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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cdc42tm1.1Rac
targeted mutation 1.1, Richard A Cerione
MGI:5495277
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cdc42tm1.1Rac/Cdc42tm1.1Rac involves: 129P2/OlaHsd * FVB/N MGI:5495324
cn2
Cdc42tm1.1Rac/Cdc42tm1.1Rac
Tg(Nes-cre)1Kln/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL MGI:5495326
cn3
Cdc42tm1.1Rac/Cdc42tm1.1Rac
Tg(GFAP-cre)25Mes/0
involves: 129P2/OlaHsd * FVB/N MGI:5495325


Genotype
MGI:5495324
hm1
Allelic
Composition
Cdc42tm1.1Rac/Cdc42tm1.1Rac
Genetic
Background
involves: 129P2/OlaHsd * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdc42tm1.1Rac mutation (0 available); any Cdc42 mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype




Genotype
MGI:5495326
cn2
Allelic
Composition
Cdc42tm1.1Rac/Cdc42tm1.1Rac
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdc42tm1.1Rac mutation (0 available); any Cdc42 mutation (45 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die within 72 hours of birth

nervous system
• more than half of mice exhibit mild or moderate hemorrhage in the lateral ventricle of the brain
• at E14.5, only sporadic proliferating cells are located in the basal ventricular zone and subventricular zone compared with wild-type mice
• at E16.5, proliferating cells are displaced from the ventricular surface and are present randomly in the basal ventricular and subventricular zone compared with wild-type mice
• decreased cell number at E16.5
• decreased cell number at E16.5
• nuclei lose their apical-basal direction
• decreased cell number at E16.5
• clustering of the ependymal cells
• lack of lining ependymal cells inside the third ventricle, aqueduct and spinal cord central canal
• more than half of mice exhibit mild or moderate hemorrhage in the lateral ventricle of the brain
• neuronal cells lining the lateral ventricle lack apical membrane domain
• lack of lining ependymal cells
• lack of lining ependymal cells
• slight increase in cell numbers with disruption of cell polarization at E14.5
• flattened surface with hypoplasia
• abnormal orientation at E16.5 indicating a folding problem
• lacking ventricular and sub-ventricular zones
• E18.5 glial cells exhibit a fried egg morphology in culture unlike wild-type cells
• decreased apical neuronal progenitor cell numbers in the cerebral cortex at E14.5 and E16.5
• collapse of the central canal and lack of differentiated ependymal cells

cellular
• at E14.5 and E16.5, radial glial cell nuclei exhibit impaired interkinetic nuclear migration compared to in wild-type cells
• at E14.5, only sporadic proliferating cells are located in the basal ventricular zone and subventricular zone compared with wild-type mice
• at E16.5, proliferating cells are displaced from the ventricular surface and are present randomly in the basal ventricular and subventricular zone compared with wild-type mice

behavior/neurological

cardiovascular system
• more than half of mice exhibit mild or moderate hemorrhage in the lateral ventricle of the brain

respiratory system
• in neonates




Genotype
MGI:5495325
cn3
Allelic
Composition
Cdc42tm1.1Rac/Cdc42tm1.1Rac
Tg(GFAP-cre)25Mes/0
Genetic
Background
involves: 129P2/OlaHsd * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdc42tm1.1Rac mutation (0 available); any Cdc42 mutation (45 available)
Tg(GFAP-cre)25Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• more than half of mice die before 3 months of age due to severe hydrocephalus

nervous system
• severe
• ependymal cells are detached from the lateral and third ventricle
• ependymal cells are detached from the lateral and third ventricle

craniofacial
• in most mice at 4 weeks

skeleton
• in most mice at 4 weeks

cellular





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory