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Mapping Data
Experiment
  • Experiment
    TEXT-QTL
  • Chromosome
    11
  • Reference
    J:102036 Bergren SK, et al., Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn 2 a. Mamm Genome. 2005 Sep;16(9):683-90
  • ID
    MGI:4353904
Genes
GeneAlleleAssay TypeDescription
Moe1
D11Mit289
Notes
  • Experiment
    The Authors carried out ten backcross generations in transferring the Scn2a<Q54 > transgene onto the C57BL/6J background, thus creating congenic line C57BL/6J.Q54 (abbreviated B6.Q54).
    Further the B6.Q54 congenic mice were crossed to strain SJL/J. Theresulting (SJL X B6)F1.Q54 offspring were abbreviated as F1.Q54. For mapping loci that modified epilepsy the F1.Q54 mice were backcrossed to C57BL/6J. Categorical trait interval mapping with a genome wide scan provided evidence for the existence of twomodifier loci one on mouse Chromosomes 11 and another on mouse 19. Moe1 mapped with Chromosome 11 and showed a peak at 54 cM (95 Mb) and is significantly associated with D11Mit289. The mouse Chromosome 19 locus Moe2 shows a peak at 24 cM (31.3 Mb) and has a significant association with D19Mit135

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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
12/10/2024
MGI 6.24
The Jackson Laboratory