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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tusc2+
wild type
MGI:2441103
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Tusc2tm1Avi/Tusc2+ involves: 129S1/Sv * C57BL/6J MGI:3707332


Genotype
MGI:3707332
ht1
Allelic
Composition
Tusc2tm1Avi/Tusc2+
Genetic
Background
involves: 129S1/Sv * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tusc2tm1Avi mutation (0 available); any Tusc2 mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 11% of mice die between 2 and 14 months of age; some show signs of systemic infection, whereas others show necrotizing arteritis in multiple organs, severe glomerulonephrits, severe nephropathy, and anemia
• some animals develop tumors and die prematurely

cardiovascular system
• some mice show a vasculitis syndrome
• 20% of mice dying before or sacrificed at 2 years of age develop arteritis in single or multiple organs
• arteritis is found in large vessels and small arteries, veins and capillaries
• multiple organs like the heart, kidney, liver, lung pancreas, spleen, lymph nodes, thyroid, gall bladder, tongue, spinal cord muscles, and omentum show arteritis; some mice develop necrotizing arteritis in pancreas, liver, spleen, small intestine, ovary, uterus, urethra, and spinal cord
• some arteritic lesions show infiltration of entire vessel with fibrinoid necrosis

hematopoietic system
• 2 mice showing arteritis and/or glomerulonephritis had low red blood cell counts

immune system
• 20% of mice dying before or sacrificed at 2 years of age develop arteritis in single or multiple organs
• arteritis is found in large vessels and small arteries, veins and capillaries
• multiple organs like the heart, kidney, liver, lung pancreas, spleen, lymph nodes, thyroid, gall bladder, tongue, spinal cord muscles, and omentum show arteritis; some mice develop necrotizing arteritis in pancreas, liver, spleen, small intestine, ovary, uterus, urethra, and spinal cord
• some arteritic lesions show infiltration of entire vessel with fibrinoid necrosis
• some mice which died prematurely showed arteritis, severe kidney abnormalities and anemia which are hallmarks of autoimmune disorder whereas wild-type mice did not display any of these
• circulating autoreactive nuclear antibodies are detected
• severe glomerulonephritis sometimes associated with extensive tubular cast formation

renal/urinary system
• glomerular lesions often include membranoproliferative changes, wire-loop-like subendothelial deposits, and intracapillary thrombi that often obstruct the capillary lumen
• severe glomerulonephritis sometimes associated with extensive tubular cast formation
• severe glomerulonephritis sometimes associated with extensive tubular cast formation

neoplasm
• no distinct tumor pattern is observed in organs outside the hematopoietic system
• ~23% of mice develop mixed hemangioma/hemangiosarcoma or either independently compared to ~4% in wild-type
• one female presented an erythroleukemia
• 2 mice develop types of lymphomas at 8 and 12 months of age, respectively compared to 0 tumors in wild-type mice

homeostasis/metabolism

adipose tissue
• one mouse presenting with vasculitis syndrome developed fat necrosis





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
03/18/2025
MGI 6.24
The Jackson Laboratory