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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:SHANK2-HMGN3

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SHANK2-HMGN3
FusionPDB ID: 81567
FusionGDB2.0 ID: 81567
HgeneTgene
Gene symbol

SHANK2

HMGN3

Gene ID

22941

9324

Gene nameSH3 and multiple ankyrin repeat domains 2high mobility group nucleosomal binding domain 3
SynonymsAUTS17|CORTBP1|CTTNBP1|ProSAP1|SHANK|SPANK-3PNAS-24|PNAS-25|TRIP7
Cytomap

11q13.3-q13.4

6q14.1

Type of geneprotein-codingprotein-coding
DescriptionSH3 and multiple ankyrin repeat domains protein 2GKAP/SAPAP interacting proteincortactin SH3 domain-binding proteincortactin-binding protein 1proline-rich synapse associated protein 1high mobility group nucleosome-binding domain-containing protein 3TR-interacting protein 7thyroid hormone receptor interacting protein 7
Modification date2020032620200313
UniProtAcc.

Q15651

Main function of 5'-partner protein: FUNCTION: Binds to nucleosomes, regulating chromatin structure and consequently, chromatin-dependent processes such as transcription, DNA replication and DNA repair. Affects both insulin and glucagon levels and modulates the expression of pancreatic genes involved in insulin secretion. Regulates the expression of the glucose transporter SLC2A2 by binding specifically to its promoter region and recruiting PDX1 and additional transcription factors. Regulates the expression of SLC6A9, a glycine transporter which regulates the glycine concentration in synaptic junctions in the central nervous system, by binding to its transcription start site. May play a role in ocular development and astrocyte function (By similarity). {ECO:0000250}.
Ensembl transtripts involved in fusion geneENST idsENST00000338508, ENST00000357171, 
ENST00000409161, ENST00000409530, 
ENST00000423696, ENST00000449116, 
ENST00000449833, ENST00000468619, 
ENST00000275036, ENST00000344726, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score50 X 31 X 10=155007 X 5 X 4=140
# samples 517
** MAII scorelog2(51/15500*10)=-4.9256271581901
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/140*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SHANK2 [Title/Abstract] AND HMGN3 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SHANK2 [Title/Abstract] AND HMGN3 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SHANK2(70505933)-HMGN3(79924739), # samples:1
Anticipated loss of major functional domain due to fusion event.SHANK2-HMGN3 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.
SHANK2-HMGN3 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.
SHANK2-HMGN3 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.
SHANK2-HMGN3 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/chr11:70505933/chr6:79924739)
- 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 SHANK2 (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 HMGN3 (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)
ENST00000449833SHANK2chr1170505933-ENST00000275036HMGN3chr679924739-103534845566173
ENST00000449833SHANK2chr1170505933-ENST00000344726HMGN3chr679924739-107634845632195
ENST00000409161SHANK2chr1170505933-ENST00000275036HMGN3chr679924739-9812940512170
ENST00000409161SHANK2chr1170505933-ENST00000344726HMGN3chr679924739-10222940578192
ENST00000423696SHANK2chr1170505933-ENST00000275036HMGN3chr679924739-1648961371179380
ENST00000423696SHANK2chr1170505933-ENST00000344726HMGN3chr679924739-1689961371245402
ENST00000338508SHANK2chr1170505933-ENST00000275036HMGN3chr679924739-2751206402282760
ENST00000338508SHANK2chr1170505933-ENST00000344726HMGN3chr679924739-2792206402348782
ENST00000409530SHANK2chr1170505933-ENST00000275036HMGN3chr679924739-9812940512170
ENST00000409530SHANK2chr1170505933-ENST00000344726HMGN3chr679924739-10222940578192
ENST00000449116SHANK2chr1170505933-ENST00000275036HMGN3chr679924739-105737067588173
ENST00000449116SHANK2chr1170505933-ENST00000344726HMGN3chr679924739-109837067654195
ENST00000357171SHANK2chr1170505933-ENST00000275036HMGN3chr679924739-103534845566173
ENST00000357171SHANK2chr1170505933-ENST00000344726HMGN3chr679924739-107634845632195

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
ENST00000449833ENST00000275036SHANK2chr1170505933-HMGN3chr679924739-0.0026073950.99739254
ENST00000449833ENST00000344726SHANK2chr1170505933-HMGN3chr679924739-0.0010071160.99899286
ENST00000409161ENST00000275036SHANK2chr1170505933-HMGN3chr679924739-0.00216190.9978381
ENST00000409161ENST00000344726SHANK2chr1170505933-HMGN3chr679924739-0.0010291210.99897087
ENST00000423696ENST00000275036SHANK2chr1170505933-HMGN3chr679924739-0.0023669220.9976331
ENST00000423696ENST00000344726SHANK2chr1170505933-HMGN3chr679924739-0.0018580130.998142
ENST00000338508ENST00000275036SHANK2chr1170505933-HMGN3chr679924739-0.0031613270.9968387
ENST00000338508ENST00000344726SHANK2chr1170505933-HMGN3chr679924739-0.0026504390.9973495
ENST00000409530ENST00000275036SHANK2chr1170505933-HMGN3chr679924739-0.00216190.9978381
ENST00000409530ENST00000344726SHANK2chr1170505933-HMGN3chr679924739-0.0010291210.99897087
ENST00000449116ENST00000275036SHANK2chr1170505933-HMGN3chr679924739-0.0024708430.9975292
ENST00000449116ENST00000344726SHANK2chr1170505933-HMGN3chr679924739-0.0009480850.99905187
ENST00000357171ENST00000275036SHANK2chr1170505933-HMGN3chr679924739-0.0026073950.99739254
ENST00000357171ENST00000344726SHANK2chr1170505933-HMGN3chr679924739-0.0010071160.99899286

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 SHANK2-HMGN3

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SHANK2chr1170505933HMGN3chr6799247392064688WQAGLRTGDFLIESPENTEGKDGSKV
SHANK2chr1170505933HMGN3chr67992473929498WQAGLRTGDFLIESPENTEGKDGSKV
SHANK2chr1170505933HMGN3chr679924739348101WQAGLRTGDFLIESPENTEGKDGSKV
SHANK2chr1170505933HMGN3chr679924739370101WQAGLRTGDFLIESPENTEGKDGSKV
SHANK2chr1170505933HMGN3chr679924739961308WQAGLRTGDFLIESPENTEGKDGSKV

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Potential FusionNeoAntigen Information of SHANK2-HMGN3 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.
SHANK2-HMGN3_70505933_79924739.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)
SHANK2-HMGN3chr1170505933chr6799247392064HLA-A02:11FLIESPENT0.96830.5372918
SHANK2-HMGN3chr1170505933chr6799247392064HLA-A02:27FLIESPENT0.96030.5477918
SHANK2-HMGN3chr1170505933chr6799247392064HLA-A02:21FLIESPENT0.95360.6245918
SHANK2-HMGN3chr1170505933chr6799247392064HLA-A02:13FLIESPENT0.94540.6413918
SHANK2-HMGN3chr1170505933chr6799247392064HLA-A02:38FLIESPENT0.89190.5602918
SHANK2-HMGN3chr1170505933chr6799247392064HLA-A02:35FLIESPENT0.88740.5077918
SHANK2-HMGN3chr1170505933chr6799247392064HLA-A02:03FLIESPENT0.96870.6731918
SHANK2-HMGN3chr1170505933chr6799247392064HLA-A02:06FLIESPENT0.95360.6245918
SHANK2-HMGN3chr1170505933chr6799247392064HLA-A02:14FLIESPENT0.95020.5125918

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Potential FusionNeoAntigen Information of SHANK2-HMGN3 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.
SHANK2-HMGN3_70505933_79924739.msa

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)
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0101TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0105TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0107TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0109TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0111TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0113TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0119TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0125TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0127TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0131TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-0464TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-1001TGDFLIESPENTEGK621
SHANK2-HMGN3chr1170505933chr6799247392064DRB1-1003TGDFLIESPENTEGK621

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Fusion breakpoint peptide structures of SHANK2-HMGN3

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
9354TGDFLIESPENTEGSHANK2HMGN3chr1170505933chr6799247392064

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SHANK2-HMGN3

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-B14:023BVN9354TGDFLIESPENTEG-7.24289-7.35629
HLA-B14:023BVN9354TGDFLIESPENTEG-6.44411-7.47941
HLA-B52:013W399354TGDFLIESPENTEG-6.85231-6.96571
HLA-B52:013W399354TGDFLIESPENTEG-5.09533-6.13063
HLA-A11:014UQ29354TGDFLIESPENTEG-8.61576-8.72916
HLA-A24:025HGA9354TGDFLIESPENTEG-6.80714-7.84244
HLA-A24:025HGA9354TGDFLIESPENTEG-6.33574-6.44914
HLA-B44:053DX89354TGDFLIESPENTEG-7.01739-7.13079
HLA-B44:053DX89354TGDFLIESPENTEG-3.37818-4.41348

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Vaccine Design for the FusionNeoAntigens of SHANK2-HMGN3

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
SHANK2-HMGN3chr1170505933chr679924739918FLIESPENTTTCTTGATTGAGTCTCCAGAGAATACA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SHANK2-HMGN3chr1170505933chr679924739621TGDFLIESPENTEGKACCGGGGACTTCTTGATTGAGTCTCCAGAGAATACAGAGGGCAAA

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Information of the samples that have these potential fusion neoantigens of SHANK2-HMGN3

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
BRCASHANK2-HMGN3chr1170505933ENST00000338508chr679924739ENST00000275036TCGA-AR-A24Z-01A

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Potential target of CAR-T therapy development for SHANK2-HMGN3

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 SHANK2-HMGN3

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 SHANK2-HMGN3

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