TNFRSF13C wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human TNFRSF13C wild-type allele is located within 22q13.1-q13.31 and is approximately 2 kb in length. This allele, which encodes tumor necrosis factor receptor superfamily member 13C protein, is involved in promoting peripheral B-cell survival. Mutations in this gene are associated with common variable immunodeficiency-4.

**Synonyms:** - BAFF-R - BAFFR - BR3 - BROMIX - CD268 - CVID4 - Prolixin Gene - TNF Receptor Superfamily Member 13C wt Allele - Tumor Necrosis Factor Receptor Superfamily, Member 13C Gene