Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8740
Gene name Gene Name - the full gene name approved by the HGNC.
TNF superfamily member 14
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TNFSF14
Synonyms (NCBI Gene) Gene synonyms aliases
CD258, HVEML, LIGHT, LTg
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the tumor necrosis factor (TNF) ligand family. This protein is a ligand for TNFRSF14, which is a member of the tumor necrosis factor receptor superfamily, and which is also known as a herpesvirus entry media
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT685905 hsa-miR-4438 HITS-CLIP 23313552
MIRT685904 hsa-miR-6504-3p HITS-CLIP 23313552
MIRT685903 hsa-miR-5095 HITS-CLIP 23313552
MIRT685902 hsa-miR-7151-3p HITS-CLIP 23313552
MIRT650331 hsa-miR-4705 HITS-CLIP 23824327
Transcription factors
Transcription factor Regulation Reference
ETS1 Activation 12215452
NFKB1 Unknown 21243522
RELA Unknown 21243522
SP1 Activation 12215452
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005102 Function Signaling receptor binding IPI 12393901
GO:0005125 Function Cytokine activity IEA
GO:0005164 Function Tumor necrosis factor receptor binding IEA
GO:0005515 Function Protein binding IPI 9462508, 10318773, 26977880, 27152329, 32296183
GO:0005615 Component Extracellular space IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604520 11930 ENSG00000125735
Protein
UniProt ID O43557
Protein name Tumor necrosis factor ligand superfamily member 14 (Herpes virus entry mediator ligand) (HVEM-L) (Herpesvirus entry mediator ligand) (CD antigen CD258) [Cleaved into: Tumor necrosis factor ligand superfamily member 14, membrane form; Tumor necrosis factor
Protein function Cytokine that binds to TNFRSF3/LTBR. Binding to the decoy receptor TNFRSF6B modulates its effects. Acts as a ligand for TNFRSF14/HVEM (PubMed:10754304, PubMed:9462508). Upon binding to TNFRSF14/HVEM, delivers costimulatory signals to T cells, le
PDB 4EN0 , 4J6G , 4KG8 , 4KGG , 4KGQ , 4RSU , 7MSG
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00229 TNF 112 240 TNF(Tumour Necrosis Factor) family Domain
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in the spleen but also found in the brain. Weakly expressed in peripheral lymphoid tissues and in heart, placenta, liver, lung, appendix, and kidney, and no expression seen in fetal tissues, endocrine glands, or
Sequence
MEESVVRPSVFVVDGQTDIPFTRLGRSHRRQSCSVARVGLGLLLLLMGAGLAVQGWFLLQ
LHWRLGEMVTRLPDGPAGSWEQLIQERRSHEVNPAAHLTGANSSLTGSGGPLLWETQLGL
AFLRGLSYHDGALVVTKAGYYYIYSKVQLGGVGCPLGLASTITHGLYKRTPRYPEELELL
VSQQSPCGRATSSSRVWWDSSFLGGVVHLEAGEKVVVRVLDERLVRLRDGTRSYFGAFMV

Sequence length 240
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Cytokine-cytokine receptor interaction
Viral protein interaction with cytokine and cytokine receptor
NF-kappa B signaling pathway
Herpes simplex virus 1 infection
  TNFR2 non-canonical NF-kB pathway
TNFs bind their physiological receptors
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Multiple sclerosis Multiple Sclerosis, Multiple Sclerosis, Acute Fulminating rs104895219, rs483353022, rs483353023, rs483353028, rs483353029, rs483353024, rs483353030, rs3207617, rs483353031, rs483353032, rs483353033, rs483353034, rs483353035, rs483353036, rs483353039
View all (4 more)
24076602, 21833088
Rheumatoid arthritis Rheumatoid Arthritis rs587776843 20008919
Unknown
Disease term Disease name Evidence References Source
Multiple Sclerosis Multiple Sclerosis GWAS
Glioblastoma Glioblastoma CRISPR screening of E3 ubiquitin ligases reveals Ring Finger Protein 185 as a novel tumor suppressor in glioblastoma repressed by promoter hypermethylation and miR-587 GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Anemia Sickle Cell Stimulate 22775554
Arthritis Rheumatoid Stimulate 33329548
Asthma Associate 29616048
Atherosclerosis Associate 30943772
Bone Diseases Associate 25460501, 30405638, 33329548
Carcinoma Hepatocellular Associate 35292636
Carcinoma Renal Cell Associate 36618968, 37762031
Chordoma Associate 38012562
Chronic Urticaria Associate 29952668
Coronary Artery Disease Associate 30943772