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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:SOGA3-LOXL2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SOGA3-LOXL2
FusionPDB ID: 85145
FusionGDB2.0 ID: 85145
HgeneTgene
Gene symbol

SOGA3

LOXL2

Gene ID

387104

4017

Gene nameSOGA family member 3lysyl oxidase like 2
SynonymsC6orf174|dJ403A15.3LOR|LOR2|WS9-14
Cytomap

6q22.33

8p21.3

Type of geneprotein-codingprotein-coding
Descriptionprotein SOGA3lysyl oxidase homolog 2lysyl oxidase related 2lysyl oxidase-like 2 delta e13lysyl oxidase-like 2 proteinlysyl oxidase-like protein 2lysyl oxidase-related protein 2lysyl oxidase-related protein WS9-14
Modification date2020031320200329
UniProtAcc.

Q9Y4K0

Main function of 5'-partner protein: FUNCTION: Mediates the post-translational oxidative deamination of lysine residues on target proteins leading to the formation of deaminated lysine (allysine) (PubMed:27735137). Acts as a transcription corepressor and specifically mediates deamination of trimethylated 'Lys-4' of histone H3 (H3K4me3), a specific tag for epigenetic transcriptional activation (PubMed:27735137). Shows no activity against histone H3 when it is trimethylated on 'Lys-9' (H3K9me3) or 'Lys-27' (H3K27me3) or when 'Lys-4' is monomethylated (H3K4me1) or dimethylated (H3K4me2) (PubMed:27735137). Also mediates deamination of methylated TAF10, a member of the transcription factor IID (TFIID) complex, which induces release of TAF10 from promoters, leading to inhibition of TFIID-dependent transcription (PubMed:25959397). LOXL2-mediated deamination of TAF10 results in transcriptional repression of genes required for embryonic stem cell pluripotency including POU5F1/OCT4, NANOG, KLF4 and SOX2 (By similarity). Involved in epithelial to mesenchymal transition (EMT) via interaction with SNAI1 and participates in repression of E-cadherin CDH1, probably by mediating deamination of histone H3 (PubMed:16096638, PubMed:27735137, PubMed:24414204). During EMT, involved with SNAI1 in negatively regulating pericentromeric heterochromatin transcription (PubMed:24239292). SNAI1 recruits LOXL2 to pericentromeric regions to oxidize histone H3 and repress transcription which leads to release of heterochromatin component CBX5/HP1A, enabling chromatin reorganization and acquisition of mesenchymal traits (PubMed:24239292). Interacts with the endoplasmic reticulum protein HSPA5 which activates the IRE1-XBP1 pathway of the unfolded protein response, leading to expression of several transcription factors involved in EMT and subsequent EMT induction (PubMed:28332555). Involved in E-cadherin repression following hypoxia, a hallmark of EMT believed to amplify tumor aggressiveness, suggesting that it may play a role in tumor progression (PubMed:20026874). When secreted into the extracellular matrix, promotes cross-linking of extracellular matrix proteins by mediating oxidative deamination of peptidyl lysine residues in precursors to fibrous collagen and elastin (PubMed:20306300). Acts as a regulator of sprouting angiogenesis, probably via collagen IV scaffolding (PubMed:21835952). Acts as a regulator of chondrocyte differentiation, probably by regulating expression of factors that control chondrocyte differentiation (By similarity). {ECO:0000250|UniProtKB:P58022, ECO:0000269|PubMed:16096638, ECO:0000269|PubMed:20026874, ECO:0000269|PubMed:20306300, ECO:0000269|PubMed:21835952, ECO:0000269|PubMed:24239292, ECO:0000269|PubMed:24414204, ECO:0000269|PubMed:25959397, ECO:0000269|PubMed:27735137}.
Ensembl transtripts involved in fusion geneENST idsENST00000368268, ENST00000481848, 
ENST00000525778, ENST00000556132, 
ENST00000474293, ENST00000465909, 
ENST00000518472, ENST00000389131, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 2 X 3=188 X 4 X 7=224
# samples 38
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(8/224*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SOGA3 [Title/Abstract] AND LOXL2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SOGA3 [Title/Abstract] AND LOXL2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SOGA3(127796438)-LOXL2(23198716), # samples:2
Anticipated loss of major functional domain due to fusion event.SOGA3-LOXL2 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.
SOGA3-LOXL2 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.
SOGA3-LOXL2 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.
SOGA3-LOXL2 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.
SOGA3-LOXL2 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
TgeneLOXL2

GO:0000122

negative regulation of transcription by RNA polymerase II

25959397

TgeneLOXL2

GO:0001837

epithelial to mesenchymal transition

16096638

TgeneLOXL2

GO:0006464

cellular protein modification process

23319596

TgeneLOXL2

GO:0018057

peptidyl-lysine oxidation

25959397|27735137|29581294

TgeneLOXL2

GO:0045892

negative regulation of transcription, DNA-templated

16096638

TgeneLOXL2

GO:0046688

response to copper ion

23319596



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/chr6:127796438/chr8:23198716)
- 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 SOGA3 (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 LOXL2 (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)
ENST00000481848SOGA3chr6127796438-ENST00000389131LOXL2chr823198716-5892324451150371508
ENST00000556132SOGA3chr6127796438-ENST00000389131LOXL2chr823198716-6246359886553911508
ENST00000368268SOGA3chr6127796438-ENST00000389131LOXL2chr823198716-53812733045261508

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
ENST00000481848ENST00000389131SOGA3chr6127796438-LOXL2chr823198716-0.0053216340.9946784
ENST00000556132ENST00000389131SOGA3chr6127796438-LOXL2chr823198716-0.0067202360.99327976
ENST00000368268ENST00000389131SOGA3chr6127796438-LOXL2chr823198716-0.0038051050.99619496

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 SOGA3-LOXL2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SOGA3chr6127796438LOXL2chr8231987162733909SADDRGAEEPISVSQNLNIQVEDIRI
SOGA3chr6127796438LOXL2chr8231987163244909SADDRGAEEPISVSQNLNIQVEDIRI
SOGA3chr6127796438LOXL2chr8231987163598909SADDRGAEEPISVSQNLNIQVEDIRI

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Potential FusionNeoAntigen Information of SOGA3-LOXL2 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.
SOGA3-LOXL2_127796438_23198716.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)
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B15:16ISVSQNLNI0.99530.54221019
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:08EPISVSQNL0.98550.7885817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:01EPISVSQNL0.98370.8535817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:03EPISVSQNL0.97890.876817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:05EPISVSQNL0.93780.5714817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:04EPISVSQNL0.89140.8993817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:02EPISVSQNL0.89140.8993817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:03EEPISVSQNL0.79650.8911717
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B44:03EEPISVSQNL0.77160.9551717
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:02EEPISVSQNL0.73950.9217717
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:04EEPISVSQNL0.73950.9217717
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B44:03AEEPISVSQNL0.99950.9767617
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B39:13AEEPISVSQNL0.9970.9548617
SOGA3-LOXL2chr6127796438chr8231987162733HLA-C15:06ISVSQNLNI0.99940.90411019
SOGA3-LOXL2chr6127796438chr8231987162733HLA-C15:06VSQNLNIQV0.99840.9611221
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:12EPISVSQNL0.89140.8993817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B51:07EPISVSQNL0.82420.6461817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B07:12EPISVSQNL0.7840.5182817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B39:10EPISVSQNL0.72710.9031817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B42:02EPISVSQNL0.70850.5426817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B42:01EPISVSQNL0.59640.5359817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B39:10EEPISVSQNL0.76580.9091717
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:12EEPISVSQNL0.73950.9217717
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B39:08AEEPISVSQNL0.99820.8203617
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B07:12AEEPISVSQNL0.97240.5358617
SOGA3-LOXL2chr6127796438chr8231987162733HLA-C15:05ISVSQNLNI0.99940.88821019
SOGA3-LOXL2chr6127796438chr8231987162733HLA-C15:02ISVSQNLNI0.99940.83121019
SOGA3-LOXL2chr6127796438chr8231987162733HLA-C15:02VSQNLNIQV0.99910.92161221
SOGA3-LOXL2chr6127796438chr8231987162733HLA-C15:05VSQNLNIQV0.99890.95191221
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:23EPISVSQNL0.98570.8476817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:77EPISVSQNL0.98370.8535817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:13EPISVSQNL0.96650.8839817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:30EPISVSQNL0.9430.7169817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:17EPISVSQNL0.9430.7169817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:11EPISVSQNL0.93890.9065817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:24EPISVSQNL0.92340.9087817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:09EPISVSQNL0.89140.8993817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B67:01EPISVSQNL0.74940.7342817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B08:12EPISVSQNL0.52050.6696817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B18:07EPISVSQNL0.140.8353817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:43EPISVSQNL0.07780.774817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B15:08EPISVSQNL0.05010.773817
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B44:26EEPISVSQNL0.77160.9551717
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B44:13EEPISVSQNL0.77160.9551717
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B44:07EEPISVSQNL0.77160.9551717
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B35:09EEPISVSQNL0.73950.9217717
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B40:04AEEPISVSQNL0.99990.7371617
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B44:13AEEPISVSQNL0.99950.9767617
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B44:26AEEPISVSQNL0.99950.9767617
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B44:07AEEPISVSQNL0.99950.9767617
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B67:01AEEPISVSQNL0.99770.9151617
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B39:02AEEPISVSQNL0.9970.9522617
SOGA3-LOXL2chr6127796438chr8231987162733HLA-B41:03AEEPISVSQNL0.98960.551617

