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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nfkb2xdr
xander
MGI:2667230
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nfkb2xdr/Nfkb2xdr C57BL/6JSfdAnu-Nfkb2xdr/Anu MGI:2667232
hm2
Nfkb2xdr/Nfkb2xdr involves: C57BL/6JSfdAnu * C57BL/10Sg * C57BR/cd * NOD MGI:2667233


Genotype
MGI:2667232
hm1
Allelic
Composition
Nfkb2xdr/Nfkb2xdr
Genetic
Background
C57BL/6JSfdAnu-Nfkb2xdr/Anu
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nfkb2xdr mutation (1 available); any Nfkb2 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
N
• homozygotes display normal B cell production in the bone marrow, as shown by normal numbers of pro-B or pre-B cells and immature B cells
• T cell numbers remain normal
• homozygotes display significantly reduced numbers of transitional T2 B cells in spleen relative to wild-type controls
• however, numbers of transitional T1 B cells are normal, suggesting that B cell emigration from the bone marrow is unaffected
• homozygotes display a significant reduction in recirculating mature B cells in spleen, blood, and all peripheral lymph nodes relative to wild-type controls
• homozygotes display significantly reduced numbers of mature B-2 B cells in spleen relative to wild-type controls
• homozygotes show significantly reduced numbers of mature recirculating (follicular) B cells in spleen relative to wild-type controls
• homozygotes show a 7-fold increase in the number of peritoneal B1 cells relative to wild-type controls
• in contrast, the number of peritoneal B-2 B cells is similar to that in wild-type controls
• homozygotes exhibit an abnormal splenic mircoarchitecture relative to wild-type controls
• homozygotes display significantly reduced numbers of marginal zone B cells in spleen relative to wild-type controls
• only a few MOMA1+ marginal metallophilic macrophages are seen in the white pulp of mutant spleens
• no follicular dendritic cell clusters are detected in mutant spleens
• mutant B cell follicles are reduced to a small ring around an apparently normal T zone

immune system
• homozygotes display significantly reduced numbers of transitional T2 B cells in spleen relative to wild-type controls
• however, numbers of transitional T1 B cells are normal, suggesting that B cell emigration from the bone marrow is unaffected
• homozygotes display a significant reduction in recirculating mature B cells in spleen, blood, and all peripheral lymph nodes relative to wild-type controls
• homozygotes display significantly reduced numbers of mature B-2 B cells in spleen relative to wild-type controls
• homozygotes show significantly reduced numbers of mature recirculating (follicular) B cells in spleen relative to wild-type controls
• homozygotes show a 7-fold increase in the number of peritoneal B1 cells relative to wild-type controls
• in contrast, the number of peritoneal B-2 B cells is similar to that in wild-type controls
• homozygotes exhibit an abnormal splenic mircoarchitecture relative to wild-type controls
• homozygotes display significantly reduced numbers of marginal zone B cells in spleen relative to wild-type controls
• only a few MOMA1+ marginal metallophilic macrophages are seen in the white pulp of mutant spleens
• no follicular dendritic cell clusters are detected in mutant spleens
• mutant B cell follicles are reduced to a small ring around an apparently normal T zone
• homozygotes display small peripheral lymph nodes relative to wild-type controls




Genotype
MGI:2667233
hm2
Allelic
Composition
Nfkb2xdr/Nfkb2xdr
Genetic
Background
involves: C57BL/6JSfdAnu * C57BL/10Sg * C57BR/cd * NOD
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nfkb2xdr mutation (1 available); any Nfkb2 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• however, numbers of immature and peritoneal B-1 B cells are normal
• homozygotes display a selective deficiency in recirculating mature B cells

immune system
• however, numbers of immature and peritoneal B-1 B cells are normal
• homozygotes display a selective deficiency in recirculating mature B cells





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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
11/19/2024
MGI 6.24
The Jackson Laboratory