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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:CHD1-MTOR

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CHD1-MTOR
FusionPDB ID: 16279
FusionGDB2.0 ID: 16279
HgeneTgene
Gene symbol

CHD1

MTOR

Gene ID

1105

2475

Gene namechromodomain helicase DNA binding protein 1mechanistic target of rapamycin kinase
SynonymsCHD-1|PILBOSFRAP|FRAP1|FRAP2|RAFT1|RAPT1|SKS
Cytomap

5q15-q21.1

1p36.22

Type of geneprotein-codingprotein-coding
Descriptionchromodomain-helicase-DNA-binding protein 1ATP-dependent helicase CHD1serine/threonine-protein kinase mTORFK506 binding protein 12-rapamycin associated protein 2FK506-binding protein 12-rapamycin complex-associated protein 1FKBP-rapamycin associated proteinFKBP12-rapamycin complex-associated protein 1mammalian target o
Modification date2020031320200329
UniProtAcc

Q86WJ1

Main function of 5'-partner protein: FUNCTION: DNA helicase which plays a role in chromatin-remodeling following DNA damage (PubMed:19661379, PubMed:29220653). Targeted to sites of DNA damage through interaction with poly(ADP-ribose) and functions to regulate chromatin during DNA repair (PubMed:19661379). Able to catalyze nucleosome sliding in an ATP-dependent manner (PubMed:19661379). Helicase activity is strongly stimulated upon poly(ADP-ribose)-binding (PubMed:19661379, PubMed:29220653). {ECO:0000269|PubMed:19661379, ECO:0000269|PubMed:29220653}.

TLDC1

Main function of 5'-partner protein: 456
Ensembl transtripts involved in fusion geneENST idsENST00000284049, ENST00000511067, 
ENST00000376838, ENST00000495435, 
ENST00000361445, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score14 X 15 X 8=168012 X 11 X 8=1056
# samples 1919
** MAII scorelog2(19/1680*10)=-3.14438990933518
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(19/1056*10)=-2.47453851102751
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CHD1 [Title/Abstract] AND MTOR [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CHD1 [Title/Abstract] AND MTOR [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CHD1(98199112)-MTOR(11273623), # samples:4
Anticipated loss of major functional domain due to fusion event.CHD1-MTOR 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.
CHD1-MTOR 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.
CHD1-MTOR 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.
CHD1-MTOR 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.
CHD1-MTOR seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
CHD1-MTOR seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CHD1-MTOR seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
CHD1-MTOR seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
CHD1-MTOR seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
CHD1-MTOR seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
CHD1-MTOR seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
CHD1-MTOR seems lost the major protein functional domain in Tgene partner, which is a kinase 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
TgeneMTOR

GO:0001558

regulation of cell growth

18762023

TgeneMTOR

GO:0001934

positive regulation of protein phosphorylation

20233713

TgeneMTOR

GO:0006468

protein phosphorylation

12150926|15467718|18925875

TgeneMTOR

GO:0009267

cellular response to starvation

28223137

TgeneMTOR

GO:0010507

negative regulation of autophagy

30704899

TgeneMTOR

GO:0016242

negative regulation of macroautophagy

25327288

TgeneMTOR

GO:0016310

phosphorylation

11853878|25327288

TgeneMTOR

GO:0031667

response to nutrient levels

29750193

TgeneMTOR

GO:0034198

cellular response to amino acid starvation

22424946

TgeneMTOR

GO:0038202

TORC1 signaling

28223137

TgeneMTOR

GO:0043200

response to amino acid

18497260

TgeneMTOR

GO:0045727

positive regulation of translation

18762023

TgeneMTOR

GO:0046777

protein autophosphorylation

15467718

TgeneMTOR

GO:0071230

cellular response to amino acid stimulus

22424946

TgeneMTOR

GO:0071233

cellular response to leucine

22424946

TgeneMTOR

GO:1990253

cellular response to leucine starvation

22424946



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/chr5:98199112/chr1:11273623)
- 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 CHD1 (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 MTOR (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)
ENST00000284049CHD1chr598204199-ENST00000361445MTORchr111273623-9881439815089302926

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

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 CHD1-MTOR

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CHD1chr598204199MTORchr11127362343981416EESEELDQKTFSIEFWVMNTSIQSTI

