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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:GON4L-IQGAP3 (FusionGDB2 ID:33993)

Fusion Gene Summary for GON4L-IQGAP3

check button Fusion gene summary
Fusion gene informationFusion gene name: GON4L-IQGAP3
Fusion gene ID: 33993
HgeneTgene
Gene symbol

GON4L

IQGAP3

Gene ID

54856

128239

Gene namegon-4 likeIQ motif containing GTPase activating protein 3
SynonymsGON-4|GON4|YARP-
Cytomap

1q22

1q22

Type of geneprotein-codingprotein-coding
DescriptionGON-4-like protein2610100B20RikYY1AP related proteinYY1AP-related protein1gon-4 homologras GTPase-activating-like protein IQGAP3
Modification date2020032020200329
UniProtAcc

Q3T8J9

Q86VI3

Ensembl transtripts involved in fusion geneENST00000271883, ENST00000361040, 
ENST00000368331, ENST00000437809, 
ENST00000471341, 
ENST00000498755, 
ENST00000361170, 
Fusion gene scores* DoF score18 X 20 X 14=50405 X 5 X 6=150
# samples 287
** MAII scorelog2(28/5040*10)=-4.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/150*10)=-1.09953567355091
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GON4L [Title/Abstract] AND IQGAP3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGON4L(155823067)-IQGAP3(156510708), # samples:2
Anticipated loss of major functional domain due to fusion event.GON4L-IQGAP3 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
GON4L-IQGAP3 seems lost the major protein functional domain in Tgene 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 GON4L (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 IQGAP3 (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-EW-A1OW-01AGON4Lchr1

155823067

-IQGAP3chr1

156510708

-
ChimerDB4BRCATCGA-EW-A1OWGON4Lchr1

155823066

-IQGAP3chr1

156510708

-


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Fusion Gene ORF analysis for GON4L-IQGAP3

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-intronENST00000271883ENST00000498755GON4Lchr1

155823067

-IQGAP3chr1

156510708

-
5CDS-intronENST00000271883ENST00000498755GON4Lchr1

155823066

-IQGAP3chr1

156510708

-
5CDS-intronENST00000361040ENST00000498755GON4Lchr1

155823067

-IQGAP3chr1

156510708

-
5CDS-intronENST00000361040ENST00000498755GON4Lchr1

155823066

-IQGAP3chr1

156510708

-
5CDS-intronENST00000368331ENST00000498755GON4Lchr1

155823067

-IQGAP3chr1

156510708

-
5CDS-intronENST00000368331ENST00000498755GON4Lchr1

155823066

-IQGAP3chr1

156510708

-
5CDS-intronENST00000437809ENST00000498755GON4Lchr1

155823067

-IQGAP3chr1

156510708

-
5CDS-intronENST00000437809ENST00000498755GON4Lchr1

155823066

-IQGAP3chr1

156510708

-
5UTR-3CDSENST00000471341ENST00000361170GON4Lchr1

155823067

-IQGAP3chr1

156510708

-
5UTR-3CDSENST00000471341ENST00000361170GON4Lchr1

155823066

-IQGAP3chr1

156510708

-
5UTR-intronENST00000471341ENST00000498755GON4Lchr1

155823067

-IQGAP3chr1

156510708

-
5UTR-intronENST00000471341ENST00000498755GON4Lchr1

155823066

-IQGAP3chr1

156510708

-
Frame-shiftENST00000271883ENST00000361170GON4Lchr1

155823067

-IQGAP3chr1

156510708

-
Frame-shiftENST00000271883ENST00000361170GON4Lchr1

155823066

-IQGAP3chr1

156510708

-
Frame-shiftENST00000361040ENST00000361170GON4Lchr1

155823067

-IQGAP3chr1

156510708

-
Frame-shiftENST00000361040ENST00000361170GON4Lchr1

155823066

-IQGAP3chr1

156510708

-
Frame-shiftENST00000368331ENST00000361170GON4Lchr1

155823067

-IQGAP3chr1

156510708

-
Frame-shiftENST00000368331ENST00000361170GON4Lchr1

155823066

-IQGAP3chr1

156510708

-
Frame-shiftENST00000437809ENST00000361170GON4Lchr1

155823067

-IQGAP3chr1

156510708

-
Frame-shiftENST00000437809ENST00000361170GON4Lchr1

155823066

-IQGAP3chr1

156510708

-

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 GON4L-IQGAP3


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.

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Fusion Protein Features for GON4L-IQGAP3


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/:155823067/:156510708)
- 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
GON4L

Q3T8J9

IQGAP3

Q86VI3

FUNCTION: Has transcriptional repressor activity, probably as part of a complex with YY1, SIN3A AND HDAC1. Required for B cell lymphopoiesis. {ECO:0000250|UniProtKB:Q9DB00}.

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 GON4L-IQGAP3


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 GON4L-IQGAP3


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 GON4L-IQGAP3


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 GON4L-IQGAP3


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