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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Furintm1Jwmc
targeted mutation 1, John W M Creemers
MGI:3700008
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Furintm1Jwmc/Furintm1Jwmc involves: 129P2/OlaHsd * C57BL/6J MGI:3700793
cn2
Furintm1Jwmc/Furintm1.1Jwmc
Tg(Mx1-cre)1Cgn/0
involves: 129P2/OlaHsd * BALB/c * C57BL/6 * C57BL/6J * CBA MGI:3700792
cn3
Furintm1Jwmc/Furintm1Jwmc
Tg(Zp3-cre)3Mrt/0
involves: 129P2/OlaHsd * C57BL/6J * CBA/J MGI:6856673
cn4
Furintm1Jwmc/Furintm1Jwmc
Tg(Gdf9-icre)5092Coo/0
involves: 129P2/OlaHsd * C57BL/6J * CBA/J MGI:6856674
cn5
Furintm1Jwmc/Furintm1Jwmc
Tg(Cd4-cre)1Cwi/0
involves: 129P2/OlaHsd * C57BL/6 * SJL MGI:5544321


Genotype
MGI:3700793
hm1
Allelic
Composition
Furintm1Jwmc/Furintm1Jwmc
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Furintm1Jwmc mutation (0 available); any Furin mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice are viable, fertile and normal in appearance




Genotype
MGI:3700792
cn2
Allelic
Composition
Furintm1Jwmc/Furintm1.1Jwmc
Tg(Mx1-cre)1Cgn/0
Genetic
Background
involves: 129P2/OlaHsd * BALB/c * C57BL/6 * C57BL/6J * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Furintm1.1Jwmc mutation (1 available); any Furin mutation (45 available)
Furintm1Jwmc mutation (0 available); any Furin mutation (45 available)
Tg(Mx1-cre)1Cgn mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
liver/biliary system
N
• conditional mice show no liver phenotype




Genotype
MGI:6856673
cn3
Allelic
Composition
Furintm1Jwmc/Furintm1Jwmc
Tg(Zp3-cre)3Mrt/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 (45 available)
Tg(Zp3-cre)3Mrt mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• loss of connexin 37 staining at the surface of oocytes indicates impaired gap junctions between oocytes and surrounding granulosa cells at the early secondary follicle stage
• metaphase II (MII) oocytes collected after superovulation exhibit poor quality with degenerated first polar bodies and severely abnormal spindles
• metaphase II (MII) oocytes collected after superovulation exhibit degenerated first polar bodies
• at P35, TUNEL analysis showed severe apoptosis of granulosa cells in late preantral follicles and antral follicles
• however, no apparent apoptosis is detected in early secondary follicles
• PCNA staining showed a severe defect in granulosa cell proliferation at 2 months of age
• at 6 and 8 weeks of age, number of early secondary follicles is significantly increased while the number of large growing (late preantral) follicles is markedly decreased
• number of antral follicles is markedly decreased
• large antral follicles exhibit degeneration at 8 weeks of age; few or almost no late growing follicles or antral follicles are observed, suggesting atresia of follicles beyond the early secondary stage
• at 6 weeks of age, the number of early secondary follicles is significantly increased while the number of large growing (late preantral) follicles and antral follicles is markedly decreased, indicating that primary follicles fail to develop beyond the early secondary follicle stage
• ovaries are smaller at P42
• metaphase II (MII) oocytes collected after superovulation exhibit severely abnormal spindles
• following induction of ovulation with exogenous PMSG + hCG, the number of ovulated oocytes per 6-wk-old female is significantly lower than that in control females
• females fail to ovulate during a natural ovulation assay
• 8-wk-old or older females cannot be induced to ovulate anymore
• when mated with fertile males for 6 months, females fail to produce any progeny indicating complete female infertility

cellular
• loss of connexin 37 staining at the surface of oocytes indicates impaired gap junctions between oocytes and surrounding granulosa cells at the early secondary follicle stage
• metaphase II (MII) oocytes collected after superovulation exhibit poor quality with degenerated first polar bodies and severely abnormal spindles
• metaphase II (MII) oocytes collected after superovulation exhibit degenerated first polar bodies
• at P35, TUNEL analysis showed severe apoptosis of granulosa cells in late preantral follicles and antral follicles
• however, no apparent apoptosis is detected in early secondary follicles
• PCNA staining showed a severe defect in granulosa cell proliferation at 2 months of age

endocrine/exocrine glands
• at P35, TUNEL analysis showed severe apoptosis of granulosa cells in late preantral follicles and antral follicles
• however, no apparent apoptosis is detected in early secondary follicles
• PCNA staining showed a severe defect in granulosa cell proliferation at 2 months of age
• at 6 and 8 weeks of age, number of early secondary follicles is significantly increased while the number of large growing (late preantral) follicles is markedly decreased
• number of antral follicles is markedly decreased
• large antral follicles exhibit degeneration at 8 weeks of age; few or almost no late growing follicles or antral follicles are observed, suggesting atresia of follicles beyond the early secondary stage
• at 6 weeks of age, the number of early secondary follicles is significantly increased while the number of large growing (late preantral) follicles and antral follicles is markedly decreased, indicating that primary follicles fail to develop beyond the early secondary follicle stage
• ovaries are smaller at P42




Genotype
MGI:6856674
cn4
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 (45 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




Genotype
MGI:5544321
cn5
Allelic
Composition
Furintm1Jwmc/Furintm1Jwmc
Tg(Cd4-cre)1Cwi/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Furintm1Jwmc mutation (0 available); any Furin mutation (45 available)
Tg(Cd4-cre)1Cwi mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• regulatory T cells fail to drive Th17 differentiation

immune system
• regulatory T cells fail to drive Th17 differentiation





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory