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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:NIPBL-NUP155

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NIPBL-NUP155
FusionPDB ID: 59208
FusionGDB2.0 ID: 59208
HgeneTgene
Gene symbol

NIPBL

NUP155

Gene ID

25836

9631

Gene nameNIPBL cohesin loading factornucleoporin 155
SynonymsCDLS|CDLS1|IDN3|IDN3-B|Scc2ATFB15|N155
Cytomap

5p13.2

5p13.2

Type of geneprotein-codingprotein-coding
Descriptionnipped-B-like proteinNipped-B homologSCC2 homologdelanginsister chromatid cohesion 2 homolognuclear pore complex protein Nup155155 kDa nucleoporinnucleoporin 155kDnucleoporin 155kDa
Modification date2020031320200329
UniProtAcc

Q6KC79

Main function of 5'-partner protein: FUNCTION: Plays an important role in the loading of the cohesin complex on to DNA. Forms a heterodimeric complex (also known as cohesin loading complex) with MAU2/SCC4 which mediates the loading of the cohesin complex onto chromatin (PubMed:22628566, PubMed:28914604). Plays a role in cohesin loading at sites of DNA damage. Its recruitment to double-strand breaks (DSBs) sites occurs in a CBX3-, RNF8- and RNF168-dependent manner whereas its recruitment to UV irradiation-induced DNA damage sites occurs in a ATM-, ATR-, RNF8- and RNF168-dependent manner (PubMed:28167679). Along with ZNF609, promotes cortical neuron migration during brain development by regulating the transcription of crucial genes in this process. Preferentially binds promoters containing paused RNA polymerase II. Up-regulates the expression of SEMA3A, NRP1, PLXND1 and GABBR2 genes, among others (By similarity). {ECO:0000250|UniProtKB:Q6KCD5, ECO:0000269|PubMed:22628566, ECO:0000269|PubMed:28167679, ECO:0000269|PubMed:28914604}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000282516, ENST00000448238, 
ENST00000504430, 
ENST00000502533, 
ENST00000513532, ENST00000231498, 
ENST00000381843, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score26 X 13 X 16=54085 X 7 X 5=175
# samples 437
** MAII scorelog2(43/5408*10)=-3.65268658669272
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/175*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: NIPBL [Title/Abstract] AND NUP155 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: NIPBL [Title/Abstract] AND NUP155 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NIPBL(36877280)-NUP155(37309369), # samples:2
Anticipated loss of major functional domain due to fusion event.NIPBL-NUP155 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.
NIPBL-NUP155 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.
NIPBL-NUP155 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.
NIPBL-NUP155 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
HgeneNIPBL

GO:0000122

negative regulation of transcription by RNA polymerase II

18854353

HgeneNIPBL

GO:0031065

positive regulation of histone deacetylation

18854353

HgeneNIPBL

GO:0045892

negative regulation of transcription, DNA-templated

18854353

HgeneNIPBL

GO:0071921

cohesin loading

22628566

TgeneNUP155

GO:0006998

nuclear envelope organization

19070573



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/chr5:36877280/chr5:37309369)
- 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 NIPBL (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 NUP155 (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)
ENST00000282516NIPBLchr537027514+ENST00000231498NUP155chr537310845-11864636149981002533
ENST00000282516NIPBLchr537027514+ENST00000381843NUP155chr537310845-8162636149981002533
ENST00000448238NIPBLchr537027514+ENST00000231498NUP155chr537310845-11833633046880692533
ENST00000448238NIPBLchr537027514+ENST00000381843NUP155chr537310845-8131633046880692533

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
ENST00000282516ENST00000231498NIPBLchr537027514+NUP155chr537310845-0.0003879470.99961203
ENST00000282516ENST00000381843NIPBLchr537027514+NUP155chr537310845-0.0006926220.9993074
ENST00000448238ENST00000231498NIPBLchr537027514+NUP155chr537310845-0.0003808020.9996191
ENST00000448238ENST00000381843NIPBLchr537027514+NUP155chr537310845-0.0006841680.99931586

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 NIPBL-NUP155

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
NIPBLchr537027514NUP155chr53731084563301954DTGYDWFEQLLQNELQEQLKITTFKD
NIPBLchr537027514NUP155chr53731084563611954DTGYDWFEQLLQNELQEQLKITTFKD

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Potential FusionNeoAntigen Information of NIPBL-NUP155 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.
NIPBL-NUP155_37027514_37310845.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)
NIPBL-NUP155chr537027514chr5373108456361HLA-B44:03NELQEQLKI0.9970.93611221
NIPBL-NUP155chr537027514chr5373108456361HLA-B48:01LQNELQEQL0.99480.61241019
NIPBL-NUP155chr537027514chr5373108456361HLA-B13:01FEQLLQNEL0.99350.9642615
NIPBL-NUP155chr537027514chr5373108456361HLA-B13:01NELQEQLKI0.99320.67691221
NIPBL-NUP155chr537027514chr5373108456361HLA-B45:01NELQEQLKI0.99210.80971221
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:01LQNELQEQL0.99080.87611019
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:22LQNELQEQL0.98740.68331019
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:01FEQLLQNEL0.95980.9175615
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:60LQNELQEQL0.95770.61461019
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:24LQNELQEQL0.95660.59691019
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:67LQNELQEQL0.95660.59691019
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:30LQNELQEQL0.95660.59691019
NIPBL-NUP155chr537027514chr5373108456361HLA-B47:01FEQLLQNEL0.95120.5672615
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:04LQNELQEQL0.94780.82271019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:24LQNELQEQL0.9470.75041019
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:01NELQEQLKI0.94550.83711221
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:21LQNELQEQL0.94240.70031019
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:17LQNELQEQL0.93650.62081019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:01LQNELQEQL0.89460.98211019
NIPBL-NUP155chr537027514chr5373108456361HLA-B13:02LQNELQEQL0.82490.78261019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:13FEQLLQNEL0.80970.9573615
NIPBL-NUP155chr537027514chr5373108456361HLA-B13:01LQNELQEQL0.80670.99011019
NIPBL-NUP155chr537027514chr5373108456361HLA-B38:02FEQLLQNEL0.79970.9871615
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:29LQNELQEQL0.79160.60061019
NIPBL-NUP155chr537027514chr5373108456361HLA-B47:01LQNELQEQL0.78510.84331019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:13LQNELQEQL0.74860.98521019
NIPBL-NUP155chr537027514chr5373108456361HLA-B38:01LQNELQEQL0.74350.99341019
NIPBL-NUP155chr537027514chr5373108456361HLA-B38:02LQNELQEQL0.72540.99411019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:03LQNELQEQL0.71460.84831019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:10LQNELQEQL0.66580.75071019
NIPBL-NUP155chr537027514chr5373108456361HLA-B41:01NELQEQLKI0.64580.9121221
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:37LQNELQEQL0.60920.76931019
NIPBL-NUP155chr537027514chr5373108456361HLA-B50:01FEQLLQNEL0.58080.851615
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:19LQNELQEQL0.55450.70591019
NIPBL-NUP155chr537027514chr5373108456361HLA-B41:01FEQLLQNEL0.50420.9849615
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:13NELQEQLKI0.23730.82671221
NIPBL-NUP155chr537027514chr5373108456361HLA-B52:01LQNELQEQL0.19850.99091019
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:22LLQNELQEQL0.99470.6696919
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:19LLQNELQEQL0.8240.7088919
NIPBL-NUP155chr537027514chr5373108456361HLA-B13:01LLQNELQEQL0.24120.9927919
NIPBL-NUP155chr537027514chr5373108456361HLA-B13:02LQNELQEQLKI0.95270.55821021
NIPBL-NUP155chr537027514chr5373108456361HLA-B13:01QLLQNELQEQL0.57550.9973819
NIPBL-NUP155chr537027514chr5373108456361HLA-B40:06FEQLLQNEL0.99920.7132615
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:02LQNELQEQL0.98860.64871019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:04LQNELQEQL0.98480.88681019
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:05LQNELQEQL0.98020.74141019
NIPBL-NUP155chr537027514chr5373108456361HLA-B44:10FEQLLQNEL0.96910.7104615
NIPBL-NUP155chr537027514chr5373108456361HLA-C08:03LQNELQEQL0.96520.99681019
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:01LQNELQEQL0.95660.59691019
NIPBL-NUP155chr537027514chr5373108456361HLA-B48:03LQNELQEQL0.91620.58721019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:09LQNELQEQL0.91260.81071019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:12LQNELQEQL0.87990.98231019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:09FEQLLQNEL0.86480.7759615
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:08LQNELQEQL0.84130.96911019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:05FEQLLQNEL0.81740.9086615
NIPBL-NUP155chr537027514chr5373108456361HLA-C02:06LQNELQEQL0.7830.9811019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:08FEQLLQNEL0.7030.9657615
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:05LQNELQEQL0.69510.97971019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:05LQNELQEQL0.38530.90141019
NIPBL-NUP155chr537027514chr5373108456361HLA-B51:07NELQEQLKI0.37080.65091221
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:08NELQEQLKI0.31770.81131221
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:02LLQNELQEQL0.99520.6456919
NIPBL-NUP155chr537027514chr5373108456361HLA-B48:03LLQNELQEQL0.25120.6206919
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:02QLLQNELQEQL0.99380.6911819
NIPBL-NUP155chr537027514chr5373108456361HLA-B40:04FEQLLQNEL0.9990.7828615
NIPBL-NUP155chr537027514chr5373108456361HLA-B44:26NELQEQLKI0.9970.93611221
NIPBL-NUP155chr537027514chr5373108456361HLA-B44:07NELQEQLKI0.9970.93611221
NIPBL-NUP155chr537027514chr5373108456361HLA-B44:13NELQEQLKI0.9970.93611221
NIPBL-NUP155chr537027514chr5373108456361HLA-B40:04NELQEQLKI0.99470.51561221
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:24LQNELQEQL0.99220.96581019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:135LQNELQEQL0.99090.86391019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:33LQNELQEQL0.99080.87611019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:34LQNELQEQL0.99080.87611019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:125LQNELQEQL0.99080.87611019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:27LQNELQEQL0.99010.89381019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:50LQNELQEQL0.98880.92231019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:73LQNELQEQL0.98310.90291019
NIPBL-NUP155chr537027514chr5373108456361HLA-C08:01LQNELQEQL0.96520.99681019
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:04FEQLLQNEL0.96460.9271615
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:07FEQLLQNEL0.96040.8763615
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:08FEQLLQNEL0.96030.9204615
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:05FEQLLQNEL0.95980.9175615
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:06FEQLLQNEL0.95470.9194615
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:03FEQLLQNEL0.94690.9071615
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:05NELQEQLKI0.94550.83711221
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:14LQNELQEQL0.94340.69711019
NIPBL-NUP155chr537027514chr5373108456361HLA-C07:04LQNELQEQL0.94310.98741019
NIPBL-NUP155chr537027514chr5373108456361HLA-A02:06LQNELQEQL0.94240.70031019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:68LQNELQEQL0.93970.75671019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:53LQNELQEQL0.93870.85871019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:30LQNELQEQL0.92970.9381019
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:11FEQLLQNEL0.92770.902615
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:12LQNELQEQL0.92510.91881019
NIPBL-NUP155chr537027514chr5373108456361HLA-B40:12LQNELQEQL0.91620.58721019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:31LQNELQEQL0.90980.98251019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:02LQNELQEQL0.90840.98511019
NIPBL-NUP155chr537027514chr5373108456361HLA-B40:49LQNELQEQL0.89720.56191019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:54LQNELQEQL0.89080.84921019
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:03NELQEQLKI0.88810.82441221
NIPBL-NUP155chr537027514chr5373108456361HLA-B40:21LQNELQEQL0.85560.59871019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:31FEQLLQNEL0.8420.9318615
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:02FEQLLQNEL0.83540.9576615
NIPBL-NUP155chr537027514chr5373108456361HLA-B18:11NELQEQLKI0.81220.76771221
NIPBL-NUP155chr537027514chr5373108456361HLA-B41:03NELQEQLKI0.78910.63031221
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:11LQNELQEQL0.78010.96071019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:11FEQLLQNEL0.75330.9438615
NIPBL-NUP155chr537027514chr5373108456361HLA-B38:05LQNELQEQL0.74350.99341019
NIPBL-NUP155chr537027514chr5373108456361HLA-B41:03FEQLLQNEL0.71150.7961615
NIPBL-NUP155chr537027514chr5373108456361HLA-B35:13LQNELQEQL0.64690.88961019
NIPBL-NUP155chr537027514chr5373108456361HLA-B48:02LQNELQEQL0.62820.93251019
NIPBL-NUP155chr537027514chr5373108456361HLA-B50:04FEQLLQNEL0.58080.851615
NIPBL-NUP155chr537027514chr5373108456361HLA-B50:05FEQLLQNEL0.58080.851615
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:09LQNELQEQL0.44280.72821019
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:20LQNELQEQL0.37840.9381019
NIPBL-NUP155chr537027514chr5373108456361HLA-B35:28LQNELQEQL0.37260.93851019
NIPBL-NUP155chr537027514chr5373108456361HLA-B39:02NELQEQLKI0.20490.8321221
NIPBL-NUP155chr537027514chr5373108456361HLA-B15:73LLQNELQEQL0.94880.9613919
NIPBL-NUP155chr537027514chr5373108456361HLA-B40:12LLQNELQEQL0.25120.6206919
NIPBL-NUP155chr537027514chr5373108456361HLA-B40:21LLQNELQEQL0.2230.6269919

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Potential FusionNeoAntigen Information of NIPBL-NUP155 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 NIPBL-NUP155

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
2346FEQLLQNELQEQLKNIPBLNUP155chr537027514chr5373108456361

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of NIPBL-NUP155

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-B14:023BVN2346FEQLLQNELQEQLK-7.9962-8.1096
HLA-B14:023BVN2346FEQLLQNELQEQLK-5.70842-6.74372
HLA-B52:013W392346FEQLLQNELQEQLK-6.83737-6.95077
HLA-B52:013W392346FEQLLQNELQEQLK-4.4836-5.5189
HLA-A11:014UQ22346FEQLLQNELQEQLK-10.0067-10.1201
HLA-A11:014UQ22346FEQLLQNELQEQLK-9.03915-10.0745
HLA-A24:025HGA2346FEQLLQNELQEQLK-6.56204-6.67544
HLA-A24:025HGA2346FEQLLQNELQEQLK-5.42271-6.45801
HLA-B44:053DX82346FEQLLQNELQEQLK-7.85648-8.89178
HLA-B44:053DX82346FEQLLQNELQEQLK-5.3978-5.5112
HLA-A02:016TDR2346FEQLLQNELQEQLK-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of NIPBL-NUP155

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
NIPBL-NUP155chr537027514chr5373108451019LQNELQEQLCTTCAAAACGAACTTCAAGAGCAGCTG
NIPBL-NUP155chr537027514chr5373108451021LQNELQEQLKICTTCAAAACGAACTTCAAGAGCAGCTGAAGATC
NIPBL-NUP155chr537027514chr5373108451221NELQEQLKIAACGAACTTCAAGAGCAGCTGAAGATC
NIPBL-NUP155chr537027514chr537310845615FEQLLQNELTTTGAGCAACTGCTTCAAAACGAACTT
NIPBL-NUP155chr537027514chr537310845819QLLQNELQEQLCAACTGCTTCAAAACGAACTTCAAGAGCAGCTG
NIPBL-NUP155chr537027514chr537310845919LLQNELQEQLCTGCTTCAAAACGAACTTCAAGAGCAGCTG

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 NIPBL-NUP155

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
BRCANIPBL-NUP155chr537027514ENST00000282516chr537310845ENST00000231498TCGA-BH-A1FM

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Potential target of CAR-T therapy development for NIPBL-NUP155

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 NIPBL-NUP155

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 NIPBL-NUP155

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