| Primary Identifier | MGI:1856329 | Allele Type | Chemically induced (ENU) |
| Gene | Dmd | Inheritance Mode | Recessive |
| Strain of Origin | C3Ha.Cg-Hpr1t<a> Pgk1<a> | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | An A to T transversion two nucleotides 5' to the intron 42/exon 43 splice accesptor site. This mutation abolishes splicing at this site and induces aberrant splice products that do not preserve the reading frame. |
