| Primary Identifier | MGI:1857924 | 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 |
| description | This mutation is associated with mottled pigmentation and a mild juvenile development and fertility phenotype (jdf2; J:56827). |
| molecularNote | This mutation involves a rearrangement detected at nucleotide ~7000 using a cDNA clone isolated from a mouse cerebellum library with a human HERC2 probe. |
