Primary Identifier | MGI:1856649 | Allele Type | Radiation induced |
Gene | Alm | Inheritance Mode | Semidominant |
Strain of Origin | (101 x C3H)F1 | Is Recombinase | false |
Is Wild Type | false |
description | This mutation arose in a (101 x C3H)F1 hybrid after gamma irradiation (J:6686), and is now extinct. Phenotypic Similarity to Human Syndrome: Dominant Cataracts in heterozygous mice (J:9528) |
molecularNote | This mutation arose in a (101 x C3H)F1 hybrid after gamma irradiation. |