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Potential FusionNeoAntigen Information of CHD1-MTOR 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.
CHD1-MTOR_98204199_11273623.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)
CHD1-MTORchr598204199chr1112736234398HLA-B57:01KTFSIEFW0.99970.9226816
CHD1-MTORchr598204199chr1112736234398HLA-B58:02KTFSIEFW0.99910.8315816
CHD1-MTORchr598204199chr1112736234398HLA-B57:03KTFSIEFW0.99830.9238816
CHD1-MTORchr598204199chr1112736234398HLA-B58:01KTFSIEFW0.99830.7839816
CHD1-MTORchr598204199chr1112736234398HLA-B15:17KTFSIEFW0.99740.8077816
CHD1-MTORchr598204199chr1112736234398HLA-B15:16KTFSIEFW0.99720.6199816
CHD1-MTORchr598204199chr1112736234398HLA-A32:13KTFSIEFW0.99490.9408816
CHD1-MTORchr598204199chr1112736234398HLA-B15:01DQKTFSIEF0.99480.8772615
CHD1-MTORchr598204199chr1112736234398HLA-B14:02DQKTFSIEF0.99330.5911615
CHD1-MTORchr598204199chr1112736234398HLA-B14:01DQKTFSIEF0.99330.5911615
CHD1-MTORchr598204199chr1112736234398HLA-B15:02DQKTFSIEF0.98020.9281615
CHD1-MTORchr598204199chr1112736234398HLA-A02:21KTFSIEFWV0.97310.7318817
CHD1-MTORchr598204199chr1112736234398HLA-B18:01DQKTFSIEF0.96980.8939615
CHD1-MTORchr598204199chr1112736234398HLA-A02:35KTFSIEFWV0.96930.6714817
CHD1-MTORchr598204199chr1112736234398HLA-A02:60KTFSIEFWV0.95230.6272817
CHD1-MTORchr598204199chr1112736234398HLA-A02:29KTFSIEFWV0.94670.6397817
CHD1-MTORchr598204199chr1112736234398HLA-A02:20KTFSIEFWV0.94530.6453817
CHD1-MTORchr598204199chr1112736234398HLA-B15:03DQKTFSIEF0.87640.7497615
CHD1-MTORchr598204199chr1112736234398HLA-B15:18DQKTFSIEF0.81550.6891615
CHD1-MTORchr598204199chr1112736234398HLA-B52:01DQKTFSIEF0.66450.7619615
CHD1-MTORchr598204199chr1112736234398HLA-B15:10DQKTFSIEF0.59180.5547615
CHD1-MTORchr598204199chr1112736234398HLA-B15:01LDQKTFSIEF0.98910.8689515
CHD1-MTORchr598204199chr1112736234398HLA-B15:07DQKTFSIEF0.98740.6709615
CHD1-MTORchr598204199chr1112736234398HLA-B15:21DQKTFSIEF0.9810.8763615
CHD1-MTORchr598204199chr1112736234398HLA-B15:04DQKTFSIEF0.94220.9019615
CHD1-MTORchr598204199chr1112736234398HLA-B15:31DQKTFSIEF0.92140.874615
CHD1-MTORchr598204199chr1112736234398HLA-B15:05DQKTFSIEF0.88230.8618615
CHD1-MTORchr598204199chr1112736234398HLA-B39:12DQKTFSIEF0.71430.9225615
CHD1-MTORchr598204199chr1112736234398HLA-B14:03DQKTFSIEF0.70640.7026615
CHD1-MTORchr598204199chr1112736234398HLA-B51:07DQKTFSIEF0.55730.7274615
CHD1-MTORchr598204199chr1112736234398HLA-B15:07LDQKTFSIEF0.99240.6824515
CHD1-MTORchr598204199chr1112736234398HLA-B57:10KTFSIEFW0.99970.9226816
CHD1-MTORchr598204199chr1112736234398HLA-B58:06KTFSIEFW0.99870.6738816
CHD1-MTORchr598204199chr1112736234398HLA-B57:04KTFSIEFW0.99820.5288816
CHD1-MTORchr598204199chr1112736234398HLA-B57:02KTFSIEFW0.99790.7747816
CHD1-MTORchr598204199chr1112736234398HLA-A32:01KTFSIEFW0.99760.919816
CHD1-MTORchr598204199chr1112736234398HLA-B15:11DQKTFSIEF0.99530.8351615
CHD1-MTORchr598204199chr1112736234398HLA-B15:08DQKTFSIEF0.99520.8349615
CHD1-MTORchr598204199chr1112736234398HLA-B15:135DQKTFSIEF0.9950.8828615
CHD1-MTORchr598204199chr1112736234398HLA-B15:125DQKTFSIEF0.99480.8772615
CHD1-MTORchr598204199chr1112736234398HLA-B15:34DQKTFSIEF0.99480.8772615
CHD1-MTORchr598204199chr1112736234398HLA-B15:33DQKTFSIEF0.99480.8772615
CHD1-MTORchr598204199chr1112736234398HLA-B35:43DQKTFSIEF0.99460.838615
CHD1-MTORchr598204199chr1112736234398HLA-B15:27DQKTFSIEF0.99390.8886615
CHD1-MTORchr598204199chr1112736234398HLA-B18:04DQKTFSIEF0.99080.9057615
CHD1-MTORchr598204199chr1112736234398HLA-B15:24DQKTFSIEF0.98910.8051615
CHD1-MTORchr598204199chr1112736234398HLA-B15:50DQKTFSIEF0.98860.8741615
CHD1-MTORchr598204199chr1112736234398HLA-B15:35DQKTFSIEF0.98850.8756615
CHD1-MTORchr598204199chr1112736234398HLA-B18:06DQKTFSIEF0.97780.9023615
CHD1-MTORchr598204199chr1112736234398HLA-B15:53DQKTFSIEF0.97760.8691615
CHD1-MTORchr598204199chr1112736234398HLA-B18:07DQKTFSIEF0.97710.8419615
CHD1-MTORchr598204199chr1112736234398HLA-A02:14KTFSIEFWV0.97370.6494817
CHD1-MTORchr598204199chr1112736234398HLA-A02:06KTFSIEFWV0.97310.7318817
CHD1-MTORchr598204199chr1112736234398HLA-B18:08DQKTFSIEF0.9730.8463615
CHD1-MTORchr598204199chr1112736234398HLA-B35:24DQKTFSIEF0.97180.8253615
CHD1-MTORchr598204199chr1112736234398HLA-B18:05DQKTFSIEF0.96980.8939615
CHD1-MTORchr598204199chr1112736234398HLA-B18:03DQKTFSIEF0.96590.8808615
CHD1-MTORchr598204199chr1112736234398HLA-B15:68DQKTFSIEF0.93830.6034615
CHD1-MTORchr598204199chr1112736234398HLA-A69:01KTFSIEFWV0.93240.9105817
CHD1-MTORchr598204199chr1112736234398HLA-B15:13DQKTFSIEF0.91910.6442615
CHD1-MTORchr598204199chr1112736234398HLA-B15:12DQKTFSIEF0.91220.8678615
CHD1-MTORchr598204199chr1112736234398HLA-B35:20DQKTFSIEF0.90230.9458615
CHD1-MTORchr598204199chr1112736234398HLA-B15:54DQKTFSIEF0.88570.8413615
CHD1-MTORchr598204199chr1112736234398HLA-B15:20DQKTFSIEF0.88070.9173615
CHD1-MTORchr598204199chr1112736234398HLA-B35:28DQKTFSIEF0.87150.9302615
CHD1-MTORchr598204199chr1112736234398HLA-B18:11DQKTFSIEF0.85070.892615
CHD1-MTORchr598204199chr1112736234398HLA-B48:02DQKTFSIEF0.70170.9182615
CHD1-MTORchr598204199chr1112736234398HLA-B08:12DQKTFSIEF0.68810.6607615
CHD1-MTORchr598204199chr1112736234398HLA-B15:54LDQKTFSIEF0.9970.8309515
CHD1-MTORchr598204199chr1112736234398HLA-B15:68LDQKTFSIEF0.99680.6222515
CHD1-MTORchr598204199chr1112736234398HLA-B15:53LDQKTFSIEF0.99460.8591515
CHD1-MTORchr598204199chr1112736234398HLA-B15:35LDQKTFSIEF0.99170.8586515
CHD1-MTORchr598204199chr1112736234398HLA-B15:24LDQKTFSIEF0.98960.8234515
CHD1-MTORchr598204199chr1112736234398HLA-B15:27LDQKTFSIEF0.98960.8681515
CHD1-MTORchr598204199chr1112736234398HLA-B15:135LDQKTFSIEF0.98920.8775515
CHD1-MTORchr598204199chr1112736234398HLA-B15:34LDQKTFSIEF0.98910.8689515
CHD1-MTORchr598204199chr1112736234398HLA-B15:125LDQKTFSIEF0.98910.8689515
CHD1-MTORchr598204199chr1112736234398HLA-B15:33LDQKTFSIEF0.98910.8689515
CHD1-MTORchr598204199chr1112736234398HLA-B15:50LDQKTFSIEF0.98330.9207515
CHD1-MTORchr598204199chr1112736234398HLA-B15:12LDQKTFSIEF0.97690.8814515
CHD1-MTORchr598204199chr1112736234398HLA-B15:13DQKTFSIEFW0.86170.6156616

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Potential FusionNeoAntigen Information of CHD1-MTOR 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.
CHD1-MTOR_98204199_11273623.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)
CHD1-MTORchr598204199chr1112736234398DRB3-0202SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0202FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0205SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0205FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0210SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0210FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0211SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0211FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0212SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0212FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0213SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0213FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0215SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0215FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0216SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0217SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0217FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0218SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0218FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0220SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0220FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0223SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0223FSIEFWVMNTSIQST1025
CHD1-MTORchr598204199chr1112736234398DRB3-0225SIEFWVMNTSIQSTI1126
CHD1-MTORchr598204199chr1112736234398DRB3-0225FSIEFWVMNTSIQST1025

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Fusion breakpoint peptide structures of CHD1-MTOR

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
1348DQKTFSIEFWVMNTCHD1MTORchr598204199chr1112736234398

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CHD1-MTOR

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-B14:023BVN1348DQKTFSIEFWVMNT-6.73316-6.85256
HLA-B14:023BVN1348DQKTFSIEFWVMNT-5.18372-6.22502
HLA-B52:013W391348DQKTFSIEFWVMNT-7.13025-8.17155
HLA-B52:013W391348DQKTFSIEFWVMNT-6.86422-6.98362
HLA-A24:025HGA1348DQKTFSIEFWVMNT-6.81438-6.93378
HLA-A24:025HGA1348DQKTFSIEFWVMNT-6.00064-7.04194
HLA-B27:056PYJ1348DQKTFSIEFWVMNT-5.12416-6.16546
HLA-B44:053DX81348DQKTFSIEFWVMNT-6.05577-6.17517
HLA-B44:053DX81348DQKTFSIEFWVMNT-5.8156-6.8569
HLA-A02:016TDR1348DQKTFSIEFWVMNT-6.6937-6.8131

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Vaccine Design for the FusionNeoAntigens of CHD1-MTOR

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
CHD1-MTORchr598204199chr111273623515LDQKTFSIEFCTGGATCAGAAGACATTCAGCATTGAATTC
CHD1-MTORchr598204199chr111273623615DQKTFSIEFGATCAGAAGACATTCAGCATTGAATTC
CHD1-MTORchr598204199chr111273623616DQKTFSIEFWGATCAGAAGACATTCAGCATTGAATTCTGG
CHD1-MTORchr598204199chr111273623816KTFSIEFWAAGACATTCAGCATTGAATTCTGG
CHD1-MTORchr598204199chr111273623817KTFSIEFWVAAGACATTCAGCATTGAATTCTGGGTC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CHD1-MTORchr598204199chr1112736231025FSIEFWVMNTSIQSTTTCAGCATTGAATTCTGGGTCATGAACACCTCAATTCAGAGCACG
CHD1-MTORchr598204199chr1112736231126SIEFWVMNTSIQSTIAGCATTGAATTCTGGGTCATGAACACCTCAATTCAGAGCACGATC

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Information of the samples that have these potential fusion neoantigens of CHD1-MTOR

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
LAMLCHD1-MTORchr598204199ENST00000284049chr111273623ENST00000361445TCGA-AB-2939_61FFWAAXX_7

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Potential target of CAR-T therapy development for CHD1-MTOR

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 CHD1-MTOR

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 CHD1-MTOR

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