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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dhx58tm1Gnb
targeted mutation 1, Glen N Barber
MGI:3837303
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Dhx58tm1Gnb/Dhx58tm1Gnb involves: 129P2/OlaHsd * C57BL/6J MGI:3837330


Genotype
MGI:3837330
hm1
Allelic
Composition
Dhx58tm1Gnb/Dhx58tm1Gnb
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dhx58tm1Gnb mutation (0 available); any Dhx58 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice exhibit decreased mortality associated with vesicular stomatitis virus (VSV) infection compared to similarly treated wild-type mice
• encephalomyocarditis virus (EMCV)-infected mice exhibit increased lethality compared to similarly treated wild-type mice

immune system
• encephalomyocarditis virus (EMCV)-infected macrophages or bone marrow-derived dendritic cells exhibit defective type I IFN production unlike similarly treated wild-type cells
• however, EMCV-infected mouse embryonic fibroblasts exhibit normal type I IFN production
• in the brains of VSV-infected mice
• polyI:C-stimulated mouse embryonic fibroblasts produce several-fold more IFN-alpha compared to similarly treated wild-type cells
• in the brains of VSV-infected mice
• polyI:C-stimulated mouse embryonic fibroblasts (MEFs) produce several-fold more IFN-beta compared to similarly treated wild-type cells
• MEFs exposed to vesicular stomatitis virus (VSV) exhibit increased IFN-beta production compared to similarly treated wild-type cells
• mouse embryonic fibroblasts (MEFs) exposed to vesicular stomatitis virus (VSV) exhibit increased IFN-beta production compared to similarly treated wild-type cells
• replication of a defective M protein VSV in MEFs is lower than in wild-type cells
• however, viral titers in VSV-infected MEFs are normal
• encephalomyocarditis virus (EMCV)-infected macrophages or bone marrow-derived dendritic cells exhibit defective type I IFN production unlike similarly treated wild-type cells
• EMCV-infected mice exhibit increased lethality compared to similarly treated wild-type mice
• however, EMCV-infected mouse embryonic fibroblasts exhibit normal type I IFN production
• mice exhibit decreased mortality associated with vesicular stomatitis virus (VSV) infection compared to similarly treated wild-type mice
• VSV-infected mice exhibit increased serum IL12 and IFN-gamma levels, decreased IFN-alpha and beta production in the brain, and lower viral titers than in similarly treated wild-type mice

homeostasis/metabolism





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory