Mecptm4.1Brd and Mecptm5.1Brd
• onset of phenotypes is gradual as compared to mice carrying Mecptm4.1Brd and Mecptm5.1Brd
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• decrease in latency to fall in 3-day accelerated rotarod-learning paradigm by day 3 as compared to controls
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• increased time in open arms of elevated plus maze as compared to controls, but not as compared to Mecptm3.1Brd (WT-GFP) control
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• increase in latency to fall in hanging wire test as compared to controls
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growth/size/body
mortality/aging
• median survival is 42 weeks
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
Rett syndrome | DOID:1206 |
OMIM:312750 OMIM:613454 |
J:227401 |