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

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome Unknown

Human Diseases

• Mutations/Alleles
  1 with disease annotations

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  17 phenotypes from multigenic genotypes
  29 phenotype references
  

• All Mutations and Alleles
  1
• Find Mice (IMSR)
  4 strains or lines available

References

• Summaries
  All 30

  Diseases 1

  Phenotypes 29
• 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:326829 Sherman KM, et al., Low bone mass and impaired fracture healing in mouse models of Trisomy21 (Down syndrome). Bone. 2022 Jun 15;162:116471