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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:BRAF-SND1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: BRAF-SND1
FusionPDB ID: 10132
FusionGDB2.0 ID: 10132
HgeneTgene
Gene symbol

BRAF

SND1

Gene ID

673

27044

Gene nameB-Raf proto-oncogene, serine/threonine kinasestaphylococcal nuclease and tudor domain containing 1
SynonymsB-RAF1|B-raf|BRAF1|NS7|RAFB1TDRD11|Tudor-SN|p100
Cytomap

7q34

7q32.1

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase B-raf94 kDa B-raf proteinB-Raf proto-oncogene serine/threonine-protein kinase (p94)B-Raf serine/threonine-proteinmurine sarcoma viral (v-raf) oncogene homolog B1proto-oncogene B-Rafv-raf murine sarcoma viral oncogene staphylococcal nuclease domain-containing protein 1EBNA2 coactivator p100testis tissue sperm-binding protein Li 82Ptudor domain-containing protein 11
Modification date2020032920200313
UniProtAcc

P15056

Main function of 5'-partner protein: FUNCTION: Protein kinase involved in the transduction of mitogenic signals from the cell membrane to the nucleus (Probable). Phosphorylates MAP2K1, and thereby activates the MAP kinase signal transduction pathway (PubMed:21441910, PubMed:29433126). May play a role in the postsynaptic responses of hippocampal neurons (PubMed:1508179). {ECO:0000269|PubMed:1508179, ECO:0000269|PubMed:21441910, ECO:0000269|PubMed:29433126, ECO:0000305}.

Q7KZF4

Main function of 5'-partner protein: FUNCTION: Endonuclease that mediates miRNA decay of both protein-free and AGO2-loaded miRNAs (PubMed:28546213, PubMed:18453631). As part of its function in miRNA decay, regulates mRNAs involved in G1-to-S phase transition (PubMed:28546213). Functions as a bridging factor between STAT6 and the basal transcription factor (PubMed:12234934). Plays a role in PIM1 regulation of MYB activity (PubMed:9809063). Functions as a transcriptional coactivator for STAT5 (By similarity). {ECO:0000250|UniProtKB:Q78PY7, ECO:0000269|PubMed:12234934, ECO:0000269|PubMed:18453631, ECO:0000269|PubMed:28546213, ECO:0000269|PubMed:9809063}.; FUNCTION: (Microbial infection) Functions as a transcriptional coactivator for the Epstein-Barr virus nuclear antigen 2 (EBNA2). {ECO:0000269|PubMed:7651391}.
Ensembl transtripts involved in fusion geneENST idsENST00000288602, ENST00000467238, 
ENST00000354725, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score28 X 21 X 11=646829 X 24 X 11=7656
# samples 3233
** MAII scorelog2(32/6468*10)=-4.3371758685863
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(33/7656*10)=-4.53605290024021
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: BRAF [Title/Abstract] AND SND1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: BRAF [Title/Abstract] AND SND1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)BRAF(140487348)-SND1(127724776), # samples:3
SND1(127361454)-BRAF(140487384), # samples:5
Anticipated loss of major functional domain due to fusion event.BRAF-SND1 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.
BRAF-SND1 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.
BRAF-SND1 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.
BRAF-SND1 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.
SND1-BRAF 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.
SND1-BRAF 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
HgeneBRAF

GO:0000186

activation of MAPKK activity

29433126

HgeneBRAF

GO:0006468

protein phosphorylation

17563371

HgeneBRAF

GO:0010828

positive regulation of glucose transmembrane transport

23010278

HgeneBRAF

GO:0033138

positive regulation of peptidyl-serine phosphorylation

19667065

HgeneBRAF

GO:0043066

negative regulation of apoptotic process

19667065

HgeneBRAF

GO:0070374

positive regulation of ERK1 and ERK2 cascade

22065586

HgeneBRAF

GO:0071277

cellular response to calcium ion

18567582

HgeneBRAF

GO:0090150

establishment of protein localization to membrane

23010278

TgeneSND1

GO:0010587

miRNA catabolic process

28546213



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/chr7:140487348/chr7:127724776)
- 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 BRAF (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 SND1 (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)
ENST00000288602BRAFchr7140487348-ENST00000354725SND1chr7127724776+24101238611860599
ENST00000288602BRAFchr7140494108-ENST00000354725SND1chr7127714554+27041201612154697

