| Primary Identifier | MGI:3581452 | Allele Type | Chemically induced (ENU) |
| Gene | Lama2 | Inheritance Mode | Recessive |
| Strain of Origin | C57BL/6J | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This mutation was shown by complementation analysis versus the original, dystrophia muscularis mutation to be an allele of Lama2. The molecular lesion is a single base change from T to C at the first position of codon 79, which converts Cys79 to Arg. |
