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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:SRBD1-ATL2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SRBD1-ATL2
FusionPDB ID: 86228
FusionGDB2.0 ID: 86228
HgeneTgene
Gene symbol

SRBD1

ATL2

Gene ID

55133

64225

Gene nameS1 RNA binding domain 1atlastin GTPase 2
Synonyms-ARL3IP2|ARL6IP2|aip-2|atlastin2
Cytomap

2p21

2p22.2-p22.1

Type of geneprotein-codingprotein-coding
DescriptionS1 RNA-binding domain-containing protein 1H_NH0576F01.1WUGSC:H_NH0576F01.1atlastin-2ADP-ribosylation factor-like protein 6-interacting protein 2ARL-6-interacting protein 2
Modification date2020031320200313
UniProtAcc.

Q8NHH9

Main function of 5'-partner protein: FUNCTION: GTPase tethering membranes through formation of trans-homooligomers and mediating homotypic fusion of endoplasmic reticulum membranes. Functions in endoplasmic reticulum tubular network biogenesis (PubMed:18270207, PubMed:19665976, PubMed:27619977). {ECO:0000269|PubMed:18270207, ECO:0000269|PubMed:19665976, ECO:0000269|PubMed:27619977}.
Ensembl transtripts involved in fusion geneENST idsENST00000263736, ENST00000535761, 
ENST00000490133, 
ENST00000332337, 
ENST00000402054, ENST00000406122, 
ENST00000419554, ENST00000452935, 
ENST00000539122, ENST00000486927, 
ENST00000546051, ENST00000378954, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 4=1446 X 5 X 4=120
# samples 56
** MAII scorelog2(5/144*10)=-1.52606881166759
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SRBD1 [Title/Abstract] AND ATL2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SRBD1 [Title/Abstract] AND ATL2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SRBD1(45704132)-ATL2(38523255), # samples:1
Anticipated loss of major functional domain due to fusion event.SRBD1-ATL2 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.
SRBD1-ATL2 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.
SRBD1-ATL2 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.
SRBD1-ATL2 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.
SRBD1-ATL2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SRBD1-ATL2 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
TgeneATL2

GO:0051260

protein homooligomerization

18270207



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/chr2:45704132/chr2:38523255)
- 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 SRBD1 (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 ATL2 (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)
ENST00000263736SRBD1chr245704132-ENST00000378954ATL2chr238523255-33462112632231722

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
ENST00000263736ENST00000378954SRBD1chr245704132-ATL2chr238523255-0.0007128840.9992872

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 SRBD1-ATL2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SRBD1chr245704132ATL2chr2385232552112682VKIEPKHIGVGMYQVLKPLGDNLMEE

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Potential FusionNeoAntigen Information of SRBD1-ATL2 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.
SRBD1-ATL2_45704132_38523255.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)
SRBD1-ATL2chr245704132chr2385232552112HLA-A02:04GMYQVLKPL0.9380.50591019
SRBD1-ATL2chr245704132chr2385232552112HLA-B39:01KHIGVGMYQVL0.99840.9238516
SRBD1-ATL2chr245704132chr2385232552112HLA-B15:10KHIGVGMYQVL0.9980.6141516
SRBD1-ATL2chr245704132chr2385232552112HLA-B39:24KHIGVGMYQVL0.99780.7763516
SRBD1-ATL2chr245704132chr2385232552112HLA-B38:01KHIGVGMYQVL0.99740.9779516
SRBD1-ATL2chr245704132chr2385232552112HLA-B38:02KHIGVGMYQVL0.99740.9754516
SRBD1-ATL2chr245704132chr2385232552112HLA-B15:37KHIGVGMYQVL0.85290.587516
SRBD1-ATL2chr245704132chr2385232552112HLA-B07:10KHIGVGMYQVL0.63540.5319516
SRBD1-ATL2chr245704132chr2385232552112HLA-B15:04GMYQVLKPL0.97610.79391019
SRBD1-ATL2chr245704132chr2385232552112HLA-B39:05KHIGVGMYQVL0.99770.9123516
SRBD1-ATL2chr245704132chr2385232552112HLA-C14:03MYQVLKPL0.8660.97121119
SRBD1-ATL2chr245704132chr2385232552112HLA-C14:02MYQVLKPL0.8660.97121119
SRBD1-ATL2chr245704132chr2385232552112HLA-A02:03GMYQVLKPL0.98380.55421019
SRBD1-ATL2chr245704132chr2385232552112HLA-B38:05KHIGVGMYQVL0.99740.9779516
SRBD1-ATL2chr245704132chr2385232552112HLA-B15:09KHIGVGMYQVL0.99310.798516

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Potential FusionNeoAntigen Information of SRBD1-ATL2 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.
SRBD1-ATL2_45704132_38523255.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)
SRBD1-ATL2chr245704132chr2385232552112DRB1-0405IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0405GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0424GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0424IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0424VGMYQVLKPLGDNLM924
SRBD1-ATL2chr245704132chr2385232552112DRB1-0429IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0429GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0430IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0430GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0445IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0445GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0448IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0448GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0457IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0457GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0477IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0477GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0480GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0480IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0480VGMYQVLKPLGDNLM924
SRBD1-ATL2chr245704132chr2385232552112DRB1-0482GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0482IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0483IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0483GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0484IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0484GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0486GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0486VGMYQVLKPLGDNLM924
SRBD1-ATL2chr245704132chr2385232552112DRB1-0486IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0489IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0489GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0803GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0804IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0805IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0805GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0814GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0818GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0818IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0823GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0827GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0831IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0832GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0832IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-0832VGMYQVLKPLGDNLM924
SRBD1-ATL2chr245704132chr2385232552112DRB1-0833GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0835GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0836GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-0838GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-1001GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-1001VGMYQVLKPLGDNLM924
SRBD1-ATL2chr245704132chr2385232552112DRB1-1001IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-1003GVGMYQVLKPLGDNL823
SRBD1-ATL2chr245704132chr2385232552112DRB1-1003VGMYQVLKPLGDNLM924
SRBD1-ATL2chr245704132chr2385232552112DRB1-1003IGVGMYQVLKPLGDN722
SRBD1-ATL2chr245704132chr2385232552112DRB1-1415IGVGMYQVLKPLGDN722

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Fusion breakpoint peptide structures of SRBD1-ATL2

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
3363HIGVGMYQVLKPLGSRBD1ATL2chr245704132chr2385232552112

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SRBD1-ATL2

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-B14:023BVN3363HIGVGMYQVLKPLG-7.9962-8.1096
HLA-B14:023BVN3363HIGVGMYQVLKPLG-5.70842-6.74372
HLA-B52:013W393363HIGVGMYQVLKPLG-6.83737-6.95077
HLA-B52:013W393363HIGVGMYQVLKPLG-4.4836-5.5189
HLA-A11:014UQ23363HIGVGMYQVLKPLG-10.0067-10.1201
HLA-A11:014UQ23363HIGVGMYQVLKPLG-9.03915-10.0745
HLA-A24:025HGA3363HIGVGMYQVLKPLG-6.56204-6.67544
HLA-A24:025HGA3363HIGVGMYQVLKPLG-5.42271-6.45801
HLA-B44:053DX83363HIGVGMYQVLKPLG-7.85648-8.89178
HLA-B44:053DX83363HIGVGMYQVLKPLG-5.3978-5.5112
HLA-A02:016TDR3363HIGVGMYQVLKPLG-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of SRBD1-ATL2

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
SRBD1-ATL2chr245704132chr2385232551019GMYQVLKPLATGTATCAGGTATTGAAGCCCCTGGGT
SRBD1-ATL2chr245704132chr2385232551119MYQVLKPLTATCAGGTATTGAAGCCCCTGGGT
SRBD1-ATL2chr245704132chr238523255516KHIGVGMYQVLCACATTGGAGTTGGAATGTATCAGGTATTGAAG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SRBD1-ATL2chr245704132chr238523255722IGVGMYQVLKPLGDNGGAGTTGGAATGTATCAGGTATTGAAGCCCCTGGGTGATAATTTG
SRBD1-ATL2chr245704132chr238523255823GVGMYQVLKPLGDNLGTTGGAATGTATCAGGTATTGAAGCCCCTGGGTGATAATTTGATG
SRBD1-ATL2chr245704132chr238523255924VGMYQVLKPLGDNLMGGAATGTATCAGGTATTGAAGCCCCTGGGTGATAATTTGATGGAG

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Information of the samples that have these potential fusion neoantigens of SRBD1-ATL2

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
SKCMSRBD1-ATL2chr245704132ENST00000263736chr238523255ENST00000378954TCGA-EB-A6L9-06A

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Potential target of CAR-T therapy development for SRBD1-ATL2

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
TgeneATL2chr2:45704132chr2:38523255ENST00000332337014477_4970567.0TransmembraneHelical
TgeneATL2chr2:45704132chr2:38523255ENST00000332337014500_5200567.0TransmembraneHelical
TgeneATL2chr2:45704132chr2:38523255ENST000004020541012477_4970413.0TransmembraneHelical
TgeneATL2chr2:45704132chr2:38523255ENST000004020541012500_5200413.0TransmembraneHelical
TgeneATL2chr2:45704132chr2:38523255ENST00000419554013477_4970580.0TransmembraneHelical
TgeneATL2chr2:45704132chr2:38523255ENST00000419554013500_5200580.0TransmembraneHelical
TgeneATL2chr2:45704132chr2:38523255ENST000005391221012477_4970413.0TransmembraneHelical
TgeneATL2chr2:45704132chr2:38523255ENST000005391221012500_5200413.0TransmembraneHelical

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 SRBD1-ATL2

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 SRBD1-ATL2

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