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
ENST00000288602ENST00000354725BRAFchr7140487348-SND1chr7127724776+0.0017271260.9982729
ENST00000288602ENST00000354725BRAFchr7140494108-SND1chr7127714554+0.0019080530.9980919

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 BRAF-SND1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
BRAFchr7140487348SND1chr71277247761238392DDLIRDQGFRGDGGTQLEKLMENMRN
BRAFchr7140494108SND1chr71277145541201380NVHINTIEPVNIDVEVEVESMDKAGN

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Potential FusionNeoAntigen Information of BRAF-SND1 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.
BRAF-SND1_140487348_127724776.msa
BRAF-SND1_140494108_127714554.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)
BRAF-SND1chr7140487348chr71277247761238HLA-B39:01FRGDGGTQL0.99750.8759817
BRAF-SND1chr7140487348chr71277247761238HLA-B39:24FRGDGGTQL0.99720.6866817
BRAF-SND1chr7140487348chr71277247761238HLA-B39:06FRGDGGTQL0.99370.8593817
BRAF-SND1chr7140487348chr71277247761238HLA-B38:02FRGDGGTQL0.99280.9567817
BRAF-SND1chr7140487348chr71277247761238HLA-B27:04FRGDGGTQL0.99280.5737817
BRAF-SND1chr7140487348chr71277247761238HLA-B38:01FRGDGGTQL0.99170.9659817
BRAF-SND1chr7140487348chr71277247761238HLA-B27:07FRGDGGTQL0.99050.6109817
BRAF-SND1chr7140487348chr71277247761238HLA-B27:05FRGDGGTQL0.98830.5674817
BRAF-SND1chr7140487348chr71277247761238HLA-B14:01FRGDGGTQL0.97940.9119817
BRAF-SND1chr7140487348chr71277247761238HLA-B14:02FRGDGGTQL0.97940.9119817
BRAF-SND1chr7140487348chr71277247761238HLA-B15:18FRGDGGTQL0.85870.6187817
BRAF-SND1chr7140487348chr71277247761238HLA-B27:07GFRGDGGTQL0.96480.7338717
BRAF-SND1chr7140487348chr71277247761238HLA-C08:15RGDGGTQL10.9812917
BRAF-SND1chr7140487348chr71277247761238HLA-C05:09RGDGGTQL10.9499917
BRAF-SND1chr7140487348chr71277247761238HLA-B39:09FRGDGGTQL0.99760.7373817
BRAF-SND1chr7140487348chr71277247761238HLA-B39:12FRGDGGTQL0.99670.8774817
BRAF-SND1chr7140487348chr71277247761238HLA-B39:05FRGDGGTQL0.99340.8543817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:05FRGDGGTQL0.98940.912817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:27FRGDGGTQL0.98920.9235817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:95FRGDGGTQL0.98790.6261817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:29FRGDGGTQL0.98320.8849817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:13FRGDGGTQL0.97150.9084817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:46FRGDGGTQL0.91570.8717817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:80FRGDGGTQL0.85340.9364817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:67FRGDGGTQL0.85340.9364817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:19FRGDGGTQL0.83990.7807817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:10FRGDGGTQL0.82080.9661817
