Analysis Tools|
Allele Symbol Allele Name Allele ID |
Dab1tm1.1Mull targeted mutation 1.1, Ulrich Mueller MGI:5141401 |
||||||||||||||||||||||||
| Summary |
5 genotypes
|
|
|
| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
|
|
| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
|
• at E14.5, neurons from mice electroporated with a cre-expressing vector at E12.5 fail to migrate into the cortical plate unlike neurons from control mice
• at E15.5, neurons from mice electroporated with a cre-expressing vector at E12.5 fail to exhibit translocating morphologies unlike neurons from control mice
• at P0, neurons from mice electroporated with a cre-expressing vector at E17.5 fail to migrate into the upper layers of the cortical plate unlike in neurons from control mice
• at P3, neurons from mice electroporated with a cre-expressing vector at E17.5 are restricted to below layer IV, near the top of layer V, of the cortical plate unlike in neurons from control mice
• at P8, neurons from mice electroporated with a cre-expressing vector at E17.5 are located below layer IV but above layers V-VI of the cortical plate unlike in neurons from control mice
• however, neurons from mice electroporated with a cre-expressing vector at E17.5 exhibit normal glia-dependent locomotion
|
|
• at E14.5, neurons from mice electroporated with a cre-expressing vector at E12.5 fail to migrate into the cortical plate unlike neurons from control mice
• at E15.5, neurons from mice electroporated with a cre-expressing vector at E12.5 fail to exhibit translocating morphologies unlike neurons from control mice
• at P0, neurons from mice electroporated with a cre-expressing vector at E17.5 fail to migrate into the upper layers of the cortical plate unlike in neurons from control mice
• at P3, neurons from mice electroporated with a cre-expressing vector at E17.5 are restricted to below layer IV, near the top of layer V, of the cortical plate unlike in neurons from control mice
• at P8, neurons from mice electroporated with a cre-expressing vector at E17.5 are located below layer IV but above layers V-VI of the cortical plate unlike in neurons from control mice
• however, neurons from mice electroporated with a cre-expressing vector at E17.5 exhibit normal glia-dependent locomotion
|
|
|
| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
|
• at E16.5, neuron layers is defective compared to in control mice
|
|
• the preplate fails to split unlike in control mice
|
|
• at E16.5, mice lack the marginal zone unlike control mice
|
|
• at E16.5
|
|
• at E16.5, neuron layers is defective compared to in control mice
|
|
|
| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
|
• at E16.5, neuron layers is defective compared to in control mice
|
|
• the preplate fails to split unlike in control mice
|
|
• at E16.5, mice lack the marginal zone unlike control mice
|
|
• at E16.5
|
|
• at E16.5, neuron layers is defective compared to in control mice
|
|
|
| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
| N |
• mice exhibit normal splitting of the cortical preplate
|
|
• late-born neurons are mislocalized deep within the cortex compared to in control mice
• however, the relative position of early-born neurons is normal
|
|
• neocortical lamination is disrupted compared to in control mice
|
|
• late-born neurons are mislocalized deep within the cortex compared to in control mice
• however, the relative position of early-born neurons is normal
|
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 09/30/2025 MGI 6.24 |
|
|
|
||


