FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:WWP2-EIF4G2 (FusionGDB2 ID:98853)

Fusion Gene Summary for WWP2-EIF4G2

check button Fusion gene summary
Fusion gene informationFusion gene name: WWP2-EIF4G2
Fusion gene ID: 98853
HgeneTgene
Gene symbol

WWP2

EIF4G2

Gene ID

11060

1982

Gene nameWW domain containing E3 ubiquitin protein ligase 2eukaryotic translation initiation factor 4 gamma 2
SynonymsAIP2|WWp2-likeAAG1|DAP5|NAT1|P97
Cytomap

16q22.1

11p15.4

Type of geneprotein-codingprotein-coding
DescriptionNEDD4-like E3 ubiquitin-protein ligase WWP2HECT-type E3 ubiquitin transferase WWP2atrophin-1 interacting protein 2eukaryotic translation initiation factor 4 gamma 2DAP-5aging-associated protein 1death-associated protein 5eIF-4-gamma 2eIF-4G 2eIF4G 2eukaryotic translation initiation factor 4G-like 1
Modification date2020032720200313
UniProtAcc.

P78344

Ensembl transtripts involved in fusion geneENST00000359154, ENST00000448661, 
ENST00000569174, ENST00000356003, 
ENST00000544162, ENST00000542271, 
ENST00000568684, 
ENST00000526148, 
ENST00000525681, ENST00000339995, 
ENST00000396525, ENST00000525995, 
Fusion gene scores* DoF score18 X 16 X 11=316826 X 29 X 7=5278
# samples 2331
** MAII scorelog2(23/3168*10)=-3.78386656913523
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(31/5278*10)=-4.08965123005203
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: WWP2 [Title/Abstract] AND EIF4G2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointWWP2(69963210)-EIF4G2(10819363), # 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
HgeneWWP2

GO:0016567

protein ubiquitination

18776082|26280536

HgeneWWP2

GO:0032410

negative regulation of transporter activity

18776082

HgeneWWP2

GO:0034765

regulation of ion transmembrane transport

17289006

HgeneWWP2

GO:0042391

regulation of membrane potential

17289006

HgeneWWP2

GO:0051865

protein autoubiquitination

24105792

HgeneWWP2

GO:1901016

regulation of potassium ion transmembrane transporter activity

17289006

TgeneEIF4G2

GO:0006446

regulation of translational initiation

11943866


check buttonFusion gene breakpoints across WWP2 (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 EIF4G2 (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
ChiTaRS5.0N/AAW020942WWP2chr16

69963210

-EIF4G2chr11

10819363

-


Top

Fusion Gene ORF analysis for WWP2-EIF4G2

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-3CDSENST00000359154ENST00000526148WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000359154ENST00000525681WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000359154ENST00000339995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000359154ENST00000396525WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-intronENST00000359154ENST00000525995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000448661ENST00000526148WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000448661ENST00000525681WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000448661ENST00000339995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000448661ENST00000396525WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-intronENST00000448661ENST00000525995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000569174ENST00000526148WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000569174ENST00000525681WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000569174ENST00000339995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000569174ENST00000396525WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-intronENST00000569174ENST00000525995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000356003ENST00000526148WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000356003ENST00000525681WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000356003ENST00000339995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000356003ENST00000396525WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-intronENST00000356003ENST00000525995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000544162ENST00000526148WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000544162ENST00000525681WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000544162ENST00000339995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000544162ENST00000396525WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-intronENST00000544162ENST00000525995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000542271ENST00000526148WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000542271ENST00000525681WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000542271ENST00000339995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000542271ENST00000396525WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-intronENST00000542271ENST00000525995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000568684ENST00000526148WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000568684ENST00000525681WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000568684ENST00000339995WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-3CDSENST00000568684ENST00000396525WWP2chr16

69963210

-EIF4G2chr11

10819363

-
intron-intronENST00000568684ENST00000525995WWP2chr16

69963210

-EIF4G2chr11

10819363

-

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

Top

Fusion Genomic Features for WWP2-EIF4G2


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)

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.

Top

Fusion Protein Features for WWP2-EIF4G2


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
.EIF4G2

P78344

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: Appears to play a role in the switch from cap-dependent to IRES-mediated translation during mitosis, apoptosis and viral infection. Cleaved by some caspases and viral proteases. {ECO:0000269|PubMed:11511540, ECO:0000269|PubMed:11943866, ECO:0000269|PubMed:9032289, ECO:0000269|PubMed:9049310}.

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


Top

Fusion Gene Sequence for WWP2-EIF4G2


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.

Top

Fusion Gene PPI Analysis for WWP2-EIF4G2


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


Top

Related Drugs for WWP2-EIF4G2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

Related Diseases for WWP2-EIF4G2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneWWP2C0409959Osteoarthritis, Knee1CTD_human