- decreased circulating glucose level / IMPC
- abnormal coat appearance / IMPC
- decreased locomotor activity / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased mean corpuscular volume / IMPC
- decreased vertical activity / IMPC
- increased urine microalbumin level / IMPC
- embryonic lethality prior to organogenesis / IMPC
129S2/SvPas-Vezttm1Smc/Orl
| Status | Available to order |
| EMMA ID | EM:01817 |
| Citation information | RRID:IMSR_EM:01817 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 | 129S2/SvPas-Vezttm1Smc/Orl |
| Alternative name | vezatinFloxed/Floxed |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Vezttm1Smc |
| Gene/Transgene symbol | Vezt |
Information from provider
| Provider | SIMMLER MARIE-CHRISTINE |
| Provider affiliation | Institut Jacques-Monod, CNRS, Equipe labellisée INSERM U950 |
| Genetic information | The mouse vezatin gene encodes several cDNA isoforms which all start at the same ATG and all contain exon 5. Vezatin is an integral protein associated to E-cadherin adherens junctions (Küssel-Anderman et al., 2000; Sousa et al., 2004; Hyenne et al., 2005; Balhoul, Simmler et al., 2009). Exon 5 encodes the transmembrane domain. We generated a vezatin allele lacking exon 5 by using a cre/loxP strategy. The vezatin targeting vector contains a 4.5 Kb EcoRI genomic fragment, a 0.7 Kb genotyping fragment (containing exon 5) flanked by a loxP site, and a 2.4 Kb ClaI/KpnI genomic fragment. A floxed pPgk-1-neo-pA cassette inserted on the right side of exon 5-fragment and a pPgk-1-DTA-pA cassette inserted on the edge of the construct were used for positive and negative selection respectively (Hyenne V et al., Mech Dev, 124, 449-462, 2007). |
| Phenotypic information | Various cre recombinase-expressing lines used for targeting the deletion in epithelial tissues that are relevant to the description of the role of vezatin in morphogenesis. A phenotype of early embryonic lethality (E4.5-E5.5) was obtained by using the Pgk1-cre line (Lallemand Y et al. 1998) and the conditional vezatin floxed line (mixed background), described in Hyenne V et al., 2007. Homozygous vezatin flox/flox mice are fully normal and fertile. |
| References |
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Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
Literature references
- Conditional knock-out reveals that zygotic vezatin-null mouse embryos die at implantation.;Hyenne Vincent, Souilhol Céline, Cohen-Tannoudji Michel, Cereghini Silvia, Petit Christine, Langa Francina, Maro Bernard, Simmler Marie-Christine, ;2007;Mechanisms of development;124;449-62; 17452094
- Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells.;Bahloul Amel, Simmler Marie-Christine, Michel Vincent, Leibovici Michel, Perfettini Isabelle, Roux Isabelle, Weil Dominique, Nouaille Sylvie, Zuo Jian, Zadro Cristina, Licastro Danilo, Gasparini Paolo, Avan Paul, Hardelin Jean-Pierre, Petit Christine, ;2009;EMBO molecular medicine;1;125-38; 20049712
- Vezatin is essential for dendritic spine morphogenesis and functional synaptic maturation.;Danglot Lydia, Freret Thomas, Le Roux Nicolas, Narboux Nême Nicolas, Burgo Andrea, Hyenne Vincent, Roumier Anne, Contremoulins Vincent, Dauphin François, Bizot Jean-Charles, Vodjdani Guilan, Gaspar Patricia, Boulouard Michel, Poncer Jean-Christophe, Galli Thierry, Simmler Marie-Christine, ;2012;The Journal of neuroscience : the official journal of the Society for Neuroscience;32;9007-22; 22745500
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