- abnormal midbrain morphology / MGI
- decreased inferior colliculus size / MGI
- abnormal hypothalamus morphology / MGI
- abnormal spatial learning / MGI
- abnormal mammillary body morphology / MGI
- behavior/neurological phenotype / MGI
- abnormal spatial working memory / MGI
- abnormal cerebellum morphology / MGI
- abnormal cerebellum anterior vermis morphology / MGI
- decreased body weight / MGI
- abnormal nursing / MGI
- abnormal maternal nurturing / MGI
- postnatal growth retardation / MGI
- maternal effect / MGI
- preweaning lethality, incomplete penetrance / MGI
- decreased body size / MGI
- abnormal sexual interaction / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
B6;129-Foxb1tm1Pgr/PgrKieg
| Status | Available to order |
| EMMA ID | EM:00071 |
| Citation information | RRID:IMSR_EM:00071 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;129-Foxb1tm1Pgr/PgrKieg |
| Alternative name | FoxB1, B6.129/SvR1-FoxB1, FoxB1 KO |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Foxb1tm1Pgr |
| Gene/Transgene symbol | Foxb1 |
Information from provider
| Provider | Peter Gruss |
| Provider affiliation | Max Planck Inst. Biophysical Chemistry |
| Genetic information | 9 Kb 5' genomic fragment, followed by PGK-neo expression cassette and 1.6 Kb 3' genomic fragment, leading to replacement of the 3' part of exon 1 and the 5' part of exon 2, including the ATG and the forkhead domain-coding sequence. |
| Phenotypic information | Homozygous animals (3 weeks of age): midbrain malformations - inferior colliculi reduced near the midline and partially covered by anterior cerebellum, hypothalamic malformations - medial mammillary nucleus absent, other nuclei less compact (this phenotype starts to be detectable at E16.5 - 18.5). Mothers neglect their pups and show neither nest-building nor nursing activities. |
| References |
|
Information from EMMA
| Archiving centre | Karolinska Institutet, Stockholm, Sweden |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal mammary gland morphology / MGI
- abnormal hypothalamus morphology / MGI
- abnormal cerebellum morphology / MGI
- abnormal cerebellum anterior vermis morphology / MGI
- abnormal midbrain morphology / MGI
- open neural tube / MGI
- decreased body weight / MGI
- decreased body size / MGI
- abnormal nursing / MGI
- abnormal maternal nurturing / MGI
- abnormal locomotor behavior / MGI
- hypoactivity / MGI
- abnormal gait / MGI
- abnormal spatial learning / MGI
- limb grasping / MGI
- decreased embryo size / MGI
- postnatal growth retardation / MGI
- abnormal brain morphology / MGI
- abnormal sexual interaction / MGI
- no phenotypic analysis / MGI
- nervous system phenotype / MGI
- maternal effect / MGI
- caudal body truncation / MGI
- abnormal mammillary body morphology / MGI
- behavior/neurological phenotype / MGI
- abnormal spatial working memory / MGI
- decreased survivor rate / MGI
- decreased inferior colliculus size / MGI
- abnormal mammary gland epithelium morphology / MGI
- abnormal mammary gland lobule morphology / MGI
- abnormal mammary gland alveolus morphology / MGI
- decreased grip strength / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- lethality throughout fetal growth and development, incomplete penetrance / MGI
- preweaning lethality, incomplete penetrance / MGI
- galactostasis / MGI
Literature references
- Fkh5-deficient mice show dysgenesis in the caudal midbrain and hypothalamic mammillary body.;Wehr R, Mansouri A, de Maeyer T, Gruss P, ;1997;Development (Cambridge, England);124;4447-56; 9409663
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).
