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Mapping Data
Experiment
  • Experiment
    CROSS
  • Chromosome
    4
  • Reference
    J:41514 Roderick TH, et al., A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse. Genomics. 1997 Jun 15;42(3):393-6
  • ID
    MGI:1095320
Genes
GeneAlleleAssay TypeDescription
Mup1 electrophoretic
In(4)56Rk visible phenotype
Notes
  • Reference
    These data have been submitted with MGD under accession numbers MGD-CREX- 621, 622, 623, and 624. Authors indicate that Rd4 may map with either the proximal or diatal inversion breakpoint in the In(4)56Rk Chromosome.
  • Experiment
    In represents the breakpoint in In(4)56Rk.Offspring types indicate alleles inherited from F1 parent.
CROSS
  • Type
    Backcross, sexes unspecified or combined
  • Female Parent
    + b/+ b
  • Strain
    Not Specified
  • Male Parent
    In a/+ b
  • Strain
    Not Specified
CROSS Data
MC #mice Mup1 In(4)56Rk
12 In a
12 + b
1 In b
1 + a
Statistics
Marker 1 Marker 2 # Recombinants Total % Recombinants Std Error
Mup1 In(4)56Rk 26 26 100.000 0.000

Contributing Projects:
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
11/12/2024
MGI 6.24
The Jackson Laboratory