| Primary Identifier | MGI:3611307 | Allele Type | Chemically induced (ENU) |
| Gene | Pde6a | Inheritance Mode | Recessive |
| Strain of Origin | A.B6-Tyr<+>/J | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This phenotypic mutation was identified in an ENU mutagenesis screen. The molecular mutation is a single nucleotide G to A missense transition in exon 16, predicted to cause an amino acid change from valine to methionine (V685M). |
