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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Prkcetm1Bsca
targeted mutation 1, Lisardo Bosca
MGI:3609215
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Prkcetm1Bsca/Prkcetm1Bsca involves: 129P2/OlaHsd * C57BL/6 MGI:3618538


Genotype
MGI:3618538
hm1
Allelic
Composition
Prkcetm1Bsca/Prkcetm1Bsca
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkcetm1Bsca mutation (0 available); any Prkce mutation (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• following culture in the presence of either LPS, LPS and IFNG, or LPS, IFNG, and 15dPGJ2 fewer than 15% of macrophages undergo apoptosis compared to from 20% to 50% of wild-type cells
• T cell proliferation in response to anti-CD3E antibody or anti-TCRalphabeta antibody is reduced to 80% of control
• macrophages produce less NO following LPS stimulation and less NO, TNF, IL1B, and PGE2 following LPS and IFNG stimulation
• serum levels of IL1B are significantly reduced
• serum levels of TNFA are significantly reduced
• survival time is decreased following exposure to either Gram-negative or Gram-positive bacteria

reproductive system
• high levels of Gram-negative bacteria are detected in the uterine fluid
• about 30% of females have distended fluid-filled uteri
• only 1 in 4 females produce a litter and second litters are even less common

growth/size/body
• 10-15% smaller than control littermates

adipose tissue
• homozygotes do not develop increased adipose tissue with age to the same extent as in wild-type mice

cardiovascular system
• in the absence of preconditioning ischemia-induced myocardial infarct size is similar to controls; however, following ischemia preconditioning (4 bouts of 4 min ischemia and 6 min reperfusion) no decrease in ischemia-induced myocardial infarct size is seen unlike in controls
• ischemia preconditioning in both controls and homozygotes does improve contractile recovery following ischemia

hematopoietic system
• following culture in the presence of either LPS, LPS and IFNG, or LPS, IFNG, and 15dPGJ2 fewer than 15% of macrophages undergo apoptosis compared to from 20% to 50% of wild-type cells
• T cell proliferation in response to anti-CD3E antibody or anti-TCRalphabeta antibody is reduced to 80% of control
• macrophages produce less NO following LPS stimulation and less NO, TNF, IL1B, and PGE2 following LPS and IFNG stimulation

homeostasis/metabolism
• in the absence of preconditioning ischemia-induced myocardial infarct size is similar to controls; however, following ischemia preconditioning (4 bouts of 4 min ischemia and 6 min reperfusion) no decrease in ischemia-induced myocardial infarct size is seen unlike in controls
• ischemia preconditioning in both controls and homozygotes does improve contractile recovery following ischemia
• macrophages produce less NO following LPS stimulation and less NO, TNF, IL1B, and PGE2 following LPS and IFNG stimulation
• serum levels of IL1B are significantly reduced
• serum levels of TNFA are significantly reduced

cellular
• following culture in the presence of either LPS, LPS and IFNG, or LPS, IFNG, and 15dPGJ2 fewer than 15% of macrophages undergo apoptosis compared to from 20% to 50% of wild-type cells
• T cell proliferation in response to anti-CD3E antibody or anti-TCRalphabeta antibody is reduced to 80% of control





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