mortality/aging
• number of viable progeny is reduced to 12.2% compared to 25% expected
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Allele Symbol Allele Name Allele ID |
Shc1tm3Paw targeted mutation 3, Tony Pawson MGI:3716777 |
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Summary |
4 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• number of viable progeny is reduced to 12.2% compared to 25% expected
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mice display motor defects more severe than than transheterozygous Shc1tm3Paw/tm4Paw mice
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• between P22 and P35, muscle spindles are abnormal and numbers are 13% of controls
• intrafusal fiber numbers are 35.9% of control numbers
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• between P22 and P35, muscle spindles are abnormal and numbers are 13% of controls
• intrafusal fiber numbers are 35.9% of control numbers
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mice display more severe motor defects than transheterozygous Shc1tm4Paw/tm7Paw mice
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• between P22 and P35, muscle spindles are abnormal and numbers are 83.3% of controls
• intrafusal fiber numbers are 66.6% of control numbers
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• between P22 and P35, muscle spindles are abnormal and numbers are 83.3% of controls
• intrafusal fiber numbers are 66.6% of control numbers
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• motor abnormalities are similar to those observed in Shc1tm7Paw homozygotes
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• between P22 and P35, muscle spindle and intrafusal fiber numbers are reduced compared to controls
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• between P22 and P35, muscle spindle and intrafusal fiber numbers are reduced compared to controls
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 11/05/2024 MGI 6.24 |
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