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Phenotypes Associated with This Genotype
Genotype
MGI:6501042
Allelic
Composition
Prdm9tm1Ymat/Prdm9tm1Ymat
Genetic
Background
B6.129P2-Prdm9tm1Ymat
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prdm9tm1Ymat mutation (3 available); any Prdm9 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• approximately 4% of P0 metaphase oocytes have a full complement of crossovers
• >98% of pachytene cells fail to properly synapse at least one pair of chromosomes
• 63.2% of (pseudo)pachytene cells show mispairing of non-homologous chromosomes in a branched 'tangled' structure
• P0 oocytes have widespread asynapsis
• females fail to reproduce, but when Chek2 is also absent then some fertility is recovered

cellular
• approximately 4% of P0 metaphase oocytes have a full complement of crossovers
• >98% of pachytene cells fail to properly synapse at least one pair of chromosomes
• 63.2% of (pseudo)pachytene cells show mispairing of non-homologous chromosomes in a branched 'tangled' structure
• P0 oocytes have widespread asynapsis
• increased DMC1 foci count from zygotene onwards indicating delayed repair of DSBs
• increased number of RAD51 foci in (pseudo)-pachytene cells

homeostasis/metabolism
• increased DMC1 foci count from zygotene onwards indicating delayed repair of DSBs
• increased number of RAD51 foci in (pseudo)-pachytene cells


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
09/17/2024
MGI 6.24
The Jackson Laboratory