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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fbxw7+
wild type
MGI:2438793
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Fbxw7tm1Sje/Fbxw7+ involves: 129S7/SvEvBrd * C57BL/6 MGI:3038805
ht2
Fbxw7tm1.1Iken/Fbxw7+ involves: C57BL/6 * C57BL/6N MGI:6157077
cn3
Fbxw7tm1Itom/Fbxw7+
Tg(Pgk1-cre)1Lni/0
involves: 129 * BALB/c * C57BL/6 * C57BL/6J MGI:5007621
cn4
Fbxw7tm1Iken/Fbxw7+
Krastm4Tyj/Kras+
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: 129S4/SvJae * C57BL/6 * C57BL/6N * DBA MGI:6157295
cn5
Fbxw7tm2Iaai/Fbxw7+
Tg(Mx1-cre)1Cgn/0
involves: C57BL/6 * CBA MGI:5524227
cn6
Fbxw7tm2Iaai/Fbxw7+
Tg(EIIa-cre)C5379Lmgd/0
involves: C57BL/6 * FVB/N MGI:5524228


Genotype
MGI:3038805
ht1
Allelic
Composition
Fbxw7tm1Sje/Fbxw7+
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fbxw7tm1Sje mutation (0 available); any Fbxw7 mutation (81 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
N
• mice did not develop spontaneous tumors for up to 1 year of age




Genotype
MGI:6157077
ht2
Allelic
Composition
Fbxw7tm1.1Iken/Fbxw7+
Genetic
Background
involves: C57BL/6 * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fbxw7tm1.1Iken mutation (0 available); any Fbxw7 mutation (81 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no living newborns are obtained, however normal ratios of E18.5 embryos are seen, indicating that mutants die around birth

respiratory system
• alveolar septa are thickened at E18.5
• increase in the number of proliferating cells (Ki67+) in the lung
• aerated lung areas are small and alveolar septa are thickened at E18.5, suggesting respiratory failure as cause of perinatal lethality

craniofacial
• 1.3% of mutants exhibit cleft palate

digestive/alimentary system
• 1.3% of mutants exhibit cleft palate

growth/size/body
• 1.3% of mutants exhibit cleft palate

vision/eye
• 17% of mutants exhibit eyes open at birth




Genotype
MGI:5007621
cn3
Allelic
Composition
Fbxw7tm1Itom/Fbxw7+
Tg(Pgk1-cre)1Lni/0
Genetic
Background
involves: 129 * BALB/c * C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fbxw7tm1Itom mutation (0 available); any Fbxw7 mutation (81 available)
Tg(Pgk1-cre)1Lni mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all pups die shortly after birth

respiratory system
• disruption of the canalicular and /or terminal sac stage of lung development
• thickened alveolar septa at E18.5

vision/eye
• in 17 of 40 mice

craniofacial
• in 30% of mice

digestive/alimentary system
• in 30% of mice

growth/size/body
• in 30% of mice




Genotype
MGI:6157295
cn4
Allelic
Composition
Fbxw7tm1Iken/Fbxw7+
Krastm4Tyj/Kras+
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * C57BL/6N * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fbxw7tm1Iken mutation (0 available); any Fbxw7 mutation (81 available)
Krastm4Tyj mutation (12 available); any Kras mutation (88 available)
Speer6-ps1Tg(Alb-cre)21Mgn mutation (6 available); any Speer6-ps1 mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• bile duct hyperplasia is seen in some mice at 8 months of age
• bile duct dilation is seen in some mice at 8 months of age

liver/biliary system
• bile duct hyperplasia is seen in some mice at 8 months of age
• bile duct dilation is seen in some mice at 8 months of age




Genotype
MGI:5524227
cn5
Allelic
Composition
Fbxw7tm2Iaai/Fbxw7+
Tg(Mx1-cre)1Cgn/0
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fbxw7tm2Iaai mutation (0 available); any Fbxw7 mutation (81 available)
Tg(Mx1-cre)1Cgn mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
N
• pIpC-treated mice do not develop leukemia
• pIpC-treated mice infected with a retrovirus expression a truncated form of Notch1 that is constitutively cleaved in a ligand-independent manner or a Notch1 lacking the PEST domain exhibit shorted latency to development of leukemia

hematopoietic system
N
• pIpC-treated mice exhibit normal numbers of hematopoietic stem cells and are more functionally competent than in cells from Fbxw7tm1Iaai/Fbxw7+ Tg(Mx1-cre)1Cgn mice

immune system
N
• pIpC-treated mice exhibit normal numbers of early T cell progenitors in the thymus




Genotype
MGI:5524228
cn6
Allelic
Composition
Fbxw7tm2Iaai/Fbxw7+
Tg(EIIa-cre)C5379Lmgd/0
Genetic
Background
involves: C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fbxw7tm2Iaai mutation (0 available); any Fbxw7 mutation (81 available)
Tg(EIIa-cre)C5379Lmgd mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
N
• mice do not develop developmental defects

neoplasm
N
• mice do not develop tumors





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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
03/18/2025
MGI 6.24
The Jackson Laboratory