| Primary Identifier | MGI:1857917 | Allele Type | Radiation induced |
| Gene | Oca2 | Inheritance Mode | Not Specified |
| Strain of Origin | (101/Rl x C3H/Rl)F1 | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This mutation is a multigene deletion extending from Herc2, at approximately nucleotide ~3300, through Oca2, Gabrg3, D7Cwr15, Gabra5 and at least part of Gabra3. |