Summary |
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Mutation origin |
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Mutation description |
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Phenotypes |
View phenotypes and curated references for all genotypes (concatenated display).
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Find Mice (IMSR) |
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Notes |
Homozygous mutant mice are viable and appear normal, healthy, and fertile with no defects in lymphocyte development (thymocytes, splenocytes, and bone-marrow derived dendritic cells). Compared to control sibs, however, macrophages and primary embryonic fibroblasts from mutant mice show reduced activation of p38 MAPK. Cytokine IL-12 (encoded for by Il12a and Il12b) is strongly reduced in mutant macrophages and dendritic cells. Mutant fibroblasts have a defective response to Tnf. Mutant mice also have defective T-helper cells with respect to the ability to produce Ifng in response to antigen stimulation of keyhole limpet hemocyanin (KLH) both in vitro and in vivo (J:54078, J:54309).
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References |
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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 11/12/2024 MGI 6.24 |
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