rd13
Chemically induced Allele Detail

Summary

• Symbol: rd13
• Name: retinal degeneration 13
• MGI ID: MGI:3045621
• Gene: rd13 Location: unknown Genetic Position: Chr15, Syntenic
• Alliance: rd13 page

Mutation origin

• Strain of Origin: C57BL/6J

Mutation description

• Allele Type: Chemically induced (ENU)
• Mutation: Undefined
• Mutation details: This retinal degeneration mutation was discovered in conjunction with Scn8a^nmf5 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.
• Inheritance: Recessive

Expression

In Structures Affected by this Mutation:

1 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 0 strains available Cell Lines: 0 lines available
• Carrying any rd13 Mutation: 0 strains or lines available

References

• Original: J:90095 Buchner DA, et al., Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Na(v)1.6) and a genetically linked retinal mutation, rd13. Mamm Genome. 2004 May;15(5):344-51
• All: 3 reference(s)