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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:BCL2L2-RPS3

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: BCL2L2-RPS3
FusionPDB ID: 9394
FusionGDB2.0 ID: 9394
HgeneTgene
Gene symbol

BCL2L2

RPS3

Gene ID

599

6188

Gene nameBCL2 like 2ribosomal protein S3
SynonymsBCL-W|BCL2-L-2|BCLW|PPP1R51S3
Cytomap

14q11.2

11q13.4

Type of geneprotein-codingprotein-coding
Descriptionbcl-2-like protein 2apoptosis regulator BCL-Wprotein phosphatase 1, regulatory subunit 5140S ribosomal protein S3IMR-90 ribosomal protein S3small ribosomal subunit protein uS3
Modification date2020031320200327
UniProtAcc

Q92843

.
Ensembl transtripts involved in fusion geneENST idsENST00000250405, ENST00000278572, 
ENST00000524851, ENST00000526608, 
ENST00000527446, ENST00000529285, 
ENST00000530164, ENST00000534440, 
ENST00000531188, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score4 X 2 X 2=1617 X 19 X 5=1615
# samples 422
** MAII scorelog2(4/16*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(22/1615*10)=-2.87595873605663
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: BCL2L2 [Title/Abstract] AND RPS3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)BCL2L2(23777078)-RPS3(75115837), # samples:1
Anticipated loss of major functional domain due to fusion event.BCL2L2-RPS3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
BCL2L2-RPS3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
BCL2L2-RPS3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
BCL2L2-RPS3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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
TgeneRPS3

GO:0006979

response to oxidative stress

23911537

TgeneRPS3

GO:0017148

negative regulation of translation

20217897

TgeneRPS3

GO:0031397

negative regulation of protein ubiquitination

19656744

TgeneRPS3

GO:0032079

positive regulation of endodeoxyribonuclease activity

18973764

TgeneRPS3

GO:0042769

DNA damage response, detection of DNA damage

23911537

TgeneRPS3

GO:0045739

positive regulation of DNA repair

23911537

TgeneRPS3

GO:0061481

response to TNF agonist

20041225

TgeneRPS3

GO:0070301

cellular response to hydrogen peroxide

23911537

TgeneRPS3

GO:1901224

positive regulation of NIK/NF-kappaB signaling

20041225

TgeneRPS3

GO:1902546

positive regulation of DNA N-glycosylase activity

15518571

TgeneRPS3

GO:1905053

positive regulation of base-excision repair

18973764

TgeneRPS3

GO:2001235

positive regulation of apoptotic signaling pathway

14988002


check buttonFusion gene breakpoints across BCL2L2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across RPS3 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4STADTCGA-CD-A4MH-01ABCL2L2chr14

23777078

+RPS3chr11

75115837

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000250405BCL2L2chr1423777078+ENST00000531188RPS3chr1175115837+19265511246728172

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
ENST00000250405ENST00000531188BCL2L2chr1423777078+RPS3chr1175115837+0.145788240.85421175

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>9394_9394_1_BCL2L2-RPS3_BCL2L2_chr14_23777078_ENST00000250405_RPS3_chr11_75115837_ENST00000531188_length(amino acids)=172AA_BP=
MFFTVLQNIIACSTNDWFHDPLREHNLGMWILMIALYCLGKFTSEPYVPSVVQANFLYTLERLINEYICKEHLEHSMTQNIMAIYIHFLC

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr14:23777078/chr11:75115837)
- 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
BCL2L2

Q92843

.
FUNCTION: Promotes cell survival. Blocks dexamethasone-induced apoptosis. Mediates survival of postmitotic Sertoli cells by suppressing death-promoting activity of BAX. {ECO:0000269|PubMed:8761287}.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.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneRPS3chr14:23777078chr11:75115837ENST000002785720721_920279.3333333333333DomainKH type-2
TgeneRPS3chr14:23777078chr11:75115837ENST000005248510621_920244.0DomainKH type-2
TgeneRPS3chr14:23777078chr11:75115837ENST000005274460721_920413.0DomainKH type-2
TgeneRPS3chr14:23777078chr11:75115837ENST000005311880721_920646.6666666666666DomainKH type-2

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneBCL2L2chr14:23777078chr11:75115837ENST00000250405+14136_1510194.0MotifNote=BH2
HgeneBCL2L2chr14:23777078chr11:75115837ENST00000250405+1485_1040194.0MotifNote=BH1
HgeneBCL2L2chr14:23777078chr11:75115837ENST00000250405+149_290194.0MotifNote=BH4


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
BCL2L2
RPS3


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to BCL2L2-RPS3


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to BCL2L2-RPS3


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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