Entrez gene ID | | 23495 |
Official gene symbol | | TNFRSF13B |
Full name | | tumor necrosis factor receptor superfamily, member 13B |
Aliases | | ,CD267,CVID,FLJ39942,MGC133214,MGC39952,TACI,TNFRSF14B, |
Gene summary | | The protein encoded by this gene is a lymphocyte-specific member of the tumor necrosis factor (TNF) receptor superfamily. It interacts with calcium-modulator and cyclophilin ligand (CAML). The protein induces activation of the transcription factors NFAT, AP1, and NF-kappa-B and plays a crucial role in humoral immunity by interacting with a TNF ligand. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq] |
Location | | Chromosome: 17 Locus: 17p11.2 |
Gene position | | 16875402 - 16842398 Map Viewer |
Gene orientation | | minus |
Gene size | | 33005 bp |
Gene sequence |
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OMIM ID | | 604907 |
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