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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:CUX2-IFT81 (FusionGDB2 ID:20754)

Fusion Gene Summary for CUX2-IFT81

check button Fusion gene summary
Fusion gene informationFusion gene name: CUX2-IFT81
Fusion gene ID: 20754
HgeneTgene
Gene symbol

CUX2

IFT81

Gene ID

23316

28981

Gene namecut like homeobox 2intraflagellar transport 81
SynonymsCDP2|CUTL2|EIEE67CDV-1|CDV-1R|CDV1|CDV1R|DV1|SRTD19
Cytomap

12q24.11-q24.12

12q24.11

Type of geneprotein-codingprotein-coding
Descriptionhomeobox protein cut-like 2homeobox protein cux-2intraflagellar transport protein 81 homologcarnitine deficiency-associated gene expressed in ventricle 1carnitine deficiency-associated protein expressed in ventricle 1
Modification date2020031320200313
UniProtAcc

O14529

Q8WYA0

Ensembl transtripts involved in fusion geneENST00000261726, ENST00000551604, 
ENST00000242591, ENST00000361948, 
ENST00000552912, ENST00000549009, 
Fusion gene scores* DoF score11 X 11 X 3=3636 X 8 X 8=384
# samples 1312
** MAII scorelog2(13/363*10)=-1.4814579249673
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/384*10)=-1.67807190511264
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CUX2 [Title/Abstract] AND IFT81 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCUX2(111472044)-IFT81(110565165), # samples:3
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneCUX2

GO:0000122

negative regulation of transcription by RNA polymerase II

15656993


check buttonFusion gene breakpoints across CUX2 (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 IFT81 (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
ChimerDB4UCSTCGA-NA-A4R1-01ACUX2chr12

111472044

-IFT81chr12

110565165

+
ChimerDB4UCSTCGA-NA-A4R1-01ACUX2chr12

111472044

+IFT81chr12

110565165

+
ChimerDB4UCSTCGA-NA-A4R1CUX2chr12

111472044

+IFT81chr12

110565164

+
ChimerDB4UCSTCGA-NA-A4R1CUX2chr12

111472044

+IFT81chr12

110565165

+


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Fusion Gene ORF analysis for CUX2-IFT81

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-5UTRENST00000261726ENST00000242591CUX2chr12

111472044

+IFT81chr12

110565165

+
5CDS-5UTRENST00000261726ENST00000242591CUX2chr12

111472044

+IFT81chr12

110565164

+
5CDS-5UTRENST00000261726ENST00000361948CUX2chr12

111472044

+IFT81chr12

110565165

+
5CDS-5UTRENST00000261726ENST00000361948CUX2chr12

111472044

+IFT81chr12

110565164

+
5CDS-5UTRENST00000261726ENST00000552912CUX2chr12

111472044

+IFT81chr12

110565165

+
5CDS-5UTRENST00000261726ENST00000552912CUX2chr12

111472044

+IFT81chr12

110565164

+
5CDS-intronENST00000261726ENST00000549009CUX2chr12

111472044

+IFT81chr12

110565165

+
5CDS-intronENST00000261726ENST00000549009CUX2chr12

111472044

+IFT81chr12

110565164

+
intron-5UTRENST00000551604ENST00000242591CUX2chr12

111472044

+IFT81chr12

110565165

+
intron-5UTRENST00000551604ENST00000242591CUX2chr12

111472044

+IFT81chr12

110565164

+
intron-5UTRENST00000551604ENST00000361948CUX2chr12

111472044

+IFT81chr12

110565165

+
intron-5UTRENST00000551604ENST00000361948CUX2chr12

111472044

+IFT81chr12

110565164

+
intron-5UTRENST00000551604ENST00000552912CUX2chr12

111472044

+IFT81chr12

110565165

+
intron-5UTRENST00000551604ENST00000552912CUX2chr12

111472044

+IFT81chr12

110565164

+
intron-intronENST00000551604ENST00000549009CUX2chr12

111472044

+IFT81chr12

110565165

+
intron-intronENST00000551604ENST00000549009CUX2chr12

111472044

+IFT81chr12

110565164

+

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 CUX2-IFT81


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)
CUX2chr12111472044+IFT81chr12110565164+0.0001323140.9998677
CUX2chr12111472044+IFT81chr12110565164+0.0001323140.9998677
CUX2chr12111472044+IFT81chr12110565164+0.0001323140.9998677
CUX2chr12111472044+IFT81chr12110565164+0.0001323140.9998677

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.
genomic feature of top 1%

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Fusion Protein Features for CUX2-IFT81


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/:111472044/:110565165)
- 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
CUX2

O14529

IFT81

Q8WYA0

FUNCTION: Transcription factor involved in the control of neuronal proliferation and differentiation in the brain. Regulates dendrite development and branching, dendritic spine formation, and synaptogenesis in cortical layers II-III. Binds to DNA in a sequence-specific manner. {ECO:0000250|UniProtKB:P70298}.FUNCTION: Component of the intraflagellar transport (IFT) complex B: together with IFT74, forms a tubulin-binding module that specifically mediates transport of tubulin within the cilium. Binds tubulin via its CH (calponin-homology)-like region (PubMed:23990561). Required for ciliogenesis (PubMed:27666822, PubMed:23990561). Required for proper regulation of SHH signaling (PubMed:27666822). {ECO:0000269|PubMed:23990561, ECO:0000269|PubMed:27666822}.

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 CUX2-IFT81


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 CUX2-IFT81


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 CUX2-IFT81


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 CUX2-IFT81


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource