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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
P2ry14tm1.1Shbg
targeted mutation 1.1, Torsten Schoneberg
MGI:5707037
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
P2ry14tm1.1Shbg/P2ry14tm1.1Shbg involves: 129S6/SvEvTac * C57BL/6 MGI:5767292


Genotype
MGI:5767292
hm1
Allelic
Composition
P2ry14tm1.1Shbg/P2ry14tm1.1Shbg
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
P2ry14tm1.1Shbg mutation (0 available); any P2ry14 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• in vitro, insulin release following stimulation with low (2.8 mM) and high glucose (16.7 mM) during a 30-min incubation is significantly reduced in isolated pancreatic islets relative wild-type controls
• both the initial insulin release peak and the sustained insulin release are significantly decreased following stimulation with a high glucose concentration (16.7mM) relative wild-type controls
• transcriptome analysis of mutant pancreatic islets revealed significantly altered expression of components involved in insulin secretion
• however, gross pancreatic islet morphology, beta-cell mass, and intracellular insulin content in lysed islets are normal
• on a standard chow diet, 16-weeks-old mice tend to have lower serum insulin levels after intraperitoneal glucose application relative wild-type controls
• after 12 weeks of western type diet, mice show significantly lower glucose-stimulated insulin secretion at both 40 and 60 min after intraperitoneal glucose injection relative wild-type controls
• under a western type diet, glucose tolerance is significantly impaired following oral and intraperitoneal glucose application relative to wild-type controls
• however, insulin sensitivity appears unaffected

endocrine/exocrine glands
• in vitro, insulin release following stimulation with low (2.8 mM) and high glucose (16.7 mM) during a 30-min incubation is significantly reduced in isolated pancreatic islets relative wild-type controls
• both the initial insulin release peak and the sustained insulin release are significantly decreased following stimulation with a high glucose concentration (16.7mM) relative wild-type controls
• transcriptome analysis of mutant pancreatic islets revealed significantly altered expression of components involved in insulin secretion
• however, gross pancreatic islet morphology, beta-cell mass, and intracellular insulin content in lysed islets are normal

growth/size/body
• mice fed a western type diet for 3 months gain significantly less weight than similarly fed wild-type controls
• however, no differences in body weight development are observed under a standard chow diet
• at 3 months of age, spleen weight is significantly increased

digestive/alimentary system
• following oral application of dye-labeled dextran, excretion of blue dextran in feces is significantly delayed relative to wild-type controls

cardiovascular system
• at 3 months of age, heart rate is increased (P < 0.01)
• at 3 months of age, mean arterial pressure is significantly increased (P < 0.001)
• at 3 months of age, diastolic pressure is significantly increased (P < 0.001)
• at 3 months of age, systolic pressure is increased (P < 0.01)

respiratory system
• reduced airway responsiveness as shown by invasive plethysmography tests
• significantly increased dynamic compliance in response to increasing inhaled doses (10-80 mg/ml) of methacholine
• however, inhaled UDP-glucose (100 uM) has no significant effect on lung resistance and dynamic compliance

hematopoietic system
• at 3 months of age, spleen weight is significantly increased

immune system
• at 3 months of age, spleen weight is significantly increased





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
04/30/2024
MGI 6.23
The Jackson Laboratory