About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pkn1tm1Ajmc
targeted mutation 1, Angus JM Cameron
MGI:5911979
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pkn1tm1Ajmc/Pkn1tm1Ajmc B6.129P2-Pkn1tm1Ajmc MGI:5912002
cx2
Pkn1tm1Ajmc/Pkn1tm1Ajmc
Pkn2tm1a(KOMP)Wtsi/Pkn2+
Pkn3tm1Ajmc/Pkn3tm1Ajmc
involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac MGI:5912007
cx3
Pkn1tm1Ajmc/Pkn1tm1Ajmc
Pkn3tm1Ajmc/Pkn3tm1Ajmc
involves: 129P2/OlaHsd * C57BL/6NTac MGI:5912005


Genotype
MGI:5912002
hm1
Allelic
Composition
Pkn1tm1Ajmc/Pkn1tm1Ajmc
Genetic
Background
B6.129P2-Pkn1tm1Ajmc
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pkn1tm1Ajmc mutation (0 available); any Pkn1 mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• hearts show a significant decrease in p42/p44-MAPK (ERK1/2) phosphorylation both at baseline and during global ischemia and reperfusion (I/R)
• the maximal rate of systolic pressure development (dP/dT max) normalized to the end diastolic pressure (EDP) is significantly lower than that in wild-type hearts
• however, the average dP/dTmax and ejection fraction are relatively normal
• the maximal rate of relaxation (dP/dT min) normalized to the end diastolic pressure (EDP) is significantly lower than that in wild-type hearts
• Doppler echocardiography revealed that left ventricular (LV) posterior wall thickness at diastole (PWTD) is significantly higher than that in wild-type hearts
• following I/R, LVDP is significantly lower than that in wild-type hearts (17.7 +/- 3.9% versus 33.6 +/- 6.1%) with no differences in end diastolic pressure (EDP) or coronary flow (CF), indicating increased injury and reduced functional recovery
• however, baseline LVDP, EDP and CF are normal
• beat-to-beat systolic pressure (SP) normalized to the end diastolic pressure (EDP) is significantly lower than that in wild-type hearts
• following global I/R injury, myocardial infarct size is nearly doubled relative to that in wild-type hearts (45.1 +/- 2.9% versus 25.5 +/- 0.8%)

homeostasis/metabolism
• following global I/R injury, myocardial infarct size is nearly doubled relative to that in wild-type hearts (45.1 +/- 2.9% versus 25.5 +/- 0.8%)
• hearts show a significant increase in basal phospholamban (PLB) Thr17 phosphorylation, ATP2A2 (ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2, aka SERCA2) expression and Jph2 (junctophilin-2) expression, suggesting a compensatory enhancement of sarcoplasmic reticulum Ca2+ uptake at baseline

muscle
• the maximal rate of systolic pressure development (dP/dT max) normalized to the end diastolic pressure (EDP) is significantly lower than that in wild-type hearts
• however, the average dP/dTmax and ejection fraction are relatively normal
• the maximal rate of relaxation (dP/dT min) normalized to the end diastolic pressure (EDP) is significantly lower than that in wild-type hearts

mortality/aging
N
• mice are viable and overtly normal

reproductive system
N
• mice are fertile




Genotype
MGI:5912007
cx2
Allelic
Composition
Pkn1tm1Ajmc/Pkn1tm1Ajmc
Pkn2tm1a(KOMP)Wtsi/Pkn2+
Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6N * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pkn1tm1Ajmc mutation (0 available); any Pkn1 mutation (45 available)
Pkn2tm1a(KOMP)Wtsi mutation (1 available); any Pkn2 mutation (84 available)
Pkn3tm1Ajmc mutation (0 available); any Pkn3 mutation (54 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• viable and fertile with no overt phenotype




Genotype
MGI:5912005
cx3
Allelic
Composition
Pkn1tm1Ajmc/Pkn1tm1Ajmc
Pkn3tm1Ajmc/Pkn3tm1Ajmc
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pkn1tm1Ajmc mutation (0 available); any Pkn1 mutation (45 available)
Pkn3tm1Ajmc mutation (0 available); any Pkn3 mutation (54 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• viable and fertile with no overt phenotype





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