Gene Symbol | TNFRSF13B |
Entrez Gene ID | 23495 |
Full Name | TNF receptor superfamily member 13B |
Synonyms | CD267,CVID,CVID2,IGAD2,RYZN,TACI,TNFRSF14B |
General protein information |
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Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
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, Jul 2008]. |
Disorder MIM: | |
Disorder Html: | Immunoglobulin A deficiency 2, 609529 (3); Immunodeficiency, common variable, 2, 240500 (3) |