About   Help   FAQ
Mapping Data
Experiment
  • Experiment
    TEXT-QTL
  • Chromosome
    17
  • Reference
    J:66474 Clapcott SJ, et al., Evidence for genomic imprinting of the major QTL controlling susceptibility to trypanosomiasis in mice. Parasite Immunol. 2000 May;22(5):259-63
  • ID
    MGI:2151135
Genes
GeneAlleleAssay TypeDescription
Tir1 reported elsewhere
D17Mit16
Notes
  • Experiment
    Four backcross populations [(C57BL/6JOlaHsd x BALB/cOlaHsd)F1 x BALB/cOlaHsd, BALB/cOlaHsd x (C57BL/6JOlaHsd x BALB/cOlaHsd)F1, (BALB/cOlaHsd x C57BL/6JolaHsd)F1 x BALB/cOlaHsd, and BALB/cOlaHsd x (C57BL/6JOlaHsd x BALB/cOlaHsd)F1] were used to assess the effect of imprinting at loci involved in trypanosomiasis survival (Tir1, Tir2, and Tir3).

    Tir1 showed significant linkage for trypanosomiasis survival time with parent of origin at D17Mit16 (LOD = 5.9). Animals from BALB/cOlaHsd fathers and (C57BL/6JOlaHsd x BALB/cOlaHsd)F1 or (C57BL/6JOlaHsd x BALB/cOlaHsd)F1 mothers exhibited higher survival rates than animals from (C57BL/6JOlaHsd x BALB/cOlaHsd)F1 or (C57BL/6JOlaHsd x BALB/cOlaHsd)F1 fathers and BALB/cOlaHsd mothers. Authors speculate that genomic imprinting may play a role in trypanosomiasis survival at Tir1.

    Tir3 showed suggestive linkage for trypanosomiasis survival time and parent of origin at D1Mit102 (LOD = 2.2-2.8), and Tir2 was not detected for linkage to survival time and parent of origin.

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
05/14/2024
MGI 6.23
The Jackson Laboratory