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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:OXSR1-ATXN7

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: OXSR1-ATXN7
FusionPDB ID: 62050
FusionGDB2.0 ID: 62050
HgeneTgene
Gene symbol

OXSR1

ATXN7

Gene ID

9943

6314

Gene nameoxidative stress responsive kinase 1ataxin 7
SynonymsOSR1ADCAII|OPCA3|SCA7|SGF73
Cytomap

3p22.2

3p14.1

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase OSR1oxidative stress responsive 1oxidative stress-responsive 1 proteinataxin-7spinocerebellar ataxia type 7 protein
Modification date2020031320200313
UniProtAcc.

Q96GX2

Main function of 5'-partner protein: FUNCTION: By binding to ENY2, interferes with the nuclear functions of the deubiquitinase (DUB) module of the SAGA complex which consists of ENY2, ATXN7, ATXN7L3 and the histone deubiquitinating component USP22. Affects USP22 DUB activity toward histones indirectly by changing the subcellular distribution of ENY2 and altering ENY2 availability for ATXN7L3 interaction. Regulates H2B monoubiquitination (H2Bub1) levels through cytoplasmic sequestration of ENY2 resulting in loss of nuclear ENY2-ATXN7L3 association which destabilizes ATXN7L3. Affects protein expression levels of ENY2 and ATXN7L3. {ECO:0000269|PubMed:27601583}.
Ensembl transtripts involved in fusion geneENST idsENST00000311806, ENST00000446845, 
ENST00000492714, 
ENST00000484332, 
ENST00000488239, ENST00000295900, 
ENST00000398590, ENST00000487717, 
ENST00000538065, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 10 X 8=7209 X 8 X 4=288
# samples 128
** MAII scorelog2(12/720*10)=-2.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/288*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: OXSR1 [Title/Abstract] AND ATXN7 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: OXSR1 [Title/Abstract] AND ATXN7 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)OXSR1(38232330)-ATXN7(63938055), # samples:3
Anticipated loss of major functional domain due to fusion event.OXSR1-ATXN7 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.
OXSR1-ATXN7 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.
OXSR1-ATXN7 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.
OXSR1-ATXN7 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
HgeneOXSR1

GO:0006468

protein phosphorylation

14707132

HgeneOXSR1

GO:0018107

peptidyl-threonine phosphorylation

24393035

HgeneOXSR1

GO:0035556

intracellular signal transduction

14707132

HgeneOXSR1

GO:0046777

protein autophosphorylation

22052202

TgeneATXN7

GO:0016578

histone deubiquitination

18206972



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/chr3:38232330/chr3:63938055)
- 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 OXSR1 (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 ATXN7 (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)
ENST00000446845OXSR1chr338232330+ENST00000398590ATXN7chr363938055+70026642013107968
ENST00000446845OXSR1chr338232330+ENST00000295900ATXN7chr363938055+69446642012948915
ENST00000446845OXSR1chr338232330+ENST00000487717ATXN7chr363938055+36896642012948915
ENST00000446845OXSR1chr338232330+ENST00000538065ATXN7chr363938055+70026642013107968
ENST00000311806OXSR1chr338232330+ENST00000398590ATXN7chr363938055+70026642013107968
ENST00000311806OXSR1chr338232330+ENST00000295900ATXN7chr363938055+69446642012948915
ENST00000311806OXSR1chr338232330+ENST00000487717ATXN7chr363938055+36896642012948915
ENST00000311806OXSR1chr338232330+ENST00000538065ATXN7chr363938055+70026642013107968

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
ENST00000446845ENST00000398590OXSR1chr338232330+ATXN7chr363938055+0.0004265050.9995735
ENST00000446845ENST00000295900OXSR1chr338232330+ATXN7chr363938055+0.0005212990.99947876
ENST00000446845ENST00000487717OXSR1chr338232330+ATXN7chr363938055+0.0041290090.995871
ENST00000446845ENST00000538065OXSR1chr338232330+ATXN7chr363938055+0.0004265050.9995735
ENST00000311806ENST00000398590OXSR1chr338232330+ATXN7chr363938055+0.0004265050.9995735
ENST00000311806ENST00000295900OXSR1chr338232330+ATXN7chr363938055+0.0005212990.99947876
ENST00000311806ENST00000487717OXSR1chr338232330+ATXN7chr363938055+0.0041290090.995871
ENST00000311806ENST00000538065OXSR1chr338232330+ATXN7chr363938055+0.0004265050.9995735

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 OXSR1-ATXN7

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
OXSR1chr338232330ATXN7chr363938055664154KDELWLVMKLLSGDMPIFGFCPAHDD

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Potential FusionNeoAntigen Information of OXSR1-ATXN7 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.
OXSR1-ATXN7_38232330_63938055.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)
OXSR1-ATXN7chr338232330chr363938055664HLA-A02:21KLLSGDMPI0.98390.5879817
OXSR1-ATXN7chr338232330chr363938055664HLA-A02:04KLLSGDMPI0.98360.5787817
OXSR1-ATXN7chr338232330chr363938055664HLA-A02:13KLLSGDMPI0.97860.5533817
OXSR1-ATXN7chr338232330chr363938055664HLA-B13:02KLLSGDMPI0.07840.6559817
OXSR1-ATXN7chr338232330chr363938055664HLA-C05:09SGDMPIFGF0.99920.84551120
OXSR1-ATXN7chr338232330chr363938055664HLA-C08:15SGDMPIFGF0.9980.90391120
OXSR1-ATXN7chr338232330chr363938055664HLA-B15:05LLSGDMPIF0.79370.7461918
OXSR1-ATXN7chr338232330chr363938055664HLA-C04:03SGDMPIFGF0.99920.72911120
OXSR1-ATXN7chr338232330chr363938055664HLA-C05:01SGDMPIFGF0.99920.84551120
OXSR1-ATXN7chr338232330chr363938055664HLA-C08:02SGDMPIFGF0.9980.90391120
OXSR1-ATXN7chr338232330chr363938055664HLA-A02:06KLLSGDMPI0.98390.5879817

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Potential FusionNeoAntigen Information of OXSR1-ATXN7 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 OXSR1-ATXN7

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
10119VMKLLSGDMPIFGFOXSR1ATXN7chr338232330chr363938055664

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of OXSR1-ATXN7

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-B14:023BVN10119VMKLLSGDMPIFGF-7.9962-8.1096
HLA-B14:023BVN10119VMKLLSGDMPIFGF-5.70842-6.74372
HLA-B52:013W3910119VMKLLSGDMPIFGF-6.83737-6.95077
HLA-B52:013W3910119VMKLLSGDMPIFGF-4.4836-5.5189
HLA-A11:014UQ210119VMKLLSGDMPIFGF-10.0067-10.1201
HLA-A11:014UQ210119VMKLLSGDMPIFGF-9.03915-10.0745
HLA-A24:025HGA10119VMKLLSGDMPIFGF-6.56204-6.67544
HLA-A24:025HGA10119VMKLLSGDMPIFGF-5.42271-6.45801
HLA-B44:053DX810119VMKLLSGDMPIFGF-7.85648-8.89178
HLA-B44:053DX810119VMKLLSGDMPIFGF-5.3978-5.5112
HLA-B35:011A1N10119VMKLLSGDMPIFGF-6.27422-6.38762
HLA-B35:011A1N10119VMKLLSGDMPIFGF-5.27424-6.30954
HLA-A02:016TDR10119VMKLLSGDMPIFGF-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of OXSR1-ATXN7

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
OXSR1-ATXN7chr338232330chr3639380551120SGDMPIFGFGTGGAGACATGCCAATATTTGGTTTCT
OXSR1-ATXN7chr338232330chr363938055817KLLSGDMPIAGCTGCTAAGTGGAGACATGCCAATAT
OXSR1-ATXN7chr338232330chr363938055918LLSGDMPIFTGCTAAGTGGAGACATGCCAATATTTG

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 OXSR1-ATXN7

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
SKCMOXSR1-ATXN7chr338232330ENST00000311806chr363938055ENST00000295900TCGA-FS-A1ZZ-06A

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Potential target of CAR-T therapy development for OXSR1-ATXN7

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 OXSR1-ATXN7

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 OXSR1-ATXN7

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