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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:ATP6V1C1-EYA1 (FusionGDB2 ID:8155)

Fusion Gene Summary for ATP6V1C1-EYA1

check button Fusion gene summary
Fusion gene informationFusion gene name: ATP6V1C1-EYA1
Fusion gene ID: 8155
HgeneTgene
Gene symbol

ATP6V1C1

EYA1

Gene ID

528

2138

Gene nameATPase H+ transporting V1 subunit C1EYA transcriptional coactivator and phosphatase 1
SynonymsATP6C|ATP6D|VATC|Vma5BOP|BOR|BOS1|OFC1
Cytomap

8q22.3

8q13.3

Type of geneprotein-codingprotein-coding
DescriptionV-type proton ATPase subunit C 1ATPase, H+ transporting, lysosomal 42kDa, V1 subunit C1H(+)-transporting two-sector ATPase, subunit CH+ -ATPase C subunitH+-transporting ATPase chain C, vacuolarV-ATPase C subunitV-ATPase subunit C 1subunit C of vacueyes absent homolog 1
Modification date2020031320200313
UniProtAcc

P21283

Q99502

Ensembl transtripts involved in fusion geneENST00000518738, ENST00000521514, 
ENST00000395862, ENST00000518857, 
ENST00000303824, ENST00000340726, 
ENST00000388740, ENST00000388741, 
ENST00000388742, ENST00000388743, 
ENST00000419131, 
Fusion gene scores* DoF score9 X 7 X 6=3783 X 4 X 2=24
# samples 115
** MAII scorelog2(11/378*10)=-1.78088271069641
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/24*10)=1.05889368905357
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: ATP6V1C1 [Title/Abstract] AND EYA1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointATP6V1C1(104033453)-EYA1(72268746), # samples:2
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
TgeneEYA1

GO:0010212

response to ionizing radiation

19234442

TgeneEYA1

GO:0016576

histone dephosphorylation

19234442


check buttonFusion gene breakpoints across ATP6V1C1 (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 EYA1 (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-BH-A0B1-01AATP6V1C1chr8

104033453

+EYA1chr8

72268746

-


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Fusion Gene ORF analysis for ATP6V1C1-EYA1

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-5UTRENST00000518738ENST00000303824ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000518738ENST00000340726ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000518738ENST00000388740ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000518738ENST00000388741ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000518738ENST00000388742ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000518738ENST00000388743ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000521514ENST00000303824ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000521514ENST00000340726ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000521514ENST00000388740ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000521514ENST00000388741ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000521514ENST00000388742ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-5UTRENST00000521514ENST00000388743ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-intronENST00000518738ENST00000419131ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
5UTR-intronENST00000521514ENST00000419131ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000395862ENST00000303824ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000395862ENST00000340726ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000395862ENST00000388740ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000395862ENST00000388741ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000395862ENST00000388742ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000395862ENST00000388743ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000518857ENST00000303824ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000518857ENST00000340726ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000518857ENST00000388740ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000518857ENST00000388741ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000518857ENST00000388742ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-5UTRENST00000518857ENST00000388743ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-intronENST00000395862ENST00000419131ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-
intron-intronENST00000518857ENST00000419131ATP6V1C1chr8

104033453

+EYA1chr8

72268746

-

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 ATP6V1C1-EYA1


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 ATP6V1C1-EYA1


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/:104033453/:72268746)
- 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
ATP6V1C1

P21283

EYA1

Q99502

FUNCTION: Subunit of the peripheral V1 complex of vacuolar ATPase. Subunit C is necessary for the assembly of the catalytic sector of the enzyme and is likely to have a specific function in its catalytic activity. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells.FUNCTION: Functions both as protein phosphatase and as transcriptional coactivator for SIX1, and probably also for SIX2, SIX4 and SIX5 (By similarity). Tyrosine phosphatase that dephosphorylates 'Tyr-142' of histone H2AX (H2AXY142ph) and promotes efficient DNA repair via the recruitment of DNA repair complexes containing MDC1. 'Tyr-142' phosphorylation of histone H2AX plays a central role in DNA repair and acts as a mark that distinguishes between apoptotic and repair responses to genotoxic stress (PubMed:19234442). Its function as histone phosphatase may contribute to its function in transcription regulation during organogenesis (By similarity). Has also phosphatase activity with proteins phosphorylated on Ser and Thr residues (in vitro) (By similarity). Required for normal embryonic development of the craniofacial and trunk skeleton, kidneys and ears (By similarity). Together with SIX1, it plays an important role in hypaxial muscle development; in this it is functionally redundant with EYA2 (By similarity). {ECO:0000250|UniProtKB:P97767, ECO:0000269|PubMed:19234442}.

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 ATP6V1C1-EYA1


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 ATP6V1C1-EYA1


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 ATP6V1C1-EYA1


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 ATP6V1C1-EYA1


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