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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:UBB-SMARCA4

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: UBB-SMARCA4
FusionPDB ID: 95965
FusionGDB2.0 ID: 95965
HgeneTgene
Gene symbol

UBB

SMARCA4

Gene ID

7314

6597

Gene nameubiquitin BSWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
SynonymsHEL-S-50BAF190|BAF190A|BRG1|CSS4|MRD16|RTPS2|SNF2|SNF2-beta|SNF2L4|SNF2LB|SWI2|hSNF2b
Cytomap

17p11.2

19p13.2

Type of geneprotein-codingprotein-coding
Descriptionpolyubiquitin-Bepididymis secretory protein Li 50polyubiquitin Btranscription activator BRG1ATP-dependent helicase SMARCA4BRG1-associated factor 190ABRM/SWI2-related gene 1SNF2-like 4brahma protein-like 1global transcription activator homologous sequencehomeotic gene regulatormitotic growth and transcription a
Modification date2020031320200315
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000302182, ENST00000395837, 
ENST00000395839, ENST00000535788, 
ENST00000578649, 
ENST00000538456, 
ENST00000413806, ENST00000450717, 
ENST00000344626, ENST00000358026, 
ENST00000429416, ENST00000444061, 
ENST00000541122, ENST00000589677, 
ENST00000590574, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 8 X 3=16820 X 28 X 15=8400
# samples 932
** MAII scorelog2(9/168*10)=-0.900464326449086
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(32/8400*10)=-4.71424551766612
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: UBB [Title/Abstract] AND SMARCA4 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: UBB [Title/Abstract] AND SMARCA4 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)UBB(16285496)-SMARCA4(11095008), # samples:1
Anticipated loss of major functional domain due to fusion event.UBB-SMARCA4 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.
UBB-SMARCA4 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.
UBB-SMARCA4 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.
UBB-SMARCA4 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.
UBB-SMARCA4 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
UBB-SMARCA4 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
UBB-SMARCA4 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
UBB-SMARCA4 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
UBB-SMARCA4 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
HgeneUBB

GO:0031398

positive regulation of protein ubiquitination

24660806

HgeneUBB

GO:0047497

mitochondrion transport along microtubule

17571083

HgeneUBB

GO:0051881

regulation of mitochondrial membrane potential

17571083

HgeneUBB

GO:0061136

regulation of proteasomal protein catabolic process

17571083

HgeneUBB

GO:1901214

regulation of neuron death

17571083

HgeneUBB

GO:1902255

positive regulation of intrinsic apoptotic signaling pathway by p53 class mediator

17571083

TgeneSMARCA4

GO:0006337

nucleosome disassembly

8895581

TgeneSMARCA4

GO:0006338

chromatin remodeling

10943845|11726552

TgeneSMARCA4

GO:0045892

negative regulation of transcription, DNA-templated

12065415

TgeneSMARCA4

GO:0045944

positive regulation of transcription by RNA polymerase II

15774904|17938176

TgeneSMARCA4

GO:0051091

positive regulation of DNA-binding transcription factor activity

11950834|17938176

TgeneSMARCA4

GO:1902661

positive regulation of glucose mediated signaling pathway

22368283



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/chr17:16285496/chr19:11095008)
- 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 UBB (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 SMARCA4 (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)
ENST00000302182UBBchr1716285496+ENST00000358026SMARCA4chr1911095008+626994490158021633
ENST00000302182UBBchr1716285496+ENST00000344626SMARCA4chr1911095008+595094490157061601
ENST00000302182UBBchr1716285496+ENST00000429416SMARCA4chr1911095008+617394490157061601
ENST00000302182UBBchr1716285496+ENST00000541122SMARCA4chr1911095008+561794490156161572
ENST00000302182UBBchr1716285496+ENST00000589677SMARCA4chr1911095008+561494490156131571
ENST00000302182UBBchr1716285496+ENST00000444061SMARCA4chr1911095008+560594490156041568
ENST00000302182UBBchr1716285496+ENST00000590574SMARCA4chr1911095008+560894490156071569
ENST00000395839UBBchr1716285496+ENST00000358026SMARCA4chr1911095008+605673168855891633
ENST00000395839UBBchr1716285496+ENST00000344626SMARCA4chr1911095008+573773168854931601
ENST00000395839UBBchr1716285496+ENST00000429416SMARCA4chr1911095008+596073168854931601
ENST00000395839UBBchr1716285496+ENST00000541122SMARCA4chr1911095008+540473168854031572
ENST00000395839UBBchr1716285496+ENST00000589677SMARCA4chr1911095008+540173168854001571
ENST00000395839UBBchr1716285496+ENST00000444061SMARCA4chr1911095008+539273168853911568
ENST00000395839UBBchr1716285496+ENST00000590574SMARCA4chr1911095008+539573168853941569
ENST00000395837UBBchr1716285496+ENST00000358026SMARCA4chr1911095008+605873369055911633
ENST00000395837UBBchr1716285496+ENST00000344626SMARCA4chr1911095008+573973369054951601
ENST00000395837UBBchr1716285496+ENST00000429416SMARCA4chr1911095008+596273369054951601
ENST00000395837UBBchr1716285496+ENST00000541122SMARCA4chr1911095008+540673369054051571
ENST00000395837UBBchr1716285496+ENST00000589677SMARCA4chr1911095008+540373369054021570
ENST00000395837UBBchr1716285496+ENST00000444061SMARCA4chr1911095008+539473369053931567
ENST00000395837UBBchr1716285496+ENST00000590574SMARCA4chr1911095008+539773369053961568

