| Primary Identifier | MGI:1857922 | 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 involves a deletion encompassing the 3' end of Herc2 and the 5' end of p. |