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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:SCYL3-CLPTM1L

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SCYL3-CLPTM1L
FusionPDB ID: 79786
FusionGDB2.0 ID: 79786
HgeneTgene
Gene symbol

SCYL3

CLPTM1L

Gene ID

57147

81037

Gene nameSCY1 like pseudokinase 3CLPTM1 like
SynonymsPACE-1|PACE1CRR9
Cytomap

1q24.2

5p15.33

Type of geneprotein-codingprotein-coding
Descriptionprotein-associating with the carboxyl-terminal domain of ezrinSCY1-like 3SCY1-like protein 3SCY1-like, kinase-like 3ezrin-binding partner PACE-1 (PACE-1)ezrin-binding protein PACE-1cleft lip and palate transmembrane protein 1-like proteinCLPTM1-like proteincisplatin resistance related protein CRR9pcisplatin resistance-related protein 9
Modification date2020031320200313
UniProtAcc.

Q96KA5

Main function of 5'-partner protein: FUNCTION: Enhