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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:ZNF696-MED16

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ZNF696-MED16
FusionPDB ID: 102731
FusionGDB2.0 ID: 102731
HgeneTgene
Gene symbol

ZNF696

MED16

Gene ID

79943

10025

Gene namezinc finger protein 696mediator complex subunit 16
Synonyms-DRIP92|THRAP5|TRAP95
Cytomap

8q24.3

19p13.3

Type of geneprotein-codingprotein-coding
Descriptionzinc finger protein 696mediator of RNA polymerase II transcription subunit 16thyroid hormone receptor-associated protein 5thyroid hormone receptor-associated protein complex 95 kDa componentthyroid hormone receptor-associated protein, 95-kD subunitvitamin D3 receptor-intera
Modification date2020031320200313
UniProtAcc.

Q9Y2X0

Main function of 5'-partner protein: FUNCTION: Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors. {ECO:0000269|PubMed:10198638, ECO:0000269|PubMed:10235266}.
Ensembl transtripts involved in fusion geneENST idsENST00000330143, ENST00000520333, 
ENST00000521537, 
ENST00000606828, 
ENST00000269814, ENST00000312090, 
ENST00000325464, ENST00000395808, 
ENST00000589119, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 2 X 2=128 X 8 X 6=384
# samples 39
** MAII scorelog2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(9/384*10)=-2.09310940439148
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ZNF696 [Title/Abstract] AND MED16 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ZNF696 [Title/Abstract] AND MED16 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ZNF696(144375235)-MED16(880148), # samples:2
Anticipated loss of major functional domain due to fusion event.ZNF696-MED16 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.
ZNF696-MED16 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.
ZNF696-MED16 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ZNF696-MED16 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
ZNF696-MED16 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
ZNF696-MED16 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
TgeneMED16

GO:0006367

transcription initiation from RNA polymerase II promoter

12218053

TgeneMED16

GO:0045893

positive regulation of transcription, DNA-templated

10198638



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/chr8:144375235/chr19:880148)
- 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 ZNF696 (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 MED16 (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)
ENST00000330143ZNF696chr8144375235+ENST00000395808MED16chr19880148-22694733731857494
ENST00000330143ZNF696chr8144375235+ENST00000589119MED16chr19880148-21044733731965530
ENST00000330143ZNF696chr8144375235+ENST00000312090MED16chr19880148-23254733731914513
ENST00000330143ZNF696chr8144375235+ENST00000269814MED16chr19880148-20744733731587404
ENST00000330143ZNF696chr8144375235+ENST00000325464MED16chr19880148-21034733731965530
ENST00000520333ZNF696chr8144375235+ENST00000395808MED16chr19880148-22364403401824494
ENST00000520333ZNF696chr8144375235+ENST00000589119MED16chr19880148-20714403401932530
ENST00000520333ZNF696chr8144375235+ENST00000312090MED16chr19880148-22924403401881513
ENST00000520333ZNF696chr8144375235+ENST00000269814MED16chr19880148-20414403401554404
ENST00000520333ZNF696chr8144375235+ENST00000325464MED16chr19880148-20704403401932530

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
ENST00000330143ENST00000395808ZNF696chr8144375235+MED16chr19880148-0.122076760.8779233
ENST00000330143ENST00000589119ZNF696chr8144375235+MED16chr19880148-0.107095510.89290446
ENST00000330143ENST00000312090ZNF696chr8144375235+MED16chr19880148-0.12801490.8719851
ENST00000330143ENST00000269814ZNF696chr8144375235+MED16chr19880148-0.2292460.77075404
ENST00000330143ENST00000325464ZNF696chr8144375235+MED16chr19880148-0.107315730.8926843
ENST00000520333ENST00000395808ZNF696chr8144375235+MED16chr19880148-0.123469450.8765306
ENST00000520333ENST00000589119ZNF696chr8144375235+MED16chr19880148-0.109239620.8907603
ENST00000520333ENST00000312090ZNF696chr8144375235+MED16chr19880148-0.12980360.8701964
ENST00000520333ENST00000269814ZNF696chr8144375235+MED16chr19880148-0.231402840.7685972
ENST00000520333ENST00000325464ZNF696chr8144375235+MED16chr19880148-0.109455790.89054424

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 ZNF696-MED16

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ZNF696chr8144375235MED16chr1988014844033GAKESSTLMESLAGLALAFHDGSVHI
ZNF696chr8144375235MED16chr1988014847333GAKESSTLMESLAGLALAFHDGSVHI

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Potential FusionNeoAntigen Information of ZNF696-MED16 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.
ZNF696-MED16_144375235_880148.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)
ZNF696-MED16chr8144375235chr19880148473HLA-B15:01SLAGLALAF0.99830.97381019
ZNF696-MED16chr8144375235chr19880148473HLA-A02:27TLMESLAGL0.99280.5595615
ZNF696-MED16chr8144375235chr19880148473HLA-A02:13TLMESLAGL0.99210.6637615
ZNF696-MED16chr8144375235chr19880148473HLA-A02:38TLMESLAGL0.98840.5409615
ZNF696-MED16chr8144375235chr19880148473HLA-B15:25SLAGLALAF0.98550.98181019
ZNF696-MED16chr8144375235chr19880148473HLA-A02:04TLMESLAGL0.98360.6006615
ZNF696-MED16chr8144375235chr19880148473HLA-B15:02SLAGLALAF0.98120.98631019
ZNF696-MED16chr8144375235chr19880148473HLA-B47:01MESLAGLAL0.97970.5582817
ZNF696-MED16chr8144375235chr19880148473HLA-A02:17TLMESLAGL0.9780.5134615
ZNF696-MED16chr8144375235chr19880148473HLA-B18:01MESLAGLAL0.93390.7729817
ZNF696-MED16chr8144375235chr19880148473HLA-B46:01SLAGLALAF0.91650.76321019
ZNF696-MED16chr8144375235chr19880148473HLA-A32:13SLAGLALAF0.91290.99281019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:03SLAGLALAF0.85180.94461019
ZNF696-MED16chr8144375235chr19880148473HLA-B39:13MESLAGLAL0.77380.9481817
ZNF696-MED16chr8144375235chr19880148473HLA-B15:10MESLAGLAL0.76420.5523817
ZNF696-MED16chr8144375235chr19880148473HLA-B39:01MESLAGLAL0.76270.9458817
ZNF696-MED16chr8144375235chr19880148473HLA-B38:02MESLAGLAL0.7320.9742817
ZNF696-MED16chr8144375235chr19880148473HLA-B15:37MESLAGLAL0.62690.5478817
ZNF696-MED16chr8144375235chr19880148473HLA-B41:01MESLAGLAL0.59360.9144817
ZNF696-MED16chr8144375235chr19880148473HLA-B50:01MESLAGLAL0.52560.8739817
ZNF696-MED16chr8144375235chr19880148473HLA-B13:01SLAGLALAF0.08380.99221019
ZNF696-MED16chr8144375235chr19880148473HLA-A26:02ESLAGLALAF0.98910.627919
ZNF696-MED16chr8144375235chr19880148473HLA-B45:01MESLAGLALA0.98460.9777818
ZNF696-MED16chr8144375235chr19880148473HLA-B50:02MESLAGLALA0.97190.9133818
ZNF696-MED16chr8144375235chr19880148473HLA-A02:38STLMESLAGL0.95250.7349515
ZNF696-MED16chr8144375235chr19880148473HLA-A02:04STLMESLAGL0.95080.5739515
ZNF696-MED16chr8144375235chr19880148473HLA-A02:13STLMESLAGL0.94310.7259515
ZNF696-MED16chr8144375235chr19880148473HLA-A02:27STLMESLAGL0.9410.6107515
ZNF696-MED16chr8144375235chr19880148473HLA-B50:01MESLAGLALA0.8550.9058818
ZNF696-MED16chr8144375235chr19880148473HLA-A02:19STLMESLAGL0.83060.5082515
ZNF696-MED16chr8144375235chr19880148473HLA-A02:27TLMESLAGLAL0.99760.5531617
ZNF696-MED16chr8144375235chr19880148473HLA-A02:38TLMESLAGLAL0.99690.5484617
ZNF696-MED16chr8144375235chr19880148473HLA-B18:01MESLAGLALAF0.99560.8133819
ZNF696-MED16chr8144375235chr19880148473HLA-A02:04TLMESLAGLAL0.99390.6463617
ZNF696-MED16chr8144375235chr19880148473HLA-A02:17TLMESLAGLAL0.99240.607617
ZNF696-MED16chr8144375235chr19880148473HLA-A02:38SSTLMESLAGL0.81280.6623415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:13SSTLMESLAGL0.7570.7098415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:27SSTLMESLAGL0.73110.5667415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:20SSTLMESLAGL0.70430.5206415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:35SSTLMESLAGL0.69190.5481415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:04SSTLMESLAGL0.67080.5812415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:29SSTLMESLAGL0.66030.5106415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:60SSTLMESLAGL0.65590.5049415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:67SSTLMESLAGL0.65250.5092415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:30SSTLMESLAGL0.65250.5092415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:24SSTLMESLAGL0.65250.5092415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:11SSTLMESLAGL0.64970.5419415
ZNF696-MED16chr8144375235chr19880148473HLA-A02:19SSTLMESLAGL0.54810.5526415
ZNF696-MED16chr8144375235chr19880148473HLA-B40:06MESLAGLAL0.99910.6813817
ZNF696-MED16chr8144375235chr19880148473HLA-B15:07SLAGLALAF0.99490.91611019
ZNF696-MED16chr8144375235chr19880148473HLA-B44:10MESLAGLAL0.99450.572817
ZNF696-MED16chr8144375235chr19880148473HLA-B15:21SLAGLALAF0.9830.9651019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:04SLAGLALAF0.9390.98361019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:31SLAGLALAF0.88210.94871019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:05SLAGLALAF0.87510.94251019
ZNF696-MED16chr8144375235chr19880148473HLA-B39:08MESLAGLAL0.83340.8857817
ZNF696-MED16chr8144375235chr19880148473HLA-B39:09MESLAGLAL0.78220.7568817
ZNF696-MED16chr8144375235chr19880148473HLA-B39:05MESLAGLAL0.74480.9288817
ZNF696-MED16chr8144375235chr19880148473HLA-A02:01SSTLMESLAGL0.65250.5092415
ZNF696-MED16chr8144375235chr19880148473HLA-B40:04MESLAGLAL0.99920.7761817
ZNF696-MED16chr8144375235chr19880148473HLA-B15:34SLAGLALAF0.99830.97381019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:125SLAGLALAF0.99830.97381019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:27SLAGLALAF0.99830.98141019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:33SLAGLALAF0.99830.97381019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:11SLAGLALAF0.9980.96591019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:135SLAGLALAF0.9980.97551019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:08SLAGLALAF0.99780.96311019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:50SLAGLALAF0.99730.98561019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:24SLAGLALAF0.99710.99031019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:35SLAGLALAF0.99650.97881019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:12SLAGLALAF0.99490.9861019
ZNF696-MED16chr8144375235chr19880148473HLA-A02:03TLMESLAGL0.99420.5263615
ZNF696-MED16chr8144375235chr19880148473HLA-B15:39SLAGLALAF0.98390.96351019
ZNF696-MED16chr8144375235chr19880148473HLA-A32:01SLAGLALAF0.96470.99211019
ZNF696-MED16chr8144375235chr19880148473HLA-B18:04MESLAGLAL0.96130.7869817
ZNF696-MED16chr8144375235chr19880148473HLA-B15:13SLAGLALAF0.95220.96311019
ZNF696-MED16chr8144375235chr19880148473HLA-B18:07MESLAGLAL0.95170.7072817
ZNF696-MED16chr8144375235chr19880148473HLA-B18:05MESLAGLAL0.93390.7729817
ZNF696-MED16chr8144375235chr19880148473HLA-B18:08MESLAGLAL0.92470.7428817
ZNF696-MED16chr8144375235chr19880148473HLA-B18:03MESLAGLAL0.92040.7529817
ZNF696-MED16chr8144375235chr19880148473HLA-B15:73SLAGLALAF0.9120.98641019
ZNF696-MED16chr8144375235chr19880148473HLA-B18:06MESLAGLAL0.90720.7924817
ZNF696-MED16chr8144375235chr19880148473HLA-B15:20SLAGLALAF0.88810.96751019
ZNF696-MED16chr8144375235chr19880148473HLA-B35:20SLAGLALAF0.85590.97461019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:73TLMESLAGL0.85190.9522615
ZNF696-MED16chr8144375235chr19880148473HLA-B35:28SLAGLALAF0.84330.9721019
ZNF696-MED16chr8144375235chr19880148473HLA-B39:11MESLAGLAL0.83310.8804817
ZNF696-MED16chr8144375235chr19880148473HLA-B18:11MESLAGLAL0.83120.8493817
ZNF696-MED16chr8144375235chr19880148473HLA-B15:30SLAGLALAF0.81860.98171019
ZNF696-MED16chr8144375235chr19880148473HLA-B15:30TLMESLAGL0.77810.958615
ZNF696-MED16chr8144375235chr19880148473HLA-B39:02MESLAGLAL0.77280.9506817
ZNF696-MED16chr8144375235chr19880148473HLA-B39:31MESLAGLAL0.77250.9456817
ZNF696-MED16chr8144375235chr19880148473HLA-B41:03MESLAGLAL0.7550.6401817
ZNF696-MED16chr8144375235chr19880148473HLA-A69:01TLMESLAGL0.73950.5425615
ZNF696-MED16chr8144375235chr19880148473HLA-B48:02MESLAGLAL0.58520.8878817
ZNF696-MED16chr8144375235chr19880148473HLA-B15:09MESLAGLAL0.55120.8049817
ZNF696-MED16chr8144375235chr19880148473HLA-B50:04MESLAGLAL0.52560.8739817
ZNF696-MED16chr8144375235chr19880148473HLA-B50:05MESLAGLAL0.52560.8739817
ZNF696-MED16chr8144375235chr19880148473HLA-B40:21SLAGLALAF0.06880.73231019
ZNF696-MED16chr8144375235chr19880148473HLA-A25:01ESLAGLALAF0.98330.9534919
ZNF696-MED16chr8144375235chr19880148473HLA-A02:03STLMESLAGL0.9710.6302515
ZNF696-MED16chr8144375235chr19880148473HLA-A69:01STLMESLAGL0.87470.6722515
ZNF696-MED16chr8144375235chr19880148473HLA-A68:02STLMESLAGL0.86330.6049515
ZNF696-MED16chr8144375235chr19880148473HLA-B50:04MESLAGLALA0.8550.9058818
ZNF696-MED16chr8144375235chr19880148473HLA-B50:05MESLAGLALA0.8550.9058818
ZNF696-MED16chr8144375235chr19880148473HLA-B18:11MESLAGLALAF0.99840.8616819
ZNF696-MED16chr8144375235chr19880148473HLA-B18:05MESLAGLALAF0.99560.8133819

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Potential FusionNeoAntigen Information of ZNF696-MED16 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.

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)

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Fusion breakpoint peptide structures of ZNF696-MED16

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
9481TLMESLAGLALAFHZNF696MED16chr8144375235chr19880148473

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ZNF696-MED16

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-B14:023BVN9481TLMESLAGLALAFH-7.15543-7.26883
HLA-B14:023BVN9481TLMESLAGLALAFH-4.77435-5.80965
HLA-B52:013W399481TLMESLAGLALAFH-6.80875-6.92215
HLA-B52:013W399481TLMESLAGLALAFH-4.20386-5.23916
HLA-A11:014UQ29481TLMESLAGLALAFH-7.5194-8.5547
HLA-A11:014UQ29481TLMESLAGLALAFH-6.9601-7.0735
HLA-A24:025HGA9481TLMESLAGLALAFH-7.52403-7.63743
HLA-A24:025HGA9481TLMESLAGLALAFH-5.82433-6.85963
HLA-B27:056PYJ9481TLMESLAGLALAFH-3.28285-4.31815
HLA-B44:053DX89481TLMESLAGLALAFH-5.91172-6.94702
HLA-B44:053DX89481TLMESLAGLALAFH-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of ZNF696-MED16

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
ZNF696-MED16chr8144375235chr198801481019SLAGLALAFCCCTTGCAGGGCTGGCCCTGGCCTTCC
ZNF696-MED16chr8144375235chr19880148415SSTLMESLAGLGCAGTACCCTGATGGAGTCCCTTGCAGGGCTGG
ZNF696-MED16chr8144375235chr19880148515STLMESLAGLGTACCCTGATGGAGTCCCTTGCAGGGCTGG
ZNF696-MED16chr8144375235chr19880148615TLMESLAGLCCCTGATGGAGTCCCTTGCAGGGCTGG
ZNF696-MED16chr8144375235chr19880148617TLMESLAGLALCCCTGATGGAGTCCCTTGCAGGGCTGGCCCTGG
ZNF696-MED16chr8144375235chr19880148817MESLAGLALTGGAGTCCCTTGCAGGGCTGGCCCTGG
ZNF696-MED16chr8144375235chr19880148818MESLAGLALATGGAGTCCCTTGCAGGGCTGGCCCTGGCCT
ZNF696-MED16chr8144375235chr19880148819MESLAGLALAFTGGAGTCCCTTGCAGGGCTGGCCCTGGCCTTCC
ZNF696-MED16chr8144375235chr19880148919ESLAGLALAFAGTCCCTTGCAGGGCTGGCCCTGGCCTTCC

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

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Information of the samples that have these potential fusion neoantigens of ZNF696-MED16

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
ESCAZNF696-MED16chr8144375235ENST00000330143chr19880148ENST00000269814TCGA-L5-A8NH

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Potential target of CAR-T therapy development for ZNF696-MED16

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 ZNF696-MED16

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 ZNF696-MED16

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