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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:CCNT1-HSPD1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CCNT1-HSPD1
FusionPDB ID: 14191
FusionGDB2.0 ID: 14191
HgeneTgene
Gene symbol

CCNT1

HSPD1

Gene ID

904

3329

Gene namecyclin T1heat shock protein family D (Hsp60) member 1
SynonymsCCNT|CYCT1|HIVE1CPN60|GROEL|HLD4|HSP-60|HSP60|HSP65|HuCHA60|SPG13
Cytomap

12q13.11-q13.12

2q33.1

Type of geneprotein-codingprotein-coding
Descriptioncyclin-T1CDK9-associated C-type proteinMLLT10/CCNT1 fusioncyclin C-related proteinhuman immunodeficiency virus type 1 (HIV-1) expression (elevated) 160 kDa heat shock protein, mitochondrial60 kDa chaperoninP60 lymphocyte proteinchaperonin 60epididymis secretory sperm binding proteinheat shock 60kDa protein 1 (chaperonin)heat shock protein 65mitochondrial matrix protein P1short heat shock prote
Modification date2020031320200315
UniProtAcc

O60563

Main function of 5'-partner protein: FUNCTION: Regulatory subunit of the cyclin-dependent kinase pair (CDK9/cyclin-T1) complex, also called positive transcription elongation factor B (P-TEFb), which is proposed to facilitate the transition from abortive to productive elongation by phosphorylating the CTD (C-terminal domain) of the large subunit of RNA polymerase II (RNA Pol II). {ECO:0000269|PubMed:16109376, ECO:0000269|PubMed:16109377}.; FUNCTION: (Microbial infection) In case of HIV or SIV infections, binds to the transactivation domain of the viral nuclear transcriptional activator, Tat, thereby increasing Tat's affinity for the transactivating response RNA element (TAR RNA). Serves as an essential cofactor for Tat, by promoting RNA Pol II activation, allowing transcription of viral genes. {ECO:0000269|PubMed:10329125, ECO:0000269|PubMed:10329126}.

P10809

Main function of 5'-partner protein: FUNCTION: Chaperonin implicated in mitochondrial protein import and macromolecular assembly. Together with Hsp10, facilitates the correct folding of imported proteins. May also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix (PubMed:1346131, PubMed:11422376). The functional units of these chaperonins consist of heptameric rings of the large subunit Hsp60, which function as a back-to-back double ring. In a cyclic reaction, Hsp60 ring complexes bind one unfolded substrate protein per ring, followed by the binding of ATP and association with 2 heptameric rings of the co-chaperonin Hsp10. This leads to sequestration of the substrate protein in the inner cavity of Hsp60 where, for a certain period of time, it can fold undisturbed by other cell components. Synchronous hydrolysis of ATP in all Hsp60 subunits results in the dissociation of the chaperonin rings and the release of ADP and the folded substrate protein (Probable). {ECO:0000269|PubMed:11422376, ECO:0000269|PubMed:1346131, ECO:0000305|PubMed:25918392}.
Ensembl transtripts involved in fusion geneENST idsENST00000261900, ENST00000544407, 
ENST00000345042, ENST00000388968, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 8 X 4=19214 X 10 X 6=840
# samples 716
** MAII scorelog2(7/192*10)=-1.45567948377619
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/840*10)=-2.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CCNT1 [Title/Abstract] AND HSPD1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CCNT1 [Title/Abstract] AND HSPD1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CCNT1(49099550)-HSPD1(198353971), # samples:1
Anticipated loss of major functional domain due to fusion event.CCNT1-HSPD1 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.
CCNT1-HSPD1 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
HgeneCCNT1

GO:0045944

positive regulation of transcription by RNA polymerase II

15563843

TgeneHSPD1

GO:0002368

B cell cytokine production

16148103

TgeneHSPD1

GO:0002755

MyD88-dependent toll-like receptor signaling pathway

16148103

TgeneHSPD1

GO:0002842

positive regulation of T cell mediated immune response to tumor cell

10663613

TgeneHSPD1

GO:0006919

activation of cysteine-type endopeptidase activity involved in apoptotic process

17823127

TgeneHSPD1

GO:0006986

response to unfolded protein

11050098

TgeneHSPD1

GO:0032727

positive regulation of interferon-alpha production

17164250

TgeneHSPD1

GO:0032729

positive regulation of interferon-gamma production

17164250

TgeneHSPD1

GO:0032733

positive regulation of interleukin-10 production

16148103

TgeneHSPD1

GO:0032735

positive regulation of interleukin-12 production

17164250

TgeneHSPD1

GO:0032755

positive regulation of interleukin-6 production

16148103

TgeneHSPD1

GO:0042026

protein refolding

11050098

TgeneHSPD1

GO:0042100

B cell proliferation

16148103

TgeneHSPD1

GO:0042110

T cell activation

15371451|17164250|18256040

TgeneHSPD1

GO:0042113

B cell activation

16148103

TgeneHSPD1

GO:0043032

positive regulation of macrophage activation

17164250

TgeneHSPD1

GO:0044406

adhesion of symbiont to host

20633027

TgeneHSPD1

GO:0048291

isotype switching to IgG isotypes

16148103

TgeneHSPD1

GO:0050870

positive regulation of T cell activation

16148103|17164250



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/chr12:49099550/chr2:198353971)
- 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 CCNT1 (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 HSPD1 (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)
ENST00000261900CCNT1chr1249099550-ENST00000388968HSPD1chr2198353971-18135952231347374
ENST00000261900CCNT1chr1249099550-ENST00000345042HSPD1chr2198353971-18085952231347374

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
ENST00000261900ENST00000388968CCNT1chr1249099550-HSPD1chr2198353971-0.0007114890.99928844
ENST00000261900ENST00000345042CCNT1chr1249099550-HSPD1chr2198353971-0.0007432950.9992567

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 CCNT1-HSPD1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CCNT1chr1249099550HSPD1chr2198353971595124LHPQESLPDTRSEVFGEEGLTLNLED

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Potential FusionNeoAntigen Information of CCNT1-HSPD1 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.
CCNT1-HSPD1_49099550_198353971.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)
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:01LPDTRSEVF0.99660.8528615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:08LPDTRSEVF0.99540.867615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:05LPDTRSEVF0.99020.5884615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:03LPDTRSEVF0.98550.8755615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:13SLPDTRSEV0.98370.6787514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:22SLPDTRSEV0.98170.5909514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:27SLPDTRSEV0.96940.6521514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:38SLPDTRSEV0.95360.726514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:29SLPDTRSEV0.94510.6052514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:30SLPDTRSEV0.94150.6045514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:24SLPDTRSEV0.94150.6045514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:67SLPDTRSEV0.94150.6045514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:60SLPDTRSEV0.94040.6325514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:11SLPDTRSEV0.9390.6178514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:21SLPDTRSEV0.91780.7199514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:20SLPDTRSEV0.91670.6047514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:35SLPDTRSEV0.91460.6146514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:04SLPDTRSEV0.89840.657514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:19SLPDTRSEV0.89130.5642514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:17SLPDTRSEV0.85690.5829514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B08:01LPDTRSEVF0.80980.6209615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B47:01SEVFGEEGL0.77320.77611120
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:02LPDTRSEVF0.76320.9354615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:04LPDTRSEVF0.76320.9354615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:13SEVFGEEGL0.210.94441120
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A66:01EVFGEEGLTL0.99630.5861222
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A26:03EVFGEEGLTL0.99470.60031222
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A26:15EVFGEEGLTL0.98950.60431222
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A26:14EVFGEEGLTL0.98950.60431222
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:08SLPDTRSEVF0.96510.841515
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B47:01SEVFGEEGLTL0.99940.73431122
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B44:03SEVFGEEGLTL0.99930.96711122
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:13SEVFGEEGLTL0.9960.91261122
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:10LPDTRSEV0.65240.9391614
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C04:07LPDTRSEVF0.99830.8979615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C04:10LPDTRSEVF0.99830.8749615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C05:09LPDTRSEVF0.99830.9298615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C08:15LPDTRSEVF0.99650.9773615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B15:31LPDTRSEVF0.99610.8337615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B44:10SEVFGEEGL0.99120.52991120
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:05SLPDTRSEV0.97410.5688514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B07:12LPDTRSEVF0.9670.629615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B14:03LPDTRSEVF0.96010.8534615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:01SLPDTRSEV0.94150.6045514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:07SLPDTRSEV0.93890.6162514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B42:02LPDTRSEVF0.89930.6452615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B42:01LPDTRSEVF0.85530.637615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:12LPDTRSEVF0.76320.9354615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C01:30SLPDTRSEV0.70450.9697514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C01:17SLPDTRSEV0.65780.9565514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C08:03LPDTRSEVF0.65370.9786615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:09LPDTRSEVF0.64680.5337615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:10LPDTRSEVF0.60620.9229615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C04:14LPDTRSEVF0.50970.8803615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:08SEVFGEEGL0.4440.79641120
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C01:17SLPDTRSEVF0.99450.9456515
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C01:30SLPDTRSEVF0.99220.9634515
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A26:01EVFGEEGLTL0.98950.60431222
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B07:12SLPDTRSEVF0.92020.6045515
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:10SLPDTRSEVF0.60420.7831515
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B44:10SEVFGEEGLTL0.99950.50051122
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:08SEVFGEEGLTL0.99690.80451122
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C04:01LPDTRSEVF0.99830.8979615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C05:01LPDTRSEVF0.99830.9298615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C04:03LPDTRSEVF0.99820.92615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:23LPDTRSEVF0.99660.8556615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:77LPDTRSEVF0.99660.8528615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C08:02LPDTRSEVF0.99650.9773615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:20LPDTRSEVF0.99620.9053615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C18:01LPDTRSEVF0.99620.9099615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B40:04SEVFGEEGL0.99550.72881120
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:03SLPDTRSEV0.99410.6488514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:30LPDTRSEVF0.99050.7485615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:17LPDTRSEVF0.99050.7485615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:24LPDTRSEVF0.9890.8631615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:11LPDTRSEVF0.98320.856615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:13LPDTRSEVF0.98210.8832615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:14SLPDTRSEV0.92080.6179514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A02:06SLPDTRSEV0.91780.7199514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C01:03SLPDTRSEV0.86390.9305514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B08:18LPDTRSEVF0.80980.6209615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:11LPDTRSEVF0.79630.8683615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:09LPDTRSEVF0.76320.9354615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B18:04LPDTRSEVF0.76080.8847615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B08:12LPDTRSEVF0.7250.7511615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C01:02SLPDTRSEV0.70480.9554514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B67:01LPDTRSEVF0.65730.755615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C08:01LPDTRSEVF0.65370.9786615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C04:04LPDTRSEVF0.55610.9199615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B18:07LPDTRSEVF0.5260.8193615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B35:43LPDTRSEVF0.19110.7954615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B15:08LPDTRSEVF0.18910.7894615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B15:11LPDTRSEVF0.17090.7911615
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:02SEVFGEEGL0.1590.95281120
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C07:04SLPDTRSEV0.04030.9623514
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B15:27SLPDTRSEVF0.99960.8831515
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C01:03SLPDTRSEVF0.99740.9025515
CCNT1-HSPD1chr1249099550chr2198353971595HLA-C01:02SLPDTRSEVF0.99660.9445515
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A25:01EVFGEEGLTL0.99520.86651222
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A68:02EVFGEEGLTL0.99280.70531222
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B15:30SLPDTRSEVF0.97930.6129515
CCNT1-HSPD1chr1249099550chr2198353971595HLA-A69:01EVFGEEGLTL0.97810.81891222
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B40:04SEVFGEEGLTL0.99980.73311122
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B44:26SEVFGEEGLTL0.99930.96711122
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B44:13SEVFGEEGLTL0.99930.96711122
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B44:07SEVFGEEGLTL0.99930.96711122
CCNT1-HSPD1chr1249099550chr2198353971595HLA-B39:02SEVFGEEGLTL0.99490.92391122

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Potential FusionNeoAntigen Information of CCNT1-HSPD1 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 CCNT1-HSPD1

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
5373LPDTRSEVFGEEGLCCNT1HSPD1chr1249099550chr2198353971595

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CCNT1-HSPD1

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-B14:023BVN5373LPDTRSEVFGEEGL-7.15543-7.26883
HLA-B14:023BVN5373LPDTRSEVFGEEGL-4.77435-5.80965
HLA-B52:013W395373LPDTRSEVFGEEGL-6.80875-6.92215
HLA-B52:013W395373LPDTRSEVFGEEGL-4.20386-5.23916
HLA-A11:014UQ25373LPDTRSEVFGEEGL-7.5194-8.5547
HLA-A11:014UQ25373LPDTRSEVFGEEGL-6.9601-7.0735
HLA-A24:025HGA5373LPDTRSEVFGEEGL-7.52403-7.63743
HLA-A24:025HGA5373LPDTRSEVFGEEGL-5.82433-6.85963
HLA-B27:056PYJ5373LPDTRSEVFGEEGL-3.28285-4.31815
HLA-B44:053DX85373LPDTRSEVFGEEGL-5.91172-6.94702
HLA-B44:053DX85373LPDTRSEVFGEEGL-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of CCNT1-HSPD1

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
CCNT1-HSPD1chr1249099550chr21983539711120SEVFGEEGLAGTGAGGTGTTTGGAGAAGAGGGATTG
CCNT1-HSPD1chr1249099550chr21983539711122SEVFGEEGLTLAGTGAGGTGTTTGGAGAAGAGGGATTGACCCTG
CCNT1-HSPD1chr1249099550chr21983539711222EVFGEEGLTLGAGGTGTTTGGAGAAGAGGGATTGACCCTG
CCNT1-HSPD1chr1249099550chr2198353971514SLPDTRSEVTCCCTTCCTGATACTAGAAGTGAGGTG
CCNT1-HSPD1chr1249099550chr2198353971515SLPDTRSEVFTCCCTTCCTGATACTAGAAGTGAGGTGTTT
CCNT1-HSPD1chr1249099550chr2198353971614LPDTRSEVCTTCCTGATACTAGAAGTGAGGTG
CCNT1-HSPD1chr1249099550chr2198353971615LPDTRSEVFCTTCCTGATACTAGAAGTGAGGTGTTT

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 CCNT1-HSPD1

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
STADCCNT1-HSPD1chr1249099550ENST00000261900chr2198353971ENST00000345042TCGA-IN-A7NT

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Potential target of CAR-T therapy development for CCNT1-HSPD1

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 CCNT1-HSPD1

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 CCNT1-HSPD1

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