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Allele : Del(2Hoxd11-Hoxd13)29Ddu deletion, Chr 2, Denis Duboule 29

Primary Identifier  MGI:1857661 Allele Type  Targeted
Attribute String  Null/knockout, Reporter Gene  Del(2Hoxd11-Hoxd13)29Ddu
Transmission  Germline Strain of Origin  129S2/SvPas
Is Recombinase  false Is Wild Type  false
molecularNote  This allele involved the use of an embryonic stem cell line carrying an ectopic Hoxd11/lacZ transgene located between the resident Hoxd13 and Evx2 genes and flanked at the 3' end by a unique loxP site. A loxPneoloxP cassette was recombined on the same chromosome, downstream of resident Hoxd11. After treatment with Cre recombinase, the resultant deletion removed Hoxd11, Hoxd12, and Hoxd13, but brought the ectopic Hoxd11/lacZ transgene back to the original Hoxd11 locus. Mice homozygous for this deficiency lacked Hoxd11, Hoxd12, and Hoxd13 loci.
  • mutations:
  • Intergenic deletion,
  • Intragenic deletion
  • synonyms:
  • HoxD<d11lacZDel3>,
  • HoxD<Del>,
  • del(11-13),
  • del(11-13),
  • Hoxd<tm2Ddu>,
  • Hoxd<Del(11-13)>,
  • Del,
  • HoxD<Del3>,
  • Hoxd<tm2Ddu>,
  • Hoxd<Del(11-13)>,
  • Del29Ddu,
  • HoxD<d11lacZDel3>,
  • HoxD<Del>,
  • Del29Ddu,
  • HoxD<Del3>,
  • Del
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1 Feature

Genome

0 Expresses

4 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

25 Publication categories