- absent mandible / MGI
- microcephaly / MGI
- abnormal forelimb morphology / MGI
- abnormal hindlimb morphology / MGI
- polydactyly / MGI
- syndactyly / MGI
- ectopic digits / MGI
- abnormal telencephalon morphology / MGI
- anophthalmia / MGI
- thick apical ectodermal ridge / MGI
- abnormal craniofacial development / MGI
- abnormal embryonic neuroepithelium morphology / MGI
- small interparietal bone / MGI
- small parietal bone / MGI
- absent nasal bone / MGI
- absent maxilla / MGI
- abnormal limb bud morphology / MGI
- absent nasal placodes / MGI
- absent optic vesicle / MGI
- abnormal first pharyngeal arch morphology / MGI
- abnormal mandibular prominence morphology / MGI
- neonatal lethality, complete penetrance / MGI
- decreased midbrain size / MGI
- decreased forebrain size / MGI
- rostral body truncation / MGI
- absent frontonasal prominence / MGI
- absent diencephalon / MGI
- abnormal anterior head development / MGI
B6;129P2(Cg)-Dkk1tm1.1Svo/Oulu
| Status | Available to order |
| EMMA ID | EM:09872 |
| Citation information | RRID:IMSR_EM:09872 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;129P2(Cg)-Dkk1tm1.1Svo/Oulu |
| Alternative name | Dkk1 (tm1.1Svo) |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Dkk1tm1.1Svo |
| Gene/Transgene symbol | Dkk1 |
Information from provider
| Provider | Christof Niehrs |
| Provider affiliation | Institute of Molecular Biology (IMB), University of Mainz |
| Genetic information | Targeted construct in 129/Ola ES cells modifies the Dkk1 allele so that Dkk1 exons 1 and 2 are flanked by loxP sites. |
| Phenotypic information | Homozygous:Homozygous Dkk1 flox/flox mice do not have any phenotypes as it requires cre recombinase activation to delete exons 1 and 2.Heterozygous:Heterozygous Dkk1 flox/+ mice do not have any phenotypes as it requires cre recombinase activation to delete exons 1 and 2. |
| Breeding history | Targeted mutation was directly maintained on a C57BL/6 background. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | University of Oulu, Oulu, Finland |
| Animals used for archiving | homozygous males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Arnold-Chiari malformation type I / Orphanet_268882
MGI phenotypes (gene matching)
Literature references
- Secreted Wnt antagonist Dickkopf-1 controls kidney papilla development coordinated by Wnt-7b signalling.;Pietilä Ilkka, Ellwanger Kristina, Railo Antti, Jokela Tiina, Barrantes Ivan Del Barco, Shan Jingdong, Niehrs Christof, Vainio Seppo J, ;2011;Developmental biology;353;50-60; 21354128
- Small-molecule Wnt agonists correct cleft palates in Pax9 mutant mice in utero.;Jia Shihai, Zhou Jing, Fanelli Christopher, Wee Yinshen, Bonds John, Schneider Pascal, Mues Gabriele, D'Souza Rena N, ;2017;Development (Cambridge, England);144;3819-3828; 28893947
- Leishmania major surface components and DKK1 signalling via LRP6 promote migration and longevity of neutrophils in the infection site.;Ihedioha Olivia C, Marcarian Haley Q, Sivakoses Anutr, Beverley Stephen M, McMahon-Pratt Diane, Bothwell Alfred L M, ;2024;Frontiers in immunology;15;1473133; 39502693
- Platelet DKK1 promotes tolerogenic dendritic cells and non-healing responses in cutaneous leishmaniasis.;Ihedioha Olivia C, Sivakoses Anutr, Marcarian Haley Q, Sajeev Malini, McMahon-Pratt Diane, Bothwell Alfred L M, ;2025;bioRxiv : the preprint server for biology;0;; 40502169
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