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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 38864

FusionGeneSummary for TNFRSF1B_FBXO6

check button Fusion gene summary
Fusion gene informationFusion gene name: TNFRSF1B_FBXO6
Fusion gene ID: 38864
HgeneTgene
Gene symbol

TNFRSF1B

FBXO6

Gene ID

7133

26270

Gene nameTNF receptor superfamily member 1BF-box protein 6
SynonymsCD120b|TBPII|TNF-R-II|TNF-R75|TNFBR|TNFR1B|TNFR2|TNFR80|p75|p75TNFRFBG2|FBS2|FBX6|Fbx6b
Cytomap

1p36.22

1p36.22

Type of geneprotein-codingprotein-coding
Descriptiontumor necrosis factor receptor superfamily member 1BTNF-R2TNF-RIIp75 TNF receptorp80 TNF-alpha receptorsoluble TNFR1B variant 1tumor necrosis factor beta receptortumor necrosis factor binding protein 2tumor necrosis factor receptor 2tumor necrosiF-box only protein 6F-box protein FBG2F-box protein Fbx6F-box protein that recognizes sugar chains 2F-box/G-domain protein 2
Modification date2018052320180519
UniProtAcc

P20333

Q9NRD1

Ensembl transtripts involved in fusion geneENST00000536782, ENST00000492361, 
ENST00000376259, 
ENST00000376753, 
Fusion gene scores* DoF score2 X 2 X 2=81 X 1 X 1=1
# samples 21
** MAII scorelog2(2/8*10)=1.32192809488736log2(1/1*10)=3.32192809488736
Context

PubMed: TNFRSF1B [Title/Abstract] AND FBXO6 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
TgeneFBXO6

GO:0031146

SCF-dependent proteasomal ubiquitin-dependent protein catabolic process

19716789


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGALDSKCMTCGA-D3-A51E-06ATNFRSF1Bchr1

12227226

+FBXO6chr1

11733334

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
Frame-shiftENST00000536782ENST00000376753TNFRSF1Bchr1

12227226

+FBXO6chr1

11733334

+
3UTR-3CDSENST00000492361ENST00000376753TNFRSF1Bchr1

12227226

+FBXO6chr1

11733334

+
Frame-shiftENST00000376259ENST00000376753TNFRSF1Bchr1

12227226

+FBXO6chr1

11733334

+

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FusionProtFeatures for TNFRSF1B_FBXO6


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TNFRSF1B

P20333

FBXO6

Q9NRD1

Receptor with high affinity for TNFSF2/TNF-alpha andapproximately 5-fold lower affinity for homotrimericTNFSF1/lymphotoxin-alpha. The TRAF1/TRAF2 complex recruits theapoptotic suppressors BIRC2 and BIRC3 to TNFRSF1B/TNFR2. Thisreceptor mediates most of the metabolic effects of TNF-alpha.Isoform 2 blocks TNF-alpha-induced apoptosis, which suggests thatit regulates TNF-alpha function by antagonizing its biologicalactivity. {ECO:0000269|PubMed:12370298}. Substrate-recognition component of some SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complexes. Involved inendoplasmic reticulum-associated degradation pathway (ERAD) formisfolded lumenal proteins by recognizing and binding sugar chainson unfolded glycoproteins that are retrotranslocated into thecytosol and promoting their ubiquitination and subsequentdegradation. Able to recognize and bind denatured glycoproteins,which are modified with not only high-mannose but also complex-type oligosaccharides. Also recognizes sulfated glycans. Alsoinvolved in DNA damage response by specifically recognizingactivated CHEK1 (phosphorylated on 'Ser-345'), promoting itsubiquitination and degradation. Ubiquitination of CHEK1 isrequired to insure that activated CHEK1 does not accumulate ascells progress through S phase, or when replication forksencounter transient impediments during normal DNA replication.{ECO:0000269|PubMed:18203720, ECO:0000269|PubMed:19716789}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

.

* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for TNFRSF1B_FBXO6


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for TNFRSF1B_FBXO6


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page

.

check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors
TNFRSF1BFANCD2, TNF, TRAF2, CAV1, KRT18, TDP2, TRAF1, TNFRSF1B, CSNK1A1, TRIM37, TRAIP, SMURF2, ASB3, TRAF3, TRAF6, TNFRSF1A, CHUK, RIPK1, TRADD, PKN1, LTA, CD14, UBQLN1, ZNF420, ADAM17, CSNK1A1LFBXO6VCP, SKP1, CUL1, ASGR2, RBX1, ATP5A1, ATP5B, ATRN, CCT3, COPS2, CRTAP, DDOST, ERLIN2, ERO1L, GLA, GLB1, COLGALT1, GNS, GRN, GUSB, H6PD, HSPA9, IGF2R, IKBIP, LAMB2, P3H1, LMNB1, MCM7, NAGLU, NOMO2, HYOU1, PIGS, PLOD1, PLOD3, PON2, PRCP, RPN1, RPN2, STT3A, STT3B, TFRC, UQCRC2, SMC1A, SMC3, ADAM17, AIFM1, ALDH1B1, ASAH1, ATP6AP1, B3GALNT2, CACHD1, CLU, CNTNAP1, COL6A1, COPA, CTPS1, DDX39A, DDX3X, EDEM3, EMILIN2, ERLIN1, ERO1LB, FARSA, FBN2, FOXRED2, FUCA2, GAA, GANAB, GBA, GGCX, GGH, HADHB, HLA-C, HNRNPC, HNRNPM, HRNR, HSP90AA1, HSP90B1, IMPDH2, ITGAV, ITGB1, EMC1, KIAA1161, LAMB1, LAMC1, LGALS3BP, LGMN, LMF2, LRIG2, MCM3, MCM5, MEGF8, MGRN1, NAGA, NCLN, NCSTN, NEDD8, NPM1, NPTN, NUP210, OAT, P4HB, PABPC1, PCBP2, PDHB, PDIA6, PLD3, PLOD2, PLXNA1, PPM1B, PPP1CC, PPT1, PRMT5, PTBP1, PTGFRN, PXDN, SCARB1, SERPINH1, SGSH, SLC25A5, SORL1, SSR1, TCTN3, TMPO, TOR1AIP2, TTC13, TUBB6, TUBG1, ACAT1, GARS, LRP1, NPC1, ASGR1, CLN5, EGFR, ORC4, A2M, ACP2, AFG3L2, ALPL, ALPP, ASS1, C1RL, CCT5, CCT6A, CCT8, CHPF2, COL4A2, COPS3, COPS7B, CPS1, CPT1A, CTSA, CTSZ, DDX3Y, ECEL1, EIF4A1, ENO1, EPRS, FLG2, GAPDH, GPR126, HSDL2, HSPA5, IGF1R, ITGA3, L1CAM, MAGT1, MET, MIR671, MRC2, PFKM, PFKP, PHB, PHGDH, PRSS21, PSMC1, PSMC3, RARS, RRM1, SLC25A1, SLC25A13, SLC25A3, SMCHD1, TCP1, TGFB1, TKT, TMEM2, TRIP13, UBA52, UGGT1, YBX1, YWHAG, YWHAQ, YWHAZ, ACACA, AASDHPPT, ABCE1, ABCF2, ABCF3, ACOT9, ACTL6A, ADAM10, ADAM15, ADAMTSL4, ADAR, AGA, AGK, AHCY, AHSA1, ALG1, ANKRD28, ARAF, ARF1, ARF4, ARHGEF2, ARIH1, ATAD3A, ATAD3B, ATF6, ATP5C1, ATP6V1A, AUP1, B4GAT1, B4GALT3, BSG, EMC7, C1QBP, APMAP, POMGNT2, C6orf89, TMEM245, CAD, CALU, CANX, CAPRIN1, CCT2, CDC37, CDC45, CDK1, CERCAM, CHPF, CHST10, CILP2, CKAP5, CLIC1, CLNS1A, CLPX, CLTC, CMAS, CNNM3, COCH, COL18A1, COMT, COPB1, COPB2, COPG2, COPS4, COPS5, COPS6, COPS7A, COPS8, CPD, CREG1, CSE1L, CTSB, CTSC, CTSD, CYC1, DARS, DDX17, DDX18, DDX21, DDX5, DDX6, DHX15, DHX9, DNAJA1, DNAJA2, DNAJB11, DNAJC11, DNASE2, DNM2, DPM1, DPP7, ECE1, EEF1B2, EEF1D, EIF2B3, EIF3A, EIF3B, EIF3E, EIF3F, EIF4A3, EIF4B, EMD, ENPP3, EPB41L3, ERLEC1, EZR, FAF2, FASN, FASTKD5, FBXW2, FDFT1, FECH, GART, GCAT, GCDH, GCN1L1, GEMIN5, COLGALT2, GMPS, GNB2L1, GNB4, GPS1, GTF2I, HEPH, HEXA, HEXB, HIST1H1D, HK2, HNRNPA2B1, HNRNPF, HNRNPH2, HNRNPL, HNRNPR, HNRNPDL, HSD17B11, HSPA1A, HSPA1B, HSPG2, HSPH1, IARS, ICAM4, ICAM5, IGF2BP1, IGF2BP3, IGSF8, ILF2, ILF3, IMMT, IPO11, IPO5, IPO7, ITFG1, ITFG3, ITGA2B, ITGA5, ITPRIP, IVNS1ABP, KARS, KDELC2, TTI1, KIAA0922, KPNB1, POGLUT1, LAMA5, LAMP1, LDHA, LEPR, LIFR, LMNA, LNPEP, SPCS2P4, LRFN4, LRPPRC, NRROS, LRRC47, LTBP1, LTBP3, LTBP4, M6PR, MAN2A2, MAN2B1, MAN2B2, MANBA, MAP2K7, MARS, MAT2A, MGAT3, MIR1181, MIR1257, MTCH2, MTHFD1, NAAA, NAMPTP1, NDUFA9, NDUFS1, NDUFS2, NDUFS7, NEU1, NGLY1, NME1, NOB1, NPEPPS, NRM, NUP133, NUP155, NUP205, NUP214, NUP85, NUP93, NUP98, OS9, PCNA, PCYOX1L, PFKL, PIGK, PLA2G15, PLBD2, PLK1, PLXNB2, POFUT1, POLR2B, PPA1, PPIB, PPM1F, PPP6C, PPT2, PRF1, PRKDC, PROS1, PRPF8, PRPS1, PSAP, PSMA1, PSMA3, PSMA4, PSMC2, PSMC5, PSMC6, PSMD3, PSMD4, PSMD7, PTGS1, PTPMT1, PTPRC, PTPRJ, PTPRS, PUM1, QPCTL, RAB27A, RAC2, RAD50, RBBP4, RBM10, RBMX, RFC3, RFC5, RHOG, RHOT2, RNASET2, RPA1, RPF2, RPL18, RPL23, RPL28, RPL32, RPL4, RPL5, RPL6, RPL7A, RPL8, RPLP2, RPS10, RPS20, RPS3, RPS4X, RPS5, RPS6, RPS7, RPS9, RUVBL1, SCAMP3, SCYL2, SDF2L1, SDHA, SEC11A, SEL1L, SEL1L3, SEMA4C, SERPINB1, SF3B1, SF3B2, SF3B3, SRSF1, SIAE, SIL1, SLC25A11, SLC25A12, SLC25A21, SLC25A22, SLC25A24, SLC25A6, SMARCA4, SMC2, SMC4, SNORA41, SNORD21, SNORD24, SNORD36C, SNORD36A, SNORD36B, SNRNP200, SPCS3, SPTLC1, SRPRB, SSR4, STK38, STOM, STOML2, STRAP, SUN1, SUSD1, SYNCRIP, TAF4, TARDBP, TCTN2, TFB2M, TFR2, TGM2, ALYREF, TIMM23, TIMM50, TIMP1, TMCO1, TMED10, EMC3, TMEM131, TMEM201, TMEM214, TMEM231, TOR1B, TPP1, TRAP1, TRIM28, TSR1, TTC17, TTC27, EMC2, TTC4, TUBA1A, TUBA1B, TUBB3, TUFM, TUSC3, TUT1, TXNDC11, TXNDC15, UCK2, UGGT2, UGT8, VAPA, VARS, VDAC2, VDAC3, VPS4A, VWDE, XPOT, YTHDF2, YWHAE, ACTG1, AMOT, ATP1A1, CAPZA1, CAPZB, CCT4, CCT7, HSPD1, CPVL, DBN1, EEF1A1, EEF1G, EFHD2, GALK1, HIST1H4A, HIST1H4D, HIST1H4E, HIST1H4H, HIST1H4I, HIST2H4A, HIST2H4B, HIST4H4, HNRNPA1, HNRNPH1, HNRNPK, HSP90AB1, HSPA8, HUWE1, IGSF3, ILK, KIF11, MIR7-1, MYO6, NOMO1, NOMO3, PCBP1, PKM, RIOK1, RUVBL2, SLC25A10, SPTBN1, STK38L, TRIM21, TUBA1C, TUBB, TUBB2B, TUBB4A, TUBG2, VIM, WDR77, UBB, HSPA13, ENTPD5, NUDT9, BTD, JMJD8, MINPP1, FAM168A, FSTL1


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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RelatedDrugs for TNFRSF1B_FBXO6


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneTNFRSF1BP20333DB11626TasonerminTumor necrosis factor receptor superfamily member 1Bbiotechapproved
HgeneTNFRSF1BP20333DB00005EtanerceptTumor necrosis factor receptor superfamily member 1Bbiotechapproved|investigational

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RelatedDiseases for TNFRSF1B_FBXO6


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTNFRSF1BC0011570Mental Depression4PSYGENET
HgeneTNFRSF1BC0011581Depressive disorder4PSYGENET
HgeneTNFRSF1BC0036341Schizophrenia2PSYGENET
HgeneTNFRSF1BC0004352Autistic Disorder1CTD_human
HgeneTNFRSF1BC0007786Brain Ischemia1CTD_human
HgeneTNFRSF1BC0011860Diabetes Mellitus, Non-Insulin-Dependent1CTD_human
HgeneTNFRSF1BC0020517Hypersensitivity1CTD_human
HgeneTNFRSF1BC0023890Liver Cirrhosis1CTD_human
HgeneTNFRSF1BC0026948Mycosis Fungoides1CTD_human;ORPHANET
HgeneTNFRSF1BC0028754Obesity1CTD_human
HgeneTNFRSF1BC0032285Pneumonia1CTD_human
HgeneTNFRSF1BC0036349Paranoid Schizophrenia1PSYGENET
HgeneTNFRSF1BC0036920Sezary Syndrome1CTD_human;ORPHANET
HgeneTNFRSF1BC0239981Hypoalbuminemia1CTD_human
HgeneTNFRSF1BC0400966Non-alcoholic Fatty Liver Disease1CTD_human
TgeneFBXO6C0038325Stevens-Johnson Syndrome1CTD_human