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Mapping Data
Experiment
  • Experiment
    TEXT-QTL
  • Chromosome
    11
  • Reference
    J:25969 Gill BM, et al., Genetic linkage of thymic T-cell proliferative unresponsiveness to mouse chromosome 11 in NOD mice. A possible role for chemokine genes. Diabetes. 1995 Jun;44(6):614-9
  • ID
    MGI:3037301
Genes
GeneAlleleAssay TypeDescription
Idd4 resistance/susceptibility
Ccl3 reported elsewhere
Ccl4 reported elsewhere
Ccl2 reported elsewhere
Mpo reported elsewhere
Xmv42 reported elsewhere
Mpmv4 reported elsewhere
D11Mit38 PCR amplified length variant
D11Nds1 PCR amplified length variant
Notes
  • Experiment
    Linkage analysis was performed on a BXD recombinant inbred (RI) panel, a (NOD x C57BL/6)F2 intercross, and on a (NOD x C57BL/6)F1 x NOD backcross population to map QTLs associated with T-cell proliferative repsonsiveness in relation to insulin dependent diabetes mellitus. Parental strain C57BL/6 exhibits high T-cell proliferation in response to stimulation of the T cell receptor/CD3 complex whereas parental strains DBA/2 and NOD exhibits low T-cell proliferative response.

    In the BXD population a statistically significant locus mapped to 49 cM on mouse Chromosome 11 near Mpo (P=0.001-0.002). This region includes Ccl2, Ccl3, Ccl4, Xmv42, and Mpmv4. In the (NOD x C57BL/6)F1 x NOD backcross and the (NOD x C57BL/6)F2 intercross, statistical significance is associated with a locus near D11Mit38 at 49 cM on mouse Chromosome 11. This locus is thought to represent Idd4. Homozygosity for C57BL/6-derived alleles confers increased T-cell proliferation at this locus.

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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
10/29/2024
MGI 6.24
The Jackson Laboratory