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Phenotypes Associated with This Genotype
Genotype
MGI:4943295
Allelic
Composition
Cfl1tm1.1Wit/Cfl1tm1.1Wit
Genetic
Background
involves: 129 * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cfl1tm1.1Wit mutation (0 available); any Cfl1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• rare survivors die by P30
• nearly all mice die by between P1 and P3

nervous system
• in rare survivors
• neuronal progenitors exit the cell cycle prematurely and differentiate
• neurite outgrowth is impaired compared to in wild-type mice
• between E13 and E19, neuronal progenitor cells in the ventricular zone exhibit a migratory defect that prevents them from entering intermediate layers unlike in wild-type mice
• at E18, radial migration of proliferating cells into the cortex is impaired compared to in wild-type mice
• neuronal progenitors fail to reach the medial pallium unlike in wild-type mice
• interkinetic nuclear migration in the ventricular zone is impaired compared to in wild-type mice
• at E14 and E16, mice exhibit impaired cell proliferation of cells in the ventricular zone compared to in wild-type mice
• large parts of layers II, III, and IV are missing compared with wild-type mice
• however, the upper molecular layer I and the inner multiform layer VI are present
• neurites are shorter than in wild-type cells

behavior/neurological
• in rare survivors
• in rare survivors

growth/size/body
• in rare survivors

cellular
• neuronal progenitors exit the cell cycle prematurely and differentiate
• neurite outgrowth is impaired compared to in wild-type mice
• between E13 and E19, neuronal progenitor cells in the ventricular zone exhibit a migratory defect that prevents them from entering intermediate layers unlike in wild-type mice
• at E18, radial migration of proliferating cells into the cortex is impaired compared to in wild-type mice
• neuronal progenitors fail to reach the medial pallium unlike in wild-type mice
• interkinetic nuclear migration in the ventricular zone is impaired compared to in wild-type mice
• at E14 and E16, mice exhibit impaired cell proliferation of cells in the ventricular zone compared to in wild-type mice


Contributing Projects:
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
03/24/2026
MGI 6.24
The Jackson Laboratory