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FLASH GENE
Symbol TNFRSF10B contributors: mct - updated : 15-10-2020
HGNC name tumor necrosis factor receptor superfamily, member 10b
HGNC id 11905
Location 8p21.3      Physical location : 22.877.647 - 22.926.700
Synonym name
  • TNF related,apoptosis induced ligand (TRAIL) receptor 2
  • apoptosis inducing receptor TRAIL-R2
  • cytotoxic TRAIL receptor-2
  • death domain containing receptor for TRAIL/Apo-2L
  • death receptor 5
  • TRAIL death receptor 5
  • Synonym symbol(s) TRAILR2, DR5, TRICK2, KILLER, KILLER/DR5 , T10B, TRICK2, TRICK2A, TRICK2B, TRICKB, ZTNFR9
    DNA
    TYPE functioning gene
    STRUCTURE 48.90 kb     10 Exon(s)
    10 Kb 5' upstream gene genomic sequence study
    regulatory sequence Promoter
    Binding site
    text structure two Sp1 binding sites responsible for the basal transcription activity
    MAPPING cloned Y linked N status confirmed
    RNA
    TRANSCRIPTS type messenger
    identificationnb exonstypebpproduct
    ProteinkDaAAspecific expressionYearPubmed
    9 - 4154 - 440 - 2007 17273769
    10 - 4067 - 411 - 2007 17273769
    EXPRESSION
    Type ubiquitous
       expressed in (based on citations)
    organ(s)
    SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
    blood / hematopoieticspleen   highly
    Cardiovascularheart   highly Homo sapiens
    Digestiveintestinelarge intestinecolon  
    Reproductivefemale systemovary  highly
     male systemprostate   
    Respiratorylung    
    tissue
    SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
    Epithelial    
    Lymphoid    
    Muscularstriatumskeletal  
    cells
    SystemCellPubmedSpeciesStageRna symbol
    Lymphoid/Immunelymphocyte
    cell lineage highly in tumor cell lineage
    cell lines
    fluid/secretion
    at STAGE
    physiological period fetal
    Text widely in fetal tissues
    PROTEIN
    PHYSICAL PROPERTIES
    STRUCTURE
    motifs/domains
  • a putative signal peptide, with two extracellular cysteine-rich pseudorepeats typical for TNFR superfamily
  • a preligand assembly domain (PLAD) in CRD1 mediating ligand-independent receptor assembly and signaling
  • a small cytoplasmic tail with an intracellular DEATH domain
  • mono polymer homomer , trimer
    HOMOLOGY
    interspecies homolog to murine Tnfrsf10b
    Homologene
    FAMILY
  • tumor necrosis factor receptor superfamily
  • CATEGORY signaling cytokine , receptor
    SUBCELLULAR LOCALIZATION     plasma membrane
    text membrane protein type 1
    basic FUNCTION
  • inducing a caspase-dependent apoptotic pathway, FADD dependent
  • acting as dosage-dependent tumor suppressor genes whose monoallelic deletion can impair TRAIL-induced apoptosis in B-cell lymphoma
  • playing a role as a regulator of megakaryocytopoiesis
  • with TNFSF10 and TNFRSF10A, play an important role in inflammation
  • TNFRSF10B- death signaling contributes to palmitate-induced apoptosis
  • importance of TNFRSF10B and CASP8 as critical signal conduits for apoptosis activation upon ER stress
  • role in the heart, which does not promote apoptosis but acts through non-canonical MMP-EGFR-ERK1/2 signaling mechanisms to contribute to cardiomyocyte hypertrophy
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
  • its signaling promotes hepatocyte lipoapoptosis
  • a component
  • death signal mediated by TNF-related apoptosis-inducing ligand (TNFSF10) receptor 2/death receptor 5 (DR5) may be a key regulator of cholestatic liver injury
  • INTERACTION
    DNA
    RNA
    small molecule metal binding,
  • FADD
  • protein
  • binding APO2L
  • receptor of TNFSF10
  • TNK2 is an essential player in the spatial regulation of TNFSR10A, TNFSR10B
  • DDIT3 and KAT2A cooperatively up-regulate TNFRSF10A and TNFRSF10B
  • YIPF2 promotes chemotherapeutic agent-mediated apoptosis via enhancing TNFRSF10B recycling to plasma membrane in Non-small cell lung cancer (NSCLC) cells
  • cell & other
    REGULATION
    induced by TP53,inducible
    by luteolin (plays a role in luteolin-induced apoptosis)
    Other only pro-apoptotic signaling through TNFRSF10A and TNFRSF10B has been found to be regulated by N- and O-glycosylation, respectively
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Other morbid association(s)
    TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
    tumoral     --over  
    in primary glioblastoma multiforme
    tumoral     --low  
    in B-cell non-Hodgkin lymphoma (B-NHL)
    tumoral somatic mutation      
    in head and neck cancer,with a mutation also present in the germ line of an affected patient
    tumoral       gain of function
    in colon cancer
    constitutional     --over  
    in patients with nonalcoholic steatohepatitis
    Susceptibility to increased risk of death in non-small cell lung cancer
    Variant & Polymorphism other polymorphisms and haplotypes associated with increased risk of death in non-small cell lung cancer
    Candidate gene
    Marker
    Therapy target
    SystemTypeDisorderPubmed
    digestiveliversteatosis
    caspase inhibitors in steatohepatitis or other approaches to reduce TNFRSF10B activation hold promise to ameliorate hepatocyte lipoapoptosis in fatty liver disease
    cancerbrainglioma/neuroblstoma
    target for future TNFSF10 therapy of glioblastoma
    cancer  
    application of TNFSF10 or anti-TNFSFR10B mAb therapies to cancer patients
    cancer  
    TNFRSF10B-stimulated JNK activation and its consequent fluxes into the pro-autophagic signaling pathways contribute to the autophagic cell death in cancer cells
    cancer  
    cytotoxic agents capable of up-regulating the expression of TNFRSF10A and TNFRSF10B can sensitize cancer cells to TNFSF10 induced apoptosis
    ANIMAL & CELL MODELS