About   Help   FAQ
Mapping Data
Experiment
  • Experiment
    TEXT-QTL
  • Chromosome
    7
  • Reference
    J:23719 Drake CG, et al., Analysis of the New Zealand Black contribution to lupus-like renal disease. Multiple genes that operate in a threshold manner. J Immunol. 1995 Mar 1;154(5):2441-7
  • ID
    MGI:5644330
Genes
GeneAlleleAssay TypeDescription
Nba3 PCR amplified length variant
D7Mit17 PCR amplified length variant
Notes
  • Experiment
    NZB and NZW mice spontaneously develop an autoimmune process remarkably simiar to human systemic lupus erythematosus. To identify additional NZB contributors to lupus like disease 90 female (NZB x SM/J)F1 x NZW backcross mice were followed for the development of sever renal disease and were comprehensively phenotyped. To identify disease associated loci the same mice were genotyped using PCR.

    A statistically significant association with disease was noted at 6 separate locations on Chrs 1, 4, 7, 10, 13 and 19. p<0.05 was the cutoff to define statistical significance. Mice carrying the NZB allele at five of these 6 positions died from severe renal disease.

    Of the six significant loci evident in the backcross, the level of association with disease at the Chromosome 1 locus was particularly strong, p<0.02, peaking with marker D1Mit111 at 61cM. This QTL has been named Nba2.

    The Chromosome 7 locus has been labeled Nba3, peaking with marker D7Mit17, p<0.008 at 45.0cM

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/28/2024
MGI 6.13
The Jackson Laboratory