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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:15765)

Fusion Gene Summary for CEP120-FBXW11

check button Fusion gene summary
Fusion gene informationFusion gene name: CEP120-FBXW11
Fusion gene ID: 15765
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

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

Q8N960

Q9UKB1

Ensembl transtripts involved in fusion geneENST00000306467, ENST00000306481, 
ENST00000328236, ENST00000395431, 
ENST00000515110, 
ENST00000522891, 
ENST00000265094, ENST00000296933, 
ENST00000393802, ENST00000425623, 
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 buttonFusion gene breakpoints across CEP120 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across FBXW11 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
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)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

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.

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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
CEP120

Q8N960

FBXW11

Q9UKB1

FUNCTION: Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors and for proper positioning of neurons during brain development. Also implicated in the migration and selfrenewal of neural progenitors. Required for centriole duplication and maturation during mitosis and subsequent ciliogenesis (By similarity). Required for the recruitment of CEP295 to the proximal end of new-born centrioles at the centriolar microtubule wall during early S phase in a PLK4-dependent manner (PubMed:27185865). {ECO:0000250|UniProtKB:Q7TSG1, ECO:0000269|PubMed:27185865}.FUNCTION: Substrate recognition component of a SCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably recognizes and binds to phosphorylated target proteins. SCF(FBXW11) mediates the ubiquitination of phosphorylated CTNNB1 and participates in Wnt signaling. SCF(FBXW11) mediates the ubiquitination of phosphorylated NFKBIA, which degradation frees the associated NFKB1 to translocate into the nucleus and to activate transcription. SCF(FBXW11) mediates the ubiquitination of IFNAR1. SCF(FBXW11) mediates the ubiquitination of CEP68; this is required for centriole separation during mitosis (PubMed:25503564). Involved in the oxidative stress-induced a ubiquitin-mediated decrease in RCAN1. Mediates the degradation of CDC25A induced by ionizing radiation in cells progressing through S phase and thus may function in the intra-S-phase checkpoint. Has an essential role in the control of the clock-dependent transcription via degradation of phosphorylated PER1 and phosphorylated PER2. SCF(FBXW11) mediates the ubiquitination of CYTH1, and probably CYTH2 (PubMed:29420262). {ECO:0000269|PubMed:10321728, ECO:0000269|PubMed:10437795, ECO:0000269|PubMed:10644755, ECO:0000269|PubMed:10648623, ECO:0000269|PubMed:14532120, ECO:0000269|PubMed:14603323, ECO:0000269|PubMed:15917222, ECO:0000269|PubMed:18575781, ECO:0000269|PubMed:19966869, ECO:0000269|PubMed:20347421, ECO:0000269|PubMed:25503564, ECO:0000269|PubMed:29420262}.; FUNCTION: (Microbial infection) Target of human immunodeficiency virus type 1 (HIV-1) protein VPU to polyubiquitinate and deplete BST2 from cells and antagonize its antiviral action. {ECO:0000269|PubMed:19730691}.

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