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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Aoc3tm1Salm
targeted mutation 1, Marko Salmi
MGI:3528069
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Aoc3tm1Salm/Aoc3tm1Salm involves: 129S6/SvEvTac * 129S7/SvEvBrd MGI:3528235


Genotype
MGI:3528235
hm1
Allelic
Composition
Aoc3tm1Salm/Aoc3tm1Salm
Genetic
Background
involves: 129S6/SvEvTac * 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aoc3tm1Salm mutation (0 available); any Aoc3 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• the overall efficiency of the extravasation process is reduced to 23% of that in wild-type
• when labeled lymphocytes are transferred into homozygous recipients significantly fewer labeled cells are found in the mesenteric lymph node and spleen compared to wild-type recipients; however, in untreated homozygotes the absolute number of leukocytes in the blood, peripheral lymph nodes, Peyer's patches, mesenteric lymph nodes, and spleen are normal
• in highly inflamed cremaster muscle transmigration of polymorphonuclear leukocytes is decreased by 71% (absolute numbers) or 47% (relative to the number of adhered leukocytes)
• in inflamed cremaster muscle the number of stably bound polymorphonuclear leukocytes is decreased by about 50% and the efficiency of the firm adhesion step is reduced 3.2-fold compared to wild-type; firm adhesion is also impaired in highly inflamed cremaster muscle
• firm adhesion is decreased in Peyer's patches
• the rolling velocity of mutant polymorphonuclear leukocytes is increased about 5-fold compared to wild-type in inflamed cremaster muscle (treated with 500 ng TNF intrascrotally for 3 hours); rolling velocity is also in creased in highly inflamed cremaster muscle (1.5 ug of TNF for 6 hours)
• rolling velocity is increased in Peyer's patches however the number of rolling cells is the same as in wild-type
• a 50% reduction in the number of infiltrating leukocytes is seen in homozygotes 6 hours after induction of peritonitis by a peritoneal injection of TNF

cellular
• the overall efficiency of the extravasation process is reduced to 23% of that in wild-type
• when labeled lymphocytes are transferred into homozygous recipients significantly fewer labeled cells are found in the mesenteric lymph node and spleen compared to wild-type recipients; however, in untreated homozygotes the absolute number of leukocytes in the blood, peripheral lymph nodes, Peyer's patches, mesenteric lymph nodes, and spleen are normal
• in highly inflamed cremaster muscle transmigration of polymorphonuclear leukocytes is decreased by 71% (absolute numbers) or 47% (relative to the number of adhered leukocytes)
• in inflamed cremaster muscle the number of stably bound polymorphonuclear leukocytes is decreased by about 50% and the efficiency of the firm adhesion step is reduced 3.2-fold compared to wild-type; firm adhesion is also impaired in highly inflamed cremaster muscle
• firm adhesion is decreased in Peyer's patches
• the rolling velocity of mutant polymorphonuclear leukocytes is increased about 5-fold compared to wild-type in inflamed cremaster muscle (treated with 500 ng TNF intrascrotally for 3 hours); rolling velocity is also in creased in highly inflamed cremaster muscle (1.5 ug of TNF for 6 hours)
• rolling velocity is increased in Peyer's patches however the number of rolling cells is the same as in wild-type

hematopoietic system
• the overall efficiency of the extravasation process is reduced to 23% of that in wild-type
• when labeled lymphocytes are transferred into homozygous recipients significantly fewer labeled cells are found in the mesenteric lymph node and spleen compared to wild-type recipients; however, in untreated homozygotes the absolute number of leukocytes in the blood, peripheral lymph nodes, Peyer's patches, mesenteric lymph nodes, and spleen are normal
• in highly inflamed cremaster muscle transmigration of polymorphonuclear leukocytes is decreased by 71% (absolute numbers) or 47% (relative to the number of adhered leukocytes)
• in inflamed cremaster muscle the number of stably bound polymorphonuclear leukocytes is decreased by about 50% and the efficiency of the firm adhesion step is reduced 3.2-fold compared to wild-type; firm adhesion is also impaired in highly inflamed cremaster muscle
• firm adhesion is decreased in Peyer's patches
• the rolling velocity of mutant polymorphonuclear leukocytes is increased about 5-fold compared to wild-type in inflamed cremaster muscle (treated with 500 ng TNF intrascrotally for 3 hours); rolling velocity is also in creased in highly inflamed cremaster muscle (1.5 ug of TNF for 6 hours)
• rolling velocity is increased in Peyer's patches however the number of rolling cells is the same as in wild-type





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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
11/05/2024
MGI 6.24
The Jackson Laboratory