irdc Gene Detail

Summary

• Symbol
  irdc
• Name
  ICR derived retinal dysfunction cone

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:4835984
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome Unknown

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  2 phenotypes from multigenic genotypes
  2 phenotype references
  

• All Mutations and Alleles
  1
• Spontaneous
  1
• Find Mice (IMSR)
  0 strains or lines available

References

• Summaries
  All 2

  Phenotypes 2
• Earliest
  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
• Latest
  J:167661 Miyamoto M, et al., IRD1 and IRD2 mice, naturally occurring models of hereditary retinal dysfunction, show late-onset and progressive retinal degeneration. Curr Eye Res. 2010 Feb;35(2):137-45