cellular
• in activated B cells, Myc/Igh translocations involving chromosomes 12 and 15 occur 10-fold less frequently with the mutant Myc allele than with the wild-type allele
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Allele Symbol Allele Name Allele ID |
Myctm39Mnz targeted mutation 39, Michel C Nussenzweig MGI:3720515 |
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Summary |
2 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• in activated B cells, Myc/Igh translocations involving chromosomes 12 and 15 occur 10-fold less frequently with the mutant Myc allele than with the wild-type allele
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• B cells within in Peyer's Patches or splenic B cells stimulated in vitro can have chromosomal translocations involving chromosomes 12 and 15
• the chromosome fusions occur precisely at the two loxP sites that exist in the Igh and Myc mutant alleles
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• B cells within in Peyer's Patches or splenic B cells stimulated in vitro can have chromosomal translocations involving chromosomes 12 and 15
• the chromosome fusions occur precisely at the two loxP sites that exist in the Igh and Myc mutant alleles
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• B cells within in Peyer's Patches or splenic B cells stimulated in vitro can have chromosomal translocations involving chromosomes 12 and 15
• the chromosome fusions occur precisely at the two loxP sites that exist in the Igh and Myc mutant alleles
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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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