| Primary Identifier | MGI:5818741 | Allele Type | Chemically induced (ENU) |
| Attribute String | Null/knockout | Gene | Me2 |
| Strain of Origin | C3HeB/FeJ | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | The molecular lesion is a A-to-G missense mutation (1400A-G) in codon 467 in exon 10. This is predicted to alter amino acid 467 from an aspartic acid to a glycine (D467G) in the encoded protein. |