BRAF-SND1chr7140487348chr71277247761238HLA-B14:03FRGDGGTQL0.65710.8432817
BRAF-SND1chr7140487348chr71277247761238HLA-C12:16FRGDGGTQL0.22110.96817
BRAF-SND1chr7140487348chr71277247761238HLA-C05:01RGDGGTQL10.9499917
BRAF-SND1chr7140487348chr71277247761238HLA-C04:03RGDGGTQL10.9548917
BRAF-SND1chr7140487348chr71277247761238HLA-C08:02RGDGGTQL10.9812917
BRAF-SND1chr7140487348chr71277247761238HLA-B39:31FRGDGGTQL0.99770.8756817
BRAF-SND1chr7140487348chr71277247761238HLA-B27:06FRGDGGTQL0.99540.6025817
BRAF-SND1chr7140487348chr71277247761238HLA-B27:10FRGDGGTQL0.9930.7107817
BRAF-SND1chr7140487348chr71277247761238HLA-B38:05FRGDGGTQL0.99170.9659817
BRAF-SND1chr7140487348chr71277247761238HLA-B27:09FRGDGGTQL0.99090.581817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:01FRGDGGTQL0.98550.63817
BRAF-SND1chr7140487348chr71277247761238HLA-C18:01FRGDGGTQL0.98220.94817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:17FRGDGGTQL0.97260.9665817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:04FRGDGGTQL0.92860.9025817
BRAF-SND1chr7140487348chr71277247761238HLA-B15:09FRGDGGTQL0.8930.8414817
BRAF-SND1chr7140487348chr71277247761238HLA-C06:08FRGDGGTQL0.89180.9834817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:22FRGDGGTQL0.860.709817
BRAF-SND1chr7140487348chr71277247761238HLA-C07:02FRGDGGTQL0.85340.9364817
BRAF-SND1chr7140487348chr71277247761238HLA-B39:11FRGDGGTQL0.8360.8322817
BRAF-SND1chr7140487348chr71277247761238HLA-C03:67FRGDGGTQL0.810.9759817
BRAF-SND1chr7140487348chr71277247761238HLA-C06:06FRGDGGTQL0.78220.9845817
BRAF-SND1chr7140487348chr71277247761238HLA-C04:04FRGDGGTQL0.70440.9388817
BRAF-SND1chr7140487348chr71277247761238HLA-C06:17FRGDGGTQL0.3360.989817
BRAF-SND1chr7140487348chr71277247761238HLA-C06:02FRGDGGTQL0.3360.989817
BRAF-SND1chr7140487348chr71277247761238HLA-B27:06GFRGDGGTQL0.97140.5969717
BRAF-SND1chr7140494108chr71277145541201HLA-B35:04EPVNIDVEV0.9050.9507716
BRAF-SND1chr7140494108chr71277145541201HLA-B35:02EPVNIDVEV0.9050.9507716
BRAF-SND1chr7140494108chr71277145541201HLA-B35:03EPVNIDVEV0.88840.8927716
BRAF-SND1chr7140494108chr71277145541201HLA-C08:15NIDVEVEV0.99820.90541018
BRAF-SND1chr7140494108chr71277145541201HLA-B35:12EPVNIDVEV0.9050.9507716
BRAF-SND1chr7140494108chr71277145541201HLA-B39:10EPVNIDVEV0.25620.8692716
BRAF-SND1chr7140494108chr71277145541201HLA-C08:02NIDVEVEV0.99820.90541018
BRAF-SND1chr7140494108chr71277145541201HLA-B35:09EPVNIDVEV0.9050.9507716
BRAF-SND1chr7140494108chr71277145541201HLA-B67:01EPVNIDVEV0.51590.5889716
BRAF-SND1chr7140494108chr71277145541201HLA-A69:01NTIEPVNIDV0.99320.5946414

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Potential FusionNeoAntigen Information of BRAF-SND1 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.
BRAF-SND1_140487348_127724776.msa
BRAF-SND1_140494108_127714554.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)
BRAF-SND1chr7140487348chr71277247761238DRB1-0338RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB1-0338DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0101RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0101DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0101IRDQGFRGDGGTQLE318
BRAF-SND1chr7140487348chr71277247761238DRB3-0101QGFRGDGGTQLEKLM621
BRAF-SND1chr7140487348chr71277247761238DRB3-0101LIRDQGFRGDGGTQL217
BRAF-SND1chr7140487348chr71277247761238DRB3-0104RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0104DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0104IRDQGFRGDGGTQLE318
BRAF-SND1chr7140487348chr71277247761238DRB3-0104QGFRGDGGTQLEKLM621
BRAF-SND1chr7140487348chr71277247761238DRB3-0104LIRDQGFRGDGGTQL217
BRAF-SND1chr7140487348chr71277247761238DRB3-0105RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0105DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0105IRDQGFRGDGGTQLE318
BRAF-SND1chr7140487348chr71277247761238DRB3-0105QGFRGDGGTQLEKLM621
BRAF-SND1chr7140487348chr71277247761238DRB3-0105LIRDQGFRGDGGTQL217
BRAF-SND1chr7140487348chr71277247761238DRB3-0108RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0108DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0108IRDQGFRGDGGTQLE318
BRAF-SND1chr7140487348chr71277247761238DRB3-0108QGFRGDGGTQLEKLM621
BRAF-SND1chr7140487348chr71277247761238DRB3-0108LIRDQGFRGDGGTQL217
BRAF-SND1chr7140487348chr71277247761238DRB3-0109RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0109DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0109IRDQGFRGDGGTQLE318
BRAF-SND1chr7140487348chr71277247761238DRB3-0109QGFRGDGGTQLEKLM621
BRAF-SND1chr7140487348chr71277247761238DRB3-0111RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0111DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0111IRDQGFRGDGGTQLE318
BRAF-SND1chr7140487348chr71277247761238DRB3-0111QGFRGDGGTQLEKLM621
BRAF-SND1chr7140487348chr71277247761238DRB3-0111LIRDQGFRGDGGTQL217
BRAF-SND1chr7140487348chr71277247761238DRB3-0112RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0112DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0112IRDQGFRGDGGTQLE318
BRAF-SND1chr7140487348chr71277247761238DRB3-0112QGFRGDGGTQLEKLM621
BRAF-SND1chr7140487348chr71277247761238DRB3-0112LIRDQGFRGDGGTQL217
BRAF-SND1chr7140487348chr71277247761238DRB3-0113RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0113DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0113IRDQGFRGDGGTQLE318
BRAF-SND1chr7140487348chr71277247761238DRB3-0113QGFRGDGGTQLEKLM621
BRAF-SND1chr7140487348chr71277247761238DRB3-0113LIRDQGFRGDGGTQL217
BRAF-SND1chr7140487348chr71277247761238DRB3-0114RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0114DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0114IRDQGFRGDGGTQLE318
BRAF-SND1chr7140487348chr71277247761238DRB3-0114QGFRGDGGTQLEKLM621
BRAF-SND1chr7140487348chr71277247761238DRB3-0209RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0209DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0216RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0216DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0221RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0221DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0303DQGFRGDGGTQLEKL520
BRAF-SND1chr7140487348chr71277247761238DRB3-0303RDQGFRGDGGTQLEK419
BRAF-SND1chr7140487348chr71277247761238DRB3-0303IRDQGFRGDGGTQLE318
BRAF-SND1chr7140494108chr71277145541201DRB1-0310TIEPVNIDVEVEVES520
BRAF-SND1chr7140494108chr71277145541201DRB1-0310IEPVNIDVEVEVESM621
BRAF-SND1chr7140494108chr71277145541201DRB1-1476TIEPVNIDVEVEVES520
BRAF-SND1chr7140494108chr71277145541201DRB1-1476IEPVNIDVEVEVESM621
BRAF-SND1chr7140494108chr71277145541201DRB1-1479TIEPVNIDVEVEVES520
BRAF-SND1chr7140494108chr71277145541201DRB1-1479IEPVNIDVEVEVESM621
BRAF-SND1chr7140494108chr71277145541201DRB3-0301NVHINTIEPVNIDVE015
BRAF-SND1chr7140494108chr71277145541201DRB4-0101IDVEVEVESMDKAGN1126
BRAF-SND1chr7140494108chr71277145541201DRB4-0101NIDVEVEVESMDKAG1025
BRAF-SND1chr7140494108chr71277145541201DRB4-0103IDVEVEVESMDKAGN1126
BRAF-SND1chr7140494108chr71277145541201DRB4-0103NIDVEVEVESMDKAG1025
BRAF-SND1chr7140494108chr71277145541201DRB4-0104IDVEVEVESMDKAGN1126
BRAF-SND1chr7140494108chr71277145541201DRB4-0104NIDVEVEVESMDKAG1025
BRAF-SND1chr7140494108chr71277145541201DRB4-0106IDVEVEVESMDKAGN1126
BRAF-SND1chr7140494108chr71277145541201DRB4-0106NIDVEVEVESMDKAG1025
BRAF-SND1chr7140494108chr71277145541201DRB4-0107IDVEVEVESMDKAGN1126
BRAF-SND1chr7140494108chr71277145541201DRB4-0107NIDVEVEVESMDKAG1025
BRAF-SND1chr7140494108chr71277145541201DRB4-0108IDVEVEVESMDKAGN1126
BRAF-SND1chr7140494108chr71277145541201DRB4-0108NIDVEVEVESMDKAG1025

