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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ctps1tm1c(KOMP)Wtsi
targeted mutation 1c, Wellcome Trust Sanger Institute
MGI:7657751
Summary 7 genotypes


Genotype
MGI:7657890
cn1
Allelic
Composition
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi
Tg(Cd8a-cre)1Itan/0
Genetic
Background
B6(129S4)-Ctps1tm1c(KOMP)Wtsi Tg(Cd8a-cre)1Itan
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctps1tm1c(KOMP)Wtsi mutation (0 available); any Ctps1 mutation (46 available)
Tg(Cd8a-cre)1Itan mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• upon activation with anti-CD3/CD28, CD8+ T cells from the spleen fail to proliferate leading to an effector memory CD8+ T cell impairment
• addition of cytidine to the culture medium during the activation rescues the proliferation defect of the CD8+ T cells
• however, no phenotypic differences are seen in the thymus and spleen, and no abnormalities are detected in blood, spleen cellularity and cell type composition

immune system
• upon activation with anti-CD3/CD28, CD8+ T cells from the spleen fail to proliferate leading to an effector memory CD8+ T cell impairment
• addition of cytidine to the culture medium during the activation rescues the proliferation defect of the CD8+ T cells
• however, no phenotypic differences are seen in the thymus and spleen, and no abnormalities are detected in blood, spleen cellularity and cell type composition

cellular
• upon activation with anti-CD3/CD28, CD8+ T cells from the spleen fail to proliferate leading to an effector memory CD8+ T cell impairment
• addition of cytidine to the culture medium during the activation rescues the proliferation defect of the CD8+ T cells
• however, no phenotypic differences are seen in the thymus and spleen, and no abnormalities are detected in blood, spleen cellularity and cell type composition




Genotype
MGI:7657888
cn2
Allelic
Composition
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi
Commd10Tg(Vav1-icre)A2Kio/0
Genetic
Background
B6.Cg-Ctps1tm1c(KOMP)Wtsi Commd10Tg(Vav1-icre)A2Kio
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Commd10Tg(Vav1-icre)A2Kio mutation (3 available); any Commd10 mutation (24 available)
Ctps1tm1c(KOMP)Wtsi mutation (0 available); any Ctps1 mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice do not survive after 6 weeks of age
• fewer than the expected numbers of mice are obtained

endocrine/exocrine glands
• cellularity of thymus is reduced

growth/size/body

hematopoietic system
• double positive cells are reduced and single positive CD4 and CD8 cells are increased, suggesting reduced proliferation of double negative thymocytes leading to double positive stage
• cellularity of thymus is reduced
• severe anemia
• bone marrow cellularity is reduced, with the percentage of Ter119+ bone marrow cells, corresponding to erythrocyte progenitors, is strongly decreased
• absolute numbers of erythroid and hematopoietic progenitors are reduced as bone marrow cellularity is reduced
• however, the percentage of LSK+ cells in bone marrow is normal
• absolute numbers of B lymphocytes are reduced in the spleen
• absolute numbers of NK cells are reduced in the spleen
• absolute numbers of T lymphocytes are reduced in the spleen
• absolute numbers of hematopoietic progenitors are reduced as bone marrow cellularity is reduced
• the percentage of Ter119+ bone marrow cells, corresponding to erythrocyte progenitors, is strongly decreased
• spleen cellularity is normal but absolute numbers of B and T lymphocytes and NK cells are reduced, while macrophages and granulocytes are not affected

immune system
• double positive cells are reduced and single positive CD4 and CD8 cells are increased, suggesting reduced proliferation of double negative thymocytes leading to double positive stage
• cellularity of thymus is reduced
• absolute numbers of B lymphocytes are reduced in the spleen
• absolute numbers of NK cells are reduced in the spleen
• absolute numbers of T lymphocytes are reduced in the spleen
• spleen cellularity is normal but absolute numbers of B and T lymphocytes and NK cells are reduced, while macrophages and granulocytes are not affected

cellular
• double positive cells are reduced and single positive CD4 and CD8 cells are increased, suggesting reduced proliferation of double negative thymocytes leading to double positive stage




Genotype
MGI:7657886
cn3
Allelic
Composition
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi
Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
Genetic
Background
B6.Cg-Ctps1tm1c(KOMP)Wtsi Gt(ROSA)26Sortm1(cre/ERT2)Tyj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctps1tm1c(KOMP)Wtsi mutation (0 available); any Ctps1 mutation (46 available)
Gt(ROSA)26Sortm1(cre/ERT2)Tyj mutation (3 available); any Gt(ROSA)26Sor mutation (993 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• mice show a drastic weight loss upon tamoxifen treatment by day 6

endocrine/exocrine glands
• tamoxifen-treated mice show numerous empty crypts and vacuoles
• thymus is smaller in tamoxifen-treated mice
• thymus cellularity is reduced 10-fold in tamoxifen-treated mice
• most cells in the thymus of tamoxifen-treated mice are CD4-/CD8- double negative, suggesting impaired proliferation capacity of early thymocytes

digestive/alimentary system
• tamoxifen-treated mice exhibit aberrant gut structures, with lamina propria that is detaching from the epithelium and abnormal cell shedding at the top of the villi
• tamoxifen-treated mice show numerous empty crypts and vacuoles
• abnormal cell shedding at the top of the villi in tamoxifen-treated mice
• length of villi is reduced in tamoxifen-treated mice

hematopoietic system
• the expansion of splenic T cells in response to CD3 and CD28 stimulation is impaired in tamoxifen-treated mice
• proliferation of sorted splenic B cells upon stimulation with LPS plus IL-4 is reduced in tamoxifen-treated mice
• thymus is smaller in tamoxifen-treated mice
• thymus cellularity is reduced 10-fold in tamoxifen-treated mice
• most cells in the thymus of tamoxifen-treated mice are CD4-/CD8- double negative, suggesting impaired proliferation capacity of early thymocytes
• red blood cell numbers are reduced in tamoxifen-treated mice
• hemoglobin is reduced in tamoxifen-treated mice
• spleen shows a slight increase of CD8+ T cells in tamoxifen-treated mice
• lymphocyte numbers are reduced in tamoxifen-treated mice
• however, no differences are seen in total number of whole blood cells and neutrophils
• CD19+CD95+GL-7+ germinal center B cells are almost absent in tamoxifen-treated mice (activated B cells)
• however, proportions of T and B cells in Peyers patches are normal
• CXCR5+PD-1+ T follicular helper cells are reduced in germinal centers of tamoxifen-treated mice
• percentage of CXCR5+PD-1+ T follicular helper cells is reduced after immunization with NP-CGG
• tamoxifen-treated mice show a drop in reticulocyte numbers
• spleen shows a cellularity and composition similar to controls except for a slight increase of CD8+ T cells
• tamoxifen-treated mice immunized with NP-CGG show a reduction of NP-specific IgM

immune system
• the expansion of splenic T cells in response to CD3 and CD28 stimulation is impaired in tamoxifen-treated mice
• proliferation of sorted splenic B cells upon stimulation with LPS plus IL-4 is reduced in tamoxifen-treated mice
• thymus is smaller in tamoxifen-treated mice
• thymus cellularity is reduced 10-fold in tamoxifen-treated mice
• most cells in the thymus of tamoxifen-treated mice are CD4-/CD8- double negative, suggesting impaired proliferation capacity of early thymocytes
• spleen shows a slight increase of CD8+ T cells in tamoxifen-treated mice
• lymphocyte numbers are reduced in tamoxifen-treated mice
• however, no differences are seen in total number of whole blood cells and neutrophils
• CD19+CD95+GL-7+ germinal center B cells are almost absent in tamoxifen-treated mice (activated B cells)
• however, proportions of T and B cells in Peyers patches are normal
• CXCR5+PD-1+ T follicular helper cells are reduced in germinal centers of tamoxifen-treated mice
• percentage of CXCR5+PD-1+ T follicular helper cells is reduced after immunization with NP-CGG
• spleen shows a cellularity and composition similar to controls except for a slight increase of CD8+ T cells
• tamoxifen-treated mice immunized with NP-CGG show a reduction of NP-specific IgM
• capacity to mount humoral immune responses against the T-dependent antigen 4-hydroxy-3-nitrophenyl (NP) hapten conjugated to chicken gamma globulin (CGG) is reduced in tamoxifen-treated mice
• spleen histology after immunization with NP-CGG shows a reduction of proliferating B cells

cellular
• the expansion of splenic T cells in response to CD3 and CD28 stimulation is impaired in tamoxifen-treated mice
• proliferation of sorted splenic B cells upon stimulation with LPS plus IL-4 is reduced in tamoxifen-treated mice




Genotype
MGI:7659098
cn4
Allelic
Composition
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi
Tg(Cd4-cre)1Cwi/0
Genetic
Background
involves: 129S/Sv * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctps1tm1c(KOMP)Wtsi mutation (0 available); any Ctps1 mutation (46 available)
Tg(Cd4-cre)1Cwi mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• both CD4 and CD8 enriched splenic T cells show a reduction in proliferation upon CD3/CD28 stimulation
• after 3 days of activation, an increase of naive (CD44-CD62L+) T cells is seen
• after 3 days of activation, a reduction of effector memory cells (CD44+CD62L-) is seen

hematopoietic system
• both CD4 and CD8 enriched splenic T cells show a reduction in proliferation upon CD3/CD28 stimulation
• after 3 days of activation, an increase of naive (CD44-CD62L+) T cells is seen
• after 3 days of activation, a reduction of effector memory cells (CD44+CD62L-) is seen

cellular
• both CD4 and CD8 enriched splenic T cells show a reduction in proliferation upon CD3/CD28 stimulation




Genotype
MGI:7659102
cn5
Allelic
Composition
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi
Ctps2tm1c(EUCOMM)Hmgu/Ctps2tm1c(EUCOMM)Hmgu
Tg(Cd4-cre)1Cwi/0
Genetic
Background
involves: 129S/Sv * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctps1tm1c(KOMP)Wtsi mutation (0 available); any Ctps1 mutation (46 available)
Ctps2tm1c(EUCOMM)Hmgu mutation (0 available); any Ctps2 mutation (17 available)
Tg(Cd4-cre)1Cwi mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• almost complete absence of activated CD4+ and CD8+ T lymphocyte proliferation
• T lymphocyte counts are diminished
• however, cellularity and cell population distribution of blood, thymus, and spleen are normal

hematopoietic system
• almost complete absence of activated CD4+ and CD8+ T lymphocyte proliferation
• T lymphocyte counts are diminished
• however, cellularity and cell population distribution of blood, thymus, and spleen are normal

cellular
• almost complete absence of activated CD4+ and CD8+ T lymphocyte proliferation




Genotype
MGI:7659103
cn6
Allelic
Composition
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi
Ctps2tm1c(EUCOMM)Hmgu/Ctps2+
Tg(Cd4-cre)1Cwi/0
Genetic
Background
involves: 129S/Sv * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctps1tm1c(KOMP)Wtsi mutation (0 available); any Ctps1 mutation (46 available)
Ctps2tm1c(EUCOMM)Hmgu mutation (0 available); any Ctps2 mutation (17 available)
Tg(Cd4-cre)1Cwi mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• T lymphocytes show reduced proliferation

hematopoietic system
• T lymphocytes show reduced proliferation

cellular
• T lymphocytes show reduced proliferation




Genotype
MGI:7659107
cn7
Allelic
Composition
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi
Tg(Cd4-cre)1Cwi/0
Foxp3sf/Y
Rag1tm1Mom/Rag1+
Genetic
Background
mixed
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctps1tm1c(KOMP)Wtsi mutation (0 available); any Ctps1 mutation (46 available)
Foxp3sf mutation (5 available); any Foxp3 mutation (58 available)
Rag1tm1Mom mutation (49 available); any Rag1 mutation (123 available)
Tg(Cd4-cre)1Cwi mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• weight does not reach control levels at 40-50 days and 60-75 days
• by day 44, mice develop enlarged spleen

endocrine/exocrine glands
• by day 44, thymus has reduced cellularity

immune system
• both CD8+ and CD4+ T cells show a reduced capacity to expand in response to CD3/CD28 stimulation
• by day 44, thymus has reduced cellularity
• by day 44, mice develop enlarged spleen
• mice exhibit a deficiency in T regulatory cells (CD4+, CD25+, FoxP3+)
• mice show prevention of the fatal systemic autoimmune and inflammatory disease that is seen in Foxp3sf/Y mice, with mice surviving at least up to 80 days and no presentation of scaly tails and ears, and no inflammation and tissue disruption at day 44
• values of total T cells return to normal and the accumulation of effector memory CD4+ and CD8+ T cells in the spleen that is seen in single Foxp3/Y mice is reduced

hematopoietic system
• both CD8+ and CD4+ T cells show a reduced capacity to expand in response to CD3/CD28 stimulation
• by day 44, thymus has reduced cellularity
• by day 44, mice develop enlarged spleen
• mice exhibit a deficiency in T regulatory cells (CD4+, CD25+, FoxP3+)

cellular
• both CD8+ and CD4+ T cells show a reduced capacity to expand in response to CD3/CD28 stimulation





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory