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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pkp2tm1Wbm
targeted mutation 1, Walter Birchmeier
MGI:3487374
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pkp2tm1Wbm/Pkp2tm1Wbm involves: C57BL/6 MGI:3510249


Genotype
MGI:3510249
hm1
Allelic
Composition
Pkp2tm1Wbm/Pkp2tm1Wbm
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pkp2tm1Wbm mutation (0 available); any Pkp2 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

E10.75 Pkp2tm1Wbm/Pkp2tm1Wbm embryos accumulate blood in pericardial and peritoneal cavities and lack red blood cells in the yolk sac vasculature

mortality/aging
• homozygous embryos begin to die around E11.5

cardiovascular system
• the adhering junctions between cardiomyocytes are abnormal and disarrayed cytoskeleton architecture is seen
• at E10.75 trabeculation is reduced
• thinner atrial walls are seen, however overt ruptures of the heart walls are not seen
• at E10.75 blood accumulates in the pericardium and peritoneum while little blood is seen in the vessels of head, dorsal trunk, and yolk sac

homeostasis/metabolism
• at E11.5-E12 peritoneal and pericardial edema are seen

muscle
• the adhering junctions between cardiomyocytes are abnormal and disarrayed cytoskeleton architecture is seen
• at E10.75 trabeculation is reduced

cellular
• the adhering junctions between cardiomyocytes are abnormal and disarrayed cytoskeleton architecture is seen





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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
04/09/2024
MGI 6.23
The Jackson Laboratory