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Phenotypes Associated with This Genotype
Genotype
MGI:3043188
cx3
Allelic
Composition
Slit1tm1.1Matl/Slit1tm1.1Matl
Slit2tm1Matl/Slit2tm1Matl
Slit3tm1.1Dor/Slit3tm1.1Dor
Genetic
Background
involves: 129S1/Sv * 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slit1tm1.1Matl mutation (0 available); any Slit1 mutation (71 available)
Slit2tm1Matl mutation (2 available); any Slit2 mutation (88 available)
Slit3tm1.1Dor mutation (1 available); any Slit3 mutation (81 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E12.5 commissural axons appear disorganized as they exit the floor plate lacking the typical bundled morphology
• at E12.5 more commissural axons stall and fail to exit the floor plate (78% versus 28% in controls) or recross the floor plate (~20% versus 0% in controls; controls in this study were Slit1tm1.1Matl homozygotes)
• the lateral funiculus (white matter tract) is significantly thinner in triple homozygous mutants compared to controls

cellular
• at E12.5 commissural axons appear disorganized as they exit the floor plate lacking the typical bundled morphology
• at E12.5 more commissural axons stall and fail to exit the floor plate (78% versus 28% in controls) or recross the floor plate (~20% versus 0% in controls; controls in this study were Slit1tm1.1Matl homozygotes)


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
12/17/2024
MGI 6.24
The Jackson Laboratory