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Ts(1716)66Yah Cytogenetic Marker Detail
Summary
  • Symbol
    Ts(1716)66Yah
  • Name
    trisomy, Chr 16 translocation to Chr 17, Yann Herault 66
  • Feature Type
    unclassified cytogenetic marker
  • IDs
    MGI:7408095
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 17, Syntenic
Human Diseases
less
  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    8 phenotypes from multigenic genotypes
    5 phenotype references
References
more
  • Summaries
    All 5
    Diseases 1
    Phenotypes 5
  • Earliest
    J:331897 Duchon A, et al., Ts66Yah, a mouse model of Down syndrome with improved construct and face validity. Dis Model Mech. 2022 Dec 1;15(12):dmm049721
  • Latest
    J:363984 Emili M, et al., Dendritic phenotype and proliferation potency in the hippocampal dentate gyrus of the Ts66Yah model of Down syndrome. Neurosci Lett. 2025 Feb 28;850:138156

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
03/25/2025
MGI 6.24
The Jackson Laboratory