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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rictortm1.1Mgn
targeted mutation 1.1, Mark A Magnuson
MGI:3703321
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ptentm1Hwu/Ptentm1Hwu
Rictortm1.1Mgn/Rictortm1.1Mgn
involves: 129S4/SvJae * 129S6/SvEvTac MGI:4848147
cn2
Ptentm1Hwu/Ptentm1Hwu
Rictortm1.1Mgn/Rictortm1.1Mgn
Tg(Ins2-cre)25Mgn/0
involves: 129S4/SvJae * 129S6/SvEvTac * BALB/c * C57BL/6 * DBA MGI:5008147
cn3
Rictortm1.1Mgn/Rictortm1.2Mgn
Meox2tm1(cre)Sor/Meox2+
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * FVB/N * SJL MGI:3706134
cn4
Rictortm1.1Mgn/Rictortm1.1Mgn
Tg(Ins2-cre)25Mgn/0
involves: 129S6/SvEvTac * BALB/c * C57BL/6 * DBA MGI:5008146


Genotype
MGI:4848147
cn1
Allelic
Composition
Ptentm1Hwu/Ptentm1Hwu
Rictortm1.1Mgn/Rictortm1.1Mgn
Genetic
Background
involves: 129S4/SvJae * 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptentm1Hwu mutation (16 available); any Pten mutation (81 available)
Rictortm1.1Mgn mutation (1 available); any Rictor mutation (140 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• prostatic ductules of mutants infected with an adenovirus expressing Cre recombinase exhibit a mixed phenotype containing mostly normal, organized epithelial cells and patches of large, disorganized hyperplastic cells; inefficient deletion of Rictor is seen in the patches of disorganized hyperplastic cells
• prostate tissue histology of mutants infected with an adenovirus expressing Cre recombinase appears normal except that epithelial cells are slightly smaller

reproductive system
• prostatic ductules of mutants infected with an adenovirus expressing Cre recombinase exhibit a mixed phenotype containing mostly normal, organized epithelial cells and patches of large, disorganized hyperplastic cells; inefficient deletion of Rictor is seen in the patches of disorganized hyperplastic cells
• prostate tissue histology of mutants infected with an adenovirus expressing Cre recombinase appears normal except that epithelial cells are slightly smaller

neoplasm
• mutants infected with an adenovirus expressing Cre recombinase do not develop prostate adenocarcinoma




Genotype
MGI:5008147
cn2
Allelic
Composition
Ptentm1Hwu/Ptentm1Hwu
Rictortm1.1Mgn/Rictortm1.1Mgn
Tg(Ins2-cre)25Mgn/0
Genetic
Background
involves: 129S4/SvJae * 129S6/SvEvTac * BALB/c * C57BL/6 * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptentm1Hwu mutation (16 available); any Pten mutation (81 available)
Rictortm1.1Mgn mutation (1 available); any Rictor mutation (140 available)
Tg(Ins2-cre)25Mgn mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• average beta cell size is increased by 31% compared to controls and by 15% compared to single conditional Pten mutants
• however, mutants show normal beta cell proliferation
• beta cell mass is about 40% lower than that of single conditional Pten mutants

growth/size/body

homeostasis/metabolism
• total glucose excursion is lower compared to single conditional Rictor mutants
• fed blood glucose concentration remains similar to the controls, however mutants show a lower blood glucose concentration at 30 and 60 min after an intraperitoneal glucose bolus compared to single conditional Rictor mutants
• mutants exhibit lower plasma insulin levels 15 min after glucose challenge and lower total insulin output compared with controls
• however, insulin secretion by glucose stimulated islets is similar to controls and pancreatic insulin content is unchanged




Genotype
MGI:3706134
cn3
Allelic
Composition
Rictortm1.1Mgn/Rictortm1.2Mgn
Meox2tm1(cre)Sor/Meox2+
Genetic
Background
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Meox2tm1(cre)Sor mutation (3 available); any Meox2 mutation (18 available)
Rictortm1.1Mgn mutation (1 available); any Rictor mutation (140 available)
Rictortm1.2Mgn mutation (0 available); any Rictor mutation (140 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• significantly lower than expected ratio of live embryos were obtained at E13.5 and E17.5, presumed to indicate embryonic lethality




Genotype
MGI:5008146
cn4
Allelic
Composition
Rictortm1.1Mgn/Rictortm1.1Mgn
Tg(Ins2-cre)25Mgn/0
Genetic
Background
involves: 129S6/SvEvTac * BALB/c * C57BL/6 * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rictortm1.1Mgn mutation (1 available); any Rictor mutation (140 available)
Tg(Ins2-cre)25Mgn mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• beta-cell mass is 28% lower than controls after adjusting for body size
• the reduction in beta cell mass is mainly due to a decrease in beta cell proliferation
• however, beta cell size is unaffected and islet number per pancreatic unit area is unchanged in mutants
• pancreatic insulin content is about 50% less than controls
• number of proliferating beta-cells is decreased by 26% compared to controls
• islets have approximately 70% lower insulin secretion in response to glucose than controls
• however, insulin sensitivity is normal

homeostasis/metabolism
• total glucose excursion is higher compared to controls
• islets have approximately 70% lower insulin secretion in response to glucose than controls
• however, insulin sensitivity is normal
• mutants exhibit hyperglycemia beginning at 12 weeks of age
• mutants show slower glucose clearance as indicated by elevated blood glucose concentrations at 15 and 30 min after an intraperitoneal glucose bolus
• impaired glucose tolerance is due to reduced pancreatic insulin content and impaired glucose-stimulated insulin secretion

cellular
• number of proliferating beta-cells is decreased by 26% compared to controls





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory