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Phenotypes Associated with This Genotype
Genotype
MGI:3839985
Allelic
Composition
Bcrtm1Hkp/Bcrtm1Hkp
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bcrtm1Hkp mutation (2 available); any Bcr mutation (51 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• LPS-treated mice exhibit cortical necrosis unlike similarly treated wild-type mice

immune system
• in the kidney and liver 6 hours after LPS-exposure unlike similarly treated wild-type mice
• 6 hours after LPS-exposure, mice exhibit a 2- to 3- fold increase in circulating neutrophils that is sustained and more pronounced than in similarly treated wild-type mice
• following activation with phorbol myristate acetate (PMA) or PMA and N-formyl-Met-Leu-Phe, neutrophils exhibit a 100% increase in respiratory burst compared to similarly treated wild-type mice
• neutrophils are more easily primed and activated compared to wild-type cells
• neutrophils exhibit spontaneous activation unlike wild-type cells
• mice exposed to LPS develop septic shock lasting at least 4 days accompanied by weight loss and intestinal edema before onset of recovery unlike similarly treated wild-type mice that recover within 24 hours of exposure
• unlike in wild-type mice, LPS exposure leads to extensive damage in multiple organs including the ileum, kidney, and liver
• however, removal of neutrophils using cyclophosphamide treatment restores normal response to LPS
• LPS-exposed mice exhibit increased plasma lactate dehydrogenase, aspartate and alanine aminotransferase, and blood nitrogen urea compared to similarly treated wild-type mice
• mice exposed to LPS develop septic shock lasting at least 4 days before recovery unlike similarly treated wild-type mice

homeostasis/metabolism
• following LPS exposure
• following LPS exposure
• higher plasma LDH levels following LPS exposure

renal/urinary system
• LPS-treated mice exhibit cortical necrosis unlike similarly treated wild-type mice
• LPS-treated mice exhibit glomerular collapse as early as 6 hours post-exposure unlike similarly treated wild-type mice
• LPS-treated mice exhibit extensive vacuolization of proximal convoluted tubules unlike similarly treated wild-type mice

liver/biliary system
• 72 hours after LPS-exposure, mice exhibit fatty vacuolization in the liver parenchyma unlike similarly treated wild-type mice

digestive/alimentary system
• unlike in wild-type mice, LPS-treated mice exhibit the presence of debris and mucus plugs in the intestinal lumen and in between microvilli indicating necrosis of mucosal epithelial cells at 24 hours post-exposure
• following LPS exposure

growth/size/body
• following LPS exposure

hematopoietic system
• 72 hours after LPS-exposure, hematopoiesis shifts to granulopoiesis unlike in similarly treated wild-type mice
• in the kidney and liver 6 hours after LPS-exposure unlike similarly treated wild-type mice
• 6 hours after LPS-exposure, mice exhibit a 2- to 3- fold increase in circulating neutrophils that is sustained and more pronounced than in similarly treated wild-type mice
• following activation with phorbol myristate acetate (PMA) or PMA and N-formyl-Met-Leu-Phe, neutrophils exhibit a 100% increase in respiratory burst compared to similarly treated wild-type mice
• neutrophils are more easily primed and activated compared to wild-type cells
• neutrophils exhibit spontaneous activation unlike wild-type cells


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
04/16/2024
MGI 6.23
The Jackson Laboratory