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Phenotypes Associated with This Genotype
Genotype
MGI:3039457
Allelic
Composition
Epha8tm1Bbd/Epha8tm1Bbd
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epha8tm1Bbd mutation (0 available); any Epha8 mutation (73 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• homozygous mutant mice were behaviorally normal and displayed no major differences in any structure of the brain, including the brainstem and cerebellum, relative to wild-type
• retrograde labeling experiments revealed a commissural defect, whereby tectal axons failed to project from the superior colliculus of the midbrain to the contralateral inferior colliculus
• notably, homozygous mutant mice exhibited an aberrant ipsilateral axonal tract that projected to the ventral region of the cervical spinal cord
• retrograde labeling revealed that these abnormal projections originated from a small subpopulation of superior colliculus neurons

cellular
• retrograde labeling experiments revealed a commissural defect, whereby tectal axons failed to project from the superior colliculus of the midbrain to the contralateral inferior colliculus


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
03/18/2025
MGI 6.24
The Jackson Laboratory