Del(2Hoxd9-Hoxd13)8Ddu
Targeted Allele Detail
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Symbol: |
Del(2Hoxd9-Hoxd13)8Ddu |
Name: |
deletion, Chr 2, Denis Duboule 8 |
MGI ID: |
MGI:3616163 |
Synonyms: |
Del8Ddu, Del(9-13) |
Gene: |
Del(2Hoxd9-Hoxd13)8Ddu Location: Chr2:74498654-74530552 bp Genetic Position: Chr2, Syntenic
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Germline Transmission: |
Earliest citation of germline transmission:
J:103924
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Parent Cell Line: |
D3 (ES Cell)
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Strain of Origin: |
129S2/SvPas
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Allele Type: |
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Targeted (Null/knockout) |
Mutations: |
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Intergenic deletion, Intragenic deletion
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Del(2Hoxd9-Hoxd13)8Ddu involves 8 genes/genome features (Hoxd13, Hoxd12, Hoxd11 ...)
View all
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Mutation details: Produced by targeted meiotic recombination in a cross between Evx2/Hoxd13 and Hoxd in the presence of Tg(Sycp1-cre)4Min. Hoxd9, Hoxd10, Hoxd11, Hoxd12, and Hoxd13 are all deleted from the Hoxd cluster.
(J:103924)
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View phenotypes and curated references for all genotypes (concatenated display).
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Mouse strains and cell lines
available from the International Mouse Strain Resource
(IMSR) |
Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available
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Carrying any Del(2Hoxd9-Hoxd13)8Ddu Mutation: |
0 strains or lines available
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Original: |
J:103924 Tarchini B, et al., HoxD cluster scanning deletions identify multiple defects leading to paralysis in the mouse mutant Ironside. Genes Dev. 2005 Dec 1;19(23):2862-76 |
All: |
1 reference(s) |
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