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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Alox15tm1Fun
targeted mutation 1, Colin D Funk
MGI:1857428
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Alox15tm1Fun/Alox15tm1Fun B6.129S2-Alox15tm1Fun MGI:5517581
hm2
Alox15tm1Fun/Alox15tm1Fun B6.129S2-Alox15tm1Fun/J MGI:3703438
hm3
Alox15tm1Fun/Alox15tm1Fun involves: 129/Sv * C57BL/6 MGI:2429456
cx4
Alox15tm1Fun/Alox15tm1Fun
Ldlrtm1Her/Ldlrtm1Her
involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6 MGI:4367211


Genotype
MGI:5517581
hm1
Allelic
Composition
Alox15tm1Fun/Alox15tm1Fun
Genetic
Background
B6.129S2-Alox15tm1Fun
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Alox15tm1Fun mutation (3 available); any Alox15 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• in a model of IgE antigen-dependent passive cutaneous anaphylaxis, mice exhibit normal dye extravasation (a measure of edema)




Genotype
MGI:3703438
hm2
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 (42 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




Genotype
MGI:2429456
hm3
Allelic
Composition
Alox15tm1Fun/Alox15tm1Fun
Genetic
Background
involves: 129/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Alox15tm1Fun mutation (3 available); any Alox15 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
N
• no defect detected in pituitary gland, adrenals, and pancreas

hematopoietic system
N
• mutants had normal total blood cell counts, normal leukocyte differentials, normal reticulocyte numbers, normal hemoglobin values, and normal hematocrit values

immune system
• 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

reproductive system
N
• mutants were fertile




Genotype
MGI:4367211
cx4
Allelic
Composition
Alox15tm1Fun/Alox15tm1Fun
Ldlrtm1Her/Ldlrtm1Her
Genetic
Background
involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Alox15tm1Fun mutation (3 available); any Alox15 mutation (42 available)
Ldlrtm1Her mutation (19 available); any Ldlr mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• reduced atherosclerotic lesions when fed a high fat diet for 3 or 9 weeks





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory