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Mapping Data
Experiment
  • Experiment
    TEXT-QTL
  • Chromosome
    5
  • Reference
    J:81197 Johnson KR, et al., Ahl2, a second locus affecting age-related hearing loss in mice. Genomics. 2002 Nov;80(5):461-4
  • ID
    MGI:2662459
Genes
GeneAlleleAssay TypeDescription
Ahl7 visible phenotype
D5Mit309 PCR amplified length variant
D5Mit235 PCR amplified length variant
Ahl2 visible phenotype
Notes
  • Experiment
    110 (NOD/LtJ x C57BL/6J)F1 x NOD/LtJ backcross animals were typed for 90 microsatellite markers to identify loci linked to age-related hearing loss. Parental strain NOD/LtJ exhibits profound hearing loss at 6 months of age as measured by auditory brainstem response (ABR) threshold. A QTL mapped to 44 cM on mouse Chromosome 5 with a LOD score of 5.5 at D5Mit309. NOD/LtJ-derived alleles confer recessively inherited hearing loss at this locus, named Ahl2.

    The authors also analyzed a (CAST/Ei x NOD/LtJ)F1 x NOD/LtJ backcross population and mapped a significant QTL with LOD=4 to 42 cM at D5Mit235. This most likely represents the same locus, Ahl2. Again, NOD/LtJ-derived alleles confer recessively inherited hearing loss at this locus.

    10.13.2015 Curators Note: Because Ahl2 was originally mapped here using the (NOD/LtJ x C57BL/6J)F1 x NOD/LtJ backcross, which differs from the second cross, we consider the second cross a separate mapping experiment and have named that QTL Ahl7.

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)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory