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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:GLE1-RBM5

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: GLE1-RBM5
FusionPDB ID: 33236
FusionGDB2.0 ID: 33236
HgeneTgene
Gene symbol

GLE1

RBM5

Gene ID

2733

10181

Gene nameGLE1 RNA export mediatorRNA binding motif protein 5
SynonymsCAAHC|CAAHD|GLE1L|LCCS|LCCS1|hGLE1G15|H37|LUCA-15|LUCA15|RMB5
Cytomap

9q34.11

3p21.31

Type of geneprotein-codingprotein-coding
Descriptionnucleoporin GLE1GLE1 RNA export mediator homologGLE1 RNA export mediator-likeGLE1-like proteinGLE1-like, RNA export mediatorRNA-binding protein 5putative tumor suppressor LUCA15renal carcinoma antigen NY-REN-9
Modification date2020031320200320
UniProtAcc

Q53GS7

Main function of 5'-partner protein: FUNCTION: Required for the export of mRNAs containing poly(A) tails from the nucleus into the cytoplasm. May be involved in the terminal step of the mRNA transport through the nuclear pore complex (NPC). {ECO:0000269|PubMed:12668658, ECO:0000269|PubMed:16000379, ECO:0000269|PubMed:9618489}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000309971, ENST00000372770, 
ENST00000539582, ENST00000494417, 
ENST00000441812, ENST00000469838, 
ENST00000347869, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score5 X 4 X 5=1008 X 7 X 5=280
# samples 58
** MAII scorelog2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/280*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: GLE1 [Title/Abstract] AND RBM5 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: GLE1 [Title/Abstract] AND RBM5 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)GLE1(131267183)-RBM5(50150816), # samples:1
Anticipated loss of major functional domain due to fusion event.GLE1-RBM5 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.
GLE1-RBM5 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.
GLE1-RBM5 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.
GLE1-RBM5 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
TgeneRBM5

GO:0000245

spliceosomal complex assembly

18951082

TgeneRBM5

GO:0000381

regulation of alternative mRNA splicing, via spliceosome

18840686|18951082

TgeneRBM5

GO:0043065

positive regulation of apoptotic process

18840686



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/chr9:131267183/chr3:50150816)
- 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 buttonRetention analysis results 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, are available here.

check buttonFusion gene breakpoints across GLE1 (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 RBM5 (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 Amino Acid Sequences


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)
ENST00000309971GLE1chr9131267183+ENST00000347869RBM5chr350150816+17632051061197363
ENST00000372770GLE1chr9131267183+ENST00000347869RBM5chr350150816+1732174751166363

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
ENST00000309971ENST00000347869GLE1chr9131267183+RBM5chr350150816+0.0014206910.99857926
ENST00000372770ENST00000347869GLE1chr9131267183+RBM5chr350150816+0.0014582380.99854183

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for GLE1-RBM5

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
GLE1chr9131267183RBM5chr35015081617433RLCYYRDWLLRREYYYNSLTQQYLYW
GLE1chr9131267183RBM5chr35015081620533RLCYYRDWLLRREYYYNSLTQQYLYW

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Potential FusionNeoAntigen Information of GLE1-RBM5 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
GLE1-RBM5_131267183_50150816.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
GLE1-RBM5chr9131267183chr350150816205HLA-B47:01REYYYNSL0.99340.50611119
GLE1-RBM5chr9131267183chr350150816205HLA-B39:13REYYYNSL0.93230.82391119
GLE1-RBM5chr9131267183chr350150816205HLA-B27:04RREYYYNSL0.9960.7911019
GLE1-RBM5chr9131267183chr350150816205HLA-B27:05RREYYYNSL0.9950.90181019
GLE1-RBM5chr9131267183chr350150816205HLA-B50:01REYYYNSLT0.01060.59081120
GLE1-RBM5chr9131267183chr350150816205HLA-B27:02YRDWLLRREY0.99890.5303414
GLE1-RBM5chr9131267183chr350150816205HLA-B27:04YRDWLLRREY0.99870.6336414
GLE1-RBM5chr9131267183chr350150816205HLA-B40:06REYYYNSL0.99940.5261119
GLE1-RBM5chr9131267183chr350150816205HLA-B39:08REYYYNSL0.86810.50791119
GLE1-RBM5chr9131267183chr350150816205HLA-C07:27RREYYYNSL0.98810.94581019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:29RREYYYNSL0.98760.93191019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:05RREYYYNSL0.98650.94561019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:95RREYYYNSL0.98560.67151019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:13RREYYYNSL0.96730.93341019
GLE1-RBM5chr9131267183chr350150816205HLA-B39:12RREYYYNSL0.92770.75791019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:67RREYYYNSL0.86470.94111019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:80RREYYYNSL0.86470.94111019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:19RREYYYNSL0.86350.68151019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:46RREYYYNSL0.85850.87081019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:10RREYYYNSL0.85150.95991019
GLE1-RBM5chr9131267183chr350150816205HLA-B44:09RDWLLRREY0.37090.522514
GLE1-RBM5chr9131267183chr350150816205HLA-C12:16RREYYYNSL0.08160.94661019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:95YRDWLLRREY0.99610.5526414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:27YRDWLLRREY0.99360.9007414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:05YRDWLLRREY0.99170.918414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:19YRDWLLRREY0.98980.5916414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:80YRDWLLRREY0.98820.8851414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:67YRDWLLRREY0.98820.8851414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:46YRDWLLRREY0.98530.7889414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:10YRDWLLRREY0.98150.9187414
GLE1-RBM5chr9131267183chr350150816205HLA-B27:03YRDWLLRREY0.97370.833414
GLE1-RBM5chr9131267183chr350150816205HLA-C12:16YRDWLLRREY0.7440.9405414
GLE1-RBM5chr9131267183chr350150816205HLA-B15:21EYYYNSLTQQY0.94370.71671223
GLE1-RBM5chr9131267183chr350150816205HLA-C07:05YYRDWLLRREY0.7830.8974314
GLE1-RBM5chr9131267183chr350150816205HLA-B40:04REYYYNSL0.9990.60941119
GLE1-RBM5chr9131267183chr350150816205HLA-B39:02REYYYNSL0.93080.83061119
GLE1-RBM5chr9131267183chr350150816205HLA-B27:06RREYYYNSL0.99730.77181019
GLE1-RBM5chr9131267183chr350150816205HLA-B27:10RREYYYNSL0.99570.88641019
GLE1-RBM5chr9131267183chr350150816205HLA-B27:08RREYYYNSL0.99550.82441019
GLE1-RBM5chr9131267183chr350150816205HLA-B27:09RREYYYNSL0.99530.88541019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:01RREYYYNSL0.99070.66561019
GLE1-RBM5chr9131267183chr350150816205HLA-B39:31RREYYYNSL0.93790.75171019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:04RREYYYNSL0.89430.74941019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:02RREYYYNSL0.86470.94111019
GLE1-RBM5chr9131267183chr350150816205HLA-C07:22RREYYYNSL0.77540.65271019
GLE1-RBM5chr9131267183chr350150816205HLA-C06:06RREYYYNSL0.44990.98181019
GLE1-RBM5chr9131267183chr350150816205HLA-C06:02RREYYYNSL0.14640.98831019
GLE1-RBM5chr9131267183chr350150816205HLA-C06:17RREYYYNSL0.14640.98831019
GLE1-RBM5chr9131267183chr350150816205HLA-B50:05REYYYNSLT0.01060.59081120
GLE1-RBM5chr9131267183chr350150816205HLA-B50:04REYYYNSLT0.01060.59081120
GLE1-RBM5chr9131267183chr350150816205HLA-B27:10YRDWLLRREY0.99840.8047414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:01YRDWLLRREY0.9960.5282414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:17YRDWLLRREY0.99020.9089414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:02YRDWLLRREY0.98820.8851414
GLE1-RBM5chr9131267183chr350150816205HLA-C07:22YRDWLLRREY0.94270.6447414
GLE1-RBM5chr9131267183chr350150816205HLA-C14:03YYRDWLLRREY0.80980.9522314
GLE1-RBM5chr9131267183chr350150816205HLA-C14:02YYRDWLLRREY0.80980.9522314

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Potential FusionNeoAntigen Information of GLE1-RBM5 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
GLE1-RBM5_131267183_50150816.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)
GLE1-RBM5chr9131267183chr350150816205DRB3-0205RREYYYNSLTQQYLY1025

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Fusion breakpoint peptide structures of GLE1-RBM5

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
1477DWLLRREYYYNSLTGLE1RBM5chr9131267183chr350150816205

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of GLE1-RBM5

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN1477DWLLRREYYYNSLT-7.15543-7.26883
HLA-B14:023BVN1477DWLLRREYYYNSLT-4.77435-5.80965
HLA-B52:013W391477DWLLRREYYYNSLT-6.80875-6.92215
HLA-B52:013W391477DWLLRREYYYNSLT-4.20386-5.23916
HLA-A11:014UQ21477DWLLRREYYYNSLT-7.5194-8.5547
HLA-A11:014UQ21477DWLLRREYYYNSLT-6.9601-7.0735
HLA-A24:025HGA1477DWLLRREYYYNSLT-7.52403-7.63743
HLA-A24:025HGA1477DWLLRREYYYNSLT-5.82433-6.85963
HLA-B27:056PYJ1477DWLLRREYYYNSLT-3.28285-4.31815
HLA-B44:053DX81477DWLLRREYYYNSLT-5.91172-6.94702
HLA-B44:053DX81477DWLLRREYYYNSLT-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of GLE1-RBM5

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
GLE1-RBM5chr9131267183chr3501508161019RREYYYNSLCGGCGCGAGTACTACTATAATTCCTTG
GLE1-RBM5chr9131267183chr3501508161119REYYYNSLCGCGAGTACTACTATAATTCCTTG
GLE1-RBM5chr9131267183chr3501508161120REYYYNSLTCGCGAGTACTACTATAATTCCTTGACC
GLE1-RBM5chr9131267183chr3501508161223EYYYNSLTQQYGAGTACTACTATAATTCCTTGACCCAGCAGTAC
GLE1-RBM5chr9131267183chr350150816314YYRDWLLRREYTACTACCGCGACTGGCTGCTGCGGCGCGAGTAC
GLE1-RBM5chr9131267183chr350150816414YRDWLLRREYTACCGCGACTGGCTGCTGCGGCGCGAGTAC
GLE1-RBM5chr9131267183chr350150816514RDWLLRREYCGCGACTGGCTGCTGCGGCGCGAGTAC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
GLE1-RBM5chr9131267183chr3501508161025RREYYYNSLTQQYLYCGGCGCGAGTACTACTATAATTCCTTGACCCAGCAGTACCTTTAC

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Information of the samples that have these potential fusion neoantigens of GLE1-RBM5

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
GBMGLE1-RBM5chr9131267183ENST00000309971chr350150816ENST00000347869TCGA-14-2554-01A

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Potential target of CAR-T therapy development for GLE1-RBM5

check button Predicted 3D structure. We used RoseTTAFold.

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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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Related Drugs to GLE1-RBM5

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 GLE1-RBM5

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