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Phenotypes Associated with This Genotype
Genotype
MGI:4839049
Allelic
Composition
Faslpr/Faslpr
Ifngtm1Ts/Ifngtm1Ts
Genetic
Background
involves: 129S7/SvEvBrd * DBA/1 * MRL/Mp
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Faslpr mutation (39 available); any Fas mutation (83 available)
Ifngtm1Ts mutation (18 available); any Ifng mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• decrease in the number of CD4-CD8-B220+ alpha beta T cells compared to mice homozygous for Faslpr and wild-type for Ifng
• lympadenopathy (based on spleen weight and cellularity) is reduced compared to mice homozygous for Faslpr and wild-type for Ifng
• at 7-8 months of age a modest increase in spleen size and cellularity is seen relative to wild-type controls
• at 3 and 7-8 months of age relative to mice homozygous for Faslpr and wild-type for Ifng
• at 3 and 7-8 months of age relative to mice homozygous for Faslpr and wild-type for Ifng
• at 3 and 7-8 months of age relative to mice homozygous for Faslpr and wild-type for Ifng
• at 3 and 7-8 months of age relative to mice homozygous for Faslpr and wild-type for Ifng
• lympadenopathy (based on lymph node weight and cellularity) is reduced compared to mice homozygous for Faslpr and wild-type for Ifng
• in young animals lymph node size is similar to wild-type controls
• at 7-8 months of age a modest increase in lymph node size and cellularity is seen relative to wild-type controls
• while mice develop the typical autoimmune lesions, end organ disease is decreased compared to mice homozygous for Faslpr and wild-type for Ifng
• lower titers of anti-snRNP and anti-rheumatoid factors antibodies relative to mice homozygous for Faslpr and wild-type for Ifng at 3 and 7-8 months of age
• at 3 and 7-8 months of age

homeostasis/metabolism
• levels are lower compared to mice homozygous for Faslpr and wild-type for Ifng

hematopoietic system
• decrease in the number of CD4-CD8-B220+ alpha beta T cells compared to mice homozygous for Faslpr and wild-type for Ifng
• lympadenopathy (based on spleen weight and cellularity) is reduced compared to mice homozygous for Faslpr and wild-type for Ifng
• at 7-8 months of age a modest increase in spleen size and cellularity is seen relative to wild-type controls
• at 3 and 7-8 months of age relative to mice homozygous for Faslpr and wild-type for Ifng
• at 3 and 7-8 months of age relative to mice homozygous for Faslpr and wild-type for Ifng
• at 3 and 7-8 months of age relative to mice homozygous for Faslpr and wild-type for Ifng
• at 3 and 7-8 months of age relative to mice homozygous for Faslpr and wild-type for Ifng

growth/size/body
• at 7-8 months of age a modest increase in spleen size and cellularity is seen relative to wild-type controls


Contributing Projects:
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
01/28/2026
MGI 6.24
The Jackson Laboratory