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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:WRB-BACE2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: WRB-BACE2
FusionPDB ID: 99392
FusionGDB2.0 ID: 99392
HgeneTgene
Gene symbol

WRB

BACE2

Gene ID

7485

25825

Gene nameguided entry of tail-anchored proteins factor 1beta-secretase 2
SynonymsCHD5|WRBAEPLC|ALP56|ASP1|ASP21|BAE2|CDA13|CEAP1|DRAP
Cytomap

21q22.2

21q22.2-q22.3

Type of geneprotein-codingprotein-coding
Descriptiontail-anchored protein insertion receptor WRBcongenital heart disease 5 proteintryptophan rich basic proteinbeta-secretase 256 kDa aspartic-like proteaseDown syndrome region aspartic proteaseSLCO3A1/BACE2 fusionaspartyl protease 1beta-site APP-cleaving enzyme 2beta-site amyloid beta A4 precursor protein-cleaving enzyme 2memapsin-1membrane-associated asp
Modification date2020031320200313
UniProtAcc.

Q9Y5Z0

Ensembl transtripts involved in fusion geneENST idsENST00000466787, ENST00000333781, 
ENST00000380708, ENST00000398753, 
ENST00000541890, 
ENST00000328735, 
ENST00000330333, ENST00000347667, 
ENST00000466122, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 4 X 6=14414 X 9 X 8=1008
# samples 814
** MAII scorelog2(8/144*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/1008*10)=-2.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: WRB [Title/Abstract] AND BACE2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)WRB(40763762)-BACE2(42647298), # samples:1
Anticipated loss of major functional domain due to fusion event.WRB-BACE2 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.
WRB-BACE2 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.
WRB-BACE2 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.
WRB-BACE2 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.
WRB-BACE2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
WRB-BACE2 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
TgeneBACE2

GO:0006509

membrane protein ectodomain proteolysis

10591213


check buttonFusion gene breakpoints across WRB (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 BACE2 (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
ChimerDB4PRADTCGA-G9-6353-01AWRBchr21

40763762

+BACE2chr21

42647298

+


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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)
ENST00000333781WRBchr2140763762+ENST00000328735BACE2chr2142647298+170447742533163
ENST00000333781WRBchr2140763762+ENST00000347667BACE2chr2142647298+762547742533163
ENST00000541890WRBchr2140763762+ENST00000328735BACE2chr2142647298+159436731423130
ENST00000541890WRBchr2140763762+ENST00000347667BACE2chr2142647298+751536752415639132
ENST00000398753WRBchr2140763762+ENST00000328735BACE2chr2142647298+15603339938996
ENST00000398753WRBchr2140763762+ENST00000347667BACE2chr2142647298+748133352075605132
ENST00000380708WRBchr2140763762+ENST00000328735BACE2chr2142647298+155232522381119
ENST00000380708WRBchr2140763762+ENST00000347667BACE2chr2142647298+747332551995597132

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
ENST00000333781ENST00000328735WRBchr2140763762+BACE2chr2142647298+0.0074384070.99256164
ENST00000333781ENST00000347667WRBchr2140763762+BACE2chr2142647298+0.0204560720.979544
ENST00000541890ENST00000328735WRBchr2140763762+BACE2chr2142647298+0.0097203340.99027973
ENST00000541890ENST00000347667WRBchr2140763762+BACE2chr2142647298+0.0201414060.97985864
ENST00000398753ENST00000328735WRBchr2140763762+BACE2chr2142647298+0.0307148430.9692852
ENST00000398753ENST00000347667WRBchr2140763762+BACE2chr2142647298+0.118932390.88106763
ENST00000380708ENST00000328735WRBchr2140763762+BACE2chr2142647298+0.0179070010.982093
ENST00000380708ENST00000347667WRBchr2140763762+BACE2chr2142647298+0.122285720.8777142

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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

>99392_99392_1_WRB-BACE2_WRB_chr21_40763762_ENST00000333781_BACE2_chr21_42647298_ENST00000328735_length(amino acids)=163AA_BP=144
MGRLASPRRRGRRCCCGPHGAAVADPAQPGASGMSSAAADHWAWLLVLSFVFGCNVLRILLPSFSSFMSRVLQKDAEQESQMRAEIQDMK

