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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
B9d2/Tgfb1tm1Flv
targeted mutation 1, Richard A Flavell
MGI:3719581
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv
Foxp3tm4(YFP/icre)Ayr/Foxp3+
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ MGI:4943576
cn2
B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv
Tnfrsf4tm2(cre)Nik/Tnfrsf4+
involves: 129S6/SvEvTac * 129X1/SvJ MGI:4943571
cn3
Foxp3tm1Flv/Foxp3+
B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv
Tg(Cd4-cre)1Cwi/?
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 MGI:3720254
cn4
B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv
Tg(Cd4-cre)1Cwi/0
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 MGI:3720255
cn5
B9d2/Tgfb1tm1Flv/B9d2/Tgfb1tm1Flv
Tg(Cd4-cre)1Cwi/0
involves: 129S6/SvEvTac * C57BL/6 * SJL MGI:5544319
cn6
B9d2/Tgfb1tm1Flv/B9d2/Tgfb1tm1Flv
Tg(CD207-cre)1Dhka/?
involves: 129S6/SvEvTac * C57BL/6J * SJL/J MGI:3761679
cn7
Tgfb1tm2Flv/B9d2/Tgfb1tm1Flv
Tg(CD207-cre)1Dhka/?
involves: 129S6/SvEvTac * C57BL/6J * SJL/J MGI:3761681


Genotype
MGI:4943576
cn1
Allelic
Composition
B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv
Foxp3tm4(YFP/icre)Ayr/Foxp3+
Genetic
Background
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
B9d2/Tgfb1tm1Flv mutation (0 available); any Tgfb1 mutation (34 available)
Foxp3tm4(YFP/icre)Ayr mutation (2 available); any Foxp3 mutation (55 available)
Tgfb1tm2Flv mutation (0 available); any Tgfb1 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
N
• mice do not exhibit wasting or inflammation unlike B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv Tg(Cd4-cre)1Cwi mice

hematopoietic system
• in the peripheral and mesenteric lymph nodes, but not the spleen
• 2-fold increase in mesenteric regulatory T cell

immune system
N
• mice do not exhibit wasting or inflammation unlike B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv Tg(Cd4-cre)1Cwi mice
• mice exhibit normal susceptibility to experimental autoimmune encephalomyelitis and Th17 cell differentiation
• in the peripheral and mesenteric lymph nodes, but not the spleen
• 2-fold increase in mesenteric regulatory T cell




Genotype
MGI:4943571
cn2
Allelic
Composition
B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv
Tnfrsf4tm2(cre)Nik/Tnfrsf4+
Genetic
Background
involves: 129S6/SvEvTac * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
B9d2/Tgfb1tm1Flv mutation (0 available); any Tgfb1 mutation (34 available)
Tgfb1tm2Flv mutation (0 available); any Tgfb1 mutation (34 available)
Tnfrsf4tm2(cre)Nik mutation (1 available); any Tnfrsf4 mutation (33 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• mild beginning at 5 months with mononuclear cell infiltrates in the mucosal lamina propria of the colon, with slight epithelial hyperplasia, and increased numbers of leukocytes in the mucosa
• mice exhibit only marginally enhanced activation and differentiation of T cells in the peripheral lymph nodes, spleen, and mesenteric lymph nodes compared with wild-type mice
• intraepithelial lymphocytes from the small intestine exhibit a high frequency of IFN-gamma-producing Th1 cells compared with wild-type mice
• in an experimental autoimmune encephalomyelitis model
• mice exhibit small foci of infiltrating mononuclear cells in the liver parenchyma unlike wild-type mice
• mice exhibit small foci of infiltrating mononuclear cells in the lung unlike wild-type mice

growth/size/body
• mild beginning at 5 months

digestive/alimentary system
• slight hyperplasia
• mild beginning at 5 months with mononuclear cell infiltrates in the mucosal lamina propria of the colon, with slight epithelial hyperplasia, and increased numbers of leukocytes in the mucosa

liver/biliary system
• mice exhibit small foci of infiltrating mononuclear cells in the liver parenchyma unlike wild-type mice

respiratory system
• mice exhibit small foci of infiltrating mononuclear cells in the lung unlike wild-type mice

hematopoietic system
• mice exhibit only marginally enhanced activation and differentiation of T cells in the peripheral lymph nodes, spleen, and mesenteric lymph nodes compared with wild-type mice
• intraepithelial lymphocytes from the small intestine exhibit a high frequency of IFN-gamma-producing Th1 cells compared with wild-type mice
• in an experimental autoimmune encephalomyelitis model

cellular
• slight hyperplasia




Genotype
MGI:3720254
cn3
Allelic
Composition
Foxp3tm1Flv/Foxp3+
B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv
Tg(Cd4-cre)1Cwi/?
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
B9d2/Tgfb1tm1Flv mutation (0 available); any Tgfb1 mutation (34 available)
Foxp3tm1Flv mutation (3 available); any Foxp3 mutation (55 available)
Tg(Cd4-cre)1Cwi mutation (10 available)
Tgfb1tm2Flv mutation (0 available); any Tgfb1 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• Foxp3+ regulatory T cells are increased 2-fold relative to wild-type mice
• the numbers of regulatory T cells is increased in the peripheral and mesenteric lymph nodes, spleens and among the lamina propria mononuclear cell infiltrate of the colon
• proliferation of Foxp3+ cells and CD4+CD8+Foxp3- cells is increased in association with the development of colitis

hematopoietic system
• Foxp3+ regulatory T cells are increased 2-fold relative to wild-type mice
• the numbers of regulatory T cells is increased in the peripheral and mesenteric lymph nodes, spleens and among the lamina propria mononuclear cell infiltrate of the colon
• proliferation of Foxp3+ cells and CD4+CD8+Foxp3- cells is increased in association with the development of colitis




