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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Exoc3tm2c(EUCOMM)Hmgu
targeted mutation 2c, Helmholtz Zentrum Muenchen GmbH
MGI:6509449
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Exoc3tm2c(EUCOMM)Hmgu/Exoc3tm2c(EUCOMM)Hmgu
Tg(Pf4-icre)Q3Rsko/0
involves: C57BL/6 * C57BL/6N MGI:6509466


Genotype
MGI:6509466
cn1
Allelic
Composition
Exoc3tm2c(EUCOMM)Hmgu/Exoc3tm2c(EUCOMM)Hmgu
Tg(Pf4-icre)Q3Rsko/0
Genetic
Background
involves: C57BL/6 * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Exoc3tm2c(EUCOMM)Hmgu mutation (0 available); any Exoc3 mutation (28 available)
Tg(Pf4-icre)Q3Rsko mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• platelets treated with a glycoprotein VI (GPVI)-selective agonist, collagen-related peptide, show defects in aggregation, integrin activation, alpha-granule, dense granule, and lysosomal granule secretion, and attenuated calcium responses
• platelets show an increase in dense granule secretion and integrin activation after protease-activated receptor 4 activation, but calcium responses are unaltered
• mice show a defect in GPVI-stimulated platelet dense granule secretion
• platelets show an increase in dense granule secretion after protease-activated receptor 4 activation
• platelet responses to GPVI stimulation show defects in platelet aggregation
• however, no difference in protease-activated receptor 4-activating peptide (PAR4-AP)-induced platelet aggregation is seen
• whole blood thrombus formation over collagen is reduced
• in a ferric chloride injury model of the carotid artery, mice show accelerated arterial thrombosis
• mice exhibit lower bleed time levels with tail tip excision, indicating improved hemostatic function

hematopoietic system
• small, but significant, 8.3% increase in mean platelet volume
• however, blood cell counts are unchanged
• platelets treated with a glycoprotein VI (GPVI)-selective agonist, collagen-related peptide, show defects in aggregation, integrin activation, alpha-granule, dense granule, and lysosomal granule secretion, and attenuated calcium responses
• platelets show an increase in dense granule secretion and integrin activation after protease-activated receptor 4 activation, but calcium responses are unaltered
• mice show a defect in GPVI-stimulated platelet dense granule secretion
• platelets show an increase in dense granule secretion after protease-activated receptor 4 activation
• platelet responses to GPVI stimulation show defects in platelet aggregation
• however, no difference in protease-activated receptor 4-activating peptide (PAR4-AP)-induced platelet aggregation is seen

cellular
• mice show a defect in GPVI-stimulated platelet dense granule secretion
• platelets show an increase in dense granule secretion after protease-activated receptor 4 activation





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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
12/10/2024
MGI 6.24
The Jackson Laboratory