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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nfatc2tm1Srf
targeted mutation 1, Edgar Serfling
MGI:2182770
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nfatc2tm1Srf/Nfatc2tm1Srf B6.Cg-Nfatc2tm1Srf MGI:3849012
hm2
Nfatc2tm1Srf/Nfatc2tm1Srf involves: 129P2/OlaHsd MGI:3849011
hm3
Nfatc2tm1Srf/Nfatc2tm1Srf involves: 129P2/OlaHsd * C57BL/6 MGI:3654100


Genotype
MGI:3849012
hm1
Allelic
Composition
Nfatc2tm1Srf/Nfatc2tm1Srf
Genetic
Background
B6.Cg-Nfatc2tm1Srf
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nfatc2tm1Srf mutation (0 available); any Nfatc2 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• as a result of infection with either Nippostrongylus brasiliensis or Mycobacterium bovis
• as a result of Nippostrongylus brasiliensis infection
• Th1 responses are decreased overall
• Th2 responses are increased overall
• Mycobacterium bovis infection results in lowered Ifn gamma secretion
• Nippostrongylus brasiliensis infection leads to significantly increased Il4 and Il5 secretion
• Nippostrongylus brasiliensis infection leads to significantly increased Il4 and Il5 secretion

hematopoietic system
• as a result of infection with either Nippostrongylus brasiliensis or Mycobacterium bovis
• as a result of Nippostrongylus brasiliensis infection
• Th1 responses are decreased overall
• Th2 responses are increased overall




Genotype
MGI:3849011
hm2
Allelic
Composition
Nfatc2tm1Srf/Nfatc2tm1Srf
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nfatc2tm1Srf mutation (0 available); any Nfatc2 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• normal immune system at birth
• two fold increase in lymphoid cells after 4-6 months
• 4 fold increase in lymph node B cells
• 10 fold increase in T lymphocytes
• 6 fold increase in lymph node cells
• increased longevity of Staphylococcal enterotoxin A stimulated T cells
• decreased synthesis of Il4 and Il5 in Staphylococcal enterotoxin A stimulated T cells
• reduced expression of IL2 receptor alpha after ConA stimulation

hematopoietic system
• normal immune system at birth
• two fold increase in lymphoid cells after 4-6 months
• 4 fold increase in lymph node B cells
• 10 fold increase in T lymphocytes
• increased longevity of Staphylococcal enterotoxin A stimulated T cells

growth/size/body




Genotype
MGI:3654100
hm3
Allelic
Composition
Nfatc2tm1Srf/Nfatc2tm1Srf
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nfatc2tm1Srf mutation (0 available); any Nfatc2 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• thymi of mice that are 6 months old show an increased cellularity compared to wild-type
• animals over 6 months of age show abnormal involution; thymi of mutants exhibit large cortical areas similar to young wild-type mice
• spleens of mutants are massively enlarged due to extended white pulp areas
• 5% of cells are mature IgM+/IgD+ B lymphocytes in these B cell areas in the thymus
• peripheral T cells in mutants older than 2 months display a preactivated phenotype; lymph node T cells express high levels of CD44 and CD69 compared to wild-type while 2 to 3-fold more T cells express low levels of CD62L
• a normal proliferative response is mounted by lymph node T cells when exposed the superantigen staphylococcal enterotoxin (SEA) or increasing CD3-specific antibodies in vitro but a 3- to 4-fold increase in proliferation is detected in the secondary response after restimulation with antigen
• 10% of mature B cells show an activated phenotype in the thymus
• mutants exhibit a gradual increase in peripheral lymphocytes; up to 2 months of age, numbers are similar to wild-type but the numbers increase 2-fold and up to 5- to 6-fold in mice older than 6 months
• after in vivo stimulation with SEA for 8 days, CD4+Vb11+ T cells show normal expansion but distinctly retarded deletion compared to wild-type (incomplete antigen response termination)
• a large increase in the size of germinal centers in the lymph nodes is observed

hematopoietic system
• thymi of mice that are 6 months old show an increased cellularity compared to wild-type
• animals over 6 months of age show abnormal involution; thymi of mutants exhibit large cortical areas similar to young wild-type mice
• spleens of mutants are massively enlarged due to extended white pulp areas
• 5% of cells are mature IgM+/IgD+ B lymphocytes in these B cell areas in the thymus
• peripheral T cells in mutants older than 2 months display a preactivated phenotype; lymph node T cells express high levels of CD44 and CD69 compared to wild-type while 2 to 3-fold more T cells express low levels of CD62L
• a normal proliferative response is mounted by lymph node T cells when exposed the superantigen staphylococcal enterotoxin (SEA) or increasing CD3-specific antibodies in vitro but a 3- to 4-fold increase in proliferation is detected in the secondary response after restimulation with antigen
• 10% of mature B cells show an activated phenotype in the thymus
• mutants exhibit a gradual increase in peripheral lymphocytes; up to 2 months of age, numbers are similar to wild-type but the numbers increase 2-fold and up to 5- to 6-fold in mice older than 6 months
• after in vivo stimulation with SEA for 8 days, CD4+Vb11+ T cells show normal expansion but distinctly retarded deletion compared to wild-type (incomplete antigen response termination)

endocrine/exocrine glands
• thymi of mice that are 6 months old show an increased cellularity compared to wild-type
• animals over 6 months of age show abnormal involution; thymi of mutants exhibit large cortical areas similar to young wild-type mice

growth/size/body
• spleens of mutants are massively enlarged due to extended white pulp areas





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