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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cdc7tm1Hmas
targeted mutation 1, Hisao Masai
MGI:2183930
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cdc7tm1Hmas/Cdc7tm1Hmas involves: 129S/Sv * C57BL/6 MGI:2662266
cx2
Cdc7tm1Hmas/Cdc7tm1Hmas
Trp53tm2Mok/Trp53tm2Mok
involves: 129S/Sv * C57BL/6 MGI:2662267
cx3
Cdc7tm1Hmas/Cdc7tm1Hmas
Tg(EF1A-Cdc7)DKO28Hmas/0
involves: 129S/Sv * C57BL/6 MGI:2681167
cx4
Cdc7tm1Hmas/Cdc7tm1Hmas
Tg(EF1A-Cdc7)DKO28Hmas/Tg(EF1A-Cdc7)DKO28Hmas
involves: 129S/Sv * C57BL/6 MGI:2681170


Genotype
MGI:2662266
hm1
Allelic
Composition
Cdc7tm1Hmas/Cdc7tm1Hmas
Genetic
Background
involves: 129S/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdc7tm1Hmas mutation (0 available); any Cdc7 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
• blastocysts grown in culture exhibit a smaller inner cell mass at E6 that continues to diminish in size such that by E8.5 it has disappeared




Genotype
MGI:2662267
cx2
Allelic
Composition
Cdc7tm1Hmas/Cdc7tm1Hmas
Trp53tm2Mok/Trp53tm2Mok
Genetic
Background
involves: 129S/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdc7tm1Hmas mutation (0 available); any Cdc7 mutation (34 available)
Trp53tm2Mok mutation (2 available); any Trp53 mutation (232 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo

growth/size/body




Genotype
MGI:2681167
cx3
Allelic
Composition
Cdc7tm1Hmas/Cdc7tm1Hmas
Tg(EF1A-Cdc7)DKO28Hmas/0
Genetic
Background
involves: 129S/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdc7tm1Hmas mutation (0 available); any Cdc7 mutation (34 available)
Tg(EF1A-Cdc7)DKO28Hmas mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• about 75% of mice born die within 3 days
• less than 25% survived to adulthood
• survivors have a normal life span

cellular
• mouse embryo fibroblast growth slowed considerably
• fewer cells in S phase
• larger numbers of cells in G0 or G1
• reduced rate of DNA replication

endocrine/exocrine glands
• lack oocytes and follicles
• ovaries are small and grossly malformed
• reduced number of seminiferous tubules
• reduced spermatogonia
• degenerating primary spermatocytes
• high levels of apoptosis

growth/size/body
• mice that survive to adulthood are 50-55% normal size
• major organs are proportional

immune system
N
• thymic and periferral lymphocytes normal

limbs/digits/tail
• tail flexion anomalies similar to curly-tail (ct) mice

reproductive system
• lack oocytes and follicles
• ovaries are small and grossly malformed
• total absence of post meiotic cells
• failure in prophase I probably in zygotene stage
• reduced number of seminiferous tubules
• reduced spermatogonia
• degenerating primary spermatocytes
• high levels of apoptosis

homeostasis/metabolism
• reduced rate of DNA replication




Genotype
MGI:2681170
cx4
Allelic
Composition
Cdc7tm1Hmas/Cdc7tm1Hmas
Tg(EF1A-Cdc7)DKO28Hmas/Tg(EF1A-Cdc7)DKO28Hmas
Genetic
Background
involves: 129S/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdc7tm1Hmas mutation (0 available); any Cdc7 mutation (34 available)
Tg(EF1A-Cdc7)DKO28Hmas mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mouse embryo fibroblast proliferation and DNA synthesis essentially normal
• body weights normal
• males were fertile
• spermatogenesis restored
• testes remain small





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