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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mob1atm1.2Asuz
targeted mutation 1.2, Akira Suzuki
MGI:5473805
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Mob1atm1.2Asuz/Mob1atm1.2Asuz
Mob1bGt(CC0690)Wtsi/Mob1b+
involves: 129P2/OlaHsd * C57BL/6 MGI:5473843
cx2
Mob1atm1.2Asuz/Mob1a+
Mob1bGt(CC0690)Wtsi/Mob1bGt(CC0690)Wtsi
involves: 129P2/OlaHsd * C57BL/6 MGI:5473844
cx3
Mob1atm1.2Asuz/Mob1atm1.2Asuz
Mob1bGt(CC0690)Wtsi/Mob1bGt(CC0690)Wtsi
involves: 129P2/OlaHsd * C57BL/6 MGI:5473845


Genotype
MGI:5473843
cx1
Allelic
Composition
Mob1atm1.2Asuz/Mob1atm1.2Asuz
Mob1bGt(CC0690)Wtsi/Mob1b+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mob1atm1.2Asuz mutation (0 available); any Mob1a mutation (18 available)
Mob1bGt(CC0690)Wtsi mutation (0 available); any Mob1b mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Tumorgenesis in Mob1atm1.2Asuz/Mob1atm1.2Asuz Mob1bGt(CC0690)Wtsi/Mob1b+ or Mob1atm1.2Asuz/Mob1a+ Mob1bGt(CC0690)Wtsi/Mob1bGt(CC0690)Wtsi mice

neoplasm
• in myofibrosarcomas some mice
• mice develop malignant outer root sheath tumors resembling trichilemmal carcinomas

skeleton
• in half of mice
• in the femur of some mice
• in the calvaria of most mice

integument

hearing/vestibular/ear

behavior/neurological
• in some mice due to disorganized inner ear hair bundles in the cochlear organ of Corti

craniofacial
• in half of mice

nervous system

respiratory system

growth/size/body
• in half of mice

digestive/alimentary system

endocrine/exocrine glands

liver/biliary system




Genotype
MGI:5473844
cx2
Allelic
Composition
Mob1atm1.2Asuz/Mob1a+
Mob1bGt(CC0690)Wtsi/Mob1bGt(CC0690)Wtsi
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mob1atm1.2Asuz mutation (0 available); any Mob1a mutation (18 available)
Mob1bGt(CC0690)Wtsi mutation (0 available); any Mob1b mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Tumorgenesis in Mob1atm1.2Asuz/Mob1atm1.2Asuz Mob1bGt(CC0690)Wtsi/Mob1b+ or Mob1atm1.2Asuz/Mob1a+ Mob1bGt(CC0690)Wtsi/Mob1bGt(CC0690)Wtsi mice

neoplasm
• in myofibrosarcomas some mice
• mice develop malignant outer root sheath tumors resembling trichilemmal carcinomas

skeleton
• in half of mice
• in the femur of some mice
• in the calvaria of most mice

integument

hearing/vestibular/ear

craniofacial
• in half of mice

behavior/neurological
• in some mice due to disorganized inner ear hair bundles in the cochlear organ of Corti

nervous system

endocrine/exocrine glands

digestive/alimentary system

growth/size/body
• in half of mice




Genotype
MGI:5473845
cx3
Allelic
Composition
Mob1atm1.2Asuz/Mob1atm1.2Asuz
Mob1bGt(CC0690)Wtsi/Mob1bGt(CC0690)Wtsi
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mob1atm1.2Asuz mutation (0 available); any Mob1a mutation (18 available)
Mob1bGt(CC0690)Wtsi mutation (0 available); any Mob1b mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• despite decidua formation, mice are absorbed by E6.5

cellular
• micronuclei in mouse embryonic fibroblasts
• in mouse embryonic fibroblasts
• after 8 days in culture, E3.5 embryos exhibit growth failure of the inner cell mass
• however, the trophoectoderm develops normally

embryo
• after 8 days in culture, E3.5 embryos exhibit growth failure of the inner cell mass
• however, the trophoectoderm develops normally





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory