| Primary Identifier | MGI:3045621 | Allele Type | Chemically induced (ENU) |
| Gene | rd13 | Inheritance Mode | Recessive |
| Strain of Origin | C57BL/6J | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This retinal degeneration mutation was discovered in conjunction with Scn8anmf5 during an ENU mutagenesis screen at the Neuroscience Mutagenesis Facility at The Jackson Laboratory. Genetic studies demonstrated that a separate gene other than Scn8a was responsible for the retinal phenotype. Candidate gene testing showed that no coding or splice site mutation was present in Pde1b. |
