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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:COQ4-TIMP1 (FusionGDB2 ID:18703)

Fusion Gene Summary for COQ4-TIMP1

check button Fusion gene summary
Fusion gene informationFusion gene name: COQ4-TIMP1
Fusion gene ID: 18703
HgeneTgene
Gene symbol

COQ4

TIMP1

Gene ID

51117

7076

Gene namecoenzyme Q4TIMP metallopeptidase inhibitor 1
SynonymsCGI-92|COQ10D7CLGI|EPA|EPO|HCI|TIMP|TIMP-1
Cytomap

9q34.11

Xp11.3

Type of geneprotein-codingprotein-coding
Descriptionubiquinone biosynthesis protein COQ4 homolog, mitochondrialcoenzyme Q biosynthesis protein 4 homologcoenzyme Q4 homologmetalloproteinase inhibitor 1collagenase inhibitorepididymis secretory sperm binding proteinerythroid potentiating activityfibroblast collagenase inhibitortissue inhibitor of metalloproteinases 1
Modification date2020031320200315
UniProtAcc

Q9Y3A0

.
Ensembl transtripts involved in fusion geneENST00000300452, ENST00000609948, 
ENST00000608951, ENST00000372875, 
ENST00000461102, 
ENST00000218388, 
ENST00000377018, ENST00000456754, 
ENST00000377017, 
Fusion gene scores* DoF score6 X 6 X 3=1084 X 5 X 4=80
# samples 65
** MAII scorelog2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
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: COQ4 [Title/Abstract] AND TIMP1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCOQ4(131087518)-TIMP1(47445920), # samples:1
Anticipated loss of major functional domain due to fusion event.COQ4-TIMP1 seems lost the major protein functional domain in Hgene 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
TgeneTIMP1

GO:0008284

positive regulation of cell proliferation

3839290

TgeneTIMP1

GO:0010951

negative regulation of endopeptidase activity

3903517

TgeneTIMP1

GO:0043086

negative regulation of catalytic activity

3903517

TgeneTIMP1

GO:0051045

negative regulation of membrane protein ectodomain proteolysis

12714508

TgeneTIMP1

GO:1905049

negative regulation of metallopeptidase activity

9573338


check buttonFusion gene breakpoints across COQ4 (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 TIMP1 (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
ChimerDB4STADTCGA-HU-A4GN-01ACOQ4chr9

131087518

+TIMP1chrX

47445920

+


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Fusion Gene ORF analysis for COQ4-TIMP1

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-shiftENST00000300452ENST00000218388COQ4chr9

131087518

+TIMP1chrX

47445920

+
5CDS-intronENST00000300452ENST00000377018COQ4chr9

131087518

+TIMP1chrX

47445920

+
5CDS-intronENST00000300452ENST00000456754COQ4chr9

131087518

+TIMP1chrX

47445920

+
5CDS-intronENST00000300452ENST00000377017COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-3CDSENST00000609948ENST00000218388COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-intronENST00000609948ENST00000377018COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-intronENST00000609948ENST00000456754COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-intronENST00000609948ENST00000377017COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-3CDSENST00000608951ENST00000218388COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-intronENST00000608951ENST00000377018COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-intronENST00000608951ENST00000456754COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-intronENST00000608951ENST00000377017COQ4chr9

131087518

+TIMP1chrX

47445920

+
Frame-shiftENST00000372875ENST00000218388COQ4chr9

131087518

+TIMP1chrX

47445920

+
5CDS-intronENST00000372875ENST00000377018COQ4chr9

131087518

+TIMP1chrX

47445920

+
5CDS-intronENST00000372875ENST00000456754COQ4chr9

131087518

+TIMP1chrX

47445920

+
5CDS-intronENST00000372875ENST00000377017COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-3CDSENST00000461102ENST00000218388COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-intronENST00000461102ENST00000377018COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-intronENST00000461102ENST00000456754COQ4chr9

131087518

+TIMP1chrX

47445920

+
intron-intronENST00000461102ENST00000377017COQ4chr9

131087518

+TIMP1chrX

47445920

+

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 COQ4-TIMP1


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)
COQ4chr9131087518+TIMP1chrX47445919+0.85638970.14361027
COQ4chr9131087518+TIMP1chrX47445919+0.85638970.14361027

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 COQ4-TIMP1


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
COQ4

Q9Y3A0

.
FUNCTION: Component of the coenzyme Q biosynthetic pathway. May play a role in organizing a multi-subunit COQ enzyme complex required for coenzyme Q biosynthesis. Required for steady-state levels of other COQ polypeptides. {ECO:0000255|HAMAP-Rule:MF_03111, ECO:0000269|PubMed:18474229}.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.

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 COQ4-TIMP1


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 COQ4-TIMP1


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 COQ4-TIMP1


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 COQ4-TIMP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCOQ4C4225392COENZYME Q10 DEFICIENCY, PRIMARY, 74CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneTIMP1C0023893Liver Cirrhosis, Experimental5CTD_human
TgeneTIMP1C0002152Alloxan Diabetes1CTD_human
TgeneTIMP1C0003504Aortic Valve Insufficiency1CTD_human
TgeneTIMP1C0004364Autoimmune Diseases1CTD_human
TgeneTIMP1C0005398Cholestasis, Extrahepatic1CTD_human
TgeneTIMP1C0006663Calcinosis1CTD_human
TgeneTIMP1C0008311Cholangitis1CTD_human
TgeneTIMP1C0011853Diabetes Mellitus, Experimental1CTD_human
TgeneTIMP1C0011860Diabetes Mellitus, Non-Insulin-Dependent1CTD_human
TgeneTIMP1C0017661IGA Glomerulonephritis1CTD_human
TgeneTIMP1C0018799Heart Diseases1CTD_human
TgeneTIMP1C0018824Heart valve disease1CTD_human
TgeneTIMP1C0019202Hepatolenticular Degeneration1CTD_human
TgeneTIMP1C0020538Hypertensive disease1CTD_human
TgeneTIMP1C0021368Inflammation1CTD_human
TgeneTIMP1C0023891Liver Cirrhosis, Alcoholic1CTD_human
TgeneTIMP1C0027626Neoplasm Invasiveness1CTD_human
TgeneTIMP1C0029172Oral Submucous Fibrosis1CTD_human
TgeneTIMP1C0034069Pulmonary Fibrosis1CTD_human
TgeneTIMP1C0035222Respiratory Distress Syndrome, Adult1CTD_human
TgeneTIMP1C0038433Streptozotocin Diabetes1CTD_human
TgeneTIMP1C0042345Varicosity1CTD_human
TgeneTIMP1C0042373Vascular Diseases1CTD_human
TgeneTIMP1C0263628Tumoral calcinosis1CTD_human
TgeneTIMP1C0521174Microcalcification1CTD_human
TgeneTIMP1C1527352Hepatic Form of Wilson Disease1CTD_human
TgeneTIMP1C1720887Female Urogenital Diseases1CTD_human
TgeneTIMP1C4721507Alveolitis, Fibrosing1CTD_human