Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tor1btm1.1Wtd mutation
(1 available);
any
Tor1b mutation
(20 available)
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normal phenotype
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• mice are indistinguishable from wild-type controls, gain weight normally and do not show brain abnormalities or gliosis, exhibit normal cortical thickness and normal limb clasping during tail suspension
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mortality/aging
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• mice exhibit early lethality beginning in the third postnatal week and endpoint of survival is P28
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growth/size/body
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• mice show reduced postnatal growth
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nervous system
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• cerebral cortex is thinner at P28, with a 64.8% reduction compared to 10.4% reduction in single conditional Tor1a homozygous mutant mice
• mice exhibit reductions of CUX1+ (cortical layer II-IV) and CTIP2+ (cortical layer V-VI) cortical neurons in sensorimotor cortex
• however, no overt brain structural abnormalities are seen at birth, cortical thickness is normal at birth, and the number of CTIP2+ (cortical layer V-VI) cortical neurons are not different at P0
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• mice exhibit gliosis in the cerebral cortex and hippocampus at P28
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• mice exhibit cell loss in the cerebral cortex and hippocampus at P28
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