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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Myo9btm1.2Bah
targeted mutation 1.2, Martin Bahler
MGI:4867915
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Myo9btm1.2Bah/Myo9btm1.2Bah B6.Cg-Myo9btm1.2Bah MGI:4867916


Genotype
MGI:4867916
hm1
Allelic
Composition
Myo9btm1.2Bah/Myo9btm1.2Bah
Genetic
Background
B6.Cg-Myo9btm1.2Bah
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myo9btm1.2Bah mutation (0 available); any Myo9b mutation (109 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• accumulation of monocytes and macrophages in the peritoneal cavity of C5a-induced peritonitis model was severely reduced
• isolated macrophages failed to spread and polarize in vitro
• isolated macrophage shows defective membrane protrusive activity
• mice have breed normal, and no detailed phenotypic analyses other than that of isolated macrophage were reported
• isolated macrophage motility and chemotaxis are impaired

hematopoietic system
• accumulation of monocytes and macrophages in the peritoneal cavity of C5a-induced peritonitis model was severely reduced
• isolated macrophages failed to spread and polarize in vitro
• isolated macrophage shows defective membrane protrusive activity
• mice have breed normal, and no detailed phenotypic analyses other than that of isolated macrophage were reported
• isolated macrophage motility and chemotaxis are impaired

cellular
• isolated macrophage motility and chemotaxis are impaired





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory