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Phenotypes Associated with This Genotype
Genotype
MGI:5140969
Allelic
Composition
Unc93b1tm1.1Kmiy/Unc93b1tm1.1Kmiy
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Unc93b1tm1.1Kmiy mutation (6 available); any Unc93b1 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• upon CpG-B-stimulation
• upon imiquimod-stimulation
• in response to anti-IgM

mortality/aging
• 50% of mice die by 30 weeks of age

immune system
• upon CpG-B-stimulation
• upon imiquimod-stimulation
• in response to anti-IgM
• progressive in moribund mice
• in moribund mice
• T cells exhibit marked differentiation into Th1 or Th7 cells compared to in wild-type mice
• T cells exhibit marked differentiation into Th1 or Th7 cells compared to in wild-type mice
• reduced percentage in the spleen
• increased percentage in the lymph nodes
• in the lymph nodes
• in the lymph nodes
• in plasmocytoid dendritic cells stimulated with CpG-A to stimulate a TLR9 response
• in plasmocytoid dendritic cells stimulated with imiquimod to stimulate a TLR7 response
• in dendritic cells stimulated with CpG-B to stimulate a TLR9 response
• in dendritic cells stimulated with loxoribine to stimulate a TLR7 response
• in bone marrow macrophages stimulated with CpG-B to stimulate a TLR9 response
• in bone marrow macrophages stimulated with loxoribine to stimulate a TLR7 response
• mice exhibit increased anti-nuclear (ANA), anti-mitochondrial (AMA), and anti-smooth muscle (ASMA) antibodies compared with wild-type mice
• CD11b+ CD11chiGr1int cells infiltrate in moribund mice
• without decreased kidney function in moribund mice

growth/size/body
• progressive in moribund mice
• in moribund mice

liver/biliary system
• CD11b+ CD11chiGr1int cells infiltrate in moribund mice
• moribund mice exhibit liver damage with pale spots unlike wild-type mice
• however, mice do not exhibit portal fibrosis indicative of chronic liver damage
• multilobular in moribund mice
• in moribund mice

homeostasis/metabolism
• weakly in moribund mice

skeleton
• mice exhibit increased erythrocyte phagocytosis in the bone marrow cells and peripheral blood compared with wild-type mice

renal/urinary system
• without decreased kidney function in moribund mice

hematopoietic system
• upon CpG-B-stimulation
• upon imiquimod-stimulation
• in response to anti-IgM
• progressive in moribund mice
• in moribund mice
• T cells exhibit marked differentiation into Th1 or Th7 cells compared to in wild-type mice
• T cells exhibit marked differentiation into Th1 or Th7 cells compared to in wild-type mice
• in moribund mice
• in the blood of moribund mice
• severe in moribund and nonmoribund mice
• reduced percentage in the spleen
• increased percentage in the lymph nodes
• in the lymph nodes
• in the lymph nodes
• mice exhibit increased erythrocyte phagocytosis in the bone marrow cells and peripheral blood compared with wild-type mice


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)
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last database update
01/06/2026
MGI 6.24
The Jackson Laboratory