Gene: TNFSF10 (tumor necrosis factor (ligand) superfamily, member 10)  Homo sapiens

Symbol: TNFSF10
Name: tumor necrosis factor (ligand) superfamily, member 10
Description: The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This protein preferentially induces apoptosis in transformed and tumor cells, but does not appear to kill normal cells although it is expressed at a significant level in most normal tissues. This protein binds to several members of TNF receptor superfamily including TNFRSF10A/TRAILR1, TNFRSF10B/TRAILR2, TNFRSF10C/TRAILR3, TNFRSF10D/TRAILR4, and possibly also to TNFRSF11B/OPG. The activity of this protein may be modulated by binding to the decoy receptors TNFRSF10C/TRAILR3, TNFRSF10D/TRAILR4, and TNFRSF11B/OPG that cannot induce apoptosis. The binding of this protein to its receptors has been shown to trigger the activation of MAPK8/JNK, caspase 8, and caspase 3. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: Apo-2 ligand; Apo-2L; APO2L; CD253; chemokine tumor necrosis factor ligand superfamily member 10; OTTHUMP00000211018; OTTHUMP00000211019; TL2; TNF-related apoptosis inducing ligand TRAIL; TNF-related apoptosis-inducing ligand; TRAIL; tumor necrosis factor (ligand) family, member 10; tumor necrosis factor apoptosis-inducing ligand splice variant delta; tumor necrosis factor ligand superfamily member 10
Orthologs: Mus musculus : Tnfsf10 (tumor necrosis factor (ligand) superfamily, member 10)  MGI
Rattus norvegicus : Tnfsf10 (tumor necrosis factor (ligand) superfamily, member 10)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_13172,085,949 - 172,103,935-NCBI
Human Genome Assembly HuRef3169,593,908 - 169,611,904-NCBI
Human Genome Assembly GRCh373172,223,298 - 172,241,297-NCBI
Human Genome Assembly Build 363173,706,158 - 173,723,963-NCBI
Human Cytogenetic Map3q26 NCBI
Human Genome Assembly3173,706,166 - 173,723,971 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on TNFSF10
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1344832
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2013-06-04
Status: ACTIVE