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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:FBXW9-TRMT1 (FusionGDB2 ID:29938)

Fusion Gene Summary for FBXW9-TRMT1

check button Fusion gene summary
Fusion gene informationFusion gene name: FBXW9-TRMT1
Fusion gene ID: 29938
HgeneTgene
Gene symbol

FBXW9

TRMT1

Gene ID

84261

55687

Gene nameF-box and WD repeat domain containing 9tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase
SynonymsFbw9|MEC-15LCAL3|MTO2|MTU1|TRMT|TRMT1
Cytomap

19p13.13

22q13.31

Type of geneprotein-codingprotein-coding
DescriptionF-box/WD repeat-containing protein 9F-box and WD-40 domain protein 9F-box and WD-40 domain-containing protein 9F-box and WD-40 repeat containing protein 9specificity factor for SCF ubiquitin ligasemitochondrial tRNA-specific 2-thiouridylase 1MTO2 homologlung cancer associated lncRNA 3mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase
Modification date2020031320200313
UniProtAcc

Q5XUX1

TRMT1L

Ensembl transtripts involved in fusion geneENST00000380339, ENST00000393261, 
ENST00000544494, ENST00000587955, 
ENST00000592892, ENST00000221504, 
ENST00000357720, ENST00000437766, 
ENST00000592062, 
Fusion gene scores* DoF score2 X 3 X 2=124 X 5 X 4=80
# samples 35
** MAII scorelog2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FBXW9 [Title/Abstract] AND TRMT1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFBXW9(12801979)-TRMT1(13218673), # samples:1
Anticipated loss of major functional domain due to fusion event.FBXW9-TRMT1 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

check buttonFusion gene breakpoints across FBXW9 (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 TRMT1 (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
ChimerDB4ESCATCGA-Z6-A8JDFBXW9chr19

12801979

-TRMT1chr19

13218673

-


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Fusion Gene ORF analysis for FBXW9-TRMT1

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-intronENST00000380339ENST00000592892FBXW9chr19

12801979

-TRMT1chr19

13218673

-
5CDS-intronENST00000393261ENST00000592892FBXW9chr19

12801979

-TRMT1chr19

13218673

-
5CDS-intronENST00000544494ENST00000592892FBXW9chr19

12801979

-TRMT1chr19

13218673

-
5CDS-intronENST00000587955ENST00000592892FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000380339ENST00000221504FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000380339ENST00000357720FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000380339ENST00000437766FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000380339ENST00000592062FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000393261ENST00000221504FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000393261ENST00000357720FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000393261ENST00000437766FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000393261ENST00000592062FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000544494ENST00000221504FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000544494ENST00000357720FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000544494ENST00000437766FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000544494ENST00000592062FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000587955ENST00000221504FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000587955ENST00000357720FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000587955ENST00000437766FBXW9chr19

12801979

-TRMT1chr19

13218673

-
Frame-shiftENST00000587955ENST00000592062FBXW9chr19

12801979

-TRMT1chr19

13218673

-

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 FBXW9-TRMT1


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 FBXW9-TRMT1


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/:12801979/:13218673)
- 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
FBXW9

Q5XUX1

TRMT1

TRMT1L

FUNCTION: Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex. {ECO:0000250}.733

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 FBXW9-TRMT1


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 FBXW9-TRMT1


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 FBXW9-TRMT1


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 FBXW9-TRMT1


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