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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:SMYD2-LPGAT1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SMYD2-LPGAT1
FusionPDB ID: 84358
FusionGDB2.0 ID: 84358
HgeneTgene
Gene symbol

SMYD2

LPGAT1

Gene ID

56950

9926

Gene nameSET and MYND domain containing 2lysophosphatidylglycerol acyltransferase 1
SynonymsHSKM-B|KMT3C|ZMYND14FAM34A|FAM34A1|NET8
Cytomap

1q32.3

1q32.3

Type of geneprotein-codingprotein-coding
DescriptionN-lysine methyltransferase SMYD2SET and MYND domain-containing protein 2histone methyltransferase SMYD2lysine N-methyltransferase 3Czinc finger, MYND domain containing 14acyl-CoA:lysophosphatidylglycerol acyltransferase 1family with sequence similarity 34, member A
Modification date2020032020200313
UniProtAcc.

Q92604

Main function of 5'-partner protein: FUNCTION: Catalyzes the transfert of an acyl group from an acyl-CoA to a lysophosphatidylglycerol (LPG) leading to biosynthesis of phosphatidylglycerol, a precursor for cardiolipin synthesis (PubMed:15485873). Uses various acyl-CoAs and LPGs as substrates but demonstrates a clear preference for long chain saturated fatty acyl-CoAs and oleoyl-CoA as acyl donors (PubMed:15485873). Prefers oleoyl-LPG over palmitoyl-LPG as an acyl receptor and oleoyl-CoA over lauroyl-CoA as an acyl donor (PubMed:15485873). In vitro can also catalyzes the transfert of an acyl group from an acyl-CoA to a monoacylglycerol leading to diacylglycerol synthesis, a precursor of triacylglycerol and plays a role in hepatic triacylglycerol synthesis and secretion (By similarity). Prefers the sn-2-monoacylglycerol to rac-1-monoacylglycerol as acyl acceptor (By similarity). {ECO:0000250|UniProtKB:Q91YX5, ECO:0000269|PubMed:15485873}.
Ensembl transtripts involved in fusion geneENST idsENST00000491455, ENST00000366957, 
ENST00000415093, 
ENST00000366996, 
ENST00000366997, ENST00000488600, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 7 X 7=4908 X 7 X 5=280
# samples 118
** MAII scorelog2(11/490*10)=-2.15527822547791
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/280*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SMYD2 [Title/Abstract] AND LPGAT1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SMYD2 [Title/Abstract] AND LPGAT1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SMYD2(214498051)-LPGAT1(211924409), # samples:3
Anticipated loss of major functional domain due to fusion event.SMYD2-LPGAT1 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.
SMYD2-LPGAT1 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.
SMYD2-LPGAT1 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.
SMYD2-LPGAT1 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
HgeneSMYD2

GO:0018026

peptidyl-lysine monomethylation

17108971|20870719



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/chr1:214498051/chr1:211924409)
- 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 SMYD2 (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 LPGAT1 (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)
ENST00000415093SMYD2chr1214498051+ENST00000366997LPGAT1chr1211924409-732562422882286
ENST00000415093SMYD2chr1214498051+ENST00000366996LPGAT1chr1211924409-98962422882286
ENST00000366957SMYD2chr1214498051+ENST00000366997LPGAT1chr1211924409-732562422882286
ENST00000366957SMYD2chr1214498051+ENST00000366996LPGAT1chr1211924409-98962422882286

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
ENST00000415093ENST00000366997SMYD2chr1214498051+LPGAT1chr1211924409-0.0004183420.99958163
ENST00000415093ENST00000366996SMYD2chr1214498051+LPGAT1chr1211924409-0.001188150.99881184
ENST00000366957ENST00000366997SMYD2chr1214498051+LPGAT1chr1211924409-0.0004183420.99958163
ENST00000366957ENST00000366996SMYD2chr1214498051+LPGAT1chr1211924409-0.001188150.99881184

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 SMYD2-LPGAT1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SMYD2chr1214498051LPGAT1chr1211924409624201EELSHLGSAIFPEIFPIKDVPLETDD

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Potential FusionNeoAntigen Information of SMYD2-LPGAT1 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.
SMYD2-LPGAT1_214498051_211924409.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)
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:21AIFPEIFPI0.98510.7042817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:38AIFPEIFPI0.98350.6832817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:22AIFPEIFPI0.97760.5348817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:60AIFPEIFPI0.97680.5102817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:24AIFPEIFPI0.97660.5453817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:30AIFPEIFPI0.97660.5453817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:67AIFPEIFPI0.97660.5453817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:11AIFPEIFPI0.97590.6058817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:04AIFPEIFPI0.97550.7453817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:27AIFPEIFPI0.97270.5717817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:13AIFPEIFPI0.97240.7364817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:29AIFPEIFPI0.96220.5552817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:35AIFPEIFPI0.96190.6216817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:16AIFPEIFPI0.9610.506817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:20AIFPEIFPI0.95330.5486817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-B57:03GSAIFPEIF0.92960.9726615
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A32:13AIFPEIFPI0.88370.9576817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-B13:02AIFPEIFPI0.49540.8134817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A30:08AIFPEIFPIK0.95290.8227818
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A74:03AIFPEIFPIK0.80690.5537818
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A74:09AIFPEIFPIK0.80690.5537818
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A74:11AIFPEIFPIK0.80690.5537818
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-B38:01SHLGSAIFPEI0.99810.9693314
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:05AIFPEIFPI0.9860.5008817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:07AIFPEIFPI0.98040.6046817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:01AIFPEIFPI0.97660.5453817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:14AIFPEIFPI0.98550.6471817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:06AIFPEIFPI0.98510.7042817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A02:03AIFPEIFPI0.97610.72817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A32:01AIFPEIFPI0.96660.972817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-B57:02GSAIFPEIF0.95730.9493615
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A69:01AIFPEIFPI0.89650.783817
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A69:01EIFPIKDVPL0.96760.5191222
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-A74:01AIFPEIFPIK0.80690.5537818
SMYD2-LPGAT1chr1214498051chr1211924409624HLA-B38:05SHLGSAIFPEI0.99810.9693314

