Primary Identifier | MGI:1857916 | 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 includes a deletion from Herc2 at nucleotide ~3000 including p, and possibly a small inversion. |