FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

leaf

Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

leaf

Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

leaf

Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:DGAT1-TONSL

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: DGAT1-TONSL
FusionPDB ID: 22392
FusionGDB2.0 ID: 22392
HgeneTgene
Gene symbol

DGAT1

TONSL

Gene ID

8694

4796

Gene namediacylglycerol O-acyltransferase 1tonsoku like, DNA repair protein
SynonymsARAT|ARGP1|DGAT|DIAR7IKBR|NFKBIL2|SEMDSP
Cytomap

8q24.3

8q24.3

Type of geneprotein-codingprotein-coding
Descriptiondiacylglycerol O-acyltransferase 1ACAT related gene product 1acyl coenzyme A:cholesterol acyltransferase related gene 1acyl-CoA retinol O-fatty-acyltransferaseacyl-CoA:diacylglycerol acyltransferasediacylglycerol O-acyltransferase homologdiglyceridetonsoku-like proteinI-kappa-B-related proteinNF-kappa-B inhibitor-like protein 2ikappaBRinhibitor of kappa B-related proteinnuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 2
Modification date2020031320200313
UniProtAcc

O75907

Main function of 5'-partner protein: FUNCTION: Catalyzes the terminal and only committed step in triacylglycerol synthesis by using diacylglycerol and fatty acyl CoA as substrates (PubMed:16214399, PubMed:18768481, PubMed:28420705, PubMed:9756920, PubMed:32433611, PubMed:32433610). Highly expressed in epithelial cells of the small intestine and its activity is essential for the absorption of dietary fats (PubMed:18768481). In liver, plays a role in esterifying exogenous fatty acids to glycerol, and is required to synthesize fat for storage (PubMed:16214399). Also present in female mammary glands, where it produces fat in the milk (By similarity). May be involved in VLDL (very low density lipoprotein) assembly (PubMed:18768481). In contrast to DGAT2 it is not essential for survival (By similarity). Functions as the major acyl-CoA retinol acyltransferase (ARAT) in the skin, where it acts to maintain retinoid homeostasis and prevent retinoid toxicity leading to skin and hair disorders (PubMed:16214399). Exhibits additional acyltransferase activities, includin acyl CoA:monoacylglycerol acyltransferase (MGAT), wax monoester and wax diester synthases (By similarity). Also able to use 1-monoalkylglycerol (1-MAkG) as an acyl acceptor for the synthesis of monoalkyl-monoacylglycerol (MAMAG) (PubMed:28420705). {ECO:0000250|UniProtKB:Q8MK44, ECO:0000250|UniProtKB:Q9Z2A7, ECO:0000269|PubMed:16214399, ECO:0000269|PubMed:18768481, ECO:0000269|PubMed:28420705, ECO:0000269|PubMed:32433610, ECO:0000269|PubMed:32433611, ECO:0000269|PubMed:9756920}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000332324, ENST00000531896, 
ENST00000527438, 
ENST00000409379, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 7 X 4=1687 X 7 X 4=196
# samples 78
** MAII scorelog2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/196*10)=-1.29278174922785
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: DGAT1 [Title/Abstract] AND TONSL [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: DGAT1 [Title/Abstract] AND TONSL [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)DGAT1(145544983)-TONSL(145662482), # samples:2
Anticipated loss of major functional domain due to fusion event.DGAT1-TONSL 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.
DGAT1-TONSL 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.
DGAT1-TONSL 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.
DGAT1-TONSL 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
HgeneDGAT1

GO:0019432

triglyceride biosynthetic process

18238778|18458083



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/chr8:145544983/chr8:145662482)
- 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 DGAT1 (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 TONSL (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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)
ENST00000332324DGAT1chr8145544983-ENST00000409379TONSLchr8145662482-33815621213045974
ENST00000531896DGAT1chr8145544983-ENST00000409379TONSLchr8145662482-3145326382809923
ENST00000332324DGAT1chr8145544984-ENST00000409379TONSLchr8145662482-33815621213045974
ENST00000531896DGAT1chr8145544984-ENST00000409379TONSLchr8145662482-3145326382809923

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
ENST00000332324ENST00000409379DGAT1chr8145544983-TONSLchr8145662482-0.0382677880.9617322
ENST00000531896ENST00000409379DGAT1chr8145544983-TONSLchr8145662482-0.044541340.95545864
ENST00000332324ENST00000409379DGAT1chr8145544984-TONSLchr8145662482-0.0382677880.9617322
ENST00000531896ENST00000409379DGAT1chr8145544984-TONSLchr8145662482-0.044541340.95545864

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

Top

Fusion Protein Breakpoint Sequences for DGAT1-TONSL

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
DGAT1chr8145544983TONSLchr814566248232696NYRGILNWCVVMLGHPLNPRDYCGWT
DGAT1chr8145544983TONSLchr814566248256216LVRRSPGLRRPAGGSGGRCLGPGGGA
DGAT1chr8145544984TONSLchr814566248232696NYRGILNWCVVMLGHPLNPRDYCGWT
DGAT1chr8145544984TONSLchr814566248256216LVRRSPGLRRPAGGSGGRCLGPGGGA

