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Tc(HSA21)1TybEmcf Other Genome Feature Detail
Summary
  • Symbol
    Tc(HSA21)1TybEmcf
  • Name
    transchromosomal, human 21, line 1, Victor Tybulewicz and Elizabeth M C Fisher
  • Synonyms
    Tc(HSA21)91-1Emcf
  • Feature Type
    unclassified other genome feature
  • IDs
    MGI:3814702
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome Unknown
Human Diseases
less
  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    17 phenotypes from multigenic genotypes
    31 phenotype references
References
more
  • Summaries
    All 32
    Diseases 1
    Phenotypes 31
  • Earliest
    J:101383 O'Doherty A, et al., An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes. Science. 2005 Sep 23;309(5743):2033-7
  • Latest
    J:363358 Wu Y, et al., Reduction of Cystatin B results in increased cathepsin B activity in disomic but not Trisomy 21 human cellular and mouse models. PLoS One. 2025;20(1):e0316822
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
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Send questions and comments to User Support. 		last database update
03/25/2025
MGI 6.24 		The Jackson Laboratory