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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:TLE4-HDAC5

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TLE4-HDAC5
FusionPDB ID: 91129
FusionGDB2.0 ID: 91129
HgeneTgene
Gene symbol

TLE4

HDAC5

Gene ID

7091

10014

Gene nameTLE family member 4, transcriptional corepressorhistone deacetylase 5
SynonymsBCE-1|BCE1|E(spI)|E(spl)|ESG|ESG4|GRG4|Grg-4HD5|NY-CO-9
Cytomap

9q21.31

17q21.31

Type of geneprotein-codingprotein-coding
Descriptiontransducin-like enhancer protein 4B lymphocyte gene 1enhancer of split groucho 4groucho-related protein 4transducin like enhancer of split 4transducin-like enhancer of split 4 (E(sp1) homolog, Drosophila)transducin-like enhancer of split 4, homolog histone deacetylase 5antigen NY-CO-9
Modification date2020031320200313
UniProtAcc.

Q9UQL6

Main function of 5'-partner protein: FUNCTION: Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Involved in muscle maturation by repressing transcription of myocyte enhancer MEF2C. During muscle differentiation, it shuttles into the cytoplasm, allowing the expression of myocyte enhancer factors. Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer. Serves as a corepressor of RARA and causes its deacetylation (PubMed:28167758). In association with RARA, plays a role in the repression of microRNA-10a and thereby in the inflammatory response (PubMed:28167758). {ECO:0000269|PubMed:24413532, ECO:0000269|PubMed:28167758}.
Ensembl transtripts involved in fusion geneENST idsENST00000376534, ENST00000265284, 
ENST00000376520, ENST00000376537, 
ENST00000376552, ENST00000376544, 
ENST00000455913, 
ENST00000225983, 
ENST00000336057, ENST00000393622, 
ENST00000586802, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 6 X 2=8413 X 11 X 8=1144
# samples 714
** MAII scorelog2(7/84*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/1144*10)=-3.03058831983342
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: TLE4 [Title/Abstract] AND HDAC5 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: TLE4 [Title/Abstract] AND HDAC5 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TLE4(82320857)-HDAC5(42165064), # samples:1
Anticipated loss of major functional domain due to fusion event.TLE4-HDAC5 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.
TLE4-HDAC5 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.
TLE4-HDAC5 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.
TLE4-HDAC5 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
TgeneHDAC5

GO:0000122

negative regulation of transcription by RNA polymerase II

16236793

TgeneHDAC5

GO:0016575

histone deacetylation

10869435



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/chr9:82320857/chr17:42165064)
- 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 TLE4 (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 HDAC5 (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)
ENST00000376552TLE4chr982320857+ENST00000225983HDAC5chr1742165064-5201180110183570850
ENST00000376552TLE4chr982320857+ENST00000393622HDAC5chr1742165064-5194180110183570850
ENST00000376552TLE4chr982320857+ENST00000336057HDAC5chr1742165064-4938180110183315765
ENST00000376552TLE4chr982320857+ENST00000586802HDAC5chr1742165064-3653180110183570850
ENST00000376520TLE4chr982320857+ENST00000225983HDAC5chr1742165064-501116118283380850
ENST00000376520TLE4chr982320857+ENST00000393622HDAC5chr1742165064-500416118283380850
ENST00000376520TLE4chr982320857+ENST00000336057HDAC5chr1742165064-474816118283125765
ENST00000376520TLE4chr982320857+ENST00000586802HDAC5chr1742165064-346316118283380850
ENST00000376537TLE4chr982320857+ENST00000225983HDAC5chr1742165064-43599591762728850
ENST00000376537TLE4chr982320857+ENST00000393622HDAC5chr1742165064-43529591762728850
ENST00000376537TLE4chr982320857+ENST00000336057HDAC5chr1742165064-40969591762473765
ENST00000376537TLE4chr982320857+ENST00000586802HDAC5chr1742165064-28119591762728850
ENST00000265284TLE4chr982320857+ENST00000225983HDAC5chr1742165064-4154754462523825
ENST00000265284TLE4chr982320857+ENST00000393622HDAC5chr1742165064-4147754462523825
ENST00000265284TLE4chr982320857+ENST00000336057HDAC5chr1742165064-3891754462268740
ENST00000265284TLE4chr982320857+ENST00000586802HDAC5chr1742165064-2606754462523825

