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TNFRSF13B

Chr 17p11.2

TNF receptor superfamily member 13B

Aliases:
TACI, CD267, IGAD2
MANE:
ENST00000261652.7

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • COVID-19 research

    BOTH monoallelic and biallelic, autosomal or pseudoautosomal
  • DDG2P

    BIALLELIC, autosomal or pseudoautosomal
  • Fetal anomalies

    BOTH monoallelic and biallelic, autosomal or pseudoautosomal
  • Primary immunodeficiency or monogenic inflammatory bowel disease

    BOTH monoallelic and biallelic, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • immunodeficiency, common variable, 2

    0.80
  • immunoglobulin A deficiency 2

    0.70
  • common variable immunodeficiency

    0.70
  • plasma cell myeloma

    0.56
  • monoclonal gammopathy

    0.47
  • immunodeficiency, common variable, 1

    0.47
  • recurrent infections associated with rare immunoglobulin isotypes deficiency

    0.46
  • Paraproteinemia

    0.44
  • amino acid metabolism disease

    0.43
  • plasma protein metabolism disease

    0.43

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Protein function (UniProt)

Tumor necrosis factor receptor superfamily member 13B

Receptor for TNFSF13/APRIL and TNFSF13B/TALL1/BAFF/BLYS that binds both ligands with similar high affinity. Mediates calcineurin-dependent activation of NF-AT, as well as activation of NF-kappa-B and AP-1. Involved in the stimulation of B- and T-cell function and the regulation of humoral immunity

Data sources: HGNC (CC BY 4.0), AlphaFold (CC BY 4.0, Jumper et al. Nature 2021), Genomics England PanelApp (CC BY 4.0), ClinGen, Open Targets (CC0), UniProt.

Not for sole clinical decision-making. Always verify against primary sources.