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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:ZNF670-SMYD3

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ZNF670-SMYD3
FusionPDB ID: 102685
FusionGDB2.0 ID: 102685
HgeneTgene
Gene symbol

ZNF670

SMYD3

Gene ID

93474

64754

Gene namezinc finger protein 670SET and MYND domain containing 3
Synonyms-KMT3E|ZMYND1|ZNFN3A1|bA74P14.1
Cytomap

1q44

1q44

Type of geneprotein-codingprotein-coding
Descriptionzinc finger protein 670histone-lysine N-methyltransferase SMYD3SET and MYND domain-containing protein 3bA74P14.1 (novel protein)zinc finger MYND domain-containing protein 1zinc finger protein, subfamily 3A (MYND domain containing), 1zinc finger, MYND domain containing 1
Modification date2020032720200320
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000366503, ENST00000388985, 
ENST00000490107, ENST00000541742, 
ENST00000366517, ENST00000403792, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 3 X 5=9029 X 14 X 17=6902
# samples 647
** MAII scorelog2(6/90*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(47/6902*10)=-3.87628181187052
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ZNF670 [Title/Abstract] AND SMYD3 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ZNF670 [Title/Abstract] AND SMYD3 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ZNF670(247241895)-SMYD3(246518396), # samples:1
ZNF670(247241896)-SMYD3(246518396), # samples:1
ZNF670(247241896)-SMYD3(246498776), # samples:1
SMYD3(246670356)-ZNF670(247109129), # samples:1
SMYD3(246670356)-ZNF670(247131094), # samples:1
Anticipated loss of major functional domain due to fusion event.ZNF670-SMYD3 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.
ZNF670-SMYD3 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.
ZNF670-SMYD3 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.
ZNF670-SMYD3 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


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/chr1:247241895/chr1:246518396)
- 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 ZNF670 (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 SMYD3 (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)
ENST00000366503ZNF670chr1247241896-ENST00000541742SMYD3chr1246498776-144416231220405
ENST00000366503ZNF670chr1247241896-ENST00000490107SMYD3chr1246498776-144216231220405
ENST00000366503ZNF670chr1247241896-ENST00000388985SMYD3chr1246498776-122116231220405

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
ENST00000366503ENST00000541742ZNF670chr1247241896-SMYD3chr1246498776-0.0023684750.99763155
ENST00000366503ENST00000490107ZNF670chr1247241896-SMYD3chr1246498776-0.0024400430.9975599
ENST00000366503ENST00000388985ZNF670chr1247241896-SMYD3chr1246498776-0.002698140.9973018

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 ZNF670-SMYD3

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ZNF670chr1247241896SMYD3chr124649877616253SLGRTPDTGDWEMKKAWPDHKRECKC

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Potential FusionNeoAntigen Information of ZNF670-SMYD3 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.
ZNF670-SMYD3_247241896_246498776.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)
ZNF670-SMYD3chr1247241896chr1246498776162HLA-B44:03GDWEMKKAW0.80410.9406817
ZNF670-SMYD3chr1247241896chr1246498776162HLA-B44:02GDWEMKKAW0.8020.6716817
ZNF670-SMYD3chr1247241896chr1246498776162HLA-B44:05GDWEMKKAW0.78280.8426817
ZNF670-SMYD3chr1247241896chr1246498776162HLA-A33:05EMKKAWPDHKR0.99160.6941122
ZNF670-SMYD3chr1247241896chr1246498776162HLA-A33:01EMKKAWPDHKR0.99160.6941122
ZNF670-SMYD3chr1247241896chr1246498776162HLA-B44:04GDWEMKKAW0.92360.5057817
ZNF670-SMYD3chr1247241896chr1246498776162HLA-B44:08GDWEMKKAW0.84530.7803817
ZNF670-SMYD3chr1247241896chr1246498776162HLA-A33:03EMKKAWPDHKR0.9770.56251122
ZNF670-SMYD3chr1247241896chr1246498776162HLA-B44:07GDWEMKKAW0.80410.9406817
ZNF670-SMYD3chr1247241896chr1246498776162HLA-B44:26GDWEMKKAW0.80410.9406817
ZNF670-SMYD3chr1247241896chr1246498776162HLA-B44:13GDWEMKKAW0.80410.9406817
ZNF670-SMYD3chr1247241896chr1246498776162HLA-B44:22GDWEMKKAW0.8020.6716817
ZNF670-SMYD3chr1247241896chr1246498776162HLA-B44:21GDWEMKKAW0.79690.569817

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Potential FusionNeoAntigen Information of ZNF670-SMYD3 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.
ZNF670-SMYD3_247241896_246498776.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)
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0801TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0801DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0801GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0801PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0802TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0803TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0803DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0803GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0803PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0805TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0805DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0807TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0807DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0808TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0808DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0808GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0808PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0809TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0811TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0811DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0811GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0811PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0813TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0814TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0814DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0814GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0814PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0815TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0816TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0816DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0816GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0816PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0818TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0821TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0823TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0823DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0823GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0823PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0826TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0826DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0826GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0826PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0827TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0827DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0827GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0827PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0830TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0832TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0832DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0832GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0832PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0833TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0833DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0833GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0833PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0834TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0835TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0835DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0835GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0835PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0836TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0836DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0836GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0836PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0837TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0837DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0837GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0838TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0838DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0838GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0838PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0839TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0839DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0839GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0839PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-0908TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1130TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1130DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1313TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1313DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1338TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1355TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1355DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1365TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1463TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1463DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1463GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1485TGDWEMKKAWPDHKR722
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1485DTGDWEMKKAWPDHK621
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1485GDWEMKKAWPDHKRE823
ZNF670-SMYD3chr1247241896chr1246498776162DRB1-1485PDTGDWEMKKAWPDH520
ZNF670-SMYD3chr1247241896chr1246498776162DRB5-0103TGDWEMKKAWPDHKR722

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Fusion breakpoint peptide structures of ZNF670-SMYD3

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
1436DTGDWEMKKAWPDHZNF670SMYD3chr1247241896chr1246498776162

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ZNF670-SMYD3

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-B14:023BVN1436DTGDWEMKKAWPDH-7.24289-7.35629
HLA-B14:023BVN1436DTGDWEMKKAWPDH-6.44411-7.47941
HLA-B52:013W391436DTGDWEMKKAWPDH-6.85231-6.96571
HLA-B52:013W391436DTGDWEMKKAWPDH-5.09533-6.13063
HLA-A11:014UQ21436DTGDWEMKKAWPDH-8.61576-8.72916
HLA-A24:025HGA1436DTGDWEMKKAWPDH-6.80714-7.84244
HLA-A24:025HGA1436DTGDWEMKKAWPDH-6.33574-6.44914
HLA-B44:053DX81436DTGDWEMKKAWPDH-7.01739-7.13079
HLA-B44:053DX81436DTGDWEMKKAWPDH-3.37818-4.41348

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Vaccine Design for the FusionNeoAntigens of ZNF670-SMYD3

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
ZNF670-SMYD3chr1247241896chr12464987761122EMKKAWPDHKRGAAATGAAAAAAGCTTGGCCAGACCACAAGCGG
ZNF670-SMYD3chr1247241896chr1246498776817GDWEMKKAWGGAGACTGGGAAATGAAAAAAGCTTGG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ZNF670-SMYD3chr1247241896chr1246498776520PDTGDWEMKKAWPDHCCAGACACCGGAGACTGGGAAATGAAAAAAGCTTGGCCAGACCAC
ZNF670-SMYD3chr1247241896chr1246498776621DTGDWEMKKAWPDHKGACACCGGAGACTGGGAAATGAAAAAAGCTTGGCCAGACCACAAG
ZNF670-SMYD3chr1247241896chr1246498776722TGDWEMKKAWPDHKRACCGGAGACTGGGAAATGAAAAAAGCTTGGCCAGACCACAAGCGG
ZNF670-SMYD3chr1247241896chr1246498776823GDWEMKKAWPDHKREGGAGACTGGGAAATGAAAAAAGCTTGGCCAGACCACAAGCGGGAA

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Information of the samples that have these potential fusion neoantigens of ZNF670-SMYD3

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
UCSZNF670-SMYD3chr1247241896ENST00000366503chr1246498776ENST00000388985TCGA-N5-A4RD

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Potential target of CAR-T therapy development for ZNF670-SMYD3

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 ZNF670-SMYD3

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 ZNF670-SMYD3

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