- absent kidney / MGI
- abnormal kidney development / MGI
- delayed kidney development / MGI
- decreased thymocyte number / MGI
- abnormal ovary morphology / MGI
- abnormal oogenesis / MGI
- secondary sex reversal / MGI
- no abnormal phenotype detected / MGI
- abnormal secondary sex determination / MGI
- abnormal adrenal gland physiology / MGI
- no phenotypic analysis / MGI
- kidney failure / MGI
- nervous system phenotype / MGI
- abnormal reproductive system development / MGI
- abnormal adenohypophysis morphology / MGI
- decreased renal glomerulus number / MGI
- decreased oocyte number / MGI
- abnormal female germ cell morphology / MGI
- absent Mullerian ducts / MGI
- decreased somatotroph cell number / MGI
- decreased gonadotroph cell number / MGI
- decreased thyrotroph cell number / MGI
- oocyte degeneration / MGI
- abnormal metanephric mesenchyme morphology / MGI
- abnormal nephrogenic mesenchyme morphogenesis / MGI
- postnatal lethality, complete penetrance / MGI
- neonatal lethality, complete penetrance / MGI
- small metanephros / MGI
B6;129P2-Wnt4tm2(EGFP/cre)Svo/Oulu
Status | Available to order |
EMMA ID | EM:10011 |
Citation information | RRID:IMSR_EM:10011 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-Wnt4tm2(EGFP/cre)Svo/Oulu |
Alternative name | Wnt-4-Cre |
Strain type | Targeted Mutant Strains : Knock-in |
Allele/Transgene symbol | Wnt4tm2(EGFP/cre)Svo |
Gene/Transgene symbol | Wnt4 |
Information from provider
Provider | Jingdong Shan |
Provider affiliation | Department of Biochemistry and Molecular Medicine, University of Oulu |
Additional owner | Dr. Seppo Vainio, University of Oulu, Oulu, Finland |
Genetic information | Targeted construct in 129/Ola ES cells replaces the Wnt4 gene after the promoter with cre recombinase. |
Phenotypic information | Homozygous:Wnt4-cre homozygotes have the same phenotype as Wnt4 knockouts. Kidney malformation and female to male sex reversal. Homozygotes die few days after birth.Heterozygous:Heterozygous mice have no reported phenotypes. |
Breeding history | Targeted mutation was directly maintained on a C57BL/6 background. |
References |
|
Homozygous fertile | not known |
Homozygous viable | no |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | University of Oulu, Oulu, Finland |
Animals used for archiving | heterozygous C57BL/6JOlaHsd males, wild-type C57BL/6NCrl females |
Stage of embryos | 2-cell |
Disease and phenotype information
MGI phenotypes (gene matching)
Literature references
- Generation of an allele to inactivate Wnt4 gene function conditionally in the mouse.;Shan Jingdong, Jokela Tiina, Peltoketo Hellevi, Vainio Seppo, ;2009;Genesis (New York, N.Y. : 2000);47;782-8; 19830824
- Mapping of the fate of cell lineages generated from cells that express the Wnt4 gene by time-lapse during kidney development.;Shan Jingdong, Jokela Tiina, Skovorodkin Ilya, Vainio Seppo, ;2010;Differentiation; research in biological diversity;79;57-64; 19740593
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