- increased bone mineral density / MGI
- abnormal long bone hypertrophic chondrocyte zone / MGI
- decreased monocyte cell number / MGI
- decreased granulocyte number / MGI
- abnormal liver morphology / MGI
- abnormal hepatocyte morphology / MGI
- increased body weight / MGI
- aggression towards inanimate objects / MGI
- abnormal stationary movement / MGI
- hypoactivity / MGI
- focal hepatic necrosis / MGI
- impaired macrophage phagocytosis / MGI
- brain inflammation / MGI
- liver inflammation / MGI
- lung inflammation / MGI
- abnormal kidney physiology / MGI
- abnormal dendritic cell physiology / MGI
- increased susceptibility to bacterial infection / MGI
- abnormal CD8-positive, alpha-beta cytotoxic T cell morphology / MGI
- abnormal leukocyte physiology / MGI
- abnormal macrophage physiology / MGI
- increased IgG level / MGI
- abnormal social/conspecific interaction / MGI
- abnormal monocyte morphology / MGI
- hepatic steatosis / MGI
- increased circulating alanine transaminase level / MGI
- increased liver weight / MGI
- abnormal long bone epiphyseal plate morphology / MGI
- peritoneal inflammation / MGI
- small intestinal inflammation / MGI
- increased hepatocellular carcinoma incidence / MGI
- liver fibrosis / MGI
- decreased width of hypertrophic chondrocyte zone / MGI
- oxidative stress / MGI
- impaired macrophage chemotaxis / MGI
- decreased macrophage cell number / MGI
- increased eosinophil cell number / MGI
- decreased lymphocyte cell number / MGI
- abnormal response to infection / MGI
- increased susceptibility to parasitic infection / MGI
- sepsis / MGI
- decreased susceptibility to injury / MGI
- reproductive system phenotype / MGI
- abnormal interferon secretion / MGI
- increased tumor necrosis factor secretion / MGI
- increased interleukin-12b secretion / MGI
- increased interleukin-6 secretion / MGI
- impaired neutrophil recruitment / MGI
- increased liver triglyceride level / MGI
- impaired cued conditioning behavior / MGI
- increased sensitivity to induced morbidity/mortality / MGI
- increased total body fat amount / MGI
- mortality/aging / MGI
- integument phenotype / MGI
- increased macrophage apoptosis / MGI
- Mallory bodies / MGI
- abnormal circadian behavior / MGI
STOCK Lgals3tm1Poi/H
| Status | Available to order |
| EMMA ID | EM:07422 |
| Citation information | RRID:IMSR_EM:07422 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 Lgals3tm1Poi/H |
| Alternative name | SJL/J Lgals3tm1Poi |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Lgals3tm1Poi |
| Gene/Transgene symbol | Lgals3 |
Information from provider
| Provider | Francis Szele |
| Provider affiliation | Department of anatomy physiology and genetics, University of Oxford |
| Genetic information | Lgals3 (Gal3) -/- 129Sv mice were generated as in Colnot, C., Fowlis, D., Ripoche, M. A., Bouchaert, I. and Poirier, F. (1998; Embryonic implantation in galectin 1/galectin 3 double mutant mice. Dev. Dyn. 211, 306-313), as follows: 3.7kb of sequence, encompassing exon 2 through to 4, was replaced by a neomycin selection cassette. The construct was electroporated into WW6 embryonic stem cells. Correctly targeted ES cells were injected into outbred MF1 blastocysts and implanted into pseudo-pregnant dames. The resultant germline chimeric male offspring were crossed with female 129/Sv mice to produce heterozygotes for the recombined allele. To generate SJL/J Lgals3 KO mice, an homozygous Gal3-/- 129/Sv was crossbred with an SJL/J mouse. Backcrosses 2-10 were heterozygous Gal3+/- SJL/J bred with SJL/J, heterozygous breeding was alternated each generation with male and female. |
| Phenotypic information | These mice are susceptible to Theiler's Murine Encephalomyelitis Virus infection and can be used to model primary progressive multiple sclerosis. During the backcrossing there was high mortality rate amongst litters and very poor breeding due to aversion to other mouse strain pheromones. SJL/J males also exhibited significant aggression often resulting in amyloidosis (sequel of social submissiveness and consequent wounds) in female breeding partners, which were often severe and required culling. |
| Breeding history | An homozygous Gal3-/- 129/Sv was crossbred with an SJL/J mouse. Backcrosses 2-10 were heterozygous Gal3+/- SJL/J bred with SJL/J, heterozygous breeding was alternated each generation with male and female. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI phenotypes (gene matching)
Literature references
- Embryonic implantation in galectin 1/galectin 3 double mutant mice.;Colnot C, Fowlis D, Ripoche M A, Bouchaert I, Poirier F, ;1998;Developmental dynamics : an official publication of the American Association of Anatomists;211;306-13; 9566950
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