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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 11626

FusionGeneSummary for ENO3_VIM

check button Fusion gene summary
Fusion gene informationFusion gene name: ENO3_VIM
Fusion gene ID: 11626
HgeneTgene
Gene symbol

ENO3

VIM

Gene ID

2027

7431

Gene nameenolase 3vimentin
SynonymsGSD13|MSE-
Cytomap

17p13.2

10p13

Type of geneprotein-codingprotein-coding
Descriptionbeta-enolase2-phospho-D-glycerate hydrolyaseenolase 3 (beta, muscle)muscle enriched enolasemuscle-specific enolaseskeletal muscle enolasevimentin
Modification date2018051920180527
UniProtAcc

P13929

P08670

Ensembl transtripts involved in fusion geneENST00000323997, ENST00000519584, 
ENST00000518175, 
ENST00000544301, 
ENST00000224237, ENST00000485947, 
Fusion gene scores* DoF score1 X 1 X 1=19 X 6 X 4=216
# samples 18
** MAII scorelog2(1/1*10)=3.32192809488736log2(8/216*10)=-1.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ENO3 [Title/Abstract] AND VIM [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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 button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1CV314769ENO3chr17

4857622

+VIMchr10

17277580

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-intronENST00000323997ENST00000544301ENO3chr17

4857622

+VIMchr10

17277580

+
intron-intronENST00000323997ENST00000224237ENO3chr17

4857622

+VIMchr10

17277580

+
intron-intronENST00000323997ENST00000485947ENO3chr17

4857622

+VIMchr10

17277580

+
intron-intronENST00000519584ENST00000544301ENO3chr17

4857622

+VIMchr10

17277580

+
intron-intronENST00000519584ENST00000224237ENO3chr17

4857622

+VIMchr10

17277580

+
intron-intronENST00000519584ENST00000485947ENO3chr17

4857622

+VIMchr10

17277580

+
intron-intronENST00000518175ENST00000544301ENO3chr17

4857622

+VIMchr10

17277580

+
intron-intronENST00000518175ENST00000224237ENO3chr17

4857622

+VIMchr10

17277580

+
intron-intronENST00000518175ENST00000485947ENO3chr17

4857622

+VIMchr10

17277580

+

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FusionProtFeatures for ENO3_VIM


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ENO3

P13929

VIM

P08670

Appears to have a function in striated muscledevelopment and regeneration.

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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FusionGeneSequence for ENO3_VIM


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for ENO3_VIM


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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RelatedDrugs for ENO3_VIM


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneVIMP08670DB11638ArtenimolVimentinsmall moleculeapproved|investigational

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RelatedDiseases for ENO3_VIM


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneENO3C0023895Liver diseases1CTD_human
HgeneENO3C2752027Glycogen Storage Disease XIII1CTD_human;ORPHANET;UNIPROT
TgeneVIMC1458155Mammary Neoplasms3CTD_human
TgeneVIMC0023890Liver Cirrhosis2CTD_human
TgeneVIMC0029408Degenerative polyarthritis2CTD_human
TgeneVIMC0033578Prostatic Neoplasms2CTD_human
TgeneVIMC0007140Carcinosarcoma1CTD_human
TgeneVIMC0007621Neoplastic Cell Transformation1CTD_human
TgeneVIMC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneVIMC0027627Neoplasm Metastasis1CTD_human
TgeneVIMC0027720Nephrosis1CTD_human
TgeneVIMC0031149Peritoneal Neoplasms1CTD_human
TgeneVIMC0035126Reperfusion Injury1CTD_human
TgeneVIMC0035309Retinal Diseases1CTD_human
TgeneVIMC0039101synovial sarcoma1CTD_human
TgeneVIMC0043094Weight Gain1CTD_human
TgeneVIMC0085084Motor Neuron Disease1CTD_human
TgeneVIMC0086543Cataract1CTD_human
TgeneVIMC0345967Malignant mesothelioma1CTD_human
TgeneVIMC0524851Neurodegenerative Disorders1CTD_human
TgeneVIMC0948089Acute Coronary Syndrome1CTD_human
TgeneVIMC1862939AMYOTROPHIC LATERAL SCLEROSIS 11CTD_human
TgeneVIMC3805411CATARACT 301UNIPROT
TgeneVIMC4277682Chemical and Drug Induced Liver Injury1CTD_human