TNFSF14 (TNF Superfamily Member 14)

LIGHT, a cytokine in immune regulation and cancer biology

Gene Information Card

Symbol TNFSF14
Full Name TNF Superfamily Member 14
Gene Type Protein coding
Chromosomal Location 19p13.3
NCBI Gene ID 8740 ncbi.nlm.nih.gov/gene/8740
Ensembl ID ENSG00000104885
UniProt ID O43557
OMIM ID 604520
HGNC ID 11925
Aliases LIGHT, HVEM-L, CD258, LTg

Description

TNFSF14 (TNF Superfamily Member 14), also known as LIGHT, is a cytokine belonging to the tumor necrosis factor (TNF) ligand family. It is expressed on activated T cells, natural killer cells, and immature dendritic cells. LIGHT binds to its receptors HVEM (TNFRSF14) and LTβR, playing critical roles in co-stimulation of T cells, lymphoid organogenesis, and immune homeostasis. Dysregulation of TNFSF14 is implicated in autoimmune diseases, graft-versus-host disease, and various cancers.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Hodgkin lymphoma LIGHT expressed on Reed-Sternberg cells may promote tumor immune evasion via HVEM signaling PMID: 15692071
Rheumatoid arthritis Elevated LIGHT levels in synovial fluid contribute to inflammatory cytokine production PMID: 12070103
Inflammatory bowel disease TNFSF14 polymorphisms associated with increased risk of Crohn's disease PMID: 21102463
Graft-versus-host disease LIGHT blockade reduces T cell alloreactivity and GVHD severity in murine models PMID: 11929768

Expression Profile

Tissue Expression
Tissue nTPM level
Spleen 12.5 Medium
Lymph node 10.8 Medium
Bone marrow 6.2 Low
Lung 4.1 Low
Small intestine 3.5 Low
Cell Line Expression
Cell Line nTPM Notes
Jurkat (T cell leukemia) 15.2 High expression
THP-1 (monocytic leukemia) 8.7 Moderate expression
HEK293 (embryonic kidney) 2.1 Low expression
K562 (chronic myeloid leukemia) 1.5 Very low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.346C>T (p.Arg116Trp) Missense <0.01% Unknown functional effect; reported in COSMIC
c.487G>A (p.Gly163Ser) Missense <0.01% Reported in COSMIC; no known disease association
Mutation functional classification

Loss of Function (LOF)

No well-characterized loss-of-function mutations reported in TNFSF14.

Gain of Function (GOF)

No gain-of-function mutations described.

Dominant Negative (DN)

No dominant-negative variants known.

Pathways

• TNF signaling pathway (KEGG: hsa04668)
• NF-kappa B signaling pathway (KEGG: hsa04064)
• LIGHT signaling via HVEM (Reactome: R-HSA-5668541)

Protein Summary

TNFSF14 encodes a 240-amino-acid type II transmembrane protein (LIGHT) with a C-terminal extracellular TNF homology domain. It forms homotrimers and binds to HVEM and LTβR. LIGHT is cleaved by metalloproteinases to generate a soluble form. The protein is involved in T cell co-stimulation, dendritic cell maturation, and lymphoid tissue development. Its dysregulation contributes to inflammatory and malignant diseases.

Related Products

Product name Cat.No. Species Gene ID
TNFSF14 Knockout HEK293 Cell Line EDJ-KQ597 Human 8740 Details Get a Quote
TNFSF14 Knockout HeLa Cell Line EDJ-KQ54994 Human 8740 Details Get a Quote
TNFSF14 Knockout A-549 Cell Line EDJ-KQ63477 Human 8740 Details Get a Quote
TNFSF14 Knockout HCT 116 Cell Line EDJ-KQ71945 Human 8740 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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