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Potential FusionNeoAntigen Information of SOGA3-LOXL2 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.
SOGA3-LOXL2_127796438_23198716.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)
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-0478EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-0904EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-0906EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-0906AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-0906GAEEPISVSQNLNIQ520
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1331EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1401EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1401AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1404EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1404AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1404GAEEPISVSQNLNIQ520
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1410EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1410AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1410GAEEPISVSQNLNIQ520
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1411EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1426EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1426AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1428EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1428AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1428GAEEPISVSQNLNIQ520
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1431EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1435EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1438EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1438AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1439EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1439AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1439GAEEPISVSQNLNIQ520
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1439EPISVSQNLNIQVED823
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1445EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1448EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1450EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1450AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1450GAEEPISVSQNLNIQ520
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1454EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1454AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1455EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1458EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1458AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1460EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1460AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1461EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1461AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1461GAEEPISVSQNLNIQ520
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1462EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1468EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1470EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1470AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1471EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1471AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1471GAEEPISVSQNLNIQ520
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1475EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1475AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1475GAEEPISVSQNLNIQ520
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1482EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1482AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1486EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1486AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1487EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1487AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1488EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1488AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1490EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1490AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1493EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1493AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1497EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1497AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1499EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1499AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1525EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1525AEEPISVSQNLNIQV621
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1525EPISVSQNLNIQVED823
SOGA3-LOXL2chr6127796438chr8231987162733DRB1-1525GAEEPISVSQNLNIQ520
SOGA3-LOXL2chr6127796438chr8231987162733DRB3-0201EPISVSQNLNIQVED823
SOGA3-LOXL2chr6127796438chr8231987162733DRB3-0201PISVSQNLNIQVEDI924
SOGA3-LOXL2chr6127796438chr8231987162733DRB3-0224EPISVSQNLNIQVED823
SOGA3-LOXL2chr6127796438chr8231987162733DRB3-0224PISVSQNLNIQVEDI924
SOGA3-LOXL2chr6127796438chr8231987162733DRB3-0301EPISVSQNLNIQVED823
SOGA3-LOXL2chr6127796438chr8231987162733DRB3-0301EEPISVSQNLNIQVE722
SOGA3-LOXL2chr6127796438chr8231987162733DRB3-0301PISVSQNLNIQVEDI924
SOGA3-LOXL2chr6127796438chr8231987162733DRB3-0301AEEPISVSQNLNIQV621

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Fusion breakpoint peptide structures of SOGA3-LOXL2

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
149AEEPISVSQNLNIQSOGA3LOXL2chr6127796438chr8231987162733

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SOGA3-LOXL2

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-B14:023BVN149AEEPISVSQNLNIQ-8.62545-8.73885
HLA-B14:023BVN149AEEPISVSQNLNIQ-3.26321-4.29851
HLA-B52:013W39149AEEPISVSQNLNIQ-6.23413-6.34753
HLA-B52:013W39149AEEPISVSQNLNIQ-4.55402-5.58932
HLA-A24:025HGA149AEEPISVSQNLNIQ-8.62578-8.73918
HLA-A24:025HGA149AEEPISVSQNLNIQ-6.438-7.4733
HLA-B44:053DX8149AEEPISVSQNLNIQ-5.68484-5.79824
HLA-B44:053DX8149AEEPISVSQNLNIQ-3.64855-4.68385
HLA-A02:016TDR149AEEPISVSQNLNIQ-5.14764-6.18294

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Vaccine Design for the FusionNeoAntigens of SOGA3-LOXL2

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
SOGA3-LOXL2chr6127796438chr8231987161019ISVSQNLNIGTGAGTCAGAACCTGAATATCCAGGTG
SOGA3-LOXL2chr6127796438chr8231987161221VSQNLNIQVCAGAACCTGAATATCCAGGTGGAGGAC
SOGA3-LOXL2chr6127796438chr823198716617AEEPISVSQNLGAGCCCATTTCCGTGAGTCAGAACCTGAATATC
SOGA3-LOXL2chr6127796438chr823198716717EEPISVSQNLCCCATTTCCGTGAGTCAGAACCTGAATATC
SOGA3-LOXL2chr6127796438chr823198716817EPISVSQNLATTTCCGTGAGTCAGAACCTGAATATC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SOGA3-LOXL2chr6127796438chr823198716520GAEEPISVSQNLNIQGAGGAGCCCATTTCCGTGAGTCAGAACCTGAATATCCAGGTGGAG
SOGA3-LOXL2chr6127796438chr823198716621AEEPISVSQNLNIQVGAGCCCATTTCCGTGAGTCAGAACCTGAATATCCAGGTGGAGGAC
SOGA3-LOXL2chr6127796438chr823198716722EEPISVSQNLNIQVECCCATTTCCGTGAGTCAGAACCTGAATATCCAGGTGGAGGACATT
SOGA3-LOXL2chr6127796438chr823198716823EPISVSQNLNIQVEDATTTCCGTGAGTCAGAACCTGAATATCCAGGTGGAGGACATTCGG
SOGA3-LOXL2chr6127796438chr823198716924PISVSQNLNIQVEDITCCGTGAGTCAGAACCTGAATATCCAGGTGGAGGACATTCGGATT

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Information of the samples that have these potential fusion neoantigens of SOGA3-LOXL2

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
STADSOGA3-LOXL2chr6127796438ENST00000368268chr823198716ENST00000389131TCGA-BR-A4IY-01A

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Potential target of CAR-T therapy development for SOGA3-LOXL2

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
HgeneSOGA3chr6:127796438chr8:23198716ENST00000368268-58915_935911698.0TransmembraneHelical

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 SOGA3-LOXL2

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 SOGA3-LOXL2

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