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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:G3BP1-PCDH9 (FusionGDB2 ID:31993)

Fusion Gene Summary for G3BP1-PCDH9

check button Fusion gene summary
Fusion gene informationFusion gene name: G3BP1-PCDH9
Fusion gene ID: 31993
HgeneTgene
Gene symbol

G3BP1

PCDH9

Gene ID

10146

5101

Gene nameG3BP stress granule assembly factor 1protocadherin 9
SynonymsG3BP|HDH-VIII-
Cytomap

5q33.1

13q21.32

Type of geneprotein-codingprotein-coding
Descriptionras GTPase-activating protein-binding protein 1ATP-dependent DNA helicase VIIIDNA helicase VIIIG3BP-1GAP SH3 domain-binding protein 1GAP binding proteinGTPase activating protein (SH3 domain) binding protein 1Ras-GTPase-activating protein SH3-domainprotocadherin-9cadherin superfamily protein VR4-11
Modification date2020031320200313
UniProtAcc

Q13283

.
Ensembl transtripts involved in fusion geneENST00000356245, ENST00000394123, 
ENST00000543466, 
ENST00000377861, 
ENST00000328454, ENST00000377865, 
ENST00000456367, ENST00000544246, 
Fusion gene scores* DoF score12 X 11 X 6=79213 X 11 X 4=572
# samples 1413
** MAII scorelog2(14/792*10)=-2.50007360313464
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/572*10)=-2.13750352374993
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: G3BP1 [Title/Abstract] AND PCDH9 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointG3BP1(151166276)-PCDH9(66879160), # samples:4
Anticipated loss of major functional domain due to fusion event.G3BP1-PCDH9 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
G3BP1-PCDH9 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
G3BP1-PCDH9 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
HgeneG3BP1

GO:0032606

type I interferon production

30804210


check buttonFusion gene breakpoints across G3BP1 (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 PCDH9 (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-85-A50M-01AG3BP1chr5

151166276

-PCDH9chr13

66879160

-
ChimerDB4LUSCTCGA-85-A50M-01AG3BP1chr5

151166276

+PCDH9chr13

66879160

-
ChimerDB4LUSCTCGA-85-A50MG3BP1chr5

151166276

+PCDH9chr13

66879160

-


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Fusion Gene ORF analysis for G3BP1-PCDH9

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-intronENST00000356245ENST00000377861G3BP1chr5

151166276

+PCDH9chr13

66879160

-
5CDS-intronENST00000394123ENST00000377861G3BP1chr5

151166276

+PCDH9chr13

66879160

-
5UTR-3CDSENST00000543466ENST00000328454G3BP1chr5

151166276

+PCDH9chr13

66879160

-
5UTR-3CDSENST00000543466ENST00000377865G3BP1chr5

151166276

+PCDH9chr13

66879160

-
5UTR-3CDSENST00000543466ENST00000456367G3BP1chr5

151166276

+PCDH9chr13

66879160

-
5UTR-3CDSENST00000543466ENST00000544246G3BP1chr5

151166276

+PCDH9chr13

66879160

-
5UTR-intronENST00000543466ENST00000377861G3BP1chr5

151166276

+PCDH9chr13

66879160

-
Frame-shiftENST00000356245ENST00000328454G3BP1chr5

151166276

+PCDH9chr13

66879160

-
Frame-shiftENST00000356245ENST00000377865G3BP1chr5

151166276

+PCDH9chr13

66879160

-
Frame-shiftENST00000356245ENST00000456367G3BP1chr5

151166276

+PCDH9chr13

66879160

-
Frame-shiftENST00000356245ENST00000544246G3BP1chr5

151166276

+PCDH9chr13

66879160

-
Frame-shiftENST00000394123ENST00000328454G3BP1chr5

151166276

+PCDH9chr13

66879160

-
Frame-shiftENST00000394123ENST00000377865G3BP1chr5

151166276

+PCDH9chr13

66879160

-
Frame-shiftENST00000394123ENST00000456367G3BP1chr5

151166276

+PCDH9chr13

66879160

-
Frame-shiftENST00000394123ENST00000544246G3BP1chr5

151166276

+PCDH9chr13

66879160

-

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 G3BP1-PCDH9


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 G3BP1-PCDH9


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/:151166276/:66879160)
- 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
G3BP1

Q13283

.
FUNCTION: ATP- and magnesium-dependent helicase that plays an essential role in innate immunity (PubMed:30510222). Participates in the DNA-triggered cGAS/STING pathway by promoting the DNA binding and activation of CGAS. Enhances also DDX58-induced type I interferon production probably by helping DDX58 at sensing pathogenic RNA (PubMed:30804210). In addition, plays an essential role in stress granule formation (PubMed:12642610, PubMed:20180778, PubMed:23279204). Unwinds preferentially partial DNA and RNA duplexes having a 17 bp annealed portion and either a hanging 3' tail or hanging tails at both 5'- and 3'-ends (PubMed:9889278). Unwinds DNA/DNA, RNA/DNA, and RNA/RNA substrates with comparable efficiency (PubMed:9889278). Acts unidirectionally by moving in the 5' to 3' direction along the bound single-stranded DNA (PubMed:9889278). Phosphorylation-dependent sequence-specific endoribonuclease in vitro (PubMed:11604510). Cleaves exclusively between cytosine and adenine and cleaves MYC mRNA preferentially at the 3'-UTR (PubMed:11604510). {ECO:0000269|PubMed:11604510, ECO:0000269|PubMed:12642610, ECO:0000269|PubMed:20180778, ECO:0000269|PubMed:23279204, ECO:0000269|PubMed:30510222, ECO:0000269|PubMed:30804210, ECO:0000269|PubMed:9889278}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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 G3BP1-PCDH9


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 G3BP1-PCDH9


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 G3BP1-PCDH9


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 G3BP1-PCDH9


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