Gene: TNFRSF13B

Alternate names for this Gene: CD267|CVID|CVID2|IGAD2|RYZN|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.

Gene is located in Chromosome: 17

Location in Chromosome : 17p11.2

Description of this Gene: TNF receptor superfamily member 13B

Type of Gene: protein-coding

Gene: TBC1D27P

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

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rs3751991 in TNFRSF13B;TBC1D27P gene and Serum albumin measurement PMID 22558069 2012 Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese.