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Mapping Data
Experiment
  • Experiment
    TEXT-QTL
  • Chromosome
    1
  • Reference
    J:40638 Vyse TJ, et al., Control of multiple autoantibodies linked with a lupus nephritis susceptibility locus in New Zealand black mice. J Immunol. 1997 Jun 1;158(11):5566-74
  • ID
    MGI:1278424
Genes
GeneAlleleAssay TypeDescription
D1Mit111 SSLP
Nba2 visible phenotype
D1Mit148 SSLP
Nba9 visible phenotype
Crp SSLP
Notes
  • Experiment
    Authors localized the Nba2 quantitative trait locus (QTL) associated with lupus nephritis and the production of multiple autoantibody specificities implicated in the pathogenesis of the disorder. This locus was mapped with the stongest linkage to mouse Chromosome 1, using 82 (NZB/BlNJ x SM/J)F1 x NZW/LacJ. Peak linkage was observed at D1Mit48 and D1Mit111 with p<0.002 at 92cM.

    Using 133 (B6.H2z x NZB)F1 x NZB backcross mice the authors map a QTL to a similar postion on Chromosome 1, peak linkage with Crp, p<0.001 at 94cM. A genome wide screen of the B6 backcross was completed with a total of 80 SSLP markers

    07.15.2015 Curator Note: Because two different crosses were used in this study we consider each a separate mapping experiment and have named the QTL identified in the B6 cross Nba9.

    When the data from both crosses was combined peak linkage was apparent between 94 and 96cM.. The 95% confidence interval is between 92 -97cM.

    Both Nba2 and Nba9 were linked (or showed a trend for linkage) with elevated serum levels of multiple autoantibodies, hypergammaglobulinemia and IgG1, IgG2a and/or IgG3 levels in each backcross.

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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
11/12/2024
MGI 6.24
The Jackson Laboratory