Ts(1716)65Dn
Radiation induced Allele Detail
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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
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Cardiovascular abnormalities in Ts(1716)65Dn/0 mice
Show the 1 phenotype image(s) involving this allele.
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Allele Type: |
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Radiation induced |
Mutation: |
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Translocation
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Ts(1716)65Dn involves 140 genes/genome features (Ncam2, 7120432I05Rik, Gm49558 ...)
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Mutation details: About 15% of the distal end of chromosome 16 (about 13.4 Mb; between Ncam2 (81,624,530 bp; NCBI37/mm9) and Mrpl39 (84,718,526; NCBI37/mm9)) is fused to less than 10% of the centromeric end of chromosome 17 (about 5 to 10 Mb; between RP23-147G23, Synj2 (5,988,977 bp; NCBI37/mm9) and D17Mit58 (10,489,635 bp; NCBI37/mm9)) 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, J:178871)
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View phenotypes and curated references for all genotypes (concatenated display).
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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: |
310 reference(s) |
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