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Mapping Data
Experiment
  • Experiment
    TEXT-Genetic Cross
  • Chromosome
    3
  • Reference
    J:104924 Pang JJ, et al., Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA). Mol Vis. 2005 Feb 28;11:152-62
  • ID
    MGI:3621810
Genes
GeneAlleleAssay TypeDescription
Rpe65
D3Mit19
Notes
  • Experiment
    To determin the genetic mapping location of the Rpe65 rd12 gene, the authors mated B6-rd12 mice to CAST/EiJ mice. The F1 mice, that exhibited no retinal abnormalities, were backcrossed (BC) to B6-rd12 mice. There were no recombinates found between Rpe65 and D3Mit19 from a total of 92 mice.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory