Del(2Hoxd10)13Ddu
Targeted Allele Detail

Summary

• Symbol: Del(2Hoxd10)13Ddu
• Name: deletion, Chr 2, Denis Duboule 13
• MGI ID: MGI:3616194
• Synonyms: Del(10), Del13Ddu
• Gene: Del(2Hoxd10)13Ddu Location: unknown Genetic Position: Chr2, Syntenic

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:103924
• Parent Cell Line: D3 (ES Cell)
• Strain of Origin: 129S2/SvPas

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutation: Intergenic deletion
• Del(2Hoxd10)13Ddu involves 2 genes/genome features (Hoxd11, Hoxd10) View all
• Mutation details: Produced by targeted meiotic recombination in a cross between Hoxd^tm5Ddu and Hoxd^tm13Ddu in the presence of Tg(Sycp1-cre)4Min. Only Hoxd10 is deleted from the Hoxd cluster. (J:103924)

Expression

In Structures Affected by this Mutation:

1 anatomical structure(s)

Find Mice (IMSR)

• 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
• Carrying any Del(2Hoxd10)13Ddu Mutation: 0 strains or lines available

References

• 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: 4 reference(s)