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Mapping Data
Experiment
  • Experiment
    TEXT-Genetic Cross
  • Chromosome
    5
  • Reference
    J:68340 Maeda YY, et al., Two interactive genes responsible for a new inherited cataract (RCT) in the mouse. Mamm Genome. 2001 Apr;12(4):278-83
  • ID
    MGI:3028178
Genes
GeneAlleleAssay TypeDescription
mrct
D5Mit239
Crybb1 reported elsewhere
Crybb2 reported elsewhere
Crybb3 reported elsewhere
Cryba4 reported elsewhere
Notes
  • Experiment
    In a RCT x (RCT x MSM/Ms)F1 backcross the a modifier of the rct phenotype was shown to be linked with with D5Mit239 (chi square 25.2). This recessively inherited locus is named mrct (modifier of Rinshoken cataract). Homozygosity for mrct accelerates the onset of cataracts in rct homozygous animals. Parental strain RCT is a cataract mutant derived from SJL/J.

    A cluster of beta-crystallin genes, Crybb1 (59 cM), Crybb2 (60 cM), Crybb3(60 cM), and Cryba4, map near mrct and are potential candidate genes. Crybb2, Crybb3, and Cryba4 eye RNA from inbred strains RCT, SJL/J, MSM/Ms, and MA/MyJwere synthesized and sequenced. However, no sequence variations were detected.

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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
04/23/2024
MGI 6.23
The Jackson Laboratory