FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

leaf

Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

leaf

Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

leaf

Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:ING3-RAD21

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ING3-RAD21
FusionPDB ID: 39743
FusionGDB2.0 ID: 39743
HgeneTgene
Gene symbol

ING3

RAD21

Gene ID

54556

5885

Gene nameinhibitor of growth family member 3RAD21 cohesin complex component
SynonymsEaf4|ING2|MEAF4|p47ING3CDLS4|HR21|HRAD21|MCD1|MGS|NXP1|SCC1|hHR21
Cytomap

7q31.31

8q24.11

Type of geneprotein-codingprotein-coding
Descriptioninhibitor of growth protein 3double-strand-break repair protein rad21 homologNXP-1RAD21 homologSCC1 homologkleisinnuclear matrix protein 1protein involved in DNA double-strand break repairsister chromatid cohesion 1
Modification date2020031320200327
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}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000315870, ENST00000339121, 
ENST00000431467, ENST00000445699, 
ENST00000523547, ENST00000517749, 
ENST00000518055, ENST00000523986, 
ENST00000297338, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 1 X 3=1810 X 11 X 6=660
# samples 612
** MAII scorelog2(6/18*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(12/660*10)=-2.4594316186373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ING3 [Title/Abstract] AND RAD21 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ING3 [Title/Abstract] AND RAD21 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ING3(120595678)-RAD21(117875498), # samples:1
Anticipated loss of major functional domain due to fusion event.ING3-RAD21 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-RAD21 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-RAD21 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-RAD21 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-RAD21 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
ING3-RAD21 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ING3-RAD21 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
ING3-RAD21 seems lost the major protein functional domain in Tgene partner, which is a CGC 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

TgeneRAD21

GO:0006357

regulation of transcription by RNA polymerase II

19468298



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/chr8:117875498)
- 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 RAD21 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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+ENST00000297338RAD21chr8117875498-37324151122166684
ENST00000339121ING3chr7120595678+ENST00000297338RAD21chr8117875498-3718401982152684
ENST00000431467ING3chr7120595678+ENST00000297338RAD21chr8117875498-3604287412038665

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
ENST00000315870ENST00000297338ING3chr7120595678+RAD21chr8117875498-0.0002909180.99970907
ENST00000339121ENST00000297338ING3chr7120595678+RAD21chr8117875498-0.0003059950.999694
ENST00000431467ENST00000297338ING3chr7120595678+RAD21chr8117875498-0.0004324340.99956757

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

Top

Fusion Protein Breakpoint Sequences for ING3-RAD21

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ING3chr7120595678RAD21chr811787549828782DEKVQLANQIYDLVKMALRTSGHLLL
ING3chr7120595678RAD21chr8117875498401101DEKVQLANQIYDLVKMALRTSGHLLL
ING3chr7120595678RAD21chr8117875498415101DEKVQLANQIYDLVKMALRTSGHLLL

Top

Potential FusionNeoAntigen Information of ING3-RAD21 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-RAD21_120595678_117875498.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-RAD21chr7120595678chr8117875498415HLA-B39:01IYDLVKMAL0.91040.8901918
ING3-RAD21chr7120595678chr8117875498415HLA-B13:01NQIYDLVKM0.84350.8539716
ING3-RAD21chr7120595678chr8117875498415HLA-B47:01NQIYDLVKM0.8230.5553716
ING3-RAD21chr7120595678chr8117875498415HLA-B15:18NQIYDLVKM0.69910.5806716
ING3-RAD21chr7120595678chr8117875498415HLA-B15:37NQIYDLVKM0.45760.5965716
ING3-RAD21chr7120595678chr8117875498415HLA-A74:11QIYDLVKMALR0.98630.8536819
ING3-RAD21chr7120595678chr8117875498415HLA-A74:03QIYDLVKMALR0.98630.8536819
ING3-RAD21chr7120595678chr8117875498415HLA-A74:09QIYDLVKMALR0.98630.8536819
ING3-RAD21chr7120595678chr8117875498415HLA-C04:10YDLVKMAL0.99940.69841018
ING3-RAD21chr7120595678chr8117875498415HLA-C05:09IYDLVKMAL0.99970.9618918
ING3-RAD21chr7120595678chr8117875498415HLA-C04:10IYDLVKMAL0.99960.6936918
ING3-RAD21chr7120595678chr8117875498415HLA-C04:07IYDLVKMAL0.99950.7087918
ING3-RAD21chr7120595678chr8117875498415HLA-C08:15IYDLVKMAL0.99940.9841918
ING3-RAD21chr7120595678chr8117875498415HLA-C01:17IYDLVKMAL0.99870.9345918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:05IYDLVKMAL0.99410.9649918
ING3-RAD21chr7120595678chr8117875498415HLA-C01:30IYDLVKMAL0.99340.9623918
ING3-RAD21chr7120595678chr8117875498415HLA-C08:13IYDLVKMAL0.99170.8926918
ING3-RAD21chr7120595678chr8117875498415HLA-C08:04IYDLVKMAL0.99170.8926918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:13IYDLVKMAL0.99160.8264918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:29IYDLVKMAL0.9880.8879918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:27IYDLVKMAL0.98630.9366918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:10IYDLVKMAL0.98560.9137918
ING3-RAD21chr7120595678chr8117875498415HLA-C04:06IYDLVKMAL0.98340.8575918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:67IYDLVKMAL0.98210.8616918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:80IYDLVKMAL0.98210.8616918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:95IYDLVKMAL0.97620.5248918
ING3-RAD21chr7120595678chr8117875498415HLA-C08:03IYDLVKMAL0.96090.9733918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:46IYDLVKMAL0.95730.715918
ING3-RAD21chr7120595678chr8117875498415HLA-B15:21NQIYDLVKM0.91270.8248716
ING3-RAD21chr7120595678chr8117875498415HLA-B14:03IYDLVKMAL0.90870.788918
ING3-RAD21chr7120595678chr8117875498415HLA-B39:09NQIYDLVKM0.90710.5196716
ING3-RAD21chr7120595678chr8117875498415HLA-B39:12IYDLVKMAL0.88360.8922918
ING3-RAD21chr7120595678chr8117875498415HLA-C04:14IYDLVKMAL0.76020.8031918
ING3-RAD21chr7120595678chr8117875498415HLA-C12:16IYDLVKMAL0.66730.9134918
ING3-RAD21chr7120595678chr8117875498415HLA-C18:01YDLVKMAL0.99920.71561018
ING3-RAD21chr7120595678chr8117875498415HLA-C05:01IYDLVKMAL0.99970.9618918
ING3-RAD21chr7120595678chr8117875498415HLA-C04:03IYDLVKMAL0.99960.7505918
ING3-RAD21chr7120595678chr8117875498415HLA-C18:01IYDLVKMAL0.99950.7014918
ING3-RAD21chr7120595678chr8117875498415HLA-C04:01IYDLVKMAL0.99950.7087918
ING3-RAD21chr7120595678chr8117875498415HLA-C08:02IYDLVKMAL0.99940.9841918
ING3-RAD21chr7120595678chr8117875498415HLA-C01:03IYDLVKMAL0.99940.944918
ING3-RAD21chr7120595678chr8117875498415HLA-C01:02IYDLVKMAL0.99910.9322918
ING3-RAD21chr7120595678chr8117875498415HLA-C03:67IYDLVKMAL0.9970.9686918
ING3-RAD21chr7120595678chr8117875498415HLA-C14:03IYDLVKMAL0.99480.9544918
ING3-RAD21chr7120595678chr8117875498415HLA-C14:02IYDLVKMAL0.99480.9544918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:02IYDLVKMAL0.98210.8616918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:04IYDLVKMAL0.98090.9643918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:17IYDLVKMAL0.98060.9408918
ING3-RAD21chr7120595678chr8117875498415HLA-C07:01IYDLVKMAL0.97890.5234918
ING3-RAD21chr7120595678chr8117875498415HLA-C04:04IYDLVKMAL0.97720.8253918
ING3-RAD21chr7120595678chr8117875498415HLA-B15:53NQIYDLVKM0.9740.7653716
ING3-RAD21chr7120595678chr8117875498415HLA-C06:06IYDLVKMAL0.96340.9774918
ING3-RAD21chr7120595678chr8117875498415HLA-C08:01IYDLVKMAL0.96090.9733918
ING3-RAD21chr7120595678chr8117875498415HLA-B39:11IYDLVKMAL0.95950.7685918
ING3-RAD21chr7120595678chr8117875498415HLA-B15:73NQIYDLVKM0.93640.6986716
ING3-RAD21chr7120595678chr8117875498415HLA-B15:30NQIYDLVKM0.84840.8173716
ING3-RAD21chr7120595678chr8117875498415HLA-B35:20NQIYDLVKM0.83980.9034716
ING3-RAD21chr7120595678chr8117875498415HLA-B35:28NQIYDLVKM0.80410.89716
ING3-RAD21chr7120595678chr8117875498415HLA-B08:12IYDLVKMAL0.80060.6551918
ING3-RAD21chr7120595678chr8117875498415HLA-B18:04NQIYDLVKM0.78390.9641716
ING3-RAD21chr7120595678chr8117875498415HLA-B48:02NQIYDLVKM0.69980.8662716
ING3-RAD21chr7120595678chr8117875498415HLA-B07:13IYDLVKMAL0.20450.6973918
ING3-RAD21chr7120595678chr8117875498415HLA-A74:01QIYDLVKMALR0.98630.8536819

Top

Potential FusionNeoAntigen Information of ING3-RAD21 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)

Top

Fusion breakpoint peptide structures of ING3-RAD21

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
463ANQIYDLVKMALRTING3RAD21chr7120595678chr8117875498415

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ING3-RAD21

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-B52:013W39463ANQIYDLVKMALRT-7.90165-7.90165
HLA-B44:053DX8463ANQIYDLVKMALRT-5.81679-5.81679

Top

Vaccine Design for the FusionNeoAntigens of ING3-RAD21

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-RAD21chr7120595678chr81178754981018YDLVKMALTATGACTTGGTGAAAATGGCATTA
ING3-RAD21chr7120595678chr8117875498716NQIYDLVKMAACCAGATATATGACTTGGTGAAAATG
ING3-RAD21chr7120595678chr8117875498819QIYDLVKMALRCAGATATATGACTTGGTGAAAATGGCATTACGG
ING3-RAD21chr7120595678chr8117875498918IYDLVKMALATATATGACTTGGTGAAAATGGCATTA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence

Top

Information of the samples that have these potential fusion neoantigens of ING3-RAD21

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-RAD21chr7120595678ENST00000315870chr8117875498ENST00000297338TCGA-BR-8372-01A

Top

Potential target of CAR-T therapy development for ING3-RAD21

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

Top

Related Drugs to ING3-RAD21

check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

Top

Related Diseases to ING3-RAD21

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