- 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
STOCK Vezttm1.1Smc/Vezttm1.2Smc/Orl
Status | Available to order |
EMMA ID | EM:04326 |
Citation information | RRID:IMSR_EM:04326 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 | STOCK Vezttm1.1Smc/Vezttm1.2Smc/Orl |
Alternative name | Vezatin flox5/null (or bi-loxP/null vezt strain) |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Vezttm1.1Smc, Vezttm1.2Smc |
Gene/Transgene symbol | Vezt, Vezt |
Information from provider
Provider | Marie-Christine SIMMLER |
Provider affiliation | Neurobiology and development, CNRS |
Genetic information | Vezatin is a integral membrane protein associated to E-cadherin adherens junctions. Exon 5 encodes the transmembranous domain. A conditional vezatin allele lacking exon 5 was generated by using a cre/loxP strategy (original vezt floxed line, EM:01817). This is an heterozygous line modified as follows: one chromosome is carrying an exon-5-only-floxed (Vezt flox5) vezatin allele, i.e. deleted of the floxed pPgk-1-neo-pA cassette (by partial cre recombinase activity) and one chromosome is carrying a null (defloxed) vezatin allele (after deletion of the exon5+neo floxed segment using the pgk1-cre). |
Phenotypic information | Ubiquitous targeted disruption of vezatin results in embryonic lethality due to a failure of epithelialization of the trophectoderm (Hyenne et al., 2007). Hairs cells targeted disruption results in noise-induced hearing loss (Balhoul et al., 2009). |
Breeding history | More than N10 breeding on a mixed/randomized 129/SvPas x B6N. Breeding procedures of heterozygous Vezt Flox5/null x Vezt Flox5/null will only produce Vezt Flox5/null (66%) and Vezt Flox5/Flox5 (33%) mice, since Vezt null/null is an embryonic lethal condition. |
References |
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Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous 129/Sv x C57BL/6N males, heterozygous 129/Sv x C57BL/6N females |
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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