MGI phenotypes (allele matching)
- no phenotypic analysis / MGI
B6.129S2-Del(2Hoxd13)3Ddu/Orl
| Status | Available to order |
| EMMA ID | EM:01228 |
| Citation information | RRID:IMSR_EM:01228 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| International strain name | B6.129S2-Del(2Hoxd13)3Ddu/Orl |
| Alternative name | P5 Del |
| Strain type | Targeted Mutant Strains : Other targeted |
| Allele/Transgene symbol | Del(2Hoxd13)3Ddu |
| Gene/Transgene symbol | Del(2Hoxd13)3Ddu |
Information from provider
| Provider | Duboule Denis |
| Provider affiliation | Laboratoire Moléculaire et Morphogenèse |
| Genetic information | Deletion of Hoxd13 by crossing mice containing loxP. |
| Phenotypic information | Malformation in digits. |
| Breeding history | Backcross: N=10; Intercross: N=10. |
| References |
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Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
Disease and phenotype information
MGI phenotypes (gene matching)
- no phenotypic analysis / MGI
Literature references
- Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbs.;Kmita Marie, Fraudeau Nadine, Hérault Yann, Duboule Denis, ;2002;Nature;420;145-50; 12432383