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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:TTLL11-NDUFA8 (FusionGDB2 ID:94494)

Fusion Gene Summary for TTLL11-NDUFA8

check button Fusion gene summary
Fusion gene informationFusion gene name: TTLL11-NDUFA8
Fusion gene ID: 94494
HgeneTgene
Gene symbol

TTLL11

NDUFA8

Gene ID

158135

4702

Gene nametubulin tyrosine ligase like 11NADH:ubiquinone oxidoreductase subunit A8
SynonymsC9orf20|bA244O19.1CI-19KD|CI-PGIV|PGIV
Cytomap

9q33.2

9q33.2

Type of geneprotein-codingprotein-coding
Descriptiontubulin polyglutamylase TTLL11tubulin tyrosine ligase like11tubulin tyrosine ligase-like family, member 11tubulin--tyrosine ligase-like protein 11NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 8, 19kDaNADH-ubiquinone oxidoreductase 19 kDa subunitNADH:ubiquinone oxidoreductase PGIV subunitcomplex I-19kDcomplex I-PGIV
Modification date2020031320200313
UniProtAcc.

P51970

Ensembl transtripts involved in fusion geneENST00000321582, ENST00000474723, 
ENST00000373776, 
ENST00000537618, 
ENST00000373768, 
Fusion gene scores* DoF score8 X 8 X 6=3848 X 5 X 6=240
# samples 99
** MAII scorelog2(9/384*10)=-2.09310940439148
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/240*10)=-1.41503749927884
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TTLL11 [Title/Abstract] AND NDUFA8 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNDUFA8(124910391)-TTLL11(124801647), # samples:1
TTLL11(124801551)-NDUFA8(124910556), # samples:2
Anticipated loss of major functional domain due to fusion event.TTLL11-NDUFA8 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 TTLL11 (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 NDUFA8 (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
ChimerDB4HNSCTCGA-BB-4227-01ATTLL11chr9

124801551

-NDUFA8chr9

124910556

-
ChimerDB4HNSCTCGA-BB-4227TTLL11chr9

124801551

-NDUFA8chr9

124910556

-
ChimerDB4HNSCTCGA-BB-4227-01ATTLL11chr9

124794002

-NDUFA8chr9

124910556

-


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Fusion Gene ORF analysis for TTLL11-NDUFA8

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-shiftENST00000321582ENST00000537618TTLL11chr9

124801551

-NDUFA8chr9

124910556

-
Frame-shiftENST00000321582ENST00000373768TTLL11chr9

124801551

-NDUFA8chr9

124910556

-
5UTR-3CDSENST00000474723ENST00000537618TTLL11chr9

124801551

-NDUFA8chr9

124910556

-
5UTR-3CDSENST00000474723ENST00000373768TTLL11chr9

124801551

-NDUFA8chr9

124910556

-
Frame-shiftENST00000373776ENST00000537618TTLL11chr9

124801551

-NDUFA8chr9

124910556

-
Frame-shiftENST00000373776ENST00000373768TTLL11chr9

124801551

-NDUFA8chr9

124910556

-
Frame-shiftENST00000321582ENST00000537618TTLL11chr9

124794002

-NDUFA8chr9

124910556

-
Frame-shiftENST00000321582ENST00000373768TTLL11chr9

124794002

-NDUFA8chr9

124910556

-
intron-3CDSENST00000474723ENST00000537618TTLL11chr9

124794002

-NDUFA8chr9

124910556

-
intron-3CDSENST00000474723ENST00000373768TTLL11chr9

124794002

-NDUFA8chr9

124910556

-
Frame-shiftENST00000373776ENST00000537618TTLL11chr9

124794002

-NDUFA8chr9

124910556

-
Frame-shiftENST00000373776ENST00000373768TTLL11chr9

124794002

-NDUFA8chr9

124910556

-

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 TTLL11-NDUFA8


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 TTLL11-NDUFA8


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.NDUFA8

P51970

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. {ECO:0000269|PubMed:27626371}.

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 TTLL11-NDUFA8


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 TTLL11-NDUFA8


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 TTLL11-NDUFA8


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneNDUFA8P51970DB00157NADHSmall moleculeApproved|Nutraceutical

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Related Diseases for TTLL11-NDUFA8


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneNDUFA8C0751651Mitochondrial Diseases1GENOMICS_ENGLAND