immune system
N |
• in a model of IgE antigen-dependent passive cutaneous anaphylaxis, mice exhibit normal dye extravasation (a measure of edema)
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Allele Symbol Allele Name Allele ID |
Alox15tm1Fun targeted mutation 1, Colin D Funk MGI:1857428 |
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Summary |
4 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
N |
• in a model of IgE antigen-dependent passive cutaneous anaphylaxis, mice exhibit normal dye extravasation (a measure of edema)
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• progressive splenomegaly is observed after 8 weeks of age
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• increase in death rate of homozygous mice as compared to controls
• 80% survival at 12 months of age
• severe anemia is most likely cause of death
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• progressive splenomegaly is observed after 8 weeks of age
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• increase in numbers of myeloid cells in bone marrow, spleen, blood and lymph nodes as compared to control
• cell cycle analysis indicates an increase in proliferative capacity of splenic myeloid cells and a decrease in the percentage of apoptotic cells
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• increase in number of myeloid cells and progenitors, as well as megkaryocytes
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• at death, cells in bone marrow of homozygous mice consist of greater than 25% myeloblasts
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• blood leukocystosis observed in asymptomatic and moribund mice
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• basophilia observed in asymptomatic and moribund mice
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• disrupted compartmentalization of red pulp
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• disrupted compartmentalization of white pulp
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• moribund mice exhibit complete loss of splenic compartmentalization
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• decrease in number of follicles
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• progressive splenomegaly is observed after 8 weeks of age
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• increase in numbers of myeloid cells in bone marrow, spleen, blood and lymph nodes as compared to control
• cell cycle analysis indicates an increase in proliferative capacity of splenic myeloid cells and a decrease in the percentage of apoptotic cells
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• blood leukocystosis observed in asymptomatic and moribund mice
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• basophilia observed in asymptomatic and moribund mice
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• disrupted compartmentalization of red pulp
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• disrupted compartmentalization of white pulp
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• moribund mice exhibit complete loss of splenic compartmentalization
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• decrease in number of follicles
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• although not enlarged, lymph nodes exhibit progressive hypercellularity
• pseudo-Gaucher cells observed in lymph nodes
• increase in GR-1+ myeloid cells as compared to controls
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• myeloid infiltrates observed in skin of moribund mice
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• mice older than 10 weeks develop a malignant myeloproliferative disease at 100% penetrance that can progress to transplantable leukemia
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• myeloid infiltrates observed in skin of moribund mice
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
N |
• no defect detected in pituitary gland, adrenals, and pancreas
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N |
• mutants had normal total blood cell counts, normal leukocyte differentials, normal reticulocyte numbers, normal hemoglobin values, and normal hematocrit values
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• altered arachadonic acid metabolism in peritoneal macrophages upon calcium ionophore stimulation: undetectable 12-hydroxyeicosatetraenoic acid (12-HETE), trace amounts of 15-hydroxyeicosatetraenoic acid (15-HETE), increased concentrations of 5-hydroxyeicosatetraenoic acid (5-HETE), however no defect detected in the spleen
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N |
• mutants were fertile
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• reduced atherosclerotic lesions when fed a high fat diet for 3 or 9 weeks
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 11/12/2024 MGI 6.24 |
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