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Phenotypes Associated with This Genotype
Genotype
MGI:4352685
Allelic
Composition
Tg(Cr2-cre)3Cgn/?
Xrcc4tm1Fwa/Xrcc4tm2Fwa
Genetic
Background
involves: 129P2/OlaHsd * 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Cr2-cre)3Cgn mutation (2 available)
Xrcc4tm1Fwa mutation (0 available); any Xrcc4 mutation (26 available)
Xrcc4tm2Fwa mutation (0 available); any Xrcc4 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• genomic stability is disrupted in activated B cells with chromosome breakage occurring in close to half of cells
• B cells undergoing class switch recombination have even greater increased risk of chromosome breakage due to aberrations at the Igh locus
• there is also increased breakage at the Igk and Igl loci with 1% of stimulated B cells demonstrating this
• Igl breaks in activated B cells are frequently fused to AID-dependent Igh breaks in the same cell to form chromosome 12/16 translocations
• there is also a five-fold increase in Igh-Myc translocations activated B cells compared to controls

hematopoietic system
• class switch recombination often leads to chromosome breakage at the Igh locus

immune system
• class switch recombination often leads to chromosome breakage at the Igh locus


Contributing Projects:
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
06/12/2024
MGI 6.13
The Jackson Laboratory