- increased susceptibility to induced arthritis / MGI
- abnormal leukocyte physiology / MGI
- joint inflammation / MGI
- increased interferon-gamma secretion / MGI
- kidney vascular congestion / MGI
- liver inflammation / MGI
- abnormal cytokine secretion / MGI
- increased vascular permeability / MGI
- pulmonary edema / MGI
- pulmonary vascular congestion / MGI
- liver vascular congestion / MGI
- spleen vascular congestion / MGI
- glomerular capillary congestion / MGI
- abnormal lung morphology / MGI
- impaired lung alveolus development / MGI
- abnormal pulmonary alveolar sac morphology / MGI
- abnormal pulmonary alveolus wall morphology / MGI
- decreased lung endothelial cell migration / MGI
B6.129P2-Pecam1tm1Mak/Cnbc
Status | Available to order |
EMMA ID | EM:07243 |
International strain name | B6.129P2-Pecam1tm1Mak/Cnbc |
Alternative name | CD31/Pecam1 |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Pecam1tm1Mak |
Gene/Transgene symbol | Pecam1 |
Information from provider
Provider | Tak W Mak |
Provider affiliation | Division of Stem Cell and Developmental Biology, Advanced Medical Discovery Institute/Ontario Cancer Institute |
Genetic information | A targeting vector was designed to disrupt exon 7 by inserting a pGK1neo resistance expression cassette in reverse orientation of CD31 transcription. |
Phenotypic information | Pecam1 (CD31)-deficient mice (CD31KO) are viable and born at the expected Mendelian frequency, remain healthy, and exhibit no obvious vascular developmental defects. In response to inflammatory challenge, polymorphonuclear leukocytes of CD31KO mice are arrested between the vascular endothelium and the basement membrane of inflammatory site mesenteric microvessels, confirming a role for CD31 in the migration of neutrophils through the subendothelial extracellular matrix. |
Breeding history | Backcrossed 10 times to C57BL/6. |
References |
|
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | not known |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous C57BL/6J |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- kidney vascular congestion / MGI
- abnormal lung morphology / MGI
- abnormal vasodilation / MGI
- liver inflammation / MGI
- abnormal leukocyte physiology / MGI
- joint inflammation / MGI
- abnormal cytokine secretion / MGI
- increased vascular permeability / MGI
- increased susceptibility to induced arthritis / MGI
- pulmonary edema / MGI
- abnormal nitric oxide homeostasis / MGI
- decreased vasodilation / MGI
- impaired lung alveolus development / MGI
- increased interferon-gamma secretion / MGI
- pulmonary vascular congestion / MGI
- liver vascular congestion / MGI
- spleen vascular congestion / MGI
- abnormal pulmonary alveolar sac morphology / MGI
- abnormal pulmonary alveolus wall morphology / MGI
- decreased lung endothelial cell migration / MGI
- glomerular capillary congestion / MGI
Literature references
- Generation and characterization of the Anp32e-deficient mouse.;Reilly Patrick T, Afzal Samia, Wakeham Andrew, Haight Jillian, You-Ten Annick, Zaugg Kathrin, Dembowy Joanna, Young Ashley, Mak Tak W, ;2010;PloS one;5;e13597; 21049064
- Genetic evidence for functional redundancy of Platelet/Endothelial cell adhesion molecule-1 (PECAM-1): CD31-deficient mice reveal PECAM-1-dependent and PECAM-1-independent functions.;Duncan G S, Andrew D P, Takimoto H, Kaufman S A, Yoshida H, Spellberg J, de la Pompa J L, Elia A, Wakeham A, Karan-Tamir B, Muller W A, Senaldi G, Zukowski M M, Mak T W, ;1999;Journal of immunology (Baltimore, Md. : 1950);162;3022-30; 10072554
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