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Fusion breakpoint peptide structures of BRAF-SND1

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
3655IEPVNIDVEVEVESBRAFSND1chr7140494108chr71277145541201
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
7275QGFRGDGGTQLEKLBRAFSND1chr7140487348chr71277247761238

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of BRAF-SND1

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-B14:023BVN3655IEPVNIDVEVEVES-7.9962-8.1096
HLA-B14:023BVN3655IEPVNIDVEVEVES-5.70842-6.74372
HLA-B52:013W393655IEPVNIDVEVEVES-6.83737-6.95077
HLA-B52:013W393655IEPVNIDVEVEVES-4.4836-5.5189
HLA-A11:014UQ23655IEPVNIDVEVEVES-10.0067-10.1201
HLA-A11:014UQ23655IEPVNIDVEVEVES-9.03915-10.0745
HLA-A24:025HGA3655IEPVNIDVEVEVES-6.56204-6.67544
HLA-A24:025HGA3655IEPVNIDVEVEVES-5.42271-6.45801
HLA-B44:053DX83655IEPVNIDVEVEVES-7.85648-8.89178
HLA-B44:053DX83655IEPVNIDVEVEVES-5.3978-5.5112
HLA-A02:016TDR3655IEPVNIDVEVEVES-3.37154-4.40684
HLA-B14:023BVN7275QGFRGDGGTQLEKL-6.78971-6.90311
HLA-B14:023BVN7275QGFRGDGGTQLEKL-6.25013-7.28543
HLA-B52:013W397275QGFRGDGGTQLEKL-6.6066-6.72
HLA-B52:013W397275QGFRGDGGTQLEKL-4.24303-5.27833
HLA-A11:014UQ27275QGFRGDGGTQLEKL-11.627-11.7404
HLA-A11:014UQ27275QGFRGDGGTQLEKL-6.05627-7.09157
HLA-A24:025HGA7275QGFRGDGGTQLEKL-7.37131-7.48471
HLA-A24:025HGA7275QGFRGDGGTQLEKL-7.11576-8.15106
HLA-B44:053DX87275QGFRGDGGTQLEKL-7.74957-7.86297
HLA-B44:053DX87275QGFRGDGGTQLEKL-2.81564-3.85094
HLA-A02:016TDR7275QGFRGDGGTQLEKL-5.7576-6.7929
HLA-A02:016TDR7275QGFRGDGGTQLEKL-4.02719-4.14059

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Vaccine Design for the FusionNeoAntigens of BRAF-SND1

