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TNFSF12

Chr 17p13.1

TNF superfamily member 12

Aliases:
TWEAK, DR3LG, APO3L, TNF12
MANE:
ENST00000293825.11

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • COVID-19 research

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Primary immunodeficiency or monogenic inflammatory bowel disease

    MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Disease associations (Open Targets)

  • atrial fibrillation

    0.40
  • hypertensive disorder

    0.39
  • eyelid disorder

    0.32
  • neurodegenerative disease

    0.27
  • cardioembolic stroke

    0.26
  • osteoarthritis, hip

    0.26
  • total hip arthroplasty

    0.25
  • pyogenic granuloma

    0.22
  • common variable immunodeficiency

    0.21
  • testicular disorder

    0.17

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

Protein function (UniProt)

Tumor necrosis factor ligand superfamily member 12

Binds to FN14 and possibly also to TNRFSF12/APO3. Weak inducer of apoptosis in some cell types. Mediates NF-kappa-B activation. Promotes angiogenesis and the proliferation of endothelial cells. Also involved in induction of inflammatory cytokines. Promotes IL8 secretion

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.