Summary |
|
||||||||||
Variant origin |
|
||||||||||
Variant description |
|
||||||||||
Notes |
Mapping and Phenotype information for this QTL, its variants and associated markersJ:81197110 (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. |
||||||||||
References |
|
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 11/05/2024 MGI 6.24 |
|
|