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Phenotypes Associated with This Genotype
Genotype
MGI:4437914
Allelic
Composition
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+
Plcg1tm1Gcrp/Plcg1tm1Rwen
Tg(Cd4-cre)1Cwi/0
Genetic
Background
involves: 129X1/SvJ * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(EYFP)Cos mutation (24 available); any Gt(ROSA)26Sor mutation (1062 available)
Plcg1tm1Gcrp mutation (0 available); any Plcg1 mutation (48 available)
Plcg1tm1Rwen mutation (0 available); any Plcg1 mutation (48 available)
Tg(Cd4-cre)1Cwi mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• following reactivation
• differentiation into CD4 or CD8 single positive thymocytes is reduced compared to in wild-type mice
• differentiation into CD4 or CD8 single positive thymocytes is reduced compared to in wild-type mice
• peripheral T cells are reduced compared to in wild-type mice
• in transplantation experiments, T cells are less competitive than wild-type T cells
• CD4+ thymocytes are more profoundly decreased than CD8+ thymocytes
• mice exhibit an increase in T cell activation compared with wild-type mice
• however, activation phenotype is not cell intrinsic
• in response to stimulation with anti-CD3m anti-CD3/anti-CD28, or anti-CD3/IL2, T cell proliferation is reduced compared to in similarly treated Plcg1tm1Gcrp/Plcg1+ Tg(CD4-cre)1Cwi Gt(ROSA)26Sortm1(EYFP)Cos mice
• however, treatment with PMA/ionomycin restores proliferation
• YFP+ T regulatory cells exhibit reduced ability to suppress naive T cell proliferation compared with wild-type T cells
• following anti-CD3/anti-CD28 stimulation, slightly fewer IFN-gamma producing single positive T cells are detected compared to in similarly treated Plcg1tm1Gcrp/Plcg1+ Tg(CD4-cre)1Cwi Gt(ROSA)26Sortm1(EYFP)Cos mice
• following anti-CD3/anti-CD28 stimulation, IL2 production by single positive T cells is reduced compared to in similarly treated Plcg1tm1Gcrp/Plcg1+ Tg(CD4-cre)1Cwi Gt(ROSA)26Sortm1(EYFP)Cos mice
• mice exhibit dermatitis unlike wild-type mice
• however, treatment with wild-type T regulatory cells prevents development of symptom

growth/size/body
• mice weight less than wild-type mice
• however, transfer of regulatory T cells restores normal weight gain

digestive/alimentary system
• mice exhibit rectal prolapse unlike wild-type mice
• however, treatment with wild-type T regulatory cells prevents development of symptom

hematopoietic system
• following reactivation
• differentiation into CD4 or CD8 single positive thymocytes is reduced compared to in wild-type mice
• differentiation into CD4 or CD8 single positive thymocytes is reduced compared to in wild-type mice
• peripheral T cells are reduced compared to in wild-type mice
• in transplantation experiments, T cells are less competitive than wild-type T cells
• CD4+ thymocytes are more profoundly decreased than CD8+ thymocytes
• mice exhibit an increase in T cell activation compared with wild-type mice
• however, activation phenotype is not cell intrinsic
• in response to stimulation with anti-CD3m anti-CD3/anti-CD28, or anti-CD3/IL2, T cell proliferation is reduced compared to in similarly treated Plcg1tm1Gcrp/Plcg1+ Tg(CD4-cre)1Cwi Gt(ROSA)26Sortm1(EYFP)Cos mice
• however, treatment with PMA/ionomycin restores proliferation
• YFP+ T regulatory cells exhibit reduced ability to suppress naive T cell proliferation compared with wild-type T cells

integument
• mice exhibit dermatitis unlike wild-type mice
• however, treatment with wild-type T regulatory cells prevents development of symptom
• mice exhibit alopecia unlike wild-type mice
• however, treatment with wild-type T regulatory cells prevents development of symptom

cellular
• following reactivation
• in response to stimulation with anti-CD3m anti-CD3/anti-CD28, or anti-CD3/IL2, T cell proliferation is reduced compared to in similarly treated Plcg1tm1Gcrp/Plcg1+ Tg(CD4-cre)1Cwi Gt(ROSA)26Sortm1(EYFP)Cos mice
• however, treatment with PMA/ionomycin restores proliferation


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
01/06/2026
MGI 6.24
The Jackson Laboratory