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Phenotypes Associated with This Genotype
Genotype
MGI:3703438
Allelic
Composition
Alox15tm1Fun/Alox15tm1Fun
Genetic
Background
B6.129S2-Alox15tm1Fun/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Alox15tm1Fun mutation (3 available); any Alox15 mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• progressive splenomegaly is observed after 8 weeks of age

mortality/aging
• 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

hematopoietic system
• progressive splenomegaly is observed after 8 weeks of age
• 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
• presumed cause of premature death
• increase in number of myeloid cells and progenitors, as well as megkaryocytes
• at death, cells in bone marrow of homozygous mice consist of greater than 25% myeloblasts
• blood leukocystosis observed in asymptomatic and moribund mice
• basophilia observed in asymptomatic and moribund mice
• disrupted compartmentalization of red pulp
• disrupted compartmentalization of white pulp
• moribund mice exhibit complete loss of splenic compartmentalization
• decrease in number of follicles

immune system
• progressive splenomegaly is observed after 8 weeks of age
• 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
• blood leukocystosis observed in asymptomatic and moribund mice
• basophilia observed in asymptomatic and moribund mice
• disrupted compartmentalization of red pulp
• disrupted compartmentalization of white pulp
• moribund mice exhibit complete loss of splenic compartmentalization
• decrease in number of follicles
• 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
• myeloid infiltrates observed in skin of moribund mice

neoplasm
• mice older than 10 weeks develop a malignant myeloproliferative disease at 100% penetrance that can progress to transplantable leukemia

integument
• myeloid infiltrates observed in skin of moribund mice


Contributing Projects:
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
03/25/2025
MGI 6.24
The Jackson Laboratory