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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:CEP120-FBXW11 (FusionGDB2 ID:HG153241TG23291)

Fusion Gene Summary for CEP120-FBXW11

check button Fusion gene summary
Fusion gene informationFusion gene name: CEP120-FBXW11
Fusion gene ID: hg153241tg23291
HgeneTgene
Gene symbol

CEP120

FBXW11

Gene ID

153241

23291

Gene namecentrosomal protein 120F-box and WD repeat domain containing 11
SynonymsCCDC100|JBTS31|SRTD13BTRC2|BTRCP2|FBW1B|FBXW1B|Fbw11|Hos
Cytomap('CEP120')('FBXW11')

5q23.2

5q35.1

Type of geneprotein-codingprotein-coding
Descriptioncentrosomal protein of 120 kDacentrosomal protein 120kDacoiled-coil domain-containing protein 100F-box/WD repeat-containing protein 11F-box and WD repeats protein beta-TrCP2F-box and WD-40 domain protein 11F-box and WD-40 domain protein 1BF-box protein Fbw1bF-box/WD repeat-containing protein 1Bbeta-transducin repeat-containing protein 2homolog
Modification date2020031320200329
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000306467, ENST00000306481, 
ENST00000328236, ENST00000395431, 
ENST00000515110, 
Fusion gene scores* DoF score2 X 3 X 2=125 X 6 X 3=90
# samples 45
** MAII scorelog2(4/12*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/90*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CEP120 [Title/Abstract] AND FBXW11 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCEP120(122700190)-FBXW11(171327104), # samples:1
Anticipated loss of major functional domain due to fusion event.CEP120-FBXW11 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CEP120-FBXW11 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
TgeneFBXW11

GO:0000209

protein polyubiquitination

20347421

TgeneFBXW11

GO:0016567

protein ubiquitination

16885022

TgeneFBXW11

GO:0031146

SCF-dependent proteasomal ubiquitin-dependent protein catabolic process

20347421

TgeneFBXW11

GO:0043161

proteasome-mediated ubiquitin-dependent protein catabolic process

20347421



check button Fusion gene information
* 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
ChimerDB4KIRCTCGA-BP-4353-01ACEP120chr5

122700190

-FBXW11chr5

171327104

-


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Fusion Gene ORF analysis for CEP120-FBXW11

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
5CDS-5UTRENST00000306467ENST00000522891CEP120chr5

122700190

-FBXW11chr5

171327104

-
5CDS-5UTRENST00000306481ENST00000522891CEP120chr5

122700190

-FBXW11chr5

171327104

-
5CDS-5UTRENST00000328236ENST00000522891CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000306467ENST00000265094CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000306467ENST00000296933CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000306467ENST00000393802CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000306467ENST00000425623CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000306481ENST00000265094CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000306481ENST00000296933CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000306481ENST00000393802CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000306481ENST00000425623CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000328236ENST00000265094CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000328236ENST00000296933CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000328236ENST00000393802CEP120chr5

122700190

-FBXW11chr5

171327104

-
Frame-shiftENST00000328236ENST00000425623CEP120chr5

122700190

-FBXW11chr5

171327104

-
intron-3CDSENST00000395431ENST00000265094CEP120chr5

122700190

-FBXW11chr5

171327104

-
intron-3CDSENST00000395431ENST00000296933CEP120chr5

122700190

-FBXW11chr5

171327104

-
intron-3CDSENST00000395431ENST00000393802CEP120chr5

122700190

-FBXW11chr5

171327104

-
intron-3CDSENST00000395431ENST00000425623CEP120chr5

122700190

-FBXW11chr5

171327104

-
intron-3CDSENST00000515110ENST00000265094CEP120chr5

122700190

-FBXW11chr5

171327104

-
intron-3CDSENST00000515110ENST00000296933CEP120chr5

122700190

-FBXW11chr5

171327104

-
intron-3CDSENST00000515110ENST00000393802CEP120chr5

122700190

-FBXW11chr5

171327104

-
intron-3CDSENST00000515110ENST00000425623CEP120chr5

122700190

-FBXW11chr5

171327104

-
intron-5UTRENST00000395431ENST00000522891CEP120chr5

122700190

-FBXW11chr5

171327104

-
intron-5UTRENST00000515110ENST00000522891CEP120chr5

122700190

-FBXW11chr5

171327104

-

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 CEP120-FBXW11


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)


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Fusion Protein Features for CEP120-FBXW11


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/:122700190/:171327104)
- 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 CEP120-FBXW11


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 CEP120-FBXW11


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 CEP120-FBXW11


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 CEP120-FBXW11


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCEP120C4225378SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY3GENOMICS_ENGLAND;UNIPROT
HgeneCEP120C0265275Jeune thoracic dystrophy2GENOMICS_ENGLAND;ORPHANET
HgeneCEP120C0431399Familial aplasia of the vermis1ORPHANET
HgeneCEP120C4274118Joubert syndrome with ocular defect1ORPHANET
HgeneCEP120C4540355JOUBERT SYNDROME 311GENOMICS_ENGLAND;UNIPROT
HgeneCEP120C4551568Joubert syndrome 11GENOMICS_ENGLAND;ORPHANET
TgeneC0557874Global developmental delay1GENOMICS_ENGLAND
TgeneC2677504AUTISM, SUSCEPTIBILITY TO, 151GENOMICS_ENGLAND
TgeneC3550704Abnormality of digit1GENOMICS_ENGLAND
TgeneC3714756Intellectual Disability1GENOMICS_ENGLAND
TgeneC4021812Abnormality of the head1GENOMICS_ENGLAND
TgeneC4316870Abnormality of the eye1GENOMICS_ENGLAND