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

>99392_99392_2_WRB-BACE2_WRB_chr21_40763762_ENST00000333781_BACE2_chr21_42647298_ENST00000347667_length(amino acids)=163AA_BP=144
MGRLASPRRRGRRCCCGPHGAAVADPAQPGASGMSSAAADHWAWLLVLSFVFGCNVLRILLPSFSSFMSRVLQKDAEQESQMRAEIQDMK

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

>99392_99392_3_WRB-BACE2_WRB_chr21_40763762_ENST00000380708_BACE2_chr21_42647298_ENST00000328735_length(amino acids)=119AA_BP=100
MAGRGFQALNGELSLLCGRRRRPMSRVLQKDAEQESQMRAEIQDMKQELSTVNMMDEFARYARLERKINKMTDKLKTHVKARTAQLAKIK

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

>99392_99392_4_WRB-BACE2_WRB_chr21_40763762_ENST00000380708_BACE2_chr21_42647298_ENST00000347667_length(amino acids)=132AA_BP=
MSIWKAPGSSYLTVSLRGTAAGPSPFPPALLSQPSPCIPNIRQLLSPECLLSETSRKGAPSCLTAVSVGALLPRLHVPGRSILSWSTPSP

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

>99392_99392_5_WRB-BACE2_WRB_chr21_40763762_ENST00000398753_BACE2_chr21_42647298_ENST00000328735_length(amino acids)=96AA_BP=77
MSRVLQKDAEQESQMRAEIQDMKQELSTVNMMDEFARYARLERKINKMTDKLKTHVKARTAQLAKIKWVISVAFYVLQKLQVLQCLKFPG

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

>99392_99392_6_WRB-BACE2_WRB_chr21_40763762_ENST00000398753_BACE2_chr21_42647298_ENST00000347667_length(amino acids)=132AA_BP=
MSIWKAPGSSYLTVSLRGTAAGPSPFPPALLSQPSPCIPNIRQLLSPECLLSETSRKGAPSCLTAVSVGALLPRLHVPGRSILSWSTPSP

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

>99392_99392_7_WRB-BACE2_WRB_chr21_40763762_ENST00000541890_BACE2_chr21_42647298_ENST00000328735_length(amino acids)=130AA_BP=111
MSSAAADHWAWLLVLSFVFGCNVLRILLPSFSSFMSRVLQKDAEQESQMRAEIQDMKQELSTVNMMDEFARYARLERKINKMTDKLKTHV

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

>99392_99392_8_WRB-BACE2_WRB_chr21_40763762_ENST00000541890_BACE2_chr21_42647298_ENST00000347667_length(amino acids)=132AA_BP=
MSIWKAPGSSYLTVSLRGTAAGPSPFPPALLSQPSPCIPNIRQLLSPECLLSETSRKGAPSCLTAVSVGALLPRLHVPGRSILSWSTPSP

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

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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/chr21:40763762/chr21:42647298)
- 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
.BACE2

Q9Y5Z0

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: Responsible for the proteolytic processing of the amyloid precursor protein (APP). Cleaves APP, between residues 690 and 691, leading to the generation and extracellular release of beta-cleaved soluble APP, and a corresponding cell-associated C-terminal fragment which is later released by gamma-secretase. It has also been shown that it can cleave APP between residues 671 and 672. Responsible also for the proteolytic processing of CLTRN in pancreatic beta cells (PubMed:21907142). {ECO:0000269|PubMed:10591213, ECO:0000269|PubMed:11083922, ECO:0000269|PubMed:11423558, ECO:0000269|PubMed:15857888, ECO:0000269|PubMed:16816112, ECO:0000269|PubMed:21907142}.

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
HgeneWRBchr21:40763762chr21:42647298ENST00000333781+3539_94112.0175.0Coiled coilOntology_term=ECO:0000255
HgeneWRBchr21:40763762chr21:42647298ENST00000333781+351_8112.0175.0Topological domainLumenal
HgeneWRBchr21:40763762chr21:42647298ENST00000333781+3530_99112.0175.0Topological domainCytoplasmic
HgeneWRBchr21:40763762chr21:42647298ENST00000380708+351_878.0141.0Topological domainLumenal
HgeneWRBchr21:40763762chr21:42647298ENST00000398753+351_878.0141.0Topological domainLumenal
HgeneWRBchr21:40763762chr21:42647298ENST00000333781+359_29112.0175.0TransmembraneHelical
HgeneWRBchr21:40763762chr21:42647298ENST00000380708+359_2978.0141.0TransmembraneHelical
HgeneWRBchr21:40763762chr21:42647298ENST00000398753+359_2978.0141.0TransmembraneHelical
TgeneBACE2chr21:40763762chr21:42647298ENST0000032873568495_518378.0397.0Topological domainCytoplasmic
TgeneBACE2chr21:40763762chr21:42647298ENST0000033033379495_518434.3333333333333519.0Topological domainCytoplasmic
TgeneBACE2chr21:40763762chr21:42647298ENST0000034766768495_518384.3333333333333469.0Topological domainCytoplasmic
TgeneBACE2chr21:40763762chr21:42647298ENST0000032873568474_494378.0397.0TransmembraneHelical
TgeneBACE2chr21:40763762chr21:42647298ENST0000033033379474_494434.3333333333333519.0TransmembraneHelical
TgeneBACE2chr21:40763762chr21:42647298ENST0000034766768474_494384.3333333333333469.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneWRBchr21:40763762chr21:42647298ENST00000380708+3539_9478.0141.0Coiled coilOntology_term=ECO:0000255
HgeneWRBchr21:40763762chr21:42647298ENST00000398753+3539_9478.0141.0Coiled coilOntology_term=ECO:0000255
HgeneWRBchr21:40763762chr21:42647298ENST00000333781+35121_148112.0175.0Topological domainLumenal
HgeneWRBchr21:40763762chr21:42647298ENST00000333781+35170_174112.0175.0Topological domainCytoplasmic
HgeneWRBchr21:40763762chr21:42647298ENST00000380708+35121_14878.0141.0Topological domainLumenal
HgeneWRBchr21:40763762chr21:42647298ENST00000380708+35170_17478.0141.0Topological domainCytoplasmic
HgeneWRBchr21:40763762chr21:42647298ENST00000380708+3530_9978.0141.0Topological domainCytoplasmic
HgeneWRBchr21:40763762chr21:42647298ENST00000398753+35121_14878.0141.0Topological domainLumenal
HgeneWRBchr21:40763762chr21:42647298ENST00000398753+35170_17478.0141.0Topological domainCytoplasmic
HgeneWRBchr21:40763762chr21:42647298ENST00000398753+3530_9978.0141.0Topological domainCytoplasmic
HgeneWRBchr21:40763762chr21:42647298ENST00000333781+35100_120112.0175.0TransmembraneHelical
HgeneWRBchr21:40763762chr21:42647298ENST00000333781+35149_169112.0175.0TransmembraneHelical
HgeneWRBchr21:40763762chr21:42647298ENST00000380708+35100_12078.0141.0TransmembraneHelical
HgeneWRBchr21:40763762chr21:42647298ENST00000380708+35149_16978.0141.0TransmembraneHelical
HgeneWRBchr21:40763762chr21:42647298ENST00000398753+35100_12078.0141.0TransmembraneHelical
HgeneWRBchr21:40763762chr21:42647298ENST00000398753+35149_16978.0141.0TransmembraneHelical
TgeneBACE2chr21:40763762chr21:42647298ENST000003287356892_429378.0397.0DomainPeptidase A1
TgeneBACE2chr21:40763762chr21:42647298ENST000003303337992_429434.3333333333333519.0DomainPeptidase A1
TgeneBACE2chr21:40763762chr21:42647298ENST000003476676892_429384.3333333333333469.0DomainPeptidase A1
TgeneBACE2chr21:40763762chr21:42647298ENST000003287356821_473378.0397.0Topological domainExtracellular
TgeneBACE2chr21:40763762chr21:42647298ENST000003303337921_473434.3333333333333519.0Topological domainExtracellular
TgeneBACE2chr21:40763762chr21:42647298ENST000003476676821_473384.3333333333333469.0Topological domainExtracellular


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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
WRB
BACE2


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
HgeneWRBchr21:40763762chr21:42647298ENST00000380708+3539_9778.0141.0GET3/TRC40
HgeneWRBchr21:40763762chr21:42647298ENST00000398753+3539_9778.0141.0GET3/TRC40


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Related Drugs to WRB-BACE2


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 WRB-BACE2


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