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Potential FusionNeoAntigen Information of SMYD2-LPGAT1 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.
SMYD2-LPGAT1_214498051_211924409.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)
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1221FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1410FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1410IFPEIFPIKDVPLET924
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1457FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1501FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1503FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1503IFPEIFPIKDVPLET924
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1503PEIFPIKDVPLETDD1126
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1504FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1504IFPEIFPIKDVPLET924
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1505FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1505IFPEIFPIKDVPLET924
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1505PEIFPIKDVPLETDD1126
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1506FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1507FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1507IFPEIFPIKDVPLET924
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1507PEIFPIKDVPLETDD1126
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1509FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1510FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1511FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1512FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1513FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1516FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1518FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1520FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1521FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1522FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1523FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1523IFPEIFPIKDVPLET924
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1523PEIFPIKDVPLETDD1126
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1524FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1525FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1525IFPEIFPIKDVPLET924
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1525PEIFPIKDVPLETDD1126
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1527FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1528FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1529FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1532FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1533FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1534FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1535FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1536FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1537FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1540FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1541FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1542FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1543FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1545FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1546FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1548FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1548IFPEIFPIKDVPLET924
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1548PEIFPIKDVPLETDD1126
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1549FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1549IFPEIFPIKDVPLET924
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1602FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1605FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1607FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1611FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1614FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1615FPEIFPIKDVPLETD1025
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1615IFPEIFPIKDVPLET924
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1615PEIFPIKDVPLETDD1126
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1615AIFPEIFPIKDVPLE823
SMYD2-LPGAT1chr1214498051chr1211924409624DRB1-1616FPEIFPIKDVPLETD1025

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Fusion breakpoint peptide structures of SMYD2-LPGAT1

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
3109GSAIFPEIFPIKDVSMYD2LPGAT1chr1214498051chr1211924409624

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SMYD2-LPGAT1

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-B14:023BVN3109GSAIFPEIFPIKDV-7.15543-7.26883
HLA-B14:023BVN3109GSAIFPEIFPIKDV-4.77435-5.80965
HLA-B52:013W393109GSAIFPEIFPIKDV-6.80875-6.92215
HLA-B52:013W393109GSAIFPEIFPIKDV-4.20386-5.23916
HLA-A11:014UQ23109GSAIFPEIFPIKDV-7.5194-8.5547
HLA-A11:014UQ23109GSAIFPEIFPIKDV-6.9601-7.0735
HLA-A24:025HGA3109GSAIFPEIFPIKDV-7.52403-7.63743
HLA-A24:025HGA3109GSAIFPEIFPIKDV-5.82433-6.85963
HLA-B27:056PYJ3109GSAIFPEIFPIKDV-3.28285-4.31815
HLA-B44:053DX83109GSAIFPEIFPIKDV-5.91172-6.94702
HLA-B44:053DX83109GSAIFPEIFPIKDV-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of SMYD2-LPGAT1

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
SMYD2-LPGAT1chr1214498051chr12119244091222EIFPIKDVPLTGAGATCTTTCCAATTAAAGATGTACCCCT
SMYD2-LPGAT1chr1214498051chr1211924409314SHLGSAIFPEITTCTCATTTGGGATCAGCGATATTTCCTGAGAT
SMYD2-LPGAT1chr1214498051chr1211924409615GSAIFPEIFGGGATCAGCGATATTTCCTGAGATCTT
SMYD2-LPGAT1chr1214498051chr1211924409817AIFPEIFPIAGCGATATTTCCTGAGATCTTTCCAAT
SMYD2-LPGAT1chr1214498051chr1211924409818AIFPEIFPIKAGCGATATTTCCTGAGATCTTTCCAATTAA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SMYD2-LPGAT1chr1214498051chr12119244091025FPEIFPIKDVPLETDATTTCCTGAGATCTTTCCAATTAAAGATGTACCCCTGGAGACTGA
SMYD2-LPGAT1chr1214498051chr12119244091126PEIFPIKDVPLETDDTCCTGAGATCTTTCCAATTAAAGATGTACCCCTGGAGACTGATGA
SMYD2-LPGAT1chr1214498051chr1211924409823AIFPEIFPIKDVPLEAGCGATATTTCCTGAGATCTTTCCAATTAAAGATGTACCCCTGGA
SMYD2-LPGAT1chr1214498051chr1211924409924IFPEIFPIKDVPLETGATATTTCCTGAGATCTTTCCAATTAAAGATGTACCCCTGGAGAC

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Information of the samples that have these potential fusion neoantigens of SMYD2-LPGAT1

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
SKCMSMYD2-LPGAT1chr1214498051ENST00000366957chr1211924409ENST00000366996TCGA-D3-A2JB-06A

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Potential target of CAR-T therapy development for SMYD2-LPGAT1

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
TgeneLPGAT1chr1:214498051chr1:211924409ENST0000036699658342_3620371.0TransmembraneHelical
TgeneLPGAT1chr1:214498051chr1:211924409ENST0000036699758342_3620371.0TransmembraneHelical

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 SMYD2-LPGAT1

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 SMYD2-LPGAT1

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