| Primary Identifier | MGI:1856695 | Allele Type | Chemically induced (other) |
| Gene | cx | Inheritance Mode | Recessive |
| Strain of Origin | (C3HA x C3H)F1 | Is Recombinase | false |
| Is Wild Type | false |
| description | This neurological mutation was found in offspring of a male mouse that had been treated with diethylsulphate. Affected mice develop slowly. They exhibit a staggering gait, ataxia, reduced mobility, cerebellar lesions, and have a narrowed face. Homozygous mutant mice mice die at 1.5 to 2 months old (J:13500). |
