irdc
Spontaneous Allele Detail

Summary

• Symbol: irdc
• Name: ICR derived retinal dysfunction cone
• MGI ID: MGI:3707707
• Gene: irdc Location: unknown
• Alliance: irdc page

Mutation origin

• Strain of Origin: ICR

Mutation description

• Allele Type: Spontaneous
• Mutation: Undefined
• Mutation details: This mutation, which is carried together with Gnat1^irdr in the IDR1 strain, affects retinal cone physiology.
• Inheritance: Recessive

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 irdc Mutation: 0 strains or lines available

Notes

Mice homozygous for this mutation have impaired cone electrophysiology but normal retinal morphology.

References

• Original: J:119862 Miyamoto M, et al., Visual electrophysiological features of two naturally occurring mouse models with retinal dysfunction. Curr Eye Res. 2006 Apr;31(4):329-35
• All: 2 reference(s)