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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Foxp3-HBEGF/EGFP)23.2Spar
transgene insertion 23.2, Tim Sparwasser
MGI:3849080
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(Foxp3-HBEGF/EGFP)23.2Spar/0 involves: C57BL/6NCrl MGI:4429143


Genotype
MGI:4429143
tg1
Allelic
Composition
Tg(Foxp3-HBEGF/EGFP)23.2Spar/0
Genetic
Background
involves: C57BL/6NCrl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Foxp3-HBEGF/EGFP)23.2Spar mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• mice exhibit normal numbers and frequencies of CD25+CD4+ T regulatory cells
• following diphtheria toxin treatment of neonates
• following diphtheria toxin treatment, CD4+ T regulatory cells are decreased in adult and neonates compared to in similarly treated wild-type mice
• however, T regulatory cell numbers rebound after cessation of diphtheria treatment in adult mice but not neonates
• following diphtheria toxin treatment of neonates
• following diphtheria toxin treatment of neonates
• following diphtheria toxin treatment of neonates
• following diphtheria toxin treatment of neonates
• diphtheria toxin treated-neonates exhibit massive inflammatory infiltrate in various organs that resembles the phenotype of Foxp3sf hemizygotes
• following diphtheria toxin treatment of neonates, mice exhibit insulitis and portal aggregates unlike similarly treated wild-type mice
• following diphtheria toxin treatment, adult mice exhibit an enhanced and prolonged delayed-type hypersensitivity response compared with similarly treated wild-type mice
• following diphtheria toxin treatment of neonates, mice exhibit peribronchial and perivascular infiltrated unlike similarly treated wild-type mice
• following diphtheria toxin treatment of neonates, the skin overlying the hyaline cartilage of the ear is thickened with epidermal hyperplasia and a dense lymphocyte infiltrate unlike in similarly treated wild-type mice

endocrine/exocrine glands
• following diphtheria toxin treatment of neonates, mice exhibit insulitis and portal aggregates unlike similarly treated wild-type mice

respiratory system
• following diphtheria toxin treatment of neonates, mice exhibit peribronchial and perivascular infiltrated unlike similarly treated wild-type mice
• following diphtheria toxin treatment of neonates, alveoli are delicate and have thin walls compared to in similarly treated wild-type mice

hematopoietic system
• following diphtheria toxin treatment of neonates
• following diphtheria toxin treatment, CD4+ T regulatory cells are decreased in adult and neonates compared to in similarly treated wild-type mice
• however, T regulatory cell numbers rebound after cessation of diphtheria treatment in adult mice but not neonates
• following diphtheria toxin treatment of neonates
• following diphtheria toxin treatment of neonates

integument
• following diphtheria toxin treatment of neonates, the skin overlying the hyaline cartilage of the ear is thickened with epidermal hyperplasia and a dense lymphocyte infiltrate unlike in similarly treated wild-type mice
• following diphtheria toxin treatment of neonates, the skin overlying the hyaline cartilage of the ear is thickened with epidermal hyperplasia and a dense lymphocyte infiltrate unlike in similarly treated wild-type mice

growth/size/body
• following diphtheria toxin treatment of neonates





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory