| Primary Identifier | MGI:4462402 | Allele Type | Chemically induced (ENU) |
| Gene | Magoh | Inheritance Mode | Not Specified |
| Strain of Origin | BALB/cJ | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This mutation was discovered in an ENU mutagenesis screen for alterations in the neurocristopathy phenotype of mice homozygous for a targeted mutation of Sox10. The molecular change is a single nucleotide deletion 198delG causing a frameshift resulting in a truncated protein. Aberrantly sized transcript by RT-PCR in brain was not observed. This is a null allele. |
