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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:VPS29-MGME1 (FusionGDB2 ID:97695)

Fusion Gene Summary for VPS29-MGME1

check button Fusion gene summary
Fusion gene informationFusion gene name: VPS29-MGME1
Fusion gene ID: 97695
HgeneTgene
Gene symbol

VPS29

MGME1

Gene ID

51699

92667

Gene nameVPS29 retromer complex componentmitochondrial genome maintenance exonuclease 1
SynonymsDC15|DC7|PEP11C20orf72|DDK1|MTDPS11|bA504H3.4
Cytomap

12q24.11

20p11.23

Type of geneprotein-codingprotein-coding
Descriptionvacuolar protein sorting-associated protein 29PEP11 homologepididymis secretory sperm binding proteinhVPS29retromer proteinvacuolar protein sorting 29 homologvacuolar sorting protein VPS29/PEP11vesicle protein sorting 29x 007 proteinmitochondrial genome maintenance exonuclease 1
Modification date2020031320200313
UniProtAcc.

Q9BQP7

Ensembl transtripts involved in fusion geneENST00000549578, ENST00000360579, 
ENST00000552130, ENST00000447578, 
ENST00000546588, ENST00000549970, 
ENST00000551655, 
ENST00000377710, 
ENST00000377709, ENST00000377704, 
ENST00000467391, 
Fusion gene scores* DoF score15 X 13 X 9=17556 X 5 X 4=120
# samples 197
** MAII scorelog2(19/1755*10)=-3.20739970686098
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/120*10)=-0.777607578663552
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: VPS29 [Title/Abstract] AND MGME1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointVPS29(110939854)-MGME1(17968809), # samples:1
Anticipated loss of major functional domain due to fusion event.VPS29-MGME1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
* 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 VPS29 (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 MGME1 (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
ChimerDB4LUSCTCGA-68-A59I-01AVPS29chr12

110939854

-MGME1chr20

17968809

+


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Fusion Gene ORF analysis for VPS29-MGME1

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
Frame-shiftENST00000549578ENST00000377710VPS29chr12

110939854

-MGME1chr20

17968809

+
Frame-shiftENST00000549578ENST00000377709VPS29chr12

110939854

-MGME1chr20

17968809

+
5CDS-intronENST00000549578ENST00000377704VPS29chr12

110939854

-MGME1chr20

17968809

+
5CDS-3UTRENST00000549578ENST00000467391VPS29chr12

110939854

-MGME1chr20

17968809

+
Frame-shiftENST00000360579ENST00000377710VPS29chr12

110939854

-MGME1chr20

17968809

+
Frame-shiftENST00000360579ENST00000377709VPS29chr12

110939854

-MGME1chr20

17968809

+
5CDS-intronENST00000360579ENST00000377704VPS29chr12

110939854

-MGME1chr20

17968809

+
5CDS-3UTRENST00000360579ENST00000467391VPS29chr12

110939854

-MGME1chr20

17968809

+
intron-3CDSENST00000552130ENST00000377710VPS29chr12

110939854

-MGME1chr20

17968809

+
intron-3CDSENST00000552130ENST00000377709VPS29chr12

110939854

-MGME1chr20

17968809

+
intron-intronENST00000552130ENST00000377704VPS29chr12

110939854

-MGME1chr20

17968809

+
intron-3UTRENST00000552130ENST00000467391VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3CDSENST00000447578ENST00000377710VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3CDSENST00000447578ENST00000377709VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-intronENST00000447578ENST00000377704VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3UTRENST00000447578ENST00000467391VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3CDSENST00000546588ENST00000377710VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3CDSENST00000546588ENST00000377709VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-intronENST00000546588ENST00000377704VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3UTRENST00000546588ENST00000467391VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3CDSENST00000549970ENST00000377710VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3CDSENST00000549970ENST00000377709VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-intronENST00000549970ENST00000377704VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3UTRENST00000549970ENST00000467391VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3CDSENST00000551655ENST00000377710VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3CDSENST00000551655ENST00000377709VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-intronENST00000551655ENST00000377704VPS29chr12

110939854

-MGME1chr20

17968809

+
5UTR-3UTRENST00000551655ENST00000467391VPS29chr12

110939854

-MGME1chr20

17968809

+

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 VPS29-MGME1


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)
VPS29chr12110939853-MGME1chr2017968808+0.0032982040.9967018
VPS29chr12110939853-MGME1chr2017968808+0.0032982040.9967018

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 VPS29-MGME1


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
.MGME1

Q9BQP7

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.FUNCTION: Metal-dependent single-stranded DNA (ssDNA) exonuclease involved in mitochondrial genome maintenance. Has preference for 5'-3' exonuclease activity but is also capable of endoduclease activity on linear substrates. Necessary for maintenance of proper 7S DNA levels. Probably involved in mitochondrial DNA (mtDNA) repair, possibly via the processing of displaced DNA containing Okazaki fragments during RNA-primed DNA synthesis on the lagging strand or via processing of DNA flaps during long-patch base excision repair. Specifically binds 5-hydroxymethylcytosine (5hmC)-containing DNA in stem cells. {ECO:0000255|HAMAP-Rule:MF_03030, ECO:0000269|PubMed:23313956, ECO:0000269|PubMed:23358826}.

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 VPS29-MGME1


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 VPS29-MGME1


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 VPS29-MGME1


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 VPS29-MGME1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMGME1C0013911Emaciation1CTD_human
TgeneMGME1C0029089Ophthalmoplegia1CTD_human
TgeneMGME1C0035229Respiratory Insufficiency1CTD_human
TgeneMGME1C0162292External Ophthalmoplegia1CTD_human
TgeneMGME1C0235063Respiratory Depression1CTD_human
TgeneMGME1C0339693Internal Ophthalmoplegia1CTD_human
TgeneMGME1C0751401Ophthalmoparesis1CTD_human
TgeneMGME1C0751651Mitochondrial Diseases1CTD_human
TgeneMGME1C0949855Electron Transport Chain Deficiencies, Mitochondrial1CTD_human
TgeneMGME1C0949856Oxidative Phosphorylation Deficiencies1CTD_human
TgeneMGME1C0949857Mitochondrial Respiratory Chain Deficiencies1CTD_human
TgeneMGME1C1145670Respiratory Failure1CTD_human
TgeneMGME1C3554462MITOCHONDRIAL DNA DEPLETION SYNDROME 111CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT