About   Help   FAQ
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 (40 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory