About   Help   FAQ
Mapping Data
Experiment
  • Experiment
    TEXT-Cytogenetic Localization
  • Chromosome
    16
  • Reference
    J:29232 Reeves RH, et al., A mouse model for Down syndrome exhibits learning and behaviour deficits [see comments]. Nat Genet. 1995 Oct;11(2):177-84
  • ID
    MGI:45659
Genes
GeneAlleleAssay TypeDescription
Pgk1-ps1 Southern analysis B24
D16Mit68 PCR amplified length variant MPC429
T(16C3-4;17A2)65Dn
App Southern analysis pDS10.1
Notes
  • Experiment
    Five mouse x Chinese hamster somatic cell hybrid lines were used to more finely map the T(16;17)65Dn translocation breakpoint. Hybrid lines H65B3.2a-2, -8, -13, and -14 carry Chromosome 16 material proximal to the translocation breakpoint, and hybrid line H65B3.2a-1 carries Chromosome 16 material distal to the breakpoint. The hybrid lines carrying the proximal chromsome material were all positive for the marker Pgk1-ps1 and negative for App, while the one hybrid carrying distal chromosome material was negative for Pgk1-ps1 and App. All 5 hybrid lines were negative for D16Mit68, which lies between Pgk1-ps1 and App. This leads the authors to conclude a small portion of Chromsome 16 may have been deleted from the chromosome at the time of the translocation.Additionally, this places the T(16;17)65Dn translocation breakpoint at the D16Mit68 locus.

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
04/16/2024
MGI 6.23
The Jackson Laboratory