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Phenotypes Associated with This Genotype
Genotype
MGI:4398747
Allelic
Composition
Os/Os
Genetic
Background
involves: 101 * C3H
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Os mutation (9 available); any Os mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
• cells of the developing embryo appear abnormal between the 7th and 8th division with suggestion of mitotic dysfunction (J:5017)
• the most striking abnormalities are seen by the middle of the 4th day when many embryonic cells contain fragmented, pycnotic chromatin and lack nuclear membrane and nucleolus (J:5017)
• in culture, blastocysts show rapid degeneration of the inner cell mass compared with control embryos (J:5768)
• noted as early as E4.5

cellular
• E4.5 embryos have an index nine times that of controls
• more than one third of cells contain mitotic figures

growth/size/body
• noted as early as E4.5


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
03/25/2025
MGI 6.24
The Jackson Laboratory