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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:HNRNPUL1-ZNF765

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: HNRNPUL1-ZNF765
FusionPDB ID: 37319
FusionGDB2.0 ID: 37319
HgeneTgene
Gene symbol

HNRNPUL1

ZNF765

Gene ID

11100

91661

Gene nameheterogeneous nuclear ribonucleoprotein U like 1zinc finger protein 765
SynonymsE1B-AP5|E1BAP5|HNRPUL1-
Cytomap

19q13.2

19q13.42

Type of geneprotein-codingprotein-coding
Descriptionheterogeneous nuclear ribonucleoprotein U-like protein 1E1B 55kDa associated protein 5E1B-55 kDa-associated protein 5adenovirus early region 1B-associated protein 5zinc finger protein 765
Modification date2020032720200313
UniProtAcc

Q9BUJ2

Main function of 5'-partner protein: FUNCTION: Acts as a basic transcriptional regulator. Represses basic transcription driven by several virus and cellular promoters. When associated with BRD7, activates transcription of glucocorticoid-responsive promoter in the absence of ligand-stimulation. Plays also a role in mRNA processing and transport. Binds avidly to poly(G) and poly(C) RNA homopolymers in vitro. {ECO:0000269|PubMed:12489984, ECO:0000269|PubMed:9733834}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000263367, ENST00000352456, 
ENST00000392006, ENST00000593587, 
ENST00000595018, ENST00000602130, 
ENST00000378215, ENST00000594207, 
ENST00000596086, ENST00000396408, 
ENST00000594030, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score18 X 14 X 12=30241 X 1 X 1=1
# samples 201
** MAII scorelog2(20/3024*10)=-3.91838623444635
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Fusion gene context

PubMed: HNRNPUL1 [Title/Abstract] AND ZNF765 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: HNRNPUL1 [Title/Abstract] AND ZNF765 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)HNRNPUL1(41787180)-ZNF765(53905318), # samples:1
Anticipated loss of major functional domain due to fusion event.HNRNPUL1-ZNF765 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.
HNRNPUL1-ZNF765 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.
HNRNPUL1-ZNF765 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.
HNRNPUL1-ZNF765 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


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/chr19:41787180/chr19:53905318)
- 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 HNRNPUL1 (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 ZNF765 (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)
ENST00000352456HNRNPUL1chr1941787180+ENST00000396408ZNF765chr1953905318+5228791112347778
ENST00000352456HNRNPUL1chr1941787180+ENST00000594030ZNF765chr1953905318+146879111958315
ENST00000595018HNRNPUL1chr1941787180+ENST00000396408ZNF765chr1953905318+5205768452324759
ENST00000595018HNRNPUL1chr1941787180+ENST00000594030ZNF765chr1953905318+144576845935296
ENST00000392006HNRNPUL1chr1941787180+ENST00000396408ZNF765chr1953905318+56091172442728894
ENST00000392006HNRNPUL1chr1941787180+ENST00000594030ZNF765chr1953905318+18491172441339431
ENST00000602130HNRNPUL1chr1941787180+ENST00000396408ZNF765chr1953905318+54891052532608851
ENST00000602130HNRNPUL1chr1941787180+ENST00000594030ZNF765chr1953905318+17291052531219388
ENST00000593587HNRNPUL1chr1941787180+ENST00000396408ZNF765chr1953905318+5230793942349751
ENST00000593587HNRNPUL1chr1941787180+ENST00000594030ZNF765chr1953905318+147079394960288
ENST00000263367HNRNPUL1chr1941787180+ENST00000396408ZNF765chr1953905318+53639261612482773
ENST00000263367HNRNPUL1chr1941787180+ENST00000594030ZNF765chr1953905318+16039261611093310

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
ENST00000352456ENST00000396408HNRNPUL1chr1941787180+ZNF765chr1953905318+0.000417490.99958247
ENST00000352456ENST00000594030HNRNPUL1chr1941787180+ZNF765chr1953905318+0.0022569630.997743
ENST00000595018ENST00000396408HNRNPUL1chr1941787180+ZNF765chr1953905318+0.0004298930.9995701
ENST00000595018ENST00000594030HNRNPUL1chr1941787180+ZNF765chr1953905318+0.0020334560.9979665
ENST00000392006ENST00000396408HNRNPUL1chr1941787180+ZNF765chr1953905318+0.0018299120.99817
ENST00000392006ENST00000594030HNRNPUL1chr1941787180+ZNF765chr1953905318+0.0064814150.99351853
ENST00000602130ENST00000396408HNRNPUL1chr1941787180+ZNF765chr1953905318+0.001781180.99821883
ENST00000602130ENST00000594030HNRNPUL1chr1941787180+ZNF765chr1953905318+0.0050788150.99492115
ENST00000593587ENST00000396408HNRNPUL1chr1941787180+ZNF765chr1953905318+0.000423610.9995764
ENST00000593587ENST00000594030HNRNPUL1chr1941787180+ZNF765chr1953905318+0.0018037820.9981962
ENST00000263367ENST00000396408HNRNPUL1chr1941787180+ZNF765chr1953905318+0.0007828650.99921715
ENST00000263367ENST00000594030HNRNPUL1chr1941787180+ZNF765chr1953905318+0.0027674560.9972325

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 HNRNPUL1-ZNF765

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
HNRNPUL1chr1941787180ZNF765chr19539053181052331YGDKFAENDVIGCFAGLLTFRDVAIE
HNRNPUL1chr1941787180ZNF765chr19539053181052333DKFAENDVIGCFAGLLTFRDVAIEFS
HNRNPUL1chr1941787180ZNF765chr19539053181172374YGDKFAENDVIGCFAGLLTFRDVAIE
HNRNPUL1chr1941787180ZNF765chr19539053181172376DKFAENDVIGCFAGLLTFRDVAIEFS
HNRNPUL1chr1941787180ZNF765chr1953905318768239YGDKFAENDVIGCFAGLLTFRDVAIE
HNRNPUL1chr1941787180ZNF765chr1953905318768241DKFAENDVIGCFAGLLTFRDVAIEFS
HNRNPUL1chr1941787180ZNF765chr1953905318791258YGDKFAENDVIGCFAGLLTFRDVAIE
HNRNPUL1chr1941787180ZNF765chr1953905318791260DKFAENDVIGCFAGLLTFRDVAIEFS
HNRNPUL1chr1941787180ZNF765chr1953905318793231YGDKFAENDVIGCFAGLLTFRDVAIE
HNRNPUL1chr1941787180ZNF765chr1953905318793233DKFAENDVIGCFAGLLTFRDVAIEFS
HNRNPUL1chr1941787180ZNF765chr1953905318926253YGDKFAENDVIGCFAGLLTFRDVAIE
HNRNPUL1chr1941787180ZNF765chr1953905318926255DKFAENDVIGCFAGLLTFRDVAIEFS

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Potential FusionNeoAntigen Information of HNRNPUL1-ZNF765 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.
HNRNPUL1-ZNF765_41787180_53905318.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)
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A66:01DVIGCFAGL0.9980.8456817
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A26:03DVIGCFAGL0.99720.8401817
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A26:02DVIGCFAGL0.99640.8246817
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B44:03AENDVIGCF0.99320.9671514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A26:14DVIGCFAGL0.99280.8478817
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A26:15DVIGCFAGL0.99280.8478817
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B13:01AENDVIGCF0.97240.7668514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A31:06CFAGLLTFR0.94840.69971221
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A31:02CFAGLLTFR0.94510.86881221
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B18:01AENDVIGCF0.91730.9043514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B50:02AENDVIGCF0.89480.5062514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B45:01AENDVIGCF0.7550.8447514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B45:01AENDVIGCFA0.98520.8423515
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B41:01AENDVIGCFA0.60060.8722515
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B50:01AENDVIGCFA0.57690.5512515
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A26:01DVIGCFAGL0.99280.8478817
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B39:08AENDVIGCF0.3940.7956514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B40:06AENDVIGCFA0.96950.5099515
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A25:01DVIGCFAGL0.99580.977817
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B44:26AENDVIGCF0.99320.9671514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B44:07AENDVIGCF0.99320.9671514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B44:13AENDVIGCF0.99320.9671514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A68:02DVIGCFAGL0.98950.7834817
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B40:04AENDVIGCF0.97720.6322514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-A69:01DVIGCFAGL0.97260.7877817
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B18:04AENDVIGCF0.94210.9206514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B18:07AENDVIGCF0.94020.8657514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B18:05AENDVIGCF0.91730.9043514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B18:08AENDVIGCF0.91710.8554514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B18:06AENDVIGCF0.87950.9152514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B18:03AENDVIGCF0.8440.8966514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B18:11AENDVIGCF0.81690.8906514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B41:03AENDVIGCF0.31880.5333514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B15:12AENDVIGCF0.28220.8693514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B35:28AENDVIGCF0.25390.8679514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B15:53AENDVIGCF0.24640.8021514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B48:02AENDVIGCF0.18210.8499514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B15:54AENDVIGCF0.04980.7434514
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B50:04AENDVIGCFA0.57690.5512515
HNRNPUL1-ZNF765chr1941787180chr1953905318926HLA-B50:05AENDVIGCFA0.57690.5512515

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Potential FusionNeoAntigen Information of HNRNPUL1-ZNF765 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 HNRNPUL1-ZNF765

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
1973ENDVIGCFAGLLTFHNRNPUL1ZNF765chr1941787180chr1953905318926

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of HNRNPUL1-ZNF765

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-B14:023BVN1973ENDVIGCFAGLLTF-7.15543-7.26883
HLA-B14:023BVN1973ENDVIGCFAGLLTF-4.77435-5.80965
HLA-B52:013W391973ENDVIGCFAGLLTF-6.80875-6.92215
HLA-B52:013W391973ENDVIGCFAGLLTF-4.20386-5.23916
HLA-A11:014UQ21973ENDVIGCFAGLLTF-7.5194-8.5547
HLA-A11:014UQ21973ENDVIGCFAGLLTF-6.9601-7.0735
HLA-A24:025HGA1973ENDVIGCFAGLLTF-7.52403-7.63743
HLA-A24:025HGA1973ENDVIGCFAGLLTF-5.82433-6.85963
HLA-B27:056PYJ1973ENDVIGCFAGLLTF-3.28285-4.31815
HLA-B44:053DX81973ENDVIGCFAGLLTF-5.91172-6.94702
HLA-B44:053DX81973ENDVIGCFAGLLTF-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of HNRNPUL1-ZNF765

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
HNRNPUL1-ZNF765chr1941787180chr19539053181221CFAGLLTFRGCGGGTCTATTGACATTCAGGGATGTG
HNRNPUL1-ZNF765chr1941787180chr1953905318514AENDVIGCFAACGATGTGATTGGCTGCTTTGCGGGT
HNRNPUL1-ZNF765chr1941787180chr1953905318515AENDVIGCFAAACGATGTGATTGGCTGCTTTGCGGGTCTA
HNRNPUL1-ZNF765chr1941787180chr1953905318817DVIGCFAGLATTGGCTGCTTTGCGGGTCTATTGACA

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 HNRNPUL1-ZNF765

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
GBMHNRNPUL1-ZNF765chr1941787180ENST00000263367chr1953905318ENST00000396408TCGA-26-5139-01A

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Potential target of CAR-T therapy development for HNRNPUL1-ZNF765

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 HNRNPUL1-ZNF765

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 HNRNPUL1-ZNF765

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