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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:XPC-RCOR1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: XPC-RCOR1
FusionPDB ID: 99632
FusionGDB2.0 ID: 99632
HgeneTgene
Gene symbol

XPC

RCOR1

Gene ID

7508

23186

Gene nameXPC complex subunit, DNA damage recognition and repair factorREST corepressor 1
SynonymsRAD4|XP3|XPCC|p125COREST|RCOR
Cytomap

3p25.1

14q32.31-q32.32

Type of geneprotein-codingprotein-coding
DescriptionDNA repair protein complementing XP-C cellsmutant xeroderma pigmentosum group Cxeroderma pigmentosum, complementation group CREST corepressor 1
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000285021, ENST00000449060, 
ENST00000262241, ENST00000570597, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score5 X 5 X 3=7513 X 15 X 4=780
# samples 515
** MAII scorelog2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/780*10)=-2.37851162325373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: XPC [Title/Abstract] AND RCOR1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: XPC [Title/Abstract] AND RCOR1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)XPC(14209757)-RCOR1(103177272), # samples:3
Anticipated loss of major functional domain due to fusion event.XPC-RCOR1 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.
XPC-RCOR1 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.
XPC-RCOR1 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.
XPC-RCOR1 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
HgeneXPC

GO:0000715

nucleotide-excision repair, DNA damage recognition

10873465|19941824

HgeneXPC

GO:0006289

nucleotide-excision repair

8168482|9734359|11259578

HgeneXPC

GO:0045893

positive regulation of transcription, DNA-templated

29973595|31527837

HgeneXPC

GO:0070914

UV-damage excision repair

8077226

TgeneRCOR1

GO:0045892

negative regulation of transcription, DNA-templated

10449787

TgeneRCOR1

GO:0070933

histone H4 deacetylation

17555596



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/chr3:14209757/chr14:103177272)
- 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 XPC (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 RCOR1 (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)
ENST00000285021XPCchr314209757-ENST00000262241RCOR1chr14103177272+55007512151429404
ENST00000285021XPCchr314209757-ENST00000570597RCOR1chr14103177272+54997512151429404
ENST00000449060XPCchr314209757-ENST00000262241RCOR1chr14103177272+517442501103367
ENST00000449060XPCchr314209757-ENST00000570597RCOR1chr14103177272+517342501103367

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
ENST00000285021ENST00000262241XPCchr314209757-RCOR1chr14103177272+0.0001597630.99984026
ENST00000285021ENST00000570597XPCchr314209757-RCOR1chr14103177272+0.0001592470.99984074
ENST00000449060ENST00000262241XPCchr314209757-RCOR1chr14103177272+0.0001533160.9998467
ENST00000449060ENST00000570597XPCchr314209757-RCOR1chr14103177272+0.0001529040.99984705

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 XPC-RCOR1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
XPCchr314209757RCOR1chr14103177272425141SENDWEEAKTRERSEDELEEANGNNP
XPCchr314209757RCOR1chr14103177272751178EIETPEQAKTRERSEDELEEANGNNP

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Potential FusionNeoAntigen Information of XPC-RCOR1 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.
XPC-RCOR1_14209757_103177272.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)
XPC-RCOR1chr314209757chr14103177272425HLA-B39:13RERSEDEL0.91760.90761018
XPC-RCOR1chr314209757chr14103177272425HLA-B39:01TRERSEDEL0.97430.8607918
XPC-RCOR1chr314209757chr14103177272425HLA-B38:02TRERSEDEL0.95050.8864918
XPC-RCOR1chr314209757chr14103177272425HLA-B38:01TRERSEDEL0.94090.8801918
XPC-RCOR1chr314209757chr14103177272425HLA-B45:01RERSEDELEEA0.99920.87771021
XPC-RCOR1chr314209757chr14103177272425HLA-B41:01RERSEDELEEA0.99810.75631021
XPC-RCOR1chr314209757chr14103177272425HLA-B50:01RERSEDELEEA0.99380.74891021
XPC-RCOR1chr314209757chr14103177272425HLA-B39:08RERSEDEL0.96260.73331018
XPC-RCOR1chr314209757chr14103177272425HLA-B39:05TRERSEDEL0.94010.8388918
XPC-RCOR1chr314209757chr14103177272425HLA-B40:06RERSEDELEEA0.99990.68131021
XPC-RCOR1chr314209757chr14103177272425HLA-B39:31TRERSEDEL0.97220.8586918
XPC-RCOR1chr314209757chr14103177272425HLA-B38:05TRERSEDEL0.94090.8801918
XPC-RCOR1chr314209757chr14103177272425HLA-B39:11TRERSEDEL0.67050.6782918
XPC-RCOR1chr314209757chr14103177272425HLA-B50:04RERSEDELEEA0.99380.74891021
XPC-RCOR1chr314209757chr14103177272425HLA-B50:05RERSEDELEEA0.99380.74891021

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Potential FusionNeoAntigen Information of XPC-RCOR1 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.
XPC-RCOR1_14209757_103177272.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)
XPC-RCOR1chr314209757chr14103177272425DRB5-0101ENDWEEAKTRERSED116
XPC-RCOR1chr314209757chr14103177272425DRB5-0101SENDWEEAKTRERSE015
XPC-RCOR1chr314209757chr14103177272425DRB5-0101NDWEEAKTRERSEDE217
XPC-RCOR1chr314209757chr14103177272425DRB5-0102ENDWEEAKTRERSED116
XPC-RCOR1chr314209757chr14103177272425DRB5-0102SENDWEEAKTRERSE015
XPC-RCOR1chr314209757chr14103177272425DRB5-0103ENDWEEAKTRERSED116
XPC-RCOR1chr314209757chr14103177272425DRB5-0103SENDWEEAKTRERSE015
XPC-RCOR1chr314209757chr14103177272425DRB5-0104ENDWEEAKTRERSED116
XPC-RCOR1chr314209757chr14103177272425DRB5-0104SENDWEEAKTRERSE015
XPC-RCOR1chr314209757chr14103177272425DRB5-0104NDWEEAKTRERSEDE217
XPC-RCOR1chr314209757chr14103177272425DRB5-0105ENDWEEAKTRERSED116
XPC-RCOR1chr314209757chr14103177272425DRB5-0105SENDWEEAKTRERSE015
XPC-RCOR1chr314209757chr14103177272425DRB5-0105NDWEEAKTRERSEDE217
XPC-RCOR1chr314209757chr14103177272425DRB5-0108NENDWEEAKTRERSED116
XPC-RCOR1chr314209757chr14103177272425DRB5-0108NSENDWEEAKTRERSE015
XPC-RCOR1chr314209757chr14103177272425DRB5-0111ENDWEEAKTRERSED116
XPC-RCOR1chr314209757chr14103177272425DRB5-0111SENDWEEAKTRERSE015
XPC-RCOR1chr314209757chr14103177272425DRB5-0111NDWEEAKTRERSEDE217
XPC-RCOR1chr314209757chr14103177272425DRB5-0112ENDWEEAKTRERSED116
XPC-RCOR1chr314209757chr14103177272425DRB5-0112SENDWEEAKTRERSE015
XPC-RCOR1chr314209757chr14103177272425DRB5-0112NDWEEAKTRERSEDE217
XPC-RCOR1chr314209757chr14103177272425DRB5-0113ENDWEEAKTRERSED116
XPC-RCOR1chr314209757chr14103177272425DRB5-0113SENDWEEAKTRERSE015
XPC-RCOR1chr314209757chr14103177272425DRB5-0113NDWEEAKTRERSEDE217
XPC-RCOR1chr314209757chr14103177272425DRB5-0114ENDWEEAKTRERSED116
XPC-RCOR1chr314209757chr14103177272425DRB5-0114SENDWEEAKTRERSE015
XPC-RCOR1chr314209757chr14103177272425DRB5-0114NDWEEAKTRERSEDE217
XPC-RCOR1chr314209757chr14103177272425DRB5-0203ENDWEEAKTRERSED116

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Fusion breakpoint peptide structures of XPC-RCOR1

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
1530EAKTRERSEDELEEXPCRCOR1chr314209757chr14103177272425

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of XPC-RCOR1

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-B14:023BVN1530EAKTRERSEDELEE-7.82647-7.93987
HLA-B14:023BVN1530EAKTRERSEDELEE-4.19548-5.23078
HLA-B52:013W391530EAKTRERSEDELEE-7.04824-7.16164
HLA-B52:013W391530EAKTRERSEDELEE-6.88601-7.92131
HLA-A11:014UQ21530EAKTRERSEDELEE-8.85724-8.97064
HLA-A24:025HGA1530EAKTRERSEDELEE-5.84033-6.87563
HLA-A24:025HGA1530EAKTRERSEDELEE-5.52087-5.63427
HLA-B27:056PYJ1530EAKTRERSEDELEE-8.42495-8.53835
HLA-B44:053DX81530EAKTRERSEDELEE-6.24277-7.27807
HLA-B44:053DX81530EAKTRERSEDELEE-5.08381-5.19721
HLA-A02:016TDR1530EAKTRERSEDELEE-5.75077-6.78607
HLA-A02:016TDR1530EAKTRERSEDELEE-5.43723-5.55063

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Vaccine Design for the FusionNeoAntigens of XPC-RCOR1

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
XPC-RCOR1chr314209757chr141031772721018RERSEDELAGAAAGAAGCGAGGATGAACTGGA
XPC-RCOR1chr314209757chr141031772721021RERSEDELEEAAGAAAGAAGCGAGGATGAACTGGAAGAGGCAAA
XPC-RCOR1chr314209757chr14103177272918TRERSEDELAAGAGAAAGAAGCGAGGATGAACTGGA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
XPC-RCOR1chr314209757chr14103177272015SENDWEEAKTRERSETGAAAATGATTGGGAAGAGGCGAAGACAAGAGAAAGAAGCGAGGA
XPC-RCOR1chr314209757chr14103177272116ENDWEEAKTRERSEDAAATGATTGGGAAGAGGCGAAGACAAGAGAAAGAAGCGAGGATGA
XPC-RCOR1chr314209757chr14103177272217NDWEEAKTRERSEDETGATTGGGAAGAGGCGAAGACAAGAGAAAGAAGCGAGGATGAACT

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Information of the samples that have these potential fusion neoantigens of XPC-RCOR1

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
BRCAXPC-RCOR1chr314209757ENST00000449060chr14103177272ENST00000262241TCGA-A8-A06Q-01A

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Potential target of CAR-T therapy development for XPC-RCOR1

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 XPC-RCOR1

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 XPC-RCOR1

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