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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:RPS24-GPC3 (FusionGDB2 ID:HG6229TG2719)

Fusion Gene Summary for RPS24-GPC3

check button Fusion gene summary
Fusion gene informationFusion gene name: RPS24-GPC3
Fusion gene ID: hg6229tg2719
HgeneTgene
Gene symbol

RPS24

GPC3

Gene ID

6229

2719

Gene nameribosomal protein S24glypican 3
SynonymsDBA3|S24|eS24DGSX|GTR2-2|MXR7|OCI-5|SDYS|SGB|SGBS|SGBS1
Cytomap('RPS24')('GPC3')

10q22.3

Xq26.2

Type of geneprotein-codingprotein-coding
Description40S ribosomal protein S24small ribosomal subunit protein eS24glypican-3glypican proteoglycan 3heparan sulphate proteoglycanintestinal protein OCI-5secreted glypican-3
Modification date2020031320200315
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000360830, ENST00000372360, 
ENST00000435275, ENST00000440692, 
ENST00000476545, 
Fusion gene scores* DoF score25 X 17 X 3=127512 X 11 X 6=792
# samples 2612
** MAII scorelog2(26/1275*10)=-2.29391371871777
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/792*10)=-2.72246602447109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: RPS24 [Title/Abstract] AND GPC3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointRPS24(79795268)-GPC3(132805330), # 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
TgeneGPC3

GO:0060828

regulation of canonical Wnt signaling pathway

14610063

TgeneGPC3

GO:0090263

positive regulation of canonical Wnt signaling pathway

24496449

TgeneGPC3

GO:2000050

regulation of non-canonical Wnt signaling pathway

14610063



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/AAI818425RPS24chr10

79795268

-GPC3chrX

132805330

-


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Fusion Gene ORF analysis for RPS24-GPC3

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-intronENST00000360830ENST00000370818RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000360830ENST00000394299RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000360830ENST00000543339RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000372360ENST00000370818RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000372360ENST00000394299RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000372360ENST00000543339RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000435275ENST00000370818RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000435275ENST00000394299RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000435275ENST00000543339RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000440692ENST00000370818RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000440692ENST00000394299RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000440692ENST00000543339RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000476545ENST00000370818RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000476545ENST00000394299RPS24chr10

79795268

-GPC3chrX

132805330

-
intron-intronENST00000476545ENST00000543339RPS24chr10

79795268

-GPC3chrX

132805330

-

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 RPS24-GPC3


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)


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Fusion Protein Features for RPS24-GPC3


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/:79795268/:132805330)
- 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: 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}.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 RPS24-GPC3


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 RPS24-GPC3


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 RPS24-GPC3


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 RPS24-GPC3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRPS24C1260899Anemia, Diamond-Blackfan8CLINGEN;GENOMICS_ENGLAND
HgeneRPS24C0265265Aase syndrome6CLINGEN
HgeneRPS24C1857719Anemia, Diamond-Blackfan, 35CTD_human;GENOMICS_ENGLAND
HgeneRPS24C2931850Aase Smith syndrome 21GENOMICS_ENGLAND
HgeneRPS24C4228778Abnormality of radial ray1GENOMICS_ENGLAND
TgeneC0796154SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 16CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneC0027708Nephroblastoma2CGI;CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneC2239176Liver carcinoma2CTD_human
TgeneC0025500Mesothelioma1CTD_human
TgeneC0152427Polydactyly1GENOMICS_ENGLAND