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Radiation induced Allele Detail
Symbol: Ts(1716)65Dn
Name: trisomy, Chr 16 translocation to Chr 17, Davisson 65
MGI ID: MGI:3512067
Synonyms: T(16C3-4;17A2)65Dn, Ts16, Ts65Dn
Gene: Ts(1716)65Dn  Location: unknown  Genetic Position: Chr16, Syntenic
Cardiovascular abnormalities in Ts(1716)65Dn/0 mice

Show the 1 phenotype image(s) involving this allele.

Strain of Origin:  DBA/2J
Allele Type:    Radiation induced
Mutation:    Translocation
Mutation detailsAbout 15% of the distal end of chromosome 16 is fused to less than 10% of the centromeric end of chromosome 17 to form a small translocation chromosome. The translocation breaks mouse Chr 16 just proximal to the amyloid precursor protein ( App ) gene and contains the HSA21-homologous genes from App to the telomere. The translocation chromosome also contains the centromere and a small portion (~5%) of Chr 17. Northern and Western blotting and enzyme activity assays demonstrate that genes on the translocation product are expressed at elevated levels in segmentally trisomic animals. (J:30229, J:71031)
View phenotypes for all genotypes (concatenated display).
Disease models
In Mice Carrying this Mutation: 6 assay results
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Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Ts(1716)65Dn Mutation:  2 strains or lines available
Original:  J:30229 Davisson MT, et al., Segmental trisomy as a mouse model for Down syndrome. Prog Clin Biol Res. 1993;384:117-33
All:  202 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.01
The Jackson Laboratory