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Phenotypes Associated with This Genotype
Genotype
MGI:3043177
Allelic
Composition
Robo1tm1Matl/Robo1tm1Matl
Genetic
Background
involves: CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Robo1tm1Matl mutation (2 available); any Robo1 mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at E11.5 misprojecting commissural axons are seen entering the doral floor plate and growing towards the ventral ventricular zone, however by E12.5 this phenotype is no longer seen
• at E12.5 many large stalled growth cones that send out multiple filopodia are seen in homozygous mutants
• the lateral funiculus (white matter tract) is significantly thicker in homozygous mutants compared to wild-type mice as a result of commissural axons growing further away from the floor plate

cellular
• at E11.5 misprojecting commissural axons are seen entering the doral floor plate and growing towards the ventral ventricular zone, however by E12.5 this phenotype is no longer seen
• at E12.5 many large stalled growth cones that send out multiple filopodia are seen in homozygous mutants


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
01/28/2026
MGI 6.24
The Jackson Laboratory