FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:ATF7IP-ATP6V0E1 (FusionGDB2 ID:7479)

Fusion Gene Summary for ATF7IP-ATP6V0E1

check button Fusion gene summary
Fusion gene informationFusion gene name: ATF7IP-ATP6V0E1
Fusion gene ID: 7479
HgeneTgene
Gene symbol

ATF7IP

ATP6V0E1

Gene ID

55729

8992

Gene nameactivating transcription factor 7 interacting proteinATPase H+ transporting V0 subunit e1
SynonymsAM|ATF-IP|MCAF|MCAF1|p621ATP6H|ATP6V0E|M9.2|Vma21|Vma21p
Cytomap

12p13.1

5q35.1

Type of geneprotein-codingprotein-coding
Descriptionactivating transcription factor 7-interacting protein 1ATF-interacting proteinATF7-interacting proteinATFa-associated modulatorMBD1-containing chromatin-associated factor 1V-type proton ATPase subunit e 1ATPase, H+ transporting, lysosomal 9kDa, V0 subunit e1H(+)-transporting two-sector ATPase, subunit HV-ATPase 9.2 kDa membrane accessory proteinV-ATPase H subunitV-ATPase M9.2 subunitV-ATPase subunit e 1vacuolar ATP s
Modification date2020031320200313
UniProtAcc

Q6VMQ6

O15342

Ensembl transtripts involved in fusion geneENST00000541654, ENST00000261168, 
ENST00000536444, ENST00000540793, 
ENST00000543189, ENST00000544627, 
ENST00000265093, ENST00000517669, 
ENST00000519374, ENST00000519911, 
Fusion gene scores* DoF score16 X 15 X 8=192014 X 14 X 4=784
# samples 2015
** MAII scorelog2(20/1920*10)=-3.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/784*10)=-2.38589115361933
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ATF7IP [Title/Abstract] AND ATP6V0E1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointATF7IP(14577454)-ATP6V0E1(172449335), # 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
HgeneATF7IP

GO:0006306

DNA methylation

12665582

HgeneATF7IP

GO:0045892

negative regulation of transcription, DNA-templated

12665582

HgeneATF7IP

GO:0045893

positive regulation of transcription, DNA-templated

12665582

HgeneATF7IP

GO:0045898

regulation of RNA polymerase II transcriptional preinitiation complex assembly

12665582


check buttonFusion gene breakpoints across ATF7IP (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 ATP6V0E1 (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
ChiTaRS5.0N/ABE077232ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-


Top

Fusion Gene ORF analysis for ATF7IP-ATP6V0E1

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
3UTR-intronENST00000541654ENST00000265093ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
3UTR-intronENST00000541654ENST00000517669ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
3UTR-intronENST00000541654ENST00000519374ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
3UTR-intronENST00000541654ENST00000519911ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000261168ENST00000265093ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000261168ENST00000517669ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000261168ENST00000519374ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000261168ENST00000519911ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000536444ENST00000265093ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000536444ENST00000517669ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000536444ENST00000519374ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000536444ENST00000519911ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000540793ENST00000265093ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000540793ENST00000517669ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000540793ENST00000519374ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000540793ENST00000519911ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000543189ENST00000265093ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000543189ENST00000517669ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000543189ENST00000519374ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000543189ENST00000519911ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000544627ENST00000265093ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000544627ENST00000517669ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000544627ENST00000519374ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-
5CDS-intronENST00000544627ENST00000519911ATF7IPchr12

14577454

-ATP6V0E1chr5

172449335

-

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

Top

Fusion Genomic Features for ATF7IP-ATP6V0E1


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.

Top

Fusion Protein Features for ATF7IP-ATP6V0E1


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/:14577454/:172449335)
- 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
ATF7IP

Q6VMQ6

ATP6V0E1

O15342

FUNCTION: Recruiter that couples transcriptional factors to general transcription apparatus and thereby modulates transcription regulation and chromatin formation. Can both act as an activator or a repressor depending on the context. Required for HUSH-mediated heterochromatin formation and gene silencing (PubMed:27732843). Mediates MBD1-dependent transcriptional repression, probably by recruiting complexes containing SETDB1 (PubMed:12665582). Stabilizes SETDB1, is required to stimulate histone methyltransferase activity of SETDB1 and facilitates the conversion of dimethylated to trimethylated H3 'Lys-9' (H3K9me3). The complex formed with MBD1 and SETDB1 represses transcription and couples DNA methylation and histone H3 'Lys-9' trimethylation (H3K9me3) (PubMed:14536086, PubMed:27732843). Facilitates telomerase TERT and TERC gene expression by SP1 in cancer cells (PubMed:19106100). {ECO:0000269|PubMed:12665582, ECO:0000269|PubMed:14536086, ECO:0000269|PubMed:19106100, ECO:0000269|PubMed:27732843}.FUNCTION: Vacuolar ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells.

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


Top

Fusion Gene Sequence for ATF7IP-ATP6V0E1


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.

Top

Fusion Gene PPI Analysis for ATF7IP-ATP6V0E1


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


Top

Related Drugs for ATF7IP-ATP6V0E1


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

Top

Related Diseases for ATF7IP-ATP6V0E1


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