MGI phenotypes (allele matching)
B6.129S2-Del(2Hoxd11-Hoxd13)29Ddu/Orl
| Status | Available to order |
| EMMA ID | EM:01222 |
| Citation information | RRID:IMSR_EM:01222 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(2Hoxd11-Hoxd13)29Ddu/Orl |
| Alternative name | B6.129 HoxD |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Del(2Hoxd11-Hoxd13)29Ddu |
| Gene/Transgene symbol | Del(2Hoxd11-Hoxd13)29Ddu |
Information from provider
| Provider | Duboule Denis |
| Provider affiliation | Laboratoire Moléculaire et Morphogenèse |
| Genetic information | Deletion of Hoxd13 and Hoxd12 genomic region and insertion of an Hoxd11-lacZ transgene. |
| Phenotypic information | Limb defect. |
| References |
|
Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
Disease and phenotype information
Literature references
- Synpolydactyly in mice with a targeted deficiency in the HoxD complex.;Zákány J, Duboule D, ;1996;Nature;384;69-71; 8900279
- Deletion of a HoxD enhancer induces transcriptional heterochrony leading to transposition of the sacrum.;Zákány J, Gérard M, Favier B, Duboule D, ;1997;The EMBO journal;16;4393-402; 9250683