Top

Potential FusionNeoAntigen Information of DGAT1-TONSL 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.
DGAT1-TONSL_145544983_145662482.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)
DGAT1-TONSLchr8145544983chr8145662482326HLA-A74:09MLGHPLNPR0.9730.80641120
DGAT1-TONSLchr8145544983chr8145662482326HLA-A74:03MLGHPLNPR0.9730.80641120
DGAT1-TONSLchr8145544983chr8145662482326HLA-A74:11MLGHPLNPR0.9730.80641120
DGAT1-TONSLchr8145544983chr8145662482326HLA-A31:06MLGHPLNPR0.97120.67191120
DGAT1-TONSLchr8145544983chr8145662482326HLA-A31:02MLGHPLNPR0.85980.7941120
DGAT1-TONSLchr8145544983chr8145662482326HLA-A74:11VMLGHPLNPR0.99260.72831020
DGAT1-TONSLchr8145544983chr8145662482326HLA-A74:09VMLGHPLNPR0.99260.72831020
DGAT1-TONSLchr8145544983chr8145662482326HLA-A74:03VMLGHPLNPR0.99260.72831020
DGAT1-TONSLchr8145544983chr8145662482326HLA-A31:06VMLGHPLNPR0.9890.62291020
DGAT1-TONSLchr8145544983chr8145662482326HLA-A31:02VMLGHPLNPR0.98240.73751020
DGAT1-TONSLchr8145544983chr8145662482562HLA-B07:05RPAGGSGGRCL0.99990.6948920
DGAT1-TONSLchr8145544983chr8145662482562HLA-B07:02RPAGGSGGRCL0.99990.6781920
DGAT1-TONSLchr8145544983chr8145662482562HLA-B81:01RPAGGSGGRCL0.66750.7223920
DGAT1-TONSLchr8145544983chr8145662482326HLA-A31:01VMLGHPLNPR0.99170.71111020
DGAT1-TONSLchr8145544983chr8145662482562HLA-B07:12RPAGGSGGRCL0.99830.7547920
DGAT1-TONSLchr8145544983chr8145662482562HLA-B07:04RPAGGSGGRCL0.98660.6211920
DGAT1-TONSLchr8145544983chr8145662482562HLA-B42:01RPAGGSGGRCL0.94650.6969920
DGAT1-TONSLchr8145544983chr8145662482326HLA-A74:01MLGHPLNPR0.9730.80641120
DGAT1-TONSLchr8145544983chr8145662482326HLA-A74:01VMLGHPLNPR0.99260.72831020
DGAT1-TONSLchr8145544983chr8145662482562HLA-B07:22RPAGGSGGRCL0.99990.6781920
DGAT1-TONSLchr8145544983chr8145662482562HLA-B07:09RPAGGSGGRCL0.99990.6844920
DGAT1-TONSLchr8145544983chr8145662482562HLA-B67:01RPAGGSGGRCL0.71450.798920

Top

Potential FusionNeoAntigen Information of DGAT1-TONSL in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)

Top

Fusion breakpoint peptide structures of DGAT1-TONSL

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
2958GLRRPAGGSGGRCLDGAT1TONSLchr8145544983chr8145662482562
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
6454NWCVVMLGHPLNPRDGAT1TONSLchr8145544983chr8145662482326

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of DGAT1-TONSL

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-B14:023BVN2958GLRRPAGGSGGRCL-7.9962-8.1096
HLA-B14:023BVN2958GLRRPAGGSGGRCL-5.70842-6.74372
HLA-B52:013W392958GLRRPAGGSGGRCL-6.83737-6.95077
HLA-B52:013W392958GLRRPAGGSGGRCL-4.4836-5.5189
HLA-A11:014UQ22958GLRRPAGGSGGRCL-10.0067-10.1201
HLA-A11:014UQ22958GLRRPAGGSGGRCL-9.03915-10.0745
HLA-A24:025HGA2958GLRRPAGGSGGRCL-6.56204-6.67544
HLA-A24:025HGA2958GLRRPAGGSGGRCL-5.42271-6.45801
HLA-B44:053DX82958GLRRPAGGSGGRCL-7.85648-8.89178
HLA-B44:053DX82958GLRRPAGGSGGRCL-5.3978-5.5112
HLA-A02:016TDR2958GLRRPAGGSGGRCL-3.37154-4.40684
HLA-B14:023BVN6454NWCVVMLGHPLNPR-7.9962-8.1096
HLA-B14:023BVN6454NWCVVMLGHPLNPR-5.70842-6.74372
HLA-B52:013W396454NWCVVMLGHPLNPR-6.83737-6.95077
HLA-B52:013W396454NWCVVMLGHPLNPR-4.4836-5.5189
HLA-A11:014UQ26454NWCVVMLGHPLNPR-10.0067-10.1201
HLA-A11:014UQ26454NWCVVMLGHPLNPR-9.03915-10.0745
HLA-A24:025HGA6454NWCVVMLGHPLNPR-6.56204-6.67544
HLA-A24:025HGA6454NWCVVMLGHPLNPR-5.42271-6.45801
HLA-B44:053DX86454NWCVVMLGHPLNPR-7.85648-8.89178
HLA-B44:053DX86454NWCVVMLGHPLNPR-5.3978-5.5112
HLA-A02:016TDR6454NWCVVMLGHPLNPR-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of DGAT1-TONSL

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
DGAT1-TONSLchr8145544983chr81456624821020VMLGHPLNPRGTGATGCTGGGCCACCCCCTTAACCCTCGG
DGAT1-TONSLchr8145544983chr81456624821120MLGHPLNPRATGCTGGGCCACCCCCTTAACCCTCGG
DGAT1-TONSLchr8145544983chr8145662482920RPAGGSGGRCLGTGGTGATGCTGGGCCACCCCCTTAACCCTCGG

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

Top

Information of the samples that have these potential fusion neoantigens of DGAT1-TONSL

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
ESCADGAT1-TONSLchr8145544983ENST00000332324chr8145662482ENST00000409379TCGA-2H-A9GN
ESCADGAT1-TONSLchr8145544983ENST00000531896chr8145662482ENST00000409379TCGA-2H-A9GN

Top

Potential target of CAR-T therapy development for DGAT1-TONSL

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

Top

Related Drugs to DGAT1-TONSL

check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

Top

Related Diseases to DGAT1-TONSL

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