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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:ACOX3-VAMP7 (FusionGDB2 ID:1533)

Fusion Gene Summary for ACOX3-VAMP7

check button Fusion gene summary
Fusion gene informationFusion gene name: ACOX3-VAMP7
Fusion gene ID: 1533
HgeneTgene
Gene symbol

ACOX3

VAMP7

Gene ID

8310

6845

Gene nameacyl-CoA oxidase 3, pristanoylvesicle associated membrane protein 7
Synonyms-SYBL1|TI-VAMP|TIVAMP|VAMP-7
Cytomap

4p16.1

Xq28 and Yq12

Type of geneprotein-codingprotein-coding
Descriptionperoxisomal acyl-coenzyme A oxidase 3BRCACoxacyl-Coenzyme A oxidase 3, pristanoylbranched-chain acyl-CoA oxidasepristanoyl-CoA oxidasevesicle-associated membrane protein 7synaptobrevin-like 1synaptobrevin-like protein 1tetanus neurotoxin-insensitive VAMPtetanus-insensitive VAMP
Modification date2020031320200313
UniProtAcc

O15254

.
Ensembl transtripts involved in fusion geneENST00000356406, ENST00000413009, 
ENST00000503233, ENST00000515797, 
ENST00000286448, ENST00000479687, 
ENST00000262640, ENST00000460621, 
Fusion gene scores* DoF score7 X 7 X 3=14710 X 10 X 5=500
# samples 711
** MAII scorelog2(7/147*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/500*10)=-2.18442457113743
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ACOX3 [Title/Abstract] AND VAMP7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointACOX3(8430078)-VAMP7(59272371), # 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
TgeneVAMP7

GO:0006906

vesicle fusion

10888671

TgeneVAMP7

GO:0008333

endosome to lysosome transport

10888671

TgeneVAMP7

GO:0016192

vesicle-mediated transport

10888671


check buttonFusion gene breakpoints across ACOX3 (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 VAMP7 (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
ChimerDB4BLCATCGA-DK-A3IS-01AACOX3chr4

8430078

-VAMP7chrY

59272371

+


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Fusion Gene ORF analysis for ACOX3-VAMP7

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
intron-3CDSENST00000356406ENST00000286448ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3UTRENST00000356406ENST00000479687ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3UTRENST00000356406ENST00000262640ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3UTRENST00000356406ENST00000460621ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3CDSENST00000413009ENST00000286448ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3UTRENST00000413009ENST00000479687ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3UTRENST00000413009ENST00000262640ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3UTRENST00000413009ENST00000460621ACOX3chr4

8430078

-VAMP7chrY

59272371

+
5UTR-3CDSENST00000503233ENST00000286448ACOX3chr4

8430078

-VAMP7chrY

59272371

+
5UTR-3UTRENST00000503233ENST00000479687ACOX3chr4

8430078

-VAMP7chrY

59272371

+
5UTR-3UTRENST00000503233ENST00000262640ACOX3chr4

8430078

-VAMP7chrY

59272371

+
5UTR-3UTRENST00000503233ENST00000460621ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3CDSENST00000515797ENST00000286448ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3UTRENST00000515797ENST00000479687ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3UTRENST00000515797ENST00000262640ACOX3chr4

8430078

-VAMP7chrY

59272371

+
intron-3UTRENST00000515797ENST00000460621ACOX3chr4

8430078

-VAMP7chrY

59272371

+

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 ACOX3-VAMP7


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)
ACOX3chr48430077-VAMP7chrY59272370+0.070871530.9291284
ACOX3chr48430077-VAMP7chrY59272370+0.070871530.9291284

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 ACOX3-VAMP7


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
ACOX3

O15254

.
FUNCTION: Oxidizes the CoA-esters of 2-methyl-branched fatty acids. {ECO:0000250|UniProtKB:Q63448}.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 ACOX3-VAMP7


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 ACOX3-VAMP7


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 ACOX3-VAMP7


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 ACOX3-VAMP7


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneACOX3C0019193Hepatitis, Toxic1CTD_human
HgeneACOX3C0860207Drug-Induced Liver Disease1CTD_human
HgeneACOX3C1262760Hepatitis, Drug-Induced1CTD_human
HgeneACOX3C3658290Drug-Induced Acute Liver Injury1CTD_human
HgeneACOX3C4277682Chemical and Drug Induced Liver Injury1CTD_human
HgeneACOX3C4279912Chemically-Induced Liver Toxicity1CTD_human
TgeneVAMP7C0343641Human papilloma virus infection1CTD_human
TgeneVAMP7C1168401Squamous cell carcinoma of the head and neck1CTD_human
TgeneVAMP7C451074446,XY partial gonadal dysgenesis1ORPHANET