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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:TMEM91-DTX4 (FusionGDB2 ID:92266)

Fusion Gene Summary for TMEM91-DTX4

check button Fusion gene summary
Fusion gene informationFusion gene name: TMEM91-DTX4
Fusion gene ID: 92266
HgeneTgene
Gene symbol

TMEM91

DTX4

Gene ID

641649

23220

Gene nametransmembrane protein 91deltex E3 ubiquitin ligase 4
SynonymsDSPC3|IFITMD6RNF155
Cytomap

19q13.2

11q12.1

Type of geneprotein-codingprotein-coding
Descriptiontransmembrane protein 91dispanin subfamily C member 3interferon induced transmembrane protein domain containing 6E3 ubiquitin-protein ligase DTX4RING finger protein 155RING-type E3 ubiquitin transferase DTX4deltex 4 homologdeltex 4, E3 ubiquitin ligasedeltex homolog 4deltex4protein deltex-4
Modification date2020031320200313
UniProtAcc.

Q9Y2E6

Ensembl transtripts involved in fusion geneENST00000413014, ENST00000356385, 
ENST00000392002, ENST00000436170, 
ENST00000447302, ENST00000539627, 
ENST00000542945, ENST00000544232, 
ENST00000604123, 
ENST00000227451, 
ENST00000532982, ENST00000531902, 
Fusion gene scores* DoF score5 X 5 X 3=754 X 4 X 3=48
# samples 55
** MAII scorelog2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/48*10)=0.0588936890535686
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TMEM91 [Title/Abstract] AND DTX4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTMEM91(41870001)-DTX4(58962681), # samples:1
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

check buttonFusion gene breakpoints across TMEM91 (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 DTX4 (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
ChiTaRS5.0N/ABM922123TMEM91chr19

41870001

+DTX4chr11

58962681

+


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Fusion Gene ORF analysis for TMEM91-DTX4

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
5UTR-3CDSENST00000413014ENST00000227451TMEM91chr19

41870001

+DTX4chr11

58962681

+
5UTR-3CDSENST00000413014ENST00000532982TMEM91chr19

41870001

+DTX4chr11

58962681

+
5UTR-intronENST00000413014ENST00000531902TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000356385ENST00000227451TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000356385ENST00000532982TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000392002ENST00000227451TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000392002ENST00000532982TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000436170ENST00000227451TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000436170ENST00000532982TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000447302ENST00000227451TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000447302ENST00000532982TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000539627ENST00000227451TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000539627ENST00000532982TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000542945ENST00000227451TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000542945ENST00000532982TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000544232ENST00000227451TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000544232ENST00000532982TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000604123ENST00000227451TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-3CDSENST00000604123ENST00000532982TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-intronENST00000356385ENST00000531902TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-intronENST00000392002ENST00000531902TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-intronENST00000436170ENST00000531902TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-intronENST00000447302ENST00000531902TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-intronENST00000539627ENST00000531902TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-intronENST00000542945ENST00000531902TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-intronENST00000544232ENST00000531902TMEM91chr19

41870001

+DTX4chr11

58962681

+
intron-intronENST00000604123ENST00000531902TMEM91chr19

41870001

+DTX4chr11

58962681

+

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 TMEM91-DTX4


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)
TMEM91chr1941870000+DTX4chr1158962680+0.0857864540.9142136
TMEM91chr1941870000+DTX4chr1158962680+0.0857864540.9142136

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 TMEM91-DTX4


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/:41870001/:58962681)
- 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
.DTX4

Q9Y2E6

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: Regulator of Notch signaling, a signaling pathway involved in cell-cell communications that regulates a broad spectrum of cell-fate determinations (By similarity). Functions as a ubiquitin ligase protein in vivo, mediating 'Lys48'-linked polyubiquitination and promoting degradation of TBK1, targeting to TBK1 requires interaction with NLRP4. {ECO:0000250, ECO:0000269|PubMed:22388039}.

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 TMEM91-DTX4


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 TMEM91-DTX4


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 TMEM91-DTX4


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 TMEM91-DTX4


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