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
BRAF-SND1chr7140487348chr7127724776717GFRGDGGTQLGATTTCGTGGTGATGGAGGCACCCAGTTGG
BRAF-SND1chr7140487348chr7127724776817FRGDGGTQLTTCGTGGTGATGGAGGCACCCAGTTGG
BRAF-SND1chr7140487348chr7127724776917RGDGGTQLGTGGTGATGGAGGCACCCAGTTGG
BRAF-SND1chr7140494108chr71277145541018NIDVEVEVAATATTGATGTGGAGGTGGAGGTG
BRAF-SND1chr7140494108chr7127714554414NTIEPVNIDVAACACAATAGAACCTGTCAATATTGATGTG
BRAF-SND1chr7140494108chr7127714554716EPVNIDVEVGAACCTGTCAATATTGATGTGGAGGTG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
BRAF-SND1chr7140487348chr7127724776217LIRDQGFRGDGGTQLTGATTAGAGACCAAGGATTTCGTGGTGATGGAGGCACCCAGTTGG
BRAF-SND1chr7140487348chr7127724776318IRDQGFRGDGGTQLETTAGAGACCAAGGATTTCGTGGTGATGGAGGCACCCAGTTGGAGA
BRAF-SND1chr7140487348chr7127724776419RDQGFRGDGGTQLEKGAGACCAAGGATTTCGTGGTGATGGAGGCACCCAGTTGGAGAAGC
BRAF-SND1chr7140487348chr7127724776520DQGFRGDGGTQLEKLACCAAGGATTTCGTGGTGATGGAGGCACCCAGTTGGAGAAGCTGA
BRAF-SND1chr7140487348chr7127724776621QGFRGDGGTQLEKLMAAGGATTTCGTGGTGATGGAGGCACCCAGTTGGAGAAGCTGATGG
BRAF-SND1chr7140494108chr7127714554015NVHINTIEPVNIDVEAATGTGCATATAAACACAATAGAACCTGTCAATATTGATGTGGAG
BRAF-SND1chr7140494108chr71277145541025NIDVEVEVESMDKAGAATATTGATGTGGAGGTGGAGGTGGAGAGCATGGACAAGGCCGGC
BRAF-SND1chr7140494108chr71277145541126IDVEVEVESMDKAGNATTGATGTGGAGGTGGAGGTGGAGAGCATGGACAAGGCCGGCAAC
BRAF-SND1chr7140494108chr7127714554520TIEPVNIDVEVEVESACAATAGAACCTGTCAATATTGATGTGGAGGTGGAGGTGGAGAGC
BRAF-SND1chr7140494108chr7127714554621IEPVNIDVEVEVESMATAGAACCTGTCAATATTGATGTGGAGGTGGAGGTGGAGAGCATG

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Information of the samples that have these potential fusion neoantigens of BRAF-SND1

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
THCABRAF-SND1chr7140487348ENST00000288602chr7127724776ENST00000354725TCGA-EL-A3ZK-01A
THCABRAF-SND1chr7140494108ENST00000288602chr7127714554ENST00000354725TCGA-KS-A41I-01A

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Potential target of CAR-T therapy development for BRAF-SND1

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 BRAF-SND1

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 BRAF-SND1

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
HgeneBRAFC0025202melanoma24CGI;CTD_human;UNIPROT
HgeneBRAFC1275081Cardio-facio-cutaneous syndrome14CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneBRAFC0009402Colorectal Carcinoma8CTD_human;UNIPROT
HgeneBRAFC0028326Noonan Syndrome8CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneBRAFC0238463Papillary thyroid carcinoma8CTD_human;ORPHANET
HgeneBRAFC0040136Thyroid Neoplasm6CGI;CTD_human
HgeneBRAFC0151468Thyroid Gland Follicular Adenoma6CTD_human
HgeneBRAFC0175704LEOPARD Syndrome6CLINGEN;GENOMICS_ENGLAND
HgeneBRAFC0549473Thyroid carcinoma6CGI;CTD_human
HgeneBRAFC3150970NOONAN SYNDROME 75CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneBRAFC0009404Colorectal Neoplasms4CTD_human
HgeneBRAFC3150971LEOPARD SYNDROME 34CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneBRAFC1519086Pilomyxoid astrocytoma3ORPHANET
HgeneBRAFC0004565Melanoma, B162CTD_human
HgeneBRAFC0009075Melanoma, Cloudman S912CTD_human
HgeneBRAFC0018598Melanoma, Harding-Passey2CTD_human
HgeneBRAFC0023443Hairy Cell Leukemia2CGI;ORPHANET
HgeneBRAFC0025205Melanoma, Experimental2CTD_human
HgeneBRAFC0033578Prostatic Neoplasms2CTD_human
HgeneBRAFC0152013Adenocarcinoma of lung (disorder)2CGI;CTD_human
HgeneBRAFC0376358Malignant neoplasm of prostate2CTD_human
HgeneBRAFC0587248Costello syndrome (disorder)2CLINGEN;CTD_human
HgeneBRAFC3501843Nonmedullary Thyroid Carcinoma2CTD_human
HgeneBRAFC3501844Familial Nonmedullary Thyroid Cancer2CTD_human
HgeneBRAFC0002448Ameloblastoma1CTD_human
HgeneBRAFC0004114Astrocytoma1CTD_human
HgeneBRAFC0010276Craniopharyngioma1CTD_human;ORPHANET
HgeneBRAFC0011860Diabetes Mellitus, Non-Insulin-Dependent1CTD_human
HgeneBRAFC0017638Glioma1CGI;CTD_human
HgeneBRAFC0019621Histiocytosis, Langerhans-Cell1CGI;ORPHANET
HgeneBRAFC0022665Kidney Neoplasm1CTD_human
HgeneBRAFC0023903Liver neoplasms1CTD_human
HgeneBRAFC0024232Lymphatic Metastasis1CTD_human
HgeneBRAFC0024694Mandibular Neoplasms1CTD_human
HgeneBRAFC0027659Neoplasms, Experimental1CTD_human
HgeneBRAFC0027962Melanocytic nevus1GENOMICS_ENGLAND
HgeneBRAFC0036920Sezary Syndrome1CTD_human
HgeneBRAFC0041409Turner Syndrome, Male1CTD_human
HgeneBRAFC0079773Lymphoma, T-Cell, Cutaneous1CTD_human
HgeneBRAFC0205768Subependymal Giant Cell Astrocytoma1CTD_human
HgeneBRAFC0206686Adrenocortical carcinoma1CTD_human
HgeneBRAFC0206754Neuroendocrine Tumors1CTD_human
HgeneBRAFC0259783mixed gliomas1CTD_human
HgeneBRAFC0278875Adult Craniopharyngioma1CTD_human
HgeneBRAFC0280783Juvenile Pilocytic Astrocytoma1CTD_human
HgeneBRAFC0280785Diffuse Astrocytoma1CTD_human
HgeneBRAFC0334579Anaplastic astrocytoma1CGI;CTD_human
HgeneBRAFC0334580Protoplasmic astrocytoma1CTD_human
HgeneBRAFC0334581Gemistocytic astrocytoma1CTD_human
HgeneBRAFC0334582Fibrillary Astrocytoma1CTD_human
HgeneBRAFC0334583Pilocytic Astrocytoma1CGI;CTD_human
HgeneBRAFC0338070Childhood Cerebral Astrocytoma1CTD_human
HgeneBRAFC0345904Malignant neoplasm of liver1CTD_human
HgeneBRAFC0376407Granulomatous Slack Skin1CTD_human
HgeneBRAFC0406803Syringocystadenoma Papilliferum1GENOMICS_ENGLAND
HgeneBRAFC0431128Papillary craniopharyngioma1CTD_human
HgeneBRAFC0431129Adamantinous Craniopharyngioma1CTD_human
HgeneBRAFC0547065Mixed oligoastrocytoma1CTD_human
HgeneBRAFC0555198Malignant Glioma1CTD_human
HgeneBRAFC0596263Carcinogenesis1CTD_human
HgeneBRAFC0684249Carcinoma of lung1CGI;UNIPROT
HgeneBRAFC0740457Malignant neoplasm of kidney1CTD_human
HgeneBRAFC0750935Cerebral Astrocytoma1CTD_human
HgeneBRAFC0750936Intracranial Astrocytoma1CTD_human
HgeneBRAFC0751061Craniopharyngioma, Child1CTD_human
HgeneBRAFC0920269Microsatellite Instability1CTD_human
HgeneBRAFC1527404Female Pseudo-Turner Syndrome1CTD_human
HgeneBRAFC1704230Grade I Astrocytoma1CTD_human
HgeneBRAFC1721098Replication Error Phenotype1CTD_human
HgeneBRAFC2239176Liver carcinoma1CTD_human
HgeneBRAFC4551484Leopard Syndrome 11GENOMICS_ENGLAND
HgeneBRAFC4551602Noonan Syndrome 11CTD_human
HgeneBRAFC4721532Lymphoma, Non-Hodgkin, Familial1UNIPROT
HgeneBRAFC4733333familial non-medullary thyroid cancer1GENOMICS_ENGLAND
TgeneSND1C0004352Autistic Disorder1CTD_human
TgeneSND1C0024121Lung Neoplasms1CTD_human
TgeneSND1C0242379Malignant neoplasm of lung1CTD_human