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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fancctm1Mgo
targeted mutation 1, Markus Grompe
MGI:1858041
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fancctm1Mgo/Fancctm1Mgo involves: 129S4/SvJaeSor * C57BL/6 MGI:2450132


Genotype
MGI:2450132
hm1
Allelic
Composition
Fancctm1Mgo/Fancctm1Mgo
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fancctm1Mgo mutation (0 available); any Fancc mutation (68 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• homozygous neonates of both sexes exhibit a developmental germ cell defect; however, germ cell depletion is more severe in females
• newborn mutant ovaries consist of granulosa cells and almost no germ cells
• newborn mutant testes contain significantly less germ cells
• at 6-8 weeks of age, mutant ovaries are almost entirely devoid of follicles
• at 6-8 weeks of age, homozygotes exhibit very small ovaries
• at 6-8 weeks of age, homozygotes show significant ovarian cortical hypoplasia as well as hyperplasia of the interstitial cells
• at 2 months, male homozygotes display a mosaic pattern of seminiferous tubules devoid of germ cells and normal tubules
• abnormal tubules that are devoid of mature sperm contain only Sertoli cells
• at 4 weeks or later, male homozygotes exhibit significantly reduced testicular weights
• at 6-8 weeks of gae, homozygotes show endometrial atrophy with reduced stroma cellularity
• female homozygotes display significantly impaired fertility
• breeding of 2-mo-old female homozygotes with heterozygous males resulted in either no litters at all or only one litter of 1-2 pups
• breeding of 4-mo-old female homozygotes with wild-type males generated only 6 pups in 4 pregnanies, with an average litter size of 1.5 pups, over a 3-mo period

endocrine/exocrine glands
• at 6-8 weeks of age, mutant ovaries are almost entirely devoid of follicles
• at 6-8 weeks of age, homozygotes exhibit very small ovaries
• at 6-8 weeks of age, homozygotes show significant ovarian cortical hypoplasia as well as hyperplasia of the interstitial cells
• at 2 months, male homozygotes display a mosaic pattern of seminiferous tubules devoid of germ cells and normal tubules
• abnormal tubules that are devoid of mature sperm contain only Sertoli cells
• at 4 weeks or later, male homozygotes exhibit significantly reduced testicular weights

hematopoietic system
• in vitro, bone marrow cultures established from 6-mo-old homozygotes display significantly reduced CFU-GM and BFU-E colony growth; however, no such differences are noted at 2-4 months
• both mutant clonal progenitors (CFU-GM and BFU-E) are hypersensitive to the mitotic inhibitory effects of IFN-gamma, independent of age
• however, no anemia or abnormal blood parameters are detected in homozygotes up to 9 months of age

cellular
• homozygous neonates of both sexes exhibit a developmental germ cell defect; however, germ cell depletion is more severe in females
• newborn mutant ovaries consist of granulosa cells and almost no germ cells
• newborn mutant testes contain significantly less germ cells
• in response to mitomycin C, mutant primary splenocytes accumulate in the G2 phase of the cell cycle, indicating a delay in cell cycle transit
• mutant skin fibroblasts are hyper-responsive to the clastogenic effect of mitomycin C and DEB, exhibiting chromosome breakage and other cytogenetic abnormalities
• some mutant skin fibroblast lines even exhibit spontaneous chromosome breakage, without exposure to clastogens
• however, homozygotes appear to remain tumor-free up to one year of age

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Fanconi anemia complementation group C DOID:0111087 OMIM:227645
J:61512





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory