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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:VMP1-RAD51C

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: VMP1-RAD51C
FusionPDB ID: 98210
FusionGDB2.0 ID: 98210
HgeneTgene
Gene symbol

VMP1

RAD51C

Gene ID

81671

5889

Gene namevacuole membrane protein 1RAD51 paralog C
SynonymsEPG3|TANGO5|TMEM49BROVCA3|FANCO|R51H3|RAD51L2
Cytomap

17q23.1

17q22

Type of geneprotein-codingprotein-coding
Descriptionvacuole membrane protein 1ectopic P-granules autophagy protein 3 homologtransmembrane protein 49transport and golgi organization 5 homologDNA repair protein RAD51 homolog 3RAD51-like protein 2yeast RAD51 homolog 3
Modification date2020032720200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000262291, ENST00000536180, 
ENST00000545362, ENST00000539763, 
ENST00000537567, ENST00000588617, 
ENST00000421782, ENST00000487921, 
ENST00000337432, ENST00000583539, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score34 X 17 X 12=693612 X 11 X 4=528
# samples 3815
** MAII scorelog2(38/6936*10)=-4.19003257489089
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/528*10)=-1.81557542886257
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: VMP1 [Title/Abstract] AND RAD51C [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)VMP1(57816308)-RAD51C(56787220), # samples:1
Anticipated loss of major functional domain due to fusion event.VMP1-RAD51C seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
VMP1-RAD51C seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
VMP1-RAD51C seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
VMP1-RAD51C seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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
TgeneRAD51C

GO:0006281

DNA repair

19451272

TgeneRAD51C

GO:0006310

DNA recombination

19451272


check buttonFusion gene breakpoints across VMP1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across RAD51C (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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-A18R-01AVMP1chr17

57816308

+RAD51Cchr17

56787220

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000262291VMP1chr1757816308+ENST00000583539RAD51Cchr1756787220+12677242531059268
ENST00000262291VMP1chr1757816308+ENST00000337432RAD51Cchr1756787220+12707242531149298
ENST00000536180VMP1chr1757816308+ENST00000583539RAD51Cchr1756787220+976433310768152
ENST00000536180VMP1chr1757816308+ENST00000337432RAD51Cchr1756787220+979433310858182
ENST00000545362VMP1chr1757816308+ENST00000583539RAD51Cchr1756787220+101046741802253
ENST00000545362VMP1chr1757816308+ENST00000337432RAD51Cchr1756787220+101346741892283

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
ENST00000262291ENST00000583539VMP1chr1757816308+RAD51Cchr1756787220+0.005196170.99480385
ENST00000262291ENST00000337432VMP1chr1757816308+RAD51Cchr1756787220+0.0035679550.99643207
ENST00000536180ENST00000583539VMP1chr1757816308+RAD51Cchr1756787220+0.0189837010.98101634
ENST00000536180ENST00000337432VMP1chr1757816308+RAD51Cchr1756787220+0.0074977570.9925022
ENST00000545362ENST00000583539VMP1chr1757816308+RAD51Cchr1756787220+0.0039231130.9960769
ENST00000545362ENST00000337432VMP1chr1757816308+RAD51Cchr1756787220+0.0020982570.9979018

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>98210_98210_1_VMP1-RAD51C_VMP1_chr17_57816308_ENST00000262291_RAD51C_chr17_56787220_ENST00000337432_length(amino acids)=298AA_BP=157
MRSGAAGVGAAPQELLIYEMAENGKNCDQRRVAMNKEHHNGNFTDPSSVNEKKRREREERQNIVLWRQPLITLQYFSLEILVILKEWTSK
LWHRQSIVVSFLLLLAVLIATYYVEGVHQQYVQRIEKQFLLYAYWIGLGILSSVGLGTGLHTFLLYLVRLVIVDGIAFPFRHDLDDLSLR
TRLLNGLAQQMISLANNHRLAVILTNQMTTKIDRNQALLVPALGESWGHAATIRLIFHWDRKQRLATLYKSPSQKECTVLFQIKPQGFRD

--------------------------------------------------------------

>98210_98210_2_VMP1-RAD51C_VMP1_chr17_57816308_ENST00000262291_RAD51C_chr17_56787220_ENST00000583539_length(amino acids)=268AA_BP=157
MRSGAAGVGAAPQELLIYEMAENGKNCDQRRVAMNKEHHNGNFTDPSSVNEKKRREREERQNIVLWRQPLITLQYFSLEILVILKEWTSK
LWHRQSIVVSFLLLLAVLIATYYVEGVHQQYVQRIEKQFLLYAYWIGLGILSSVGLGTGLHTFLLYLVRLVIVDGIAFPFRHDLDDLSLR

--------------------------------------------------------------

>98210_98210_3_VMP1-RAD51C_VMP1_chr17_57816308_ENST00000536180_RAD51C_chr17_56787220_ENST00000337432_length(amino acids)=182AA_BP=41
MDLKYVQRIEKQFLLYAYWIGLGILSSVGLGTGLHTFLLYLVRLVIVDGIAFPFRHDLDDLSLRTRLLNGLAQQMISLANNHRLAVILTN
QMTTKIDRNQALLVPALGESWGHAATIRLIFHWDRKQRLATLYKSPSQKECTVLFQIKPQGFRDTVVTSACSLQTEGSLSTRKRSRDPEE

--------------------------------------------------------------

>98210_98210_4_VMP1-RAD51C_VMP1_chr17_57816308_ENST00000536180_RAD51C_chr17_56787220_ENST00000583539_length(amino acids)=152AA_BP=41
MDLKYVQRIEKQFLLYAYWIGLGILSSVGLGTGLHTFLLYLVRLVIVDGIAFPFRHDLDDLSLRTRLLNGLAQQMISLANNHRLAVILTN

--------------------------------------------------------------

>98210_98210_5_VMP1-RAD51C_VMP1_chr17_57816308_ENST00000545362_RAD51C_chr17_56787220_ENST00000337432_length(amino acids)=283AA_BP=142
MIYEMAENGKNCDQRRVAMNKEHHNGNFTDPSSVNEKKRREREERQNIVLWRQPLITLQYFSLEILVILKEWTSKLWHRQSIVVSFLLLL
AVLIATYYVEGVHQQYVQRIEKQFLLYAYWIGLGILSSVGLGTGLHTFLLYLVRLVIVDGIAFPFRHDLDDLSLRTRLLNGLAQQMISLA
NNHRLAVILTNQMTTKIDRNQALLVPALGESWGHAATIRLIFHWDRKQRLATLYKSPSQKECTVLFQIKPQGFRDTVVTSACSLQTEGSL

--------------------------------------------------------------

>98210_98210_6_VMP1-RAD51C_VMP1_chr17_57816308_ENST00000545362_RAD51C_chr17_56787220_ENST00000583539_length(amino acids)=253AA_BP=142
MIYEMAENGKNCDQRRVAMNKEHHNGNFTDPSSVNEKKRREREERQNIVLWRQPLITLQYFSLEILVILKEWTSKLWHRQSIVVSFLLLL
AVLIATYYVEGVHQQYVQRIEKQFLLYAYWIGLGILSSVGLGTGLHTFLLYLVRLVIVDGIAFPFRHDLDDLSLRTRLLNGLAQQMISLA

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr17:57816308/chr17:56787220)
- 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
..
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: 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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+5122_43138.0407.0Topological domainCytoplasmic
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+51265_77138.0407.0Topological domainExtracellular
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+51299_109138.0407.0Topological domainCytoplasmic
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512110_130138.0407.0TransmembraneHelical
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+51244_64138.0407.0TransmembraneHelical
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+51278_98138.0407.0TransmembraneHelical
TgeneRAD51Cchr17:57816308chr17:56787220ENST0000033743239366_370235.0377.0MotifNuclear localization signal
TgeneRAD51Cchr17:57816308chr17:56787220ENST0000042178202366_3700136.0MotifNuclear localization signal
TgeneRAD51Cchr17:57816308chr17:56787220ENST0000042178202125_1320136.0Nucleotide bindingATP
TgeneRAD51Cchr17:57816308chr17:56787220ENST00000421782021_1260136.0RegionNote=Required for Holliday junction resolution activity

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512173_316138.0407.0RegionVTT domain
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512131_250138.0407.0Topological domainExtracellular
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512272_273138.0407.0Topological domainCytoplasmic
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512295_305138.0407.0Topological domainExtracellular
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512327_363138.0407.0Topological domainCytoplasmic
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512385_406138.0407.0Topological domainExtracellular
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512251_271138.0407.0TransmembraneHelical
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512274_294138.0407.0TransmembraneHelical
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512306_326138.0407.0TransmembraneHelical
HgeneVMP1chr17:57816308chr17:56787220ENST00000262291+512364_384138.0407.0TransmembraneHelical
TgeneRAD51Cchr17:57816308chr17:56787220ENST0000033743239125_132235.0377.0Nucleotide bindingATP
TgeneRAD51Cchr17:57816308chr17:56787220ENST00000337432391_126235.0377.0RegionNote=Required for Holliday junction resolution activity


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
VMP1
RAD51C


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
TgeneRAD51Cchr17:57816308chr17:56787220ENST000003374323979_136235.0377.0RAD51B%2C RAD51D and XRCC3


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Related Drugs to VMP1-RAD51C


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to VMP1-RAD51C


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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