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Phenotypes Associated with This Genotype
Genotype
MGI:6856674
Allelic
Composition
Furintm1Jwmc/Furintm1Jwmc
Tg(Gdf9-icre)5092Coo/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Furintm1Jwmc mutation (0 available); any Furin mutation (49 available)
Tg(Gdf9-icre)5092Coo mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• PCNA staining showed a severe defect in granulosa cell proliferation at 2 months of age
• number of early secondary follicles is significantly increased at 6 weeks of age
• ovarian follicle development is arrested at the early secondary follicle stage
• however, number of primordial follicles is normal at 2 months of age, suggesting that survival and activation of primordial follicles is unaffected

cellular
• PCNA staining showed a severe defect in granulosa cell proliferation at 2 months of age

endocrine/exocrine glands
• PCNA staining showed a severe defect in granulosa cell proliferation at 2 months of age
• number of early secondary follicles is significantly increased at 6 weeks of age
• ovarian follicle development is arrested at the early secondary follicle stage
• however, number of primordial follicles is normal at 2 months of age, suggesting that survival and activation of primordial follicles is unaffected


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
01/28/2026
MGI 6.24
The Jackson Laboratory