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
ENST00000302182ENST00000358026UBBchr1716285496+SMARCA4chr1911095008+0.0184646340.98153543
ENST00000302182ENST00000344626UBBchr1716285496+SMARCA4chr1911095008+0.0186694540.9813306
ENST00000302182ENST00000429416UBBchr1716285496+SMARCA4chr1911095008+0.0167110660.98328894
ENST00000302182ENST00000541122UBBchr1716285496+SMARCA4chr1911095008+0.0174815650.98251843
ENST00000302182ENST00000589677UBBchr1716285496+SMARCA4chr1911095008+0.0177729730.982227
ENST00000302182ENST00000444061UBBchr1716285496+SMARCA4chr1911095008+0.0177835880.98221636
ENST00000302182ENST00000590574UBBchr1716285496+SMARCA4chr1911095008+0.0175849140.98241514
ENST00000395839ENST00000358026UBBchr1716285496+SMARCA4chr1911095008+0.0180052970.9819947
ENST00000395839ENST00000344626UBBchr1716285496+SMARCA4chr1911095008+0.0183597710.9816403
ENST00000395839ENST00000429416UBBchr1716285496+SMARCA4chr1911095008+0.0160894020.98391056
ENST00000395839ENST00000541122UBBchr1716285496+SMARCA4chr1911095008+0.0176079120.98239213
ENST00000395839ENST00000589677UBBchr1716285496+SMARCA4chr1911095008+0.0178210980.98217887
ENST00000395839ENST00000444061UBBchr1716285496+SMARCA4chr1911095008+0.0177240760.98227596
ENST00000395839ENST00000590574UBBchr1716285496+SMARCA4chr1911095008+0.0177207480.98227924
ENST00000395837ENST00000358026UBBchr1716285496+SMARCA4chr1911095008+0.0177044590.9822955
ENST00000395837ENST00000344626UBBchr1716285496+SMARCA4chr1911095008+0.0180308950.9819692
ENST00000395837ENST00000429416UBBchr1716285496+SMARCA4chr1911095008+0.015859860.98414016
ENST00000395837ENST00000541122UBBchr1716285496+SMARCA4chr1911095008+0.0171740690.98282593
ENST00000395837ENST00000589677UBBchr1716285496+SMARCA4chr1911095008+0.017418450.9825815
ENST00000395837ENST00000444061UBBchr1716285496+SMARCA4chr1911095008+0.0173123240.98268765
ENST00000395837ENST00000590574UBBchr1716285496+SMARCA4chr1911095008+0.0173376130.98266244

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 UBB-SMARCA4

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
UBBchr1716285496SMARCA4chr191109500873113MNLFKMLIKVSLHGTGGYPQDNMHQM
UBBchr1716285496SMARCA4chr191109500873313MNLFKMLIKVSLHGTGGYPQDNMHQM
UBBchr1716285496SMARCA4chr191109500894413MNLFKMLIKVSLHGTGGYPQDNMHQM

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Potential FusionNeoAntigen Information of UBB-SMARCA4 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.
UBB-SMARCA4_16285496_11095008.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)
UBB-SMARCA4chr1716285496chr1911095008944HLA-B15:17VSLHGTGGY0.98010.9621918

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Potential FusionNeoAntigen Information of UBB-SMARCA4 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 UBB-SMARCA4

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
5107LIKVSLHGTGGYPQUBBSMARCA4chr1716285496chr1911095008944

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of UBB-SMARCA4

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-B14:023BVN5107LIKVSLHGTGGYPQ-7.9962-8.1096
HLA-B14:023BVN5107LIKVSLHGTGGYPQ-5.70842-6.74372
HLA-B52:013W395107LIKVSLHGTGGYPQ-6.83737-6.95077
HLA-B52:013W395107LIKVSLHGTGGYPQ-4.4836-5.5189
HLA-A11:014UQ25107LIKVSLHGTGGYPQ-10.0067-10.1201
HLA-A11:014UQ25107LIKVSLHGTGGYPQ-9.03915-10.0745
HLA-A24:025HGA5107LIKVSLHGTGGYPQ-6.56204-6.67544
HLA-A24:025HGA5107LIKVSLHGTGGYPQ-5.42271-6.45801
HLA-B44:053DX85107LIKVSLHGTGGYPQ-7.85648-8.89178
HLA-B44:053DX85107LIKVSLHGTGGYPQ-5.3978-5.5112
HLA-A02:016TDR5107LIKVSLHGTGGYPQ-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of UBB-SMARCA4

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
UBB-SMARCA4chr1716285496chr1911095008918VSLHGTGGYCGTTGCATGGTACTGGAGGGTACCCTC

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 UBB-SMARCA4

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
N/AUBB-SMARCA4chr1716285496ENST00000302182chr1911095008ENST00000344626DB041801

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Potential target of CAR-T therapy development for UBB-SMARCA4

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 UBB-SMARCA4

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 UBB-SMARCA4

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