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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:BUB1B-THBS1 (FusionGDB2 ID:HG701TG7057)

Fusion Gene Summary for BUB1B-THBS1

check button Fusion gene summary
Fusion gene informationFusion gene name: BUB1B-THBS1
Fusion gene ID: hg701tg7057
HgeneTgene
Gene symbol

BUB1B

THBS1

Gene ID

701

7057

Gene nameBUB1 mitotic checkpoint serine/threonine kinase Bthrombospondin 1
SynonymsBUB1beta|BUBR1|Bub1A|MAD3L|MVA1|SSK1|hBUBR1THBS|THBS-1|TSP|TSP-1|TSP1
Cytomap('BUB1B')('THBS1')

15q15.1

15q14

Type of geneprotein-codingprotein-coding
Descriptionmitotic checkpoint serine/threonine-protein kinase BUB1 betaBUB1B, mitotic checkpoint serine/threonine kinaseMAD3/BUB1-related protein kinasebudding uninhibited by benzimidazoles 1 homolog betamitotic checkpoint kinase MAD3Lthrombospondin-1glycoprotein Gthrombospondin-1p180thrombospondin-p50
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000560120, ENST00000287598, 
ENST00000412359, 
Fusion gene scores* DoF score5 X 6 X 5=15012 X 13 X 5=780
# samples 1212
** MAII scorelog2(12/150*10)=-0.321928094887362
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/780*10)=-2.70043971814109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: BUB1B [Title/Abstract] AND THBS1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointBUB1B(40462882)-THBS1(39879548), # samples:1
Anticipated loss of major functional domain due to fusion event.BUB1B-THBS1 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
BUB1B-THBS1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
BUB1B-THBS1 seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
BUB1B-THBS1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* 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
TgeneTHBS1

GO:0001937

negative regulation of endothelial cell proliferation

16150726|17996481

TgeneTHBS1

GO:0001953

negative regulation of cell-matrix adhesion

16150726|17416590

TgeneTHBS1

GO:0002581

negative regulation of antigen processing and presentation of peptide or polysaccharide antigen via MHC class II

16882710

TgeneTHBS1

GO:0002605

negative regulation of dendritic cell antigen processing and presentation

16882710

TgeneTHBS1

GO:0006954

inflammatory response

23144964

TgeneTHBS1

GO:0007050

cell cycle arrest

17596205

TgeneTHBS1

GO:0008284

positive regulation of cell proliferation

24615654

TgeneTHBS1

GO:0009749

response to glucose

18096704

TgeneTHBS1

GO:0010595

positive regulation of endothelial cell migration

18555217

TgeneTHBS1

GO:0010596

negative regulation of endothelial cell migration

18555217

TgeneTHBS1

GO:0010748

negative regulation of plasma membrane long-chain fatty acid transport

17416590

TgeneTHBS1

GO:0010751

negative regulation of nitric oxide mediated signal transduction

16150726|17416590

TgeneTHBS1

GO:0010754

negative regulation of cGMP-mediated signaling

17416590

TgeneTHBS1

GO:0010757

negative regulation of plasminogen activation

6438154

TgeneTHBS1

GO:0010763

positive regulation of fibroblast migration

18555217

TgeneTHBS1

GO:0016477

cell migration

18555217

TgeneTHBS1

GO:0016525

negative regulation of angiogenesis

16150726|17596205|17996481|18726995

TgeneTHBS1

GO:0018149

peptide cross-linking

3997886

TgeneTHBS1

GO:0030194

positive regulation of blood coagulation

3997886

TgeneTHBS1

GO:0030335

positive regulation of cell migration

15700281

TgeneTHBS1

GO:0030511

positive regulation of transforming growth factor beta receptor signaling pathway

18555217

TgeneTHBS1

GO:0032026

response to magnesium ion

6777381

TgeneTHBS1

GO:0032695

negative regulation of interleukin-12 production

16882710

TgeneTHBS1

GO:0040037

negative regulation of fibroblast growth factor receptor signaling pathway

17996481

TgeneTHBS1

GO:0042535

positive regulation of tumor necrosis factor biosynthetic process

18726995

TgeneTHBS1

GO:0043032

positive regulation of macrophage activation

18757424

TgeneTHBS1

GO:0043066

negative regulation of apoptotic process

18653767

TgeneTHBS1

GO:0043154

negative regulation of cysteine-type endopeptidase activity involved in apoptotic process

18653767

TgeneTHBS1

GO:0043536

positive regulation of blood vessel endothelial cell migration

18555217

TgeneTHBS1

GO:0043537

negative regulation of blood vessel endothelial cell migration

18555217

TgeneTHBS1

GO:0043652

engulfment of apoptotic cell

16882710

TgeneTHBS1

GO:0045727

positive regulation of translation

15700281

TgeneTHBS1

GO:0048661

positive regulation of smooth muscle cell proliferation

24615654

TgeneTHBS1

GO:0050921

positive regulation of chemotaxis

18555217

TgeneTHBS1

GO:0051592

response to calcium ion

6777381|18757424

TgeneTHBS1

GO:0051897

positive regulation of protein kinase B signaling

18653767

TgeneTHBS1

GO:0051918

negative regulation of fibrinolysis

6438154

TgeneTHBS1

GO:1902043

positive regulation of extrinsic apoptotic signaling pathway via death domain receptors

18726995

TgeneTHBS1

GO:2000353

positive regulation of endothelial cell apoptotic process

18726995

TgeneTHBS1

GO:2000379

positive regulation of reactive oxygen species metabolic process

18757424

TgeneTHBS1

GO:2001027

negative regulation of endothelial cell chemotaxis

16150726



check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4BRCATCGA-AR-A256-01ABUB1Bchr15

40462882

+THBS1chr15

39879548

+


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Fusion Gene ORF analysis for BUB1B-THBS1

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
3UTR-3CDSENST00000560120ENST00000260356BUB1Bchr15

40462882

+THBS1chr15

39879548

+
Frame-shiftENST00000287598ENST00000260356BUB1Bchr15

40462882

+THBS1chr15

39879548

+
Frame-shiftENST00000412359ENST00000260356BUB1Bchr15

40462882

+THBS1chr15

39879548

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for BUB1B-THBS1


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
BUB1Bchr1540462882+THBS1chr1539879547+3.79E-060.9999962
BUB1Bchr1540462882+THBS1chr1539879547+3.79E-060.9999962


check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.
genomic feature of top 1%

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Fusion Protein Features for BUB1B-THBS1


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:40462882/:39879548)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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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Fusion Gene Sequence for BUB1B-THBS1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for BUB1B-THBS1


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


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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Related Drugs for BUB1B-THBS1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for BUB1B-THBS1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneBUB1BC1850343Mosaic variegated aneuploidy syndrome 16CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneBUB1BC0018273Growth Disorders1CTD_human
HgeneBUB1BC0025958Microcephaly1CTD_human
HgeneBUB1BC0027654Embryonal Neoplasm1CTD_human
HgeneBUB1BC0027658Neoplasms, Germ Cell and Embryonal1CTD_human
HgeneBUB1BC0205851Germ cell tumor1CTD_human
HgeneBUB1BC0205852Neoplasms, Embryonal and Mixed1CTD_human
HgeneBUB1BC0206656Embryonal Rhabdomyosarcoma1CTD_human
HgeneBUB1BC0279626Squamous cell carcinoma of esophagus1CTD_human
HgeneBUB1BC0740345Germ Cell Cancer1CTD_human
HgeneBUB1BC0751364Cancer, Embryonal1CTD_human
HgeneBUB1BC0751365Cancer, Embryonal and Mixed1CTD_human
HgeneBUB1BC1864389PREMATURE CHROMATID SEPARATION TRAIT1CTD_human;UNIPROT
HgeneBUB1BC1956147Microlissencephaly1CTD_human
HgeneBUB1BC2239176Liver carcinoma1CTD_human
HgeneBUB1BC2931286Warburton Anyane Yeboa syndrome1ORPHANET
HgeneBUB1BC2931383Chromosomal mosaicism due to mitotic instability1CTD_human
HgeneBUB1BC3853041Severe Congenital Microcephaly1CTD_human
TgeneC0006142Malignant neoplasm of breast1CTD_human
TgeneC0011875Diabetic Angiopathies1CTD_human
TgeneC0011884Diabetic Retinopathy1CTD_human
TgeneC0016059Fibrosis1CTD_human
TgeneC0023890Liver Cirrhosis1CTD_human
TgeneC0025945Microangiopathy, Diabetic1CTD_human
TgeneC0027707Nephritis, Interstitial1CTD_human
TgeneC0035126Reperfusion Injury1CTD_human
TgeneC0036341Schizophrenia1CTD_human
TgeneC0041349Nephritis, Tubulointerstitial1CTD_human
TgeneC0087031Juvenile-Onset Still Disease1CTD_human
TgeneC0239946Fibrosis, Liver1CTD_human
TgeneC0678222Breast Carcinoma1CTD_human
TgeneC1257931Mammary Neoplasms, Human1CTD_human
TgeneC1458155Mammary Neoplasms1CTD_human
TgeneC1623038Cirrhosis1CTD_human
TgeneC3495559Juvenile arthritis1CTD_human
TgeneC3714758Juvenile psoriatic arthritis1CTD_human
TgeneC4552091Polyarthritis, Juvenile, Rheumatoid Factor Negative1CTD_human
TgeneC4704862Polyarthritis, Juvenile, Rheumatoid Factor Positive1CTD_human
TgeneC4704874Mammary Carcinoma, Human1CTD_human