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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:VPS35-SLC6A2 (FusionGDB2 ID:98391)

Fusion Gene Summary for VPS35-SLC6A2

check button Fusion gene summary
Fusion gene informationFusion gene name: VPS35-SLC6A2
Fusion gene ID: 98391
HgeneTgene
Gene symbol

VPS35

SLC6A2

Gene ID

55737

6530

Gene nameVPS35 retromer complex componentsolute carrier family 6 member 2
SynonymsMEM3|PARK17NAT1|NET|NET1|SLC6A5
Cytomap

16q11.2

16q12.2

Type of geneprotein-codingprotein-coding
Descriptionvacuolar protein sorting-associated protein 35hVPS35maternal-embryonic 3vacuolar protein sorting 35 homologsodium-dependent noradrenaline transporterneurotransmitter transporternorepinephrine transportersolute carrier family 6 (neurotransmitter transporter), member 2solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2solute carri
Modification date2020031320200315
UniProtAcc

VPS35L

P23975

Ensembl transtripts involved in fusion geneENST00000299138, ENST00000568642, 
ENST00000219833, ENST00000379906, 
ENST00000414754, ENST00000561820, 
ENST00000568943, ENST00000566163, 
ENST00000567238, 
Fusion gene scores* DoF score6 X 7 X 4=1683 X 3 X 2=18
# samples 83
** MAII scorelog2(8/168*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: VPS35 [Title/Abstract] AND SLC6A2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointVPS35(46702842)-SLC6A2(55690556), # samples:3
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
HgeneVPS35

GO:0010628

positive regulation of gene expression

26618722

HgeneVPS35

GO:0032268

regulation of cellular protein metabolic process

26618722

HgeneVPS35

GO:0045056

transcytosis

15247922

HgeneVPS35

GO:0060161

positive regulation of dopamine receptor signaling pathway

27460146

HgeneVPS35

GO:0099639

neurotransmitter receptor transport, endosome to plasma membrane

27460146

TgeneSLC6A2

GO:0015844

monoamine transport

16024787


check buttonFusion gene breakpoints across VPS35 (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 SLC6A2 (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-E2-A109-01AVPS35chr16

46702842

-SLC6A2chr16

55690556

+


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Fusion Gene ORF analysis for VPS35-SLC6A2

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
5CDS-5UTRENST00000299138ENST00000219833VPS35chr16

46702842

-SLC6A2chr16

55690556

+
5CDS-5UTRENST00000299138ENST00000379906VPS35chr16

46702842

-SLC6A2chr16

55690556

+
5CDS-5UTRENST00000299138ENST00000414754VPS35chr16

46702842

-SLC6A2chr16

55690556

+
5CDS-5UTRENST00000299138ENST00000561820VPS35chr16

46702842

-SLC6A2chr16

55690556

+
5CDS-5UTRENST00000299138ENST00000568943VPS35chr16

46702842

-SLC6A2chr16

55690556

+
5CDS-intronENST00000299138ENST00000566163VPS35chr16

46702842

-SLC6A2chr16

55690556

+
5CDS-intronENST00000299138ENST00000567238VPS35chr16

46702842

-SLC6A2chr16

55690556

+
intron-5UTRENST00000568642ENST00000219833VPS35chr16

46702842

-SLC6A2chr16

55690556

+
intron-5UTRENST00000568642ENST00000379906VPS35chr16

46702842

-SLC6A2chr16

55690556

+
intron-5UTRENST00000568642ENST00000414754VPS35chr16

46702842

-SLC6A2chr16

55690556

+
intron-5UTRENST00000568642ENST00000561820VPS35chr16

46702842

-SLC6A2chr16

55690556

+
intron-5UTRENST00000568642ENST00000568943VPS35chr16

46702842

-SLC6A2chr16

55690556

+
intron-intronENST00000568642ENST00000566163VPS35chr16

46702842

-SLC6A2chr16

55690556

+
intron-intronENST00000568642ENST00000567238VPS35chr16

46702842

-SLC6A2chr16

55690556

+

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 VPS35-SLC6A2


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)
VPS35chr1646702841-SLC6A2chr1655690555+0.0001921630.9998079
VPS35chr1646702841-SLC6A2chr1655690555+0.0001921630.9998079

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 VPS35-SLC6A2


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/:46702842/:55690556)
- 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
VPS35

VPS35L

SLC6A2

P23975

963FUNCTION: Amine transporter. Terminates the action of noradrenaline by its high affinity sodium-dependent reuptake into presynaptic terminals. {ECO:0000269|PubMed:2008212}.

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 VPS35-SLC6A2


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 VPS35-SLC6A2


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 VPS35-SLC6A2


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 VPS35-SLC6A2


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