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Mapping Data
Experiment
  • Experiment
    TEXT-Genetic Cross
  • Chromosome
    13
  • Reference
    J:747 Holcombe RF, et al., Linkage of loci associated with two pigment mutations on mouse chromosome 13. Genet Res. 1991 Aug;58(1):41-50
  • ID
    MGI:45295
Genes
GeneAlleleAssay TypeDescription
Lyst visible phenotype
Tcrg-C Southern analysis Tcrg-C probe
H3c7 electrophoretic
Prl Southern analysis pIT200
Fim1 Southern analysis 167-PP15
Dhfr Southern analysis pdhfr3.2
Ap3b1 visible phenotype
Gzma Southern analysis Ctla3 cDNA
Notes
  • Reference
    A recombination between loci reported for this reference are recorded in both the summary haplotype data and in the 2x2 recombination tables. Authors use Muhf instead of Ctla3.
  • Experiment
    Progeny from one intra and two inter-specific backcrosses was used to map bg and pe to mouse Chromosome 13. The following recombination phenotype between adjacent loci was determined as bg - 3.2 +/- 1.2 - Tcrg-C - 6.3 +/- 3.5 - Hist1h3f - 2.2 +/- 2.1 - Prl - 2.8 +/- 1.8 - Fim1 - 42.3 +/- 9.7 - Dhfr - 8.6 +/- 4.7 - pl - 5.4 +/- 3.0 - Ctla3

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
10/29/2024
MGI 6.24
The Jackson Laboratory