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
ENST00000376552ENST00000225983TLE4chr982320857+HDAC5chr1742165064-0.0013761870.99862385
ENST00000376552ENST00000393622TLE4chr982320857+HDAC5chr1742165064-0.0014027370.9985972
ENST00000376552ENST00000336057TLE4chr982320857+HDAC5chr1742165064-0.0017625420.9982375
ENST00000376552ENST00000586802TLE4chr982320857+HDAC5chr1742165064-0.0031400230.99686
ENST00000376520ENST00000225983TLE4chr982320857+HDAC5chr1742165064-0.0013286630.9986714
ENST00000376520ENST00000393622TLE4chr982320857+HDAC5chr1742165064-0.0013541550.99864584
ENST00000376520ENST00000336057TLE4chr982320857+HDAC5chr1742165064-0.0017047280.99829525
ENST00000376520ENST00000586802TLE4chr982320857+HDAC5chr1742165064-0.003131470.99686855
ENST00000376537ENST00000225983TLE4chr982320857+HDAC5chr1742165064-0.0022633380.9977367
ENST00000376537ENST00000393622TLE4chr982320857+HDAC5chr1742165064-0.0023125820.99768746
ENST00000376537ENST00000336057TLE4chr982320857+HDAC5chr1742165064-0.0028501330.9971499
ENST00000376537ENST00000586802TLE4chr982320857+HDAC5chr1742165064-0.0078951330.9921049
ENST00000265284ENST00000225983TLE4chr982320857+HDAC5chr1742165064-0.0014982930.9985018
ENST00000265284ENST00000393622TLE4chr982320857+HDAC5chr1742165064-0.0015427020.9984573
ENST00000265284ENST00000336057TLE4chr982320857+HDAC5chr1742165064-0.0013428130.9986572
ENST00000265284ENST00000586802TLE4chr982320857+HDAC5chr1742165064-0.0054853770.9945147

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 TLE4-HDAC5

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
TLE4chr982320857HDAC5chr17421650641611261KSDDNLVVDVSNEILTKTGELPRQPT
TLE4chr982320857HDAC5chr17421650641801261KSDDNLVVDVSNEILTKTGELPRQPT
TLE4chr982320857HDAC5chr1742165064754236KSDDNLVVDVSNEILTKTGELPRQPT
TLE4chr982320857HDAC5chr1742165064959261KSDDNLVVDVSNEILTKTGELPRQPT

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Potential FusionNeoAntigen Information of TLE4-HDAC5 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.
TLE4-HDAC5_82320857_42165064.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)
TLE4-HDAC5chr982320857chr1742165064754HLA-A02:21LVVDVSNEI0.97370.5815514
TLE4-HDAC5chr982320857chr1742165064754HLA-B08:01EILTKTGEL0.97340.93721221
TLE4-HDAC5chr982320857chr1742165064754HLA-C05:09VVDVSNEI10.9534614
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:10VVDVSNEI10.7203614
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:07VVDVSNEI10.7229614
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:15VVDVSNEI0.99990.9731614
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:06VVDVSNEI0.99730.7624614
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:04VVDVSNEI0.95260.9711614
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:13VVDVSNEI0.95260.9711614
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:03VVDVSNEI0.86450.9851614
TLE4-HDAC5chr982320857chr1742165064754HLA-C05:09VVDVSNEIL0.99990.9683615
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:10VVDVSNEIL0.99980.8287615
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:07VVDVSNEIL0.99980.8274615
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:15VVDVSNEIL0.99970.9837615
TLE4-HDAC5chr982320857chr1742165064754HLA-C03:07LVVDVSNEI0.99930.9822514
TLE4-HDAC5chr982320857chr1742165064754HLA-C03:19LVVDVSNEI0.99810.9815514
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:06VVDVSNEIL0.98460.8242615
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:13VVDVSNEIL0.93970.9806615
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:04VVDVSNEIL0.93970.9806615
TLE4-HDAC5chr982320857chr1742165064754HLA-C02:06LVVDVSNEI0.90960.9777514
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:14VVDVSNEIL0.90070.8262615
TLE4-HDAC5chr982320857chr1742165064754HLA-A02:07VVDVSNEIL0.75690.5095615
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:03VVDVSNEIL0.72390.9898615
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:03VVDVSNEI10.7588614
TLE4-HDAC5chr982320857chr1742165064754HLA-C05:01VVDVSNEI10.9534614
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:01VVDVSNEI10.7229614
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:02VVDVSNEI0.99990.9731614
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:01VVDVSNEI0.86450.9851614
TLE4-HDAC5chr982320857chr1742165064754HLA-B07:13VVDVSNEI0.53640.7032614
TLE4-HDAC5chr982320857chr1742165064754HLA-C05:01VVDVSNEIL0.99990.9683615
TLE4-HDAC5chr982320857chr1742165064754HLA-C18:01VVDVSNEIL0.99980.8102615
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:01VVDVSNEIL0.99980.8274615
TLE4-HDAC5chr982320857chr1742165064754HLA-C04:03VVDVSNEIL0.99980.8385615
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:02VVDVSNEIL0.99970.9837615
TLE4-HDAC5chr982320857chr1742165064754HLA-C01:03VVDVSNEIL0.99960.9573615
TLE4-HDAC5chr982320857chr1742165064754HLA-C03:06LVVDVSNEI0.99310.9881514
TLE4-HDAC5chr982320857chr1742165064754HLA-A69:01LVVDVSNEI0.9770.6373514
TLE4-HDAC5chr982320857chr1742165064754HLA-A02:06LVVDVSNEI0.97370.5815514
TLE4-HDAC5chr982320857chr1742165064754HLA-B08:18EILTKTGEL0.97340.93721221
TLE4-HDAC5chr982320857chr1742165064754HLA-C03:06VVDVSNEIL0.94760.9912615
TLE4-HDAC5chr982320857chr1742165064754HLA-C17:01VVDVSNEIL0.790.9646615
TLE4-HDAC5chr982320857chr1742165064754HLA-B08:12EILTKTGEL0.74880.94841221
TLE4-HDAC5chr982320857chr1742165064754HLA-C17:01LVVDVSNEI0.73450.935514
TLE4-HDAC5chr982320857chr1742165064754HLA-C08:01VVDVSNEIL0.72390.9898615
TLE4-HDAC5chr982320857chr1742165064754HLA-B07:13VVDVSNEIL0.18360.8235615

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Potential FusionNeoAntigen Information of TLE4-HDAC5 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.
TLE4-HDAC5_82320857_42165064.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)
TLE4-HDAC5chr982320857chr1742165064754DRB1-0301DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0305DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0310DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0310SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB1-0310KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB1-0313DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0318DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0320DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0322DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0324DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0326DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0328DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0330DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0332DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0334DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0336DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0338DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0338SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB1-0340DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0342DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0342SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB1-0344DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0346DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0348DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0350DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0352DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0354DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0422DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0466DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0472DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-0704DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1438DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1439DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1447DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1448DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1448SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB1-1449DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1450DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1476DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1476SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB1-1476KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB1-1476DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB1-1479DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1479SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB1-1479KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB1-1479DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB1-1482DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1493DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1493SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB1-1525DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB1-1525SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB1-1525DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB1-1525KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0101DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0101SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0101KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0101DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB3-0104DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0104SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0104KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0104DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB3-0105DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0105SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0105KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0105DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB3-0108DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0108SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0108KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0108DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB3-0109DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0109SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0109KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0109DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB3-0111DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0111SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0111KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0111DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB3-0112DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0112SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0112KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0112DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB3-0113DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0113SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0113KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0113DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB3-0114DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0114SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0114KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0114DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB3-0201DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0204DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0209DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0209SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0213DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0214DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0216DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0221DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0221SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0224DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0301DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0301SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0301DNLVVDVSNEILTKT318
TLE4-HDAC5chr982320857chr1742165064754DRB3-0301KSDDNLVVDVSNEIL015
TLE4-HDAC5chr982320857chr1742165064754DRB3-0303DDNLVVDVSNEILTK217
TLE4-HDAC5chr982320857chr1742165064754DRB3-0303SDDNLVVDVSNEILT116
TLE4-HDAC5chr982320857chr1742165064754DRB3-0303DNLVVDVSNEILTKT318

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Fusion breakpoint peptide structures of TLE4-HDAC5

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
10343VVDVSNEILTKTGETLE4HDAC5chr982320857chr1742165064754

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of TLE4-HDAC5

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-B14:023BVN10343VVDVSNEILTKTGE-7.15543-7.26883
HLA-B14:023BVN10343VVDVSNEILTKTGE-4.77435-5.80965
HLA-B52:013W3910343VVDVSNEILTKTGE-6.80875-6.92215
HLA-B52:013W3910343VVDVSNEILTKTGE-4.20386-5.23916
HLA-A11:014UQ210343VVDVSNEILTKTGE-7.5194-8.5547
HLA-A11:014UQ210343VVDVSNEILTKTGE-6.9601-7.0735
HLA-A24:025HGA10343VVDVSNEILTKTGE-7.52403-7.63743
HLA-A24:025HGA10343VVDVSNEILTKTGE-5.82433-6.85963
HLA-B27:056PYJ10343VVDVSNEILTKTGE-3.28285-4.31815
HLA-B44:053DX810343VVDVSNEILTKTGE-5.91172-6.94702
HLA-B44:053DX810343VVDVSNEILTKTGE-4.24346-4.35686
HLA-B35:011A1N10343VVDVSNEILTKTGE-5.9251-6.0385
HLA-B35:011A1N10343VVDVSNEILTKTGE-4.80237-5.83767

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Vaccine Design for the FusionNeoAntigens of TLE4-HDAC5

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
TLE4-HDAC5chr982320857chr17421650641221EILTKTGELGAGATCCTCACCAAGACAGGGGAGCTG
TLE4-HDAC5chr982320857chr1742165064514LVVDVSNEITTGGTGGTTGACGTTTCCAATGAGATC
TLE4-HDAC5chr982320857chr1742165064614VVDVSNEIGTGGTTGACGTTTCCAATGAGATC
TLE4-HDAC5chr982320857chr1742165064615VVDVSNEILGTGGTTGACGTTTCCAATGAGATCCTC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
TLE4-HDAC5chr982320857chr1742165064015KSDDNLVVDVSNEILAAAAGTGATGACAACTTGGTGGTTGACGTTTCCAATGAGATCCTC
TLE4-HDAC5chr982320857chr1742165064116SDDNLVVDVSNEILTAGTGATGACAACTTGGTGGTTGACGTTTCCAATGAGATCCTCACC
TLE4-HDAC5chr982320857chr1742165064217DDNLVVDVSNEILTKGATGACAACTTGGTGGTTGACGTTTCCAATGAGATCCTCACCAAG
TLE4-HDAC5chr982320857chr1742165064318DNLVVDVSNEILTKTGACAACTTGGTGGTTGACGTTTCCAATGAGATCCTCACCAAGACA

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Information of the samples that have these potential fusion neoantigens of TLE4-HDAC5

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
GBMTLE4-HDAC5chr982320857ENST00000265284chr1742165064ENST00000225983TCGA-06-0749-01A

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Potential target of CAR-T therapy development for TLE4-HDAC5

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 TLE4-HDAC5

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 TLE4-HDAC5

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