- increased T cell number / IMPC
- hyperactivity / IMPC
- decreased hemoglobin content / IMPC
- abnormal glucose homeostasis / IMPC
- thrombocytosis / IMPC
- decreased hematocrit / IMPC
- decreased circulating cholesterol level / IMPC
- decreased IgG3 level / IMPC
- decreased mature B cell number / IMPC
- decreased circulating free fatty acids level / IMPC
- increased IgM level / IMPC
- increased IgG1 level / IMPC
- decreased circulating triglyceride level / IMPC
- decreased bone mineral density / IMPC
- increased IgG2b level / IMPC
- decreased erythrocyte cell number / IMPC
B10.Cg-Plcg2tm1Jni H2d Tg(BCL2)36Wehi Tg(Igh2k3-83)1Nemz/H
Status | Available to order |
EMMA ID | EM:01892 |
Citation information | RRID:IMSR_EM:01892 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 | B10.Cg-Plcg2tm1Jni H2d Tg(BCL2)36Wehi Tg(Igh2k3-83)1Nemz/H |
Alternative name | Plcg2 |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Plcg2tm1Jni, H2d, Tg(BCL2)36Wehi, Tg(Igh2k3-83)1Nemz |
Gene/Transgene symbol | Plcg2, H2, Tg(BCL2)36Wehi, Tg(Igh2 |
Information from provider
Provider | Martin Turner |
Provider affiliation | The Babraham Institute, Babraham, Cambridge, CB2 4PB |
Genetic information | These mice have a null mutation in Plcg2 and display defects in B-lymphocyte function. They also contain a transgene encoding a specific B-cell receptor and a transgene that directs expression of the anti-apoptotic protein Bcl2 to both B- and T-cells. |
Phenotypic information | Defects in B-lymphocyte development. High incidence of perinatal lethality. Homozygotes are infertile. |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- PLCG2-associated antibody deficiency and immune dysregulation / Orphanet_300359
- Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation / Orphanet_324530
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- decreased hematocrit / MGI
- abnormal liver physiology / MGI
- abnormal T cell differentiation / MGI
- abnormal cytokine secretion / MGI
- increased autoantibody level / MGI
- decreased susceptibility to parasitic infection / MGI
- arrested B cell differentiation / MGI
- abnormal dendritic cell physiology / MGI
- abnormal B cell physiology / MGI
- decreased susceptibility to induced arthritis / MGI
- decreased B cell proliferation / MGI
- abnormal dendritic cell morphology / MGI
- decreased follicular B cell number / MGI
- increased pro-B cell number / MGI
- decreased mature B cell number / MGI
- increased B cell apoptosis / MGI
- decreased platelet aggregation / MGI
- increased transitional stage T2 B cell number / MGI
- abnormal dendritic cell chemotaxis / MGI
- abnormal trabecular bone morphology / MGI
- abnormal B cell differentiation / MGI
- increased susceptibility to viral infection / MGI
- increased pre-B cell number / MGI
- decreased osteoclast cell number / MGI
- impaired natural killer cell mediated cytotoxicity / MGI
- increased B cell proliferation / MGI
- abnormal osteoclast differentiation / MGI
- decreased interferon-gamma secretion / MGI
- increased trabecular bone thickness / MGI
- increased trabecular bone volume / MGI
MGI phenotypes (gene matching)
- decreased hematocrit / MGI
- abnormal liver physiology / MGI
- abnormal T cell differentiation / MGI
- increased susceptibility to bacterial infection / MGI
- abnormal immunoglobulin level / MGI
- increased IgM level / MGI
- abnormal cytokine secretion / MGI
- thyroid inflammation / MGI
- increased autoantibody level / MGI
- insulitis / MGI
- increased susceptibility to autoimmune diabetes / MGI
- decreased susceptibility to autoimmune diabetes / MGI
- decreased susceptibility to parasitic infection / MGI
- immune system phenotype / MGI
- periinsulitis / MGI
- abnormal T cell number / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- increased CD8-positive, alpha-beta T cell number / MGI
- decreased IgG1 level / MGI
- decreased IgG2a level / MGI
- increased physiological sensitivity to xenobiotic / MGI
- decreased physiological sensitivity to xenobiotic / MGI
- increased sensitivity to induced morbidity/mortality / MGI
- abnormal trabecular bone morphology / MGI
- abnormal foot pad morphology / MGI
- spleen hyperplasia / MGI
- dermatitis / MGI
- internal hemorrhage / MGI
- abnormal humoral immune response / MGI
- arrested B cell differentiation / MGI
- decreased IgM level / MGI
- abnormal inflammatory response / MGI
- abnormal lymphatic vessel morphology / MGI
- premature death / MGI
- abnormal B cell differentiation / MGI
- abnormal dendritic cell physiology / MGI
- increased susceptibility to viral infection / MGI
- abnormal B cell physiology / MGI
- chronic inflammation / MGI
- glomerulonephritis / MGI
- increased pre-B cell number / MGI
- decreased susceptibility to induced arthritis / MGI
- osteoarthritis / MGI
- decreased osteoclast cell number / MGI
- impaired natural killer cell mediated cytotoxicity / MGI
- decreased B cell proliferation / MGI
- increased B cell proliferation / MGI
- immune system phenotype / MGI
- abnormal dendritic cell morphology / MGI
- decreased B-1a cell number / MGI
- decreased follicular B cell number / MGI
- increased pro-B cell number / MGI
- decreased transitional stage B cell number / MGI
- decreased B-2 B cell number / MGI
- decreased mature B cell number / MGI
- abnormal osteoclast differentiation / MGI
- decreased tumor necrosis factor secretion / MGI
- decreased interferon-gamma secretion / MGI
- increased B cell apoptosis / MGI
- increased trabecular bone thickness / MGI
- decreased platelet aggregation / MGI
- increased transitional stage T2 B cell number / MGI
- abnormal dendritic cell chemotaxis / MGI
- abnormal NK cell physiology / MGI
- increased trabecular bone volume / MGI
- chylous ascites / MGI
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