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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:EXOSC8-NDUFS1 (FusionGDB2 ID:27994)

Fusion Gene Summary for EXOSC8-NDUFS1

check button Fusion gene summary
Fusion gene informationFusion gene name: EXOSC8-NDUFS1
Fusion gene ID: 27994
HgeneTgene
Gene symbol

EXOSC8

NDUFS1

Gene ID

11340

4719

Gene nameexosome component 8NADH:ubiquinone oxidoreductase core subunit S1
SynonymsCIP3|EAP2|OIP2|PCH1C|RRP43|Rrp43p|bA421P11.3|p9CI-75Kd|CI-75k|MC1DN5|PRO1304
Cytomap

13q13.3

2q33.3

Type of geneprotein-codingprotein-coding
Descriptionexosome complex component RRP43CBP-interacting protein 3OIP-2Opa interacting protein 2exosome complex exonuclease RRP43ribosomal RNA-processing protein 43NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrialNADH dehydrogenase (ubiquinone) Fe-S protein 1, 75kDa (NADH-coenzyme Q reductase)complex I 75kDa subunitcomplex I, mitochondrial respiratory chain, 75-kD subunitmitochondrial NADH-ubiquinone
Modification date2020031320200313
UniProtAcc

Q96B26

P28331

Ensembl transtripts involved in fusion geneENST00000389704, ENST00000489088, 
ENST00000233190, ENST00000423725, 
ENST00000432169, ENST00000440274, 
ENST00000449699, ENST00000455934, 
ENST00000457011, 
Fusion gene scores* DoF score1 X 1 X 1=17 X 7 X 6=294
# samples 17
** MAII scorelog2(1/1*10)=3.32192809488736log2(7/294*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: EXOSC8 [Title/Abstract] AND NDUFS1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointEXOSC8(37574959)-NDUFS1(206997829), # samples:1
Anticipated loss of major functional domain due to fusion event.EXOSC8-NDUFS1 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
EXOSC8-NDUFS1 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
EXOSC8-NDUFS1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
EXOSC8-NDUFS1 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
TgeneNDUFS1

GO:0008637

apoptotic mitochondrial changes

15186778


check buttonFusion gene breakpoints across EXOSC8 (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 NDUFS1 (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
ChimerDB4BRCATCGA-C8-A1HEEXOSC8chr13

37574959

+NDUFS1chr2

206997829

-


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Fusion Gene ORF analysis for EXOSC8-NDUFS1

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
Frame-shiftENST00000389704ENST00000233190EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
Frame-shiftENST00000389704ENST00000423725EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
Frame-shiftENST00000389704ENST00000432169EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
Frame-shiftENST00000389704ENST00000440274EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
Frame-shiftENST00000389704ENST00000449699EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
Frame-shiftENST00000389704ENST00000455934EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
Frame-shiftENST00000389704ENST00000457011EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
intron-3CDSENST00000489088ENST00000233190EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
intron-3CDSENST00000489088ENST00000423725EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
intron-3CDSENST00000489088ENST00000432169EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
intron-3CDSENST00000489088ENST00000440274EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
intron-3CDSENST00000489088ENST00000449699EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
intron-3CDSENST00000489088ENST00000455934EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-
intron-3CDSENST00000489088ENST00000457011EXOSC8chr13

37574959

+NDUFS1chr2

206997829

-

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 EXOSC8-NDUFS1


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 EXOSC8-NDUFS1


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/:37574959/:206997829)
- 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
EXOSC8

Q96B26

NDUFS1

P28331

FUNCTION: Non-catalytic component of the RNA exosome complex which has 3'->5' exoribonuclease activity and participates in a multitude of cellular RNA processing and degradation events. In the nucleus, the RNA exosome complex is involved in proper maturation of stable RNA species such as rRNA, snRNA and snoRNA, in the elimination of RNA processing by-products and non-coding 'pervasive' transcripts, such as antisense RNA species and promoter-upstream transcripts (PROMPTs), and of mRNAs with processing defects, thereby limiting or excluding their export to the cytoplasm. The RNA exosome may be involved in Ig class switch recombination (CSR) and/or Ig variable region somatic hypermutation (SHM) by targeting AICDA deamination activity to transcribed dsDNA substrates. In the cytoplasm, the RNA exosome complex is involved in general mRNA turnover and specifically degrades inherently unstable mRNAs containing AU-rich elements (AREs) within their 3' untranslated regions, and in RNA surveillance pathways, preventing translation of aberrant mRNAs. It seems to be involved in degradation of histone mRNA. The catalytic inactive RNA exosome core complex of 9 subunits (Exo-9) is proposed to play a pivotal role in the binding and presentation of RNA for ribonucleolysis, and to serve as a scaffold for the association with catalytic subunits and accessory proteins or complexes. EXOSC8 binds to ARE-containing RNAs. {ECO:0000269|PubMed:16912217, ECO:0000269|PubMed:17545563}.FUNCTION: Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which catalyzes electron transfer from NADH through the respiratory chain, using ubiquinone as an electron acceptor (PubMed:30879903, PubMed:31557978). Essential for catalysing the entry and efficient transfer of electrons within complex I (PubMed:31557978). Plays a key role in the assembly and stability of complex I and participates in the association of complex I with ubiquinol-cytochrome reductase complex (Complex III) to form supercomplexes (PubMed:30879903, PubMed:31557978). {ECO:0000269|PubMed:30879903, ECO:0000269|PubMed:31557978}.

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 EXOSC8-NDUFS1


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 EXOSC8-NDUFS1


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 EXOSC8-NDUFS1


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 EXOSC8-NDUFS1


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