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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:ING3-SHARPIN

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ING3-SHARPIN
FusionPDB ID: 39744
FusionGDB2.0 ID: 39744
HgeneTgene
Gene symbol

ING3

SHARPIN

Gene ID

54556

81858

Gene nameinhibitor of growth family member 3SHANK associated RH domain interactor
SynonymsEaf4|ING2|MEAF4|p47ING3SIPL1
Cytomap

7q31.31

8q24.3

Type of geneprotein-codingprotein-coding
Descriptioninhibitor of growth protein 3sharpinhSIPL1shank-associated RH domain-interacting proteinshank-interacting protein-like 1
Modification date2020031320200313
UniProtAcc

Q9NXR8

Main function of 5'-partner protein: FUNCTION: Component of the NuA4 histone acetyltransferase (HAT) complex which is involved in transcriptional activation of select genes principally by acetylation of nucleosomal histones H4 and H2A. This modification may both alter nucleosome - DNA interactions and promote interaction of the modified histones with other proteins which positively regulate transcription. This complex may be required for the activation of transcriptional programs associated with oncogene and proto-oncogene mediated growth induction, tumor suppressor mediated growth arrest and replicative senescence, apoptosis, and DNA repair. NuA4 may also play a direct role in DNA repair when directly recruited to sites of DNA damage. Component of a SWR1-like complex that specifically mediates the removal of histone H2A.Z/H2AZ1 from the nucleosome. {ECO:0000269|PubMed:12545155, ECO:0000269|PubMed:14966270, ECO:0000269|PubMed:24463511}.

SHARPIN

Main function of 5'-partner protein: 387
Ensembl transtripts involved in fusion geneENST idsENST00000315870, ENST00000339121, 
ENST00000431467, ENST00000445699, 
ENST00000533948, ENST00000398712, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 1 X 3=187 X 2 X 4=56
# samples 67
** MAII scorelog2(6/18*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(7/56*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Fusion gene context

PubMed: ING3 [Title/Abstract] AND SHARPIN [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ING3 [Title/Abstract] AND SHARPIN [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ING3(120595678)-SHARPIN(145158128), # samples:1
Anticipated loss of major functional domain due to fusion event.ING3-SHARPIN 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.
ING3-SHARPIN 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.
ING3-SHARPIN 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.
ING3-SHARPIN 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.
ING3-SHARPIN seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
ING3-SHARPIN seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ING3-SHARPIN seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
ING3-SHARPIN seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneING3

GO:0043065

positive regulation of apoptotic process

16387653

HgeneING3

GO:0043967

histone H4 acetylation

14966270|16387653

HgeneING3

GO:0043968

histone H2A acetylation

14966270|16387653

TgeneSHARPIN

GO:0010803

regulation of tumor necrosis factor-mediated signaling pathway

21455173

TgeneSHARPIN

GO:0043123

positive regulation of I-kappaB kinase/NF-kappaB signaling

21455173

TgeneSHARPIN

GO:0097039

protein linear polyubiquitination

21455173|21455180|21455181

TgeneSHARPIN

GO:2000348

regulation of CD40 signaling pathway

21455173



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/chr7:120595678/chr8:145158128)
- 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 ING3 (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 SHARPIN (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)
ENST00000315870ING3chr7120595678+ENST00000398712SHARPINchr8145158128-15424151121377421
ENST00000339121ING3chr7120595678+ENST00000398712SHARPINchr8145158128-1528401981363421
ENST00000431467ING3chr7120595678+ENST00000398712SHARPINchr8145158128-1414287411249402

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
ENST00000315870ENST00000398712ING3chr7120595678+SHARPINchr8145158128-0.0342410580.9657589
ENST00000339121ENST00000398712ING3chr7120595678+SHARPINchr8145158128-0.0336802040.96631986
ENST00000431467ENST00000398712ING3chr7120595678+SHARPINchr8145158128-0.042900780.9570992

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 ING3-SHARPIN

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ING3chr7120595678SHARPINchr814515812828782DEKVQLANQIYDLVNLEWPLESVSYT
ING3chr7120595678SHARPINchr8145158128401101DEKVQLANQIYDLVNLEWPLESVSYT
ING3chr7120595678SHARPINchr8145158128415101DEKVQLANQIYDLVNLEWPLESVSYT

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Potential FusionNeoAntigen Information of ING3-SHARPIN 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.
ING3-SHARPIN_120595678_145158128.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)
ING3-SHARPINchr7120595678chr8145158128415HLA-B58:02IYDLVNLEW0.99360.9058918
ING3-SHARPINchr7120595678chr8145158128415HLA-B58:01IYDLVNLEW0.9830.9493918
ING3-SHARPINchr7120595678chr8145158128415HLA-A32:13IYDLVNLEW0.9820.9783918
ING3-SHARPINchr7120595678chr8145158128415HLA-B39:01NQIYDLVNL0.97890.9464716
ING3-SHARPINchr7120595678chr8145158128415HLA-B39:13NQIYDLVNL0.95860.9579716
ING3-SHARPINchr7120595678chr8145158128415HLA-A02:21NQIYDLVNL0.90460.7321716
ING3-SHARPINchr7120595678chr8145158128415HLA-B13:01NQIYDLVNL0.79830.8069716
ING3-SHARPINchr7120595678chr8145158128415HLA-B15:10NQIYDLVNL0.74690.6084716
ING3-SHARPINchr7120595678chr8145158128415HLA-A24:14IYDLVNLEW0.64120.5182918
ING3-SHARPINchr7120595678chr8145158128415HLA-B15:37NQIYDLVNL0.55670.6469716
ING3-SHARPINchr7120595678chr8145158128415HLA-B57:01QIYDLVNLEW0.99860.9976818
ING3-SHARPINchr7120595678chr8145158128415HLA-B58:01QIYDLVNLEW0.99440.9962818
ING3-SHARPINchr7120595678chr8145158128415HLA-B57:03QIYDLVNLEW0.98320.9988818
ING3-SHARPINchr7120595678chr8145158128415HLA-A31:08QIYDLVNLEW0.98220.7579818
ING3-SHARPINchr7120595678chr8145158128415HLA-A24:17QIYDLVNLEW0.97410.7516818
ING3-SHARPINchr7120595678chr8145158128415HLA-A24:10QIYDLVNLEW0.96660.5835818
ING3-SHARPINchr7120595678chr8145158128415HLA-A32:13QIYDLVNLEW0.950.9901818
ING3-SHARPINchr7120595678chr8145158128415HLA-B53:01QIYDLVNLEW0.92750.8684818
ING3-SHARPINchr7120595678chr8145158128415HLA-A24:31QIYDLVNLEW0.90340.7842818
ING3-SHARPINchr7120595678chr8145158128415HLA-A24:15QIYDLVNLEW0.87840.7869818
ING3-SHARPINchr7120595678chr8145158128415HLA-A24:14QIYDLVNLEW0.70090.7971818
ING3-SHARPINchr7120595678chr8145158128415HLA-B39:09NQIYDLVNL0.98170.6471716
ING3-SHARPINchr7120595678chr8145158128415HLA-B39:05NQIYDLVNL0.92730.9331716
ING3-SHARPINchr7120595678chr8145158128415HLA-C04:07IYDLVNLEW0.75360.8215918
ING3-SHARPINchr7120595678chr8145158128415HLA-C04:10IYDLVNLEW0.75290.8266918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:19IYDLVNLEW0.74210.8093918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:10IYDLVNLEW0.73240.9816918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:46IYDLVNLEW0.7030.9273918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:80IYDLVNLEW0.69840.9736918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:67IYDLVNLEW0.69840.9736918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:05IYDLVNLEW0.6620.9743918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:27IYDLVNLEW0.64060.9741918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:13IYDLVNLEW0.33630.967918
ING3-SHARPINchr7120595678chr8145158128415HLA-C04:14IYDLVNLEW0.17640.9021918
ING3-SHARPINchr7120595678chr8145158128415HLA-C04:10IYDLVNLEWPL0.99940.8946920
ING3-SHARPINchr7120595678chr8145158128415HLA-C04:07IYDLVNLEWPL0.99940.8863920
ING3-SHARPINchr7120595678chr8145158128415HLA-C04:14IYDLVNLEWPL0.97390.9169920
ING3-SHARPINchr7120595678chr8145158128415HLA-B39:02NQIYDLVNL0.98330.9595716
ING3-SHARPINchr7120595678chr8145158128415HLA-B39:31NQIYDLVNL0.98290.9472716
ING3-SHARPINchr7120595678chr8145158128415HLA-B57:02IYDLVNLEW0.94940.8716918
ING3-SHARPINchr7120595678chr8145158128415HLA-B15:73NQIYDLVNL0.94690.8785716
ING3-SHARPINchr7120595678chr8145158128415HLA-A02:14NQIYDLVNL0.90740.6809716
ING3-SHARPINchr7120595678chr8145158128415HLA-A02:06NQIYDLVNL0.90460.7321716
ING3-SHARPINchr7120595678chr8145158128415HLA-B15:30NQIYDLVNL0.89270.9053716
ING3-SHARPINchr7120595678chr8145158128415HLA-B39:11NQIYDLVNL0.76450.8578716
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:17IYDLVNLEW0.7580.9857918
ING3-SHARPINchr7120595678chr8145158128415HLA-C04:01IYDLVNLEW0.75360.8215918
ING3-SHARPINchr7120595678chr8145158128415HLA-C18:01IYDLVNLEW0.73220.8251918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:02IYDLVNLEW0.69840.9736918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:01IYDLVNLEW0.69120.7765918
ING3-SHARPINchr7120595678chr8145158128415HLA-B15:09NQIYDLVNL0.6780.5237716
ING3-SHARPINchr7120595678chr8145158128415HLA-B15:13IYDLVNLEW0.6390.7548918
ING3-SHARPINchr7120595678chr8145158128415HLA-C14:02IYDLVNLEW0.30020.984918
ING3-SHARPINchr7120595678chr8145158128415HLA-C14:03IYDLVNLEW0.30020.984918
ING3-SHARPINchr7120595678chr8145158128415HLA-C07:04IYDLVNLEW0.2430.9716918
ING3-SHARPINchr7120595678chr8145158128415HLA-C04:04IYDLVNLEW0.17490.9269918
ING3-SHARPINchr7120595678chr8145158128415HLA-B57:04QIYDLVNLEW0.99870.9574818
ING3-SHARPINchr7120595678chr8145158128415HLA-B57:10QIYDLVNLEW0.99860.9976818
ING3-SHARPINchr7120595678chr8145158128415HLA-B15:24QIYDLVNLEW0.99390.9927818
ING3-SHARPINchr7120595678chr8145158128415HLA-B57:02QIYDLVNLEW0.990.9971818
ING3-SHARPINchr7120595678chr8145158128415HLA-A32:01QIYDLVNLEW0.98820.9953818
ING3-SHARPINchr7120595678chr8145158128415HLA-B15:13QIYDLVNLEW0.98270.9427818
ING3-SHARPINchr7120595678chr8145158128415HLA-A25:01QIYDLVNLEW0.7390.9747818
ING3-SHARPINchr7120595678chr8145158128415HLA-C04:01IYDLVNLEWPL0.99940.8863920
ING3-SHARPINchr7120595678chr8145158128415HLA-C18:01IYDLVNLEWPL0.9990.8923920

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Potential FusionNeoAntigen Information of ING3-SHARPIN 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 ING3-SHARPIN

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
464ANQIYDLVNLEWPLING3SHARPINchr7120595678chr8145158128415

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ING3-SHARPIN

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-B14:023BVN464ANQIYDLVNLEWPL-4.62424-5.65954
HLA-B14:023BVN464ANQIYDLVNLEWPL-4.1114-4.2248
HLA-B52:013W39464ANQIYDLVNLEWPL-6.8001-6.9135
HLA-B52:013W39464ANQIYDLVNLEWPL-6.46104-7.49634
HLA-A24:025HGA464ANQIYDLVNLEWPL-9.1447-9.2581
HLA-A24:025HGA464ANQIYDLVNLEWPL-6.01279-7.04809
HLA-B44:053DX8464ANQIYDLVNLEWPL-5.02862-5.14202
HLA-B44:053DX8464ANQIYDLVNLEWPL-4.60714-5.64244

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Vaccine Design for the FusionNeoAntigens of ING3-SHARPIN

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
ING3-SHARPINchr7120595678chr8145158128716NQIYDLVNLAACCAGATATATGACTTGGTTAATTTG
ING3-SHARPINchr7120595678chr8145158128818QIYDLVNLEWCAGATATATGACTTGGTTAATTTGGAGTGG
ING3-SHARPINchr7120595678chr8145158128918IYDLVNLEWATATATGACTTGGTTAATTTGGAGTGG
ING3-SHARPINchr7120595678chr8145158128920IYDLVNLEWPLATATATGACTTGGTTAATTTGGAGTGGCCCCTG

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 ING3-SHARPIN

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
STADING3-SHARPINchr7120595678ENST00000315870chr8145158128ENST00000398712TCGA-D7-5577-01A

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Potential target of CAR-T therapy development for ING3-SHARPIN

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 ING3-SHARPIN

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 ING3-SHARPIN

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