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| Nomenclature |
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Symbol:
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Tc(HSA21)1TybEmcf
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Name:
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transchromosomal, human 21, line 1, Victor Tybulewicz and Elizabeth M C Fisher
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MGI ID: |
MGI:3814712 |
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Synonyms: |
Tc1, Tc(HSA21)91-1Emcf |
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Gene:
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Tc(Hsa21)1TybEmcf
Location:
unknown
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Mutation origin |
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Mutant Cell Line:
| 91-1 (Not Specified) |
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Germline Transmission:
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Earliest citation of germline transmission:
J:101383
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Parent Cell Line:
| Other (see notes) (ES Cell) |
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Strain of Origin:
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129S2/SvPas
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Mutation description |
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Allele
Type: | |
Not Applicable |
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Mutation: | |
Other |
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Mutation details: A freely segregating chromosome composed of 42 Mb, or 90%, of human chromosome 21 (spanning D21S5-CXADR, D21S1922-IFNAR1 and RUNX1-COL6A1) was created in MPI-VI (129S2/SvPas) ES cells using irradiated microcell-mediated chromosome transfer. (J:101383)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Notes |
ES cell line = MPI-VI.
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| References |
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Original: |
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
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All: |
11 reference(s)
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