| Primary Identifier | MGI:1857918 | Allele Type | Radiation induced |
| Gene | Oca2 | Inheritance Mode | Not Specified |
| Strain of Origin | (101/Rl x C3H/Rl)F1 x p STOCK | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This mutation includes a deletion from Herc2 at nucleotide ~2600 ending before the 5-prime end of p, and possibly an inversion. |