- abnormal T cell physiology / MGI
- abnormal positive T cell selection / MGI
- decreased T cell number / MGI
- impaired natural killer cell mediated cytotoxicity / MGI
- decreased double-positive T cell number / MGI
- immune system phenotype / MGI
- decreased NK T cell number / MGI
- abnormal CD4-positive T cell differentiation / MGI
- decreased interleukin-4 secretion / MGI
- decreased IgG level / MGI
- abnormal T cell differentiation / MGI
- abnormal B cell number / MGI
- decreased B-1 B cell number / MGI
- abnormal response to infection / MGI
- increased double-negative T cell number / MGI
- decreased B cell proliferation / MGI
- abnormal T cell number / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- decreased CD8-positive, alpha-beta T cell number / MGI
- increased transitional stage B cell number / MGI
- decreased IgG1 level / MGI
- decreased IgG2a level / MGI
- decreased IgG3 level / MGI
- abnormal splenic cell ratio / MGI
- abnormal lymph node cell ratio / MGI
- thymus hypoplasia / MGI
- abnormal T cell activation / MGI
- decreased T cell proliferation / MGI
- decreased interleukin-2 secretion / MGI
- abnormal iridocorneal angle / MGI
- ocular hypertension / MGI
- anterior iris synechia / MGI
- decreased mature B cell number / MGI
STOCK Vav2tm1Kdf Vav1tm2Bbd/Cnbc
Status | Available to order |
EMMA ID | EM:08030 |
International strain name | STOCK Vav2tm1Kdf Vav1tm2Bbd/Cnbc |
Alternative name | Double KO: vav1_KO; vav2_KO or Vav1tm2Bbd; Vav2tm1Kdf |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Vav2tm1Kdf, |
Gene/Transgene symbol | Vav2 |
Information from provider
Provider | Mariano Barbacid |
Provider affiliation | Molecular Oncology, Centro Nacional de Investigaciones Oncologicas |
Genetic information | In the Vav1 allele sequences encoding amino acids 135-195 comprising the entire acidic domain were replaced with a PGK-neo cassette via homologous recombination. Gene expression was absent in thymocytes of homozygous mutant animals. In the Vav2 allele a lacZ-neo cassette was fused in-frame to amino acids 150-155 of exon 5 and introduced via homologous recombination. Western blot analysis of spleen tissue from homozygous mutant animals confirmed the absence of gene expression. |
Phenotypic information | Homozygous:Combined deletion of both Vav1 and Vav2 in mice results in a marked reduction in mature B lymphocyte numbers. Vav1(-/-),Vav-2(-/-) B cells are unresponsive to B cell antigen receptor (BCR)-driven proliferation in vitro and to thymus-independent antigen in vivo. BCR-stimulated intracellular calcium mobilization is greatly impaired in Vav1(-/-),Vav-2(-/-) B cells.Heterozygous:Heterozygous mice are viable |
Breeding history | Chimeras were crossed with CD1 females for germ-line transmission analysis. Heterozygous animals for each allele were crossed among themselves to generate corresponding homozygous animals. To obtain the double mutant strain homozygous animals for each allele were crossbred. Currently maintained as mixed CD1 and 129. |
References |
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Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | homozygous CD-1 outbred stock (syn.: outbr. CD-1 or CD1, Swiss CD-1 or CD1, ICR(CD-1), etc.), homozygous CD-1 outbred stock (syn.: outbr. CD-1 or CD1, Swiss CD-1 or CD1, ICR(CD-1), etc.) |
Stage of embryos | 4/8-cell |
Disease and phenotype information
MGI phenotypes (allele matching)
Literature references
- Vav is a regulator of cytoskeletal reorganization mediated by the T-cell receptor.;Fischer K D, Kong Y Y, Nishina H, Tedford K, Marengère L E, Kozieradzki I, Sasaki T, Starr M, Chan G, Gardener S, Nghiem M P, Bouchard D, Barbacid M, Bernstein A, Penninger J M, ;1998;Current biology : CB;8;554-62; 9601639
- Compensation between Vav-1 and Vav-2 in B cell development and antigen receptor signaling.;Tedford K, Nitschke L, Girkontaite I, Charlesworth A, Chan G, Sakk V, Barbacid M, Fischer K D, ;2001;Nature immunology;2;548-55; 11376343
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