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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:COA1-HECW1 (FusionGDB2 ID:17947)

Fusion Gene Summary for COA1-HECW1

check button Fusion gene summary
Fusion gene informationFusion gene name: COA1-HECW1
Fusion gene ID: 17947
HgeneTgene
Gene symbol

COA1

HECW1

Gene ID

55744

23072

Gene namecytochrome c oxidase assembly factor 1 homologHECT, C2 and WW domain containing E3 ubiquitin protein ligase 1
SynonymsC7orf44|MITRAC15NEDL1
Cytomap

7p13

7p14.1-p13

Type of geneprotein-codingprotein-coding
Descriptioncytochrome c oxidase assembly factor 1 homologcytochrome c oxidase assembly protein 1 homologmitochondrial translation regulation assembly intermediate of cytochrome c oxidase protein of 15 kDaE3 ubiquitin-protein ligase HECW1HECT type E3 ubiquitin ligaseHECT-type E3 ubiquitin transferase HECW1NEDD4-like ubiquitin-protein ligase 1
Modification date2020031320200313
UniProtAcc

Q9GZY4

Q76N89

Ensembl transtripts involved in fusion geneENST00000223336, ENST00000310564, 
ENST00000395880, ENST00000395879, 
ENST00000488813, 
ENST00000395891, 
ENST00000453890, ENST00000471043, 
Fusion gene scores* DoF score14 X 10 X 7=9808 X 10 X 6=480
# samples 189
** MAII scorelog2(18/980*10)=-2.4447848426729
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/480*10)=-2.41503749927884
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: COA1 [Title/Abstract] AND HECW1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCOA1(43769028)-HECW1(43580762), # samples:3
HECW1(43519343)-COA1(43649094), # 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 COA1 (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 HECW1 (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
ChimerDB4GBMTCGA-06-0210-01ACOA1chr7

43769028

-HECW1chr7

43580762

+
ChimerDB4GBMTCGA-06-0210-02ACOA1chr7

43769028

-HECW1chr7

43580762

+


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Fusion Gene ORF analysis for COA1-HECW1

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-3CDSENST00000223336ENST00000395891COA1chr7

43769028

-HECW1chr7

43580762

+
5UTR-3CDSENST00000223336ENST00000453890COA1chr7

43769028

-HECW1chr7

43580762

+
5UTR-3CDSENST00000310564ENST00000395891COA1chr7

43769028

-HECW1chr7

43580762

+
5UTR-3CDSENST00000310564ENST00000453890COA1chr7

43769028

-HECW1chr7

43580762

+
5UTR-3CDSENST00000395880ENST00000395891COA1chr7

43769028

-HECW1chr7

43580762

+
5UTR-3CDSENST00000395880ENST00000453890COA1chr7

43769028

-HECW1chr7

43580762

+
5UTR-intronENST00000223336ENST00000471043COA1chr7

43769028

-HECW1chr7

43580762

+
5UTR-intronENST00000310564ENST00000471043COA1chr7

43769028

-HECW1chr7

43580762

+
5UTR-intronENST00000395880ENST00000471043COA1chr7

43769028

-HECW1chr7

43580762

+
intron-3CDSENST00000395879ENST00000395891COA1chr7

43769028

-HECW1chr7

43580762

+
intron-3CDSENST00000395879ENST00000453890COA1chr7

43769028

-HECW1chr7

43580762

+
intron-3CDSENST00000488813ENST00000395891COA1chr7

43769028

-HECW1chr7

43580762

+
intron-3CDSENST00000488813ENST00000453890COA1chr7

43769028

-HECW1chr7

43580762

+
intron-intronENST00000395879ENST00000471043COA1chr7

43769028

-HECW1chr7

43580762

+
intron-intronENST00000488813ENST00000471043COA1chr7

43769028

-HECW1chr7

43580762

+

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 COA1-HECW1


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)
COA1chr743769027-HECW1chr743580761+3.23E-050.9999677
COA1chr743769027-HECW1chr743580761+3.23E-050.9999677
COA1chr743769027-HECW1chr743580761+3.23E-050.9999677
COA1chr743769027-HECW1chr743580761+3.23E-050.9999677

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 COA1-HECW1


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/:43769028/:43580762)
- 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
COA1

Q9GZY4

HECW1

Q76N89

FUNCTION: Component of the MITRAC (mitochondrial translation regulation assembly intermediate of cytochrome c oxidase complex) complex, that regulates cytochrome c oxidase assembly. MITRAC complexes regulate both translation of mitochondrial encoded components and assembly of nuclear-encoded components imported in mitochondrion. Required for assembly of mitochondrial respiratory chain complex I and complex IV. {ECO:0000269|PubMed:23260140}.FUNCTION: E3 ubiquitin-protein ligase that mediates ubiquitination and subsequent degradation of DVL1. Also targets the mutant SOD1 protein involved in familial amyotrophic lateral sclerosis (FALS). Forms cytotoxic aggregates with DVL1, SSR3 and mutant SOD1 that lead to motor neuron death in FALS. {ECO:0000269|PubMed:14684739}.

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 COA1-HECW1


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 COA1-HECW1


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 COA1-HECW1


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 COA1-HECW1


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