HCSGD entry for TNFSF15


1. General information

Official gene symbolTNFSF15
Entrez ID9966
Gene full nametumor necrosis factor (ligand) superfamily, member 15
Other gene symbolsTL1 TL1A VEGI VEGI192A
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0005102Receptor bindingTASmolecular_function
GO:0005123Death receptor bindingIEAmolecular_function
GO:0005125Cytokine activityIEAmolecular_function
GO:0005164Tumor necrosis factor receptor bindingIEAmolecular_function
GO:0005615Extracellular spaceIEAcellular_component
GO:0005886Plasma membraneIDAcellular_component
GO:0005887Integral component of plasma membraneTAScellular_component
GO:0006919Activation of cysteine-type endopeptidase activity involved in apoptotic processIDAbiological_process
GO:0006955Immune responseIEAbiological_process
GO:0007165Signal transductionNASbiological_process
GO:0007250Activation of NF-kappaB-inducing kinase activityIDAbiological_process
GO:0016021Integral component of membraneNAScellular_component
GO:0042107Cytokine metabolic processIDAbiological_process
GO:0050715Positive regulation of cytokine secretionIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.00000685760.76212638960.01157777781.0000000000

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Up0.5056622829
GSE13712_SHEARUp0.8596657441
GSE13712_STATICUp1.4051765310
GSE19018Down-0.5944119553
GSE19899_A1Up7.5998315391
GSE19899_A2Up8.9136202416
PubMed_21979375_A1Up9.2946409325
PubMed_21979375_A2Up9.7325836560
GSE35957Down-1.3846646248
GSE36640Up4.2746076893
GSE54402Up5.7281324216
GSE9593Down-0.3778613610
GSE43922Up5.9051924732
GSE24585Down-0.1314442767
GSE37065Up0.1721510593
GSE28863_A1Up0.1197675131
GSE28863_A2Up0.3700727098
GSE28863_A3Up0.0250248644
GSE28863_A4Up0.2031096341
GSE48662Up0.2562730057

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-26b-5pMIMAT0000083MIRT029860MicroarrayFunctional MTI (Weak)19088304
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  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

20675618Two functionally distinct isoforms of TL1A (TNFSF15) generated by differential ectodomain shedding
20675618Tumor necrosis factor-like cytokine 1A (TL1A) is expressed in endothelial cells and contributes to T-cell activation, via an extracellular fragment TL1A(L72-L251), generated by ectodomain shedding
20675618Fragments of TL1A, referred to as vascular endothelial growth inhibitor, were found to induce growth arrest and apoptosis in endothelial cells; however, the underlying mechanisms remained obscure
20675618Here, we show that full-length TL1A is the major detectable gene product in both human umbilical vein endothelial cells and circulating endothelial progenitor cells
20675618TL1A expression was significantly enhanced in senescent circulating endothelial progenitor cells, and knockdown of TL1A partially reverted senescence
20675618TL1A overexpression induced premature senescence in both circulating endothelial progenitor cells and human umbilical vein endothelial cells
20675618We also identified a novel extracellular fragment of TL1A, TL1A(V84-L251), resulting from differential ectodomain shedding, which induced growth arrest and apoptosis in human umbilical vein endothelial cells
20675618These findings suggest that TL1A is involved in the regulation of endothelial cell senescence, via a novel fragment produced by differential ectodomain shedding
16626901In particular, a significant upregulation of interleukin-8, VEGI, and the IGF-binding proteins 3 and 5 was observed
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