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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Sarm1tm1.1Diam
targeted mutation 1.1, Michael S Diamond
MGI:5507721
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Sarm1tm1.1Diam/Sarm1tm1.1Diam involves: 129X1/SvJ * C57BL/6 MGI:5507810


Genotype
MGI:5507810
hm1
Allelic
Composition
Sarm1tm1.1Diam/Sarm1tm1.1Diam
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sarm1tm1.1Diam mutation (0 available); any Sarm1 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 36% survival as compared to 63% survival for controls after infection with WNV

immune system
N
• La Crosse virus (LACV) replication is normal (J:196200)
• no difference in vial burden as compared to controls in spleen, brain, or spinal cord after infection with 102 PFU of West Nile Virus (WNV) (J:200140)
• no difference in virus specific IgG or IgM at 6, 8, and 10 days after infection (J:200140)
• no difference in CD8+ T cells in the brain (J:200140)
• fewer activated microglia, particularly in brainstem and cerebral cortex but not in cerebellum after WNV infection
• macrophage and resting microglia numbers are unchanged
• 10 fold lower levels of TNF alpha in brain homogenates relative to controls afer WNV infection
• increased vulnerability to infection with 102 PFU of West Nile Virus (WNV)
• elevated WNV RNA in the brainstem but not in the cortex
• 36% survival as compared to 63% survival for controls after infection with WNV

hematopoietic system
N
• normal hematopoietc cell development after WNV infection
• typical B and T cell maturation profiles
• fewer activated microglia, particularly in brainstem and cerebral cortex but not in cerebellum after WNV infection
• macrophage and resting microglia numbers are unchanged

homeostasis/metabolism
• 10 fold lower levels of TNF alpha in brain homogenates relative to controls afer WNV infection

nervous system
• 100% of controls infected with 103 PFU of LACV develop neurological disease by 3 weeks whereas homozygous mutant mice develop disease at a significantly lower level
• levels of virus RNA are similar to control levels
• no mitochondrial damage, unlike control mice
• apoptosis is reduced in neurons from homozygotes infected with La Crosse virus, LACV, relative to controls (in culture)
• delayed neuronal death
• increased apoptosis in the brainstem 8-10 days after infection with WNV but not in the cortex, hippocampus, or cerebellum
• fewer activated microglia, particularly in brainstem and cerebral cortex but not in cerebellum after WNV infection
• macrophage and resting microglia numbers are unchanged

cellular
• apoptosis is reduced in neurons from homozygotes infected with La Crosse virus, LACV, relative to controls (in culture)
• delayed neuronal death
• increased apoptosis in the brainstem 8-10 days after infection with WNV but not in the cortex, hippocampus, or cerebellum





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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
10/29/2024
MGI 6.24
The Jackson Laboratory