normal phenotype
• mutants are fertile and indistinguishable from wild-type mice
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Allele Symbol Allele Name Allele ID |
Hoxb1tm7Mrc targeted mutation 7, Mario R Capecchi MGI:3046794 |
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Summary |
3 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mutants are fertile and indistinguishable from wild-type mice
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
N |
• no behavioral abnormalities are seen
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• the average number of motor neurons is significantly reduced in mutants compared to wild-type mice although not to the same extent as in compound heterozygous mutants carrying Tg(Wnt1-cre)11Rth
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• some mutants are unable to move their ears
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• some mutants are unable to blink their eyes
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• some mutants are unable to move their whiskers
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• 35% of mutants show total facial paralysis and another 10% show partial facial paralysis
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• increased motor neuron loss is seen from E14.5 to E16.5 when motor neuron pruning normally occurs resulting a significant decrease in the average number of motor neurons in mutants compared to wild-type mice
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• loss of VII th cranial nerve branches is seen
• at E12.5 the average number of axonal branch points is decreased
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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 12/10/2024 MGI 6.24 |
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