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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gper1tm1.1Lmlf
targeted mutation 1.1, L M Leeb-Lundberg
MGI:3837567
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gper1tm1.1Lmlf/Gper1tm1.1Lmlf B6.129-Gper1tm1.1Lmlf MGI:3837658


Genotype
MGI:3837658
hm1
Allelic
Composition
Gper1tm1.1Lmlf/Gper1tm1.1Lmlf
Genetic
Background
B6.129-Gper1tm1.1Lmlf
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gper1tm1.1Lmlf mutation (0 available); any Gper1 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• however, male mice exhibit normal glucagons secretion in response to glucose stimulation
• female mice exhibit slightly reduced glucagons release in response to low (18%) and high-glucose (12%) compared to in wild-type mice
• PGE2-treated islet cells fail to exhibit decreased glucagons in response to glucose stimulation unlike wild-type cells
• in response to low and high glucose levels, female mice exhibit a 35% and 57%, respectively, decrease in insulin release compared to similarly treated wild-type mice
• however, the fold stimulation by glucose, tolbutamide and high potassium ion is normal
• ovariectomized female mice failed to exhibit an increase in pancreatic insulin content unlike similarly treated wild-type mice
• treatment of ovariectomized female mice with PGE2 fail to increase pancreatic insulin content unlike in similarly treated wild-type mice
• PGE2-treated islet cells fails to increases insulin release in response to glucose stimulation unlike in similarly treated wild-type cells
• 13% in female mice at 6 months of age
• female mice exhibit depressed glucagons levels 10 minutes after glucose challenge compared to wild-type mice
• in female mice, but not in male mice, at 6 months of age
• female mice exhibit diminished first-phase insulin response to glucose challenge compared to similarly treated wild-type mice
• however, male mice exhibit normal glucose tolerance
• normal insulin and glucagon response to PGE2 is abolished

endocrine/exocrine glands
• female mice exhibit slightly reduced glucagons release in response to low (18%) and high-glucose (12%) compared to in wild-type mice
• however, male mice exhibit normal glucagons secretion in response to glucose stimulation
• PGE2-treated islet cells fail to exhibit decreased glucagons in response to glucose stimulation unlike wild-type cells
• in response to low and high glucose levels, female mice exhibit a 35% and 57%, respectively, decrease in insulin release compared to similarly treated wild-type mice
• however, the fold stimulation by glucose, tolbutamide and high potassium ion is normal
• ovariectomized female mice failed to exhibit an increase in pancreatic insulin content unlike similarly treated wild-type mice
• treatment of ovariectomized female mice with PGE2 fail to increase pancreatic insulin content unlike in similarly treated wild-type mice
• PGE2-treated islet cells fails to increases insulin release in response to glucose stimulation unlike in similarly treated wild-type cells

growth/size/body
• in female mice only
• in female mice only

cardiovascular system
• at 9 months, the lumen circumference of resistance arteries is reduced 23% and media to lumen ratio is increased 45% compared to in wild-type mice
• however, mice exhibit normal thoracic arteries dimensions and media thickness
• at 9 months, female mice exhibit a 23% elevation in mean arterial blood pressure compared to in wild-type mice

limbs/digits/tail
• in female mice only

skeleton
• in female mice only





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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
04/23/2024
MGI 6.23
The Jackson Laboratory