About   Help   FAQ
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 (24 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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory