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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:SCAF1-ETV7

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SCAF1-ETV7
FusionPDB ID: 79403
FusionGDB2.0 ID: 79403
HgeneTgene
Gene symbol

SCAF1

ETV7

Gene ID

58506

51513

Gene nameSR-related CTD associated factor 1ETS variant transcription factor 7
SynonymsSRA1TEL-2|TEL2|TELB
Cytomap

19q13.33

6p21.31

Type of geneprotein-codingprotein-coding
Descriptionsplicing factor, arginine/serine-rich 19SCAFSR-related C-terminal domain-associated factor 1SR-related and CTD-associated factor 1SR-related-CTD-associated factorserine arginine-rich pre-mRNA splicing factor SR-A1transcription factor ETV7ETS translocation variant 7ETS variant 7ETS-related protein Tel2Ets transcription factor TEL-2bTEL2 oncogeneets variant gene 7 (TEL2 oncogene)tel-related Ets factor
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000360565, ENST00000538992, 
ENST00000339796, ENST00000340181, 
ENST00000373737, ENST00000373738, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score9 X 8 X 9=6484 X 4 X 4=64
# samples 135
** MAII scorelog2(13/648*10)=-2.31748218985617
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/64*10)=-0.356143810225275
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SCAF1 [Title/Abstract] AND ETV7 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SCAF1 [Title/Abstract] AND ETV7 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SCAF1(50155926)-ETV7(36343378), # samples:1
SCAF1(50150087)-ETV7(36341355), # samples:1
Anticipated loss of major functional domain due to fusion event.SCAF1-ETV7 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.
SCAF1-ETV7 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.
SCAF1-ETV7 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.
SCAF1-ETV7 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
TgeneETV7

GO:0000122

negative regulation of transcription by RNA polymerase II

11108721



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/chr19:50155926/chr6:36343378)
- 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 SCAF1 (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 ETV7 (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)
ENST00000360565SCAF1chr1950150087+ENST00000339796ETV7chr636341355-1249602491248400
ENST00000360565SCAF1chr1950150087+ENST00000373737ETV7chr636341355-1541602491089346
ENST00000360565SCAF1chr1950150087+ENST00000340181ETV7chr636341355-1772602491320423
ENST00000360565SCAF1chr1950150087+ENST00000373738ETV7chr636341355-1771602491320423

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
ENST00000360565ENST00000339796SCAF1chr1950150087+ETV7chr636341355-0.035361280.9646387
ENST00000360565ENST00000373737SCAF1chr1950150087+ETV7chr636341355-0.0089925690.9910074
ENST00000360565ENST00000340181SCAF1chr1950150087+ETV7chr636341355-0.0185383020.9814617
ENST00000360565ENST00000373738SCAF1chr1950150087+ETV7chr636341355-0.0182920270.98170793

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 SCAF1-ETV7

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SCAF1chr1950150087ETV7chr636341355602184LLPRLRAWRTGKTGDVLYELLQYIKT

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Potential FusionNeoAntigen Information of SCAF1-ETV7 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.
SCAF1-ETV7_50150087_36341355.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)
SCAF1-ETV7chr1950150087chr636341355602HLA-B58:01KTGDVLYEL0.99120.97931120
SCAF1-ETV7chr1950150087chr636341355602HLA-B15:17KTGDVLYEL0.99020.97241120
SCAF1-ETV7chr1950150087chr636341355602HLA-B15:16KTGDVLYEL0.98410.96381120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:24KTGDVLYEL0.97620.60721120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:30KTGDVLYEL0.97620.60721120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:67KTGDVLYEL0.97620.60721120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:60KTGDVLYEL0.97530.54291120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:04KTGDVLYEL0.97520.60581120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:21KTGDVLYEL0.97470.72141120
SCAF1-ETV7chr1950150087chr636341355602HLA-B58:02KTGDVLYEL0.97260.9761120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:11KTGDVLYEL0.97210.64181120
SCAF1-ETV7chr1950150087chr636341355602HLA-B57:03KTGDVLYEL0.9720.99411120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:35KTGDVLYEL0.96160.62531120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:16KTGDVLYEL0.94790.60541120
SCAF1-ETV7chr1950150087chr636341355602HLA-A32:13KTGDVLYEL0.92610.95281120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:29KTGDVLYEL0.91320.61061120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:20KTGDVLYEL0.88450.61341120
SCAF1-ETV7chr1950150087chr636341355602HLA-B13:01KTGDVLYEL0.21410.99291120
SCAF1-ETV7chr1950150087chr636341355602HLA-B15:17RTGKTGDVLY0.98050.9507818
SCAF1-ETV7chr1950150087chr636341355602HLA-B27:02WRTGKTGDVLY0.99970.5861718
SCAF1-ETV7chr1950150087chr636341355602HLA-C05:09TGDVLYEL10.96641220
SCAF1-ETV7chr1950150087chr636341355602HLA-C08:15TGDVLYEL10.9771220
SCAF1-ETV7chr1950150087chr636341355602HLA-C05:09TGDVLYELL0.99990.95611221
SCAF1-ETV7chr1950150087chr636341355602HLA-C08:15TGDVLYELL0.99980.98031221
SCAF1-ETV7chr1950150087chr636341355602HLA-C15:06KTGDVLYEL0.99950.96831120
SCAF1-ETV7chr1950150087chr636341355602HLA-C15:04KTGDVLYEL0.99930.96521120
SCAF1-ETV7chr1950150087chr636341355602HLA-C03:07KTGDVLYEL0.9990.99161120
SCAF1-ETV7chr1950150087chr636341355602HLA-C04:06KTGDVLYEL0.99870.92771120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:01KTGDVLYEL0.97620.60721120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:07KTGDVLYEL0.97570.62631120
SCAF1-ETV7chr1950150087chr636341355602HLA-C06:03KTGDVLYEL0.88130.99511120
SCAF1-ETV7chr1950150087chr636341355602HLA-C12:04KTGDVLYEL0.87960.99431120
SCAF1-ETV7chr1950150087chr636341355602HLA-C02:06KTGDVLYEL0.45930.97631120
SCAF1-ETV7chr1950150087chr636341355602HLA-C04:03TGDVLYEL10.90791220
SCAF1-ETV7chr1950150087chr636341355602HLA-C08:02TGDVLYEL10.9771220
SCAF1-ETV7chr1950150087chr636341355602HLA-C05:01TGDVLYEL10.96641220
SCAF1-ETV7chr1950150087chr636341355602HLA-C04:03TGDVLYELL0.99990.93031221
SCAF1-ETV7chr1950150087chr636341355602HLA-C05:01TGDVLYELL0.99990.95611221
SCAF1-ETV7chr1950150087chr636341355602HLA-C08:02TGDVLYELL0.99980.98031221
SCAF1-ETV7chr1950150087chr636341355602HLA-C15:02KTGDVLYEL0.99950.93611120
SCAF1-ETV7chr1950150087chr636341355602HLA-C15:05KTGDVLYEL0.99950.93771120
SCAF1-ETV7chr1950150087chr636341355602HLA-C15:09KTGDVLYEL0.99930.96521120
SCAF1-ETV7chr1950150087chr636341355602HLA-C16:02KTGDVLYEL0.99520.99571120
SCAF1-ETV7chr1950150087chr636341355602HLA-B57:04KTGDVLYEL0.98790.8561120
SCAF1-ETV7chr1950150087chr636341355602HLA-A32:01KTGDVLYEL0.98620.9711120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:14KTGDVLYEL0.97580.59531120
SCAF1-ETV7chr1950150087chr636341355602HLA-A02:06KTGDVLYEL0.97470.72141120
SCAF1-ETV7chr1950150087chr636341355602HLA-B58:06KTGDVLYEL0.9660.96591120
SCAF1-ETV7chr1950150087chr636341355602HLA-B57:02KTGDVLYEL0.95370.97071120
SCAF1-ETV7chr1950150087chr636341355602HLA-C17:01KTGDVLYEL0.6540.97491120
SCAF1-ETV7chr1950150087chr636341355602HLA-C02:10KTGDVLYEL0.32280.98541120
SCAF1-ETV7chr1950150087chr636341355602HLA-C02:02KTGDVLYEL0.32280.98541120
SCAF1-ETV7chr1950150087chr636341355602HLA-B57:04RTGKTGDVLY0.99540.7592818
SCAF1-ETV7chr1950150087chr636341355602HLA-B15:135RTGKTGDVLY0.98730.8923818
SCAF1-ETV7chr1950150087chr636341355602HLA-B58:06RTGKTGDVLY0.97540.7489818

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Potential FusionNeoAntigen Information of SCAF1-ETV7 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.
SCAF1-ETV7_50150087_36341355.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)
SCAF1-ETV7chr1950150087chr636341355602DRB1-0437LPRLRAWRTGKTGDV116
SCAF1-ETV7chr1950150087chr636341355602DRB1-0437LLPRLRAWRTGKTGD015
SCAF1-ETV7chr1950150087chr636341355602DRB1-1457LPRLRAWRTGKTGDV116
SCAF1-ETV7chr1950150087chr636341355602DRB1-1457LLPRLRAWRTGKTGD015

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Fusion breakpoint peptide structures of SCAF1-ETV7

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
732AWRTGKTGDVLYELSCAF1ETV7chr1950150087chr636341355602

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SCAF1-ETV7

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-B14:023BVN732AWRTGKTGDVLYEL-7.63753-7.75093
HLA-B14:023BVN732AWRTGKTGDVLYEL-4.36349-5.39879
HLA-B52:013W39732AWRTGKTGDVLYEL-6.74822-6.86162
HLA-B52:013W39732AWRTGKTGDVLYEL-4.96916-6.00446
HLA-A24:025HGA732AWRTGKTGDVLYEL-8.26666-9.30196
HLA-A24:025HGA732AWRTGKTGDVLYEL-7.6208-7.7342
HLA-B27:036PZ5732AWRTGKTGDVLYEL0.0420189-0.993281
HLA-B44:053DX8732AWRTGKTGDVLYEL-5.06122-5.17462
HLA-B44:053DX8732AWRTGKTGDVLYEL-4.87073-5.90603

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Vaccine Design for the FusionNeoAntigens of SCAF1-ETV7

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
SCAF1-ETV7chr1950150087chr6363413551120KTGDVLYELAAACGGGTGACGTCCTGTATGAGCTGC
SCAF1-ETV7chr1950150087chr6363413551220TGDVLYELCGGGTGACGTCCTGTATGAGCTGC
SCAF1-ETV7chr1950150087chr6363413551221TGDVLYELLCGGGTGACGTCCTGTATGAGCTGCTCC
SCAF1-ETV7chr1950150087chr636341355718WRTGKTGDVLYGGAGGACGGGCAAAACGGGTGACGTCCTGTATG
SCAF1-ETV7chr1950150087chr636341355818RTGKTGDVLYGGACGGGCAAAACGGGTGACGTCCTGTATG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SCAF1-ETV7chr1950150087chr636341355015LLPRLRAWRTGKTGDTGCTGCCCCGTCTCAGGGCCTGGAGGACGGGCAAAACGGGTGACG
SCAF1-ETV7chr1950150087chr636341355116LPRLRAWRTGKTGDVTGCCCCGTCTCAGGGCCTGGAGGACGGGCAAAACGGGTGACGTCC

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Information of the samples that have these potential fusion neoantigens of SCAF1-ETV7

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
LGGSCAF1-ETV7chr1950150087ENST00000360565chr636341355ENST00000339796TCGA-TM-A7CF

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Potential target of CAR-T therapy development for SCAF1-ETV7

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 SCAF1-ETV7

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 SCAF1-ETV7

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