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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Ins2-GP)#Psoh
transgene insertion, Pamela Ohashi
MGI:5568709
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Tg(Ins2-GP)#Psoh/0
Tg(TcrLCMV)327Sdz/0
involves: C57BL/6 * DBA/2 MGI:5568711
cx2
Tg(Ins1-Cd80)378Psoh/0
Tg(Ins2-GP)#Psoh/0
Tg(TcrLCMV)327Sdz/0
involves: C57BL/6 * DBA/2 * FVB/N MGI:5569019
cx3
Tg(Ins1-Cd80)378Psoh/0
Tg(Ins2-GP)#Psoh/0
involves: C57BL/6 * FVB/N MGI:5569021
tg4
Tg(Ins2-GP)#Psoh/0 involves: C57BL/6 MGI:5568710


Genotype
MGI:5568711
cx1
Allelic
Composition
Tg(Ins2-GP)#Psoh/0
Tg(TcrLCMV)327Sdz/0
Genetic
Background
involves: C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Ins2-GP)#Psoh mutation (0 available)
Tg(TcrLCMV)327Sdz mutation (8 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• skewing of thymocytes to the single CD8+ mature phenotype, indicating that thymocytes are positively selected
• however, double transgenic mice are able to respond by proliferation to LCMV antigens at the same magnitude as single Tg(TcrLCMV)327Sdz mice and cytotoxic T lymphocytes are able to respond to LCMV infection as in controls

homeostasis/metabolism
N
• mice do not develop diabetes and exhibit normal islet architecture with no evidence of insulitis
• mice immunized with lymphocytic choriomeningitis virus (LCMV) develop hyperglycemia 3 to 4 days after infection
• a variant LCM virus, 8.7, does not induce diabetes in mice
• mice immunized with LCMV develop glucosuria 3 to 4 days after infection

immune system
• skewing of thymocytes to the single CD8+ mature phenotype, indicating that thymocytes are positively selected
• however, double transgenic mice are able to respond by proliferation to LCMV antigens at the same magnitude as single Tg(TcrLCMV)327Sdz mice and cytotoxic T lymphocytes are able to respond to LCMV infection as in controls

renal/urinary system
• mice immunized with LCMV develop glucosuria 3 to 4 days after infection




Genotype
MGI:5569019
cx2
Allelic
Composition
Tg(Ins1-Cd80)378Psoh/0
Tg(Ins2-GP)#Psoh/0
Tg(TcrLCMV)327Sdz/0
Genetic
Background
involves: C57BL/6 * DBA/2 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Ins1-Cd80)378Psoh mutation (0 available)
Tg(Ins2-GP)#Psoh mutation (0 available)
Tg(TcrLCMV)327Sdz mutation (8 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• hyperglycemia is followed by ketosis, wasting, and death

endocrine/exocrine glands
• complete beta-cell destruction
• ongoing insulitis is seen at 10 weeks of age, with a diminished, but still present, mass of beta cells
• 4 week old mice show a mixture of a few cD8+ and CD4+ T lymphocytes and an increase in the number of macrophages surrounding pancreatic islets, while 9 week old mice show severe insulitis and periinsulitis with CD8+ and CD4+ T lymphocytes, macrophages and B lymphocytes infiltrating the islets
• 9 week old mice show severe periinsulitis

growth/size/body
• hyperglycemia is wasting

homeostasis/metabolism
• mice spontaneously become diabetic with a median age of hyperglycemia onset of 9-10 weeks of age
• hyperglycemia is followed by ketosis

immune system
• ongoing insulitis is seen at 10 weeks of age, with a diminished, but still present, mass of beta cells
• 4 week old mice show a mixture of a few cD8+ and CD4+ T lymphocytes and an increase in the number of macrophages surrounding pancreatic islets, while 9 week old mice show severe insulitis and periinsulitis with CD8+ and CD4+ T lymphocytes, macrophages and B lymphocytes infiltrating the islets
• 9 week old mice show severe periinsulitis

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
type 1 diabetes mellitus DOID:9744 OMIM:222100
J:209714




Genotype
MGI:5569021
cx3
Allelic
Composition
Tg(Ins1-Cd80)378Psoh/0
Tg(Ins2-GP)#Psoh/0
Genetic
Background
involves: C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• mice infected with a recombinant vaccinia virus expressing GP develop diabetes 6-10 days after infection
• however, mice do not develop spontaneous diabetes and exhibit normal islet architecture with no evidence of isulitis




Genotype
MGI:5568710
tg4
Allelic
Composition
Tg(Ins2-GP)#Psoh/0
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice immunized with LCMV die 15-20 days after infection

homeostasis/metabolism
• mice immunized with lymphocytic choriomeningitis virus (LCMV) develop hyperglycemia 9-11 days after infection
• treatment with either CD4 or CD8 antibodies one day before or after LCMV infection results in no signs of increased glucose levels
• treatment with poly-IC to induce IFN-alpha and IFN-beta or with IFN-alpha to enhance expression of class I and class II MHC does not induce diabetes in mutants
• mice immunized with LCMV develop glucosuria 9-11 days after infection

immune system
• mice immunized with LCMV show lymphocytic infiltration of the islets of Langerhans; CD4+ T cells are seen around the islets of Langerhans while CD8+ T cells infiltrate the entire islets of the pancreas

endocrine/exocrine glands
• mice immunized with LCMV show lymphocytic infiltration of the islets of Langerhans; CD4+ T cells are seen around the islets of Langerhans while CD8+ T cells infiltrate the entire islets of the pancreas

renal/urinary system
• mice immunized with LCMV develop glucosuria 9-11 days after infection





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