Genotype
MGI:3720255
cn4
Allelic
Composition
B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv
Tg(Cd4-cre)1Cwi/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
B9d2/Tgfb1tm1Flv mutation (0 available); any Tgfb1 mutation (34 available)
Tg(Cd4-cre)1Cwi mutation (10 available)
Tgfb1tm2Flv mutation (0 available); any Tgfb1 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice begin to die at 6 months of age due to wasting and diarrhea

immune system
• T cells Th1, Th2 and CTL (cytotoxic T lymphocyte) differentiation is enhanced while Th17-cell differentiation is inhibited
• in the experimental autoimmune encephalomyelitis model, the number of IL-17 producing T cells is reduced in animals that do and those that do not develop encephalomyelitis
• as determined by transplantation experiments, defects in Th17 cell differentiation occur in an autocrine manner
• T cell activation is enhanced
• following activation, interferon-gamma levels are increased relative to in control cells
• in the experimental autoimmune encephalomyelitis model, only mice that develop encephalomyelitis produce great amounts of interferon-gamma
• following activation, IL-4 levels are increased whereas IL-17 levels are decreased relative to in control cells
• 6 of 8 mice did not develop encephalomyelitis and only 2 showed mild disease compared to controls which all develop severe disease
• the number of IL-17 producing T cells is reduced in animals that do and those that do not develop encephalomyelitis
• only mice that develop encephalomyelitis produce great amounts of interferon-gamma
• mice present with mononuclear infiltrate in the lungs, parenchyma of the liver, and colon
• severe colitis is associated with disruption of the crypt architecture, crypt abscess formation and epithelium hyperplasia

digestive/alimentary system
• epithelium hyperplasia is associated with colitis
• disruption of crypt architecture is associated with colitis
• associated with colitis
• at 4 to 12 months of age, heavy mononuclear cell infiltrate of the lamina propria and subglandular areas of the colon is detected
• at 4 months of age
• severe colitis is associated with disruption of the crypt architecture, crypt abscess formation and epithelium hyperplasia

growth/size/body
• at 4 months of age mice display signs of wasting

liver/biliary system
• mononuclear cell clusters are detected in the parenchyma of mice with colitis

renal/urinary system
• IgG deposits accumulate in the glomeruli

respiratory system
• mononuclear cell infiltrate is present in the lungs of mice with colitis

endocrine/exocrine glands
• disruption of crypt architecture is associated with colitis
• associated with colitis

hematopoietic system
• T cells Th1, Th2 and CTL (cytotoxic T lymphocyte) differentiation is enhanced while Th17-cell differentiation is inhibited
• in the experimental autoimmune encephalomyelitis model, the number of IL-17 producing T cells is reduced in animals that do and those that do not develop encephalomyelitis
• as determined by transplantation experiments, defects in Th17 cell differentiation occur in an autocrine manner
• T cell activation is enhanced

homeostasis/metabolism
• following activation, interferon-gamma levels are increased relative to in control cells
• in the experimental autoimmune encephalomyelitis model, only mice that develop encephalomyelitis produce great amounts of interferon-gamma
• following activation, IL-4 levels are increased whereas IL-17 levels are decreased relative to in control cells

cellular




Genotype
MGI:5544319
cn5
Allelic
Composition
B9d2/Tgfb1tm1Flv/B9d2/Tgfb1tm1Flv
Tg(Cd4-cre)1Cwi/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
B9d2/Tgfb1tm1Flv mutation (0 available); any Tgfb1 mutation (34 available)
Tg(Cd4-cre)1Cwi mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• regulatory T cells fail to drive Th17 differentiation

immune system
• regulatory T cells fail to drive Th17 differentiation




Genotype
MGI:3761679
cn6
Allelic
Composition
B9d2/Tgfb1tm1Flv/B9d2/Tgfb1tm1Flv
Tg(CD207-cre)1Dhka/?
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
B9d2/Tgfb1tm1Flv mutation (0 available); any Tgfb1 mutation (34 available)
Tg(CD207-cre)1Dhka mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• although the number of Langerhans cells is substantially reduced compared to in wild-type mice, a variable number of Langerhans cells are present in the epidermis (0.02% to 0.1% of total epidermal cells compared to 0.42% to 1.17% in wild-type mice)
• Langerhans cells are absent from the vast majority of the ear with Langerhans cells being found at the edge of the ear in clusters

hematopoietic system
• although the number of Langerhans cells is substantially reduced compared to in wild-type mice, a variable number of Langerhans cells are present in the epidermis (0.02% to 0.1% of total epidermal cells compared to 0.42% to 1.17% in wild-type mice)
• Langerhans cells are absent from the vast majority of the ear with Langerhans cells being found at the edge of the ear in clusters




Genotype
MGI:3761681
cn7
Allelic
Composition
Tgfb1tm2Flv/B9d2/Tgfb1tm1Flv
Tg(CD207-cre)1Dhka/?
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
B9d2/Tgfb1tm1Flv mutation (0 available); any Tgfb1 mutation (34 available)
Tg(CD207-cre)1Dhka mutation (1 available)
Tgfb1tm2Flv mutation (0 available); any Tgfb1 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• mice are indistinguishable from Tg(CD207-cre)1Mjs B9d2/Tgfb1tm1Flv mice

hematopoietic system
• mice are indistinguishable from Tg(CD207-cre)1Mjs B9d2/Tgfb1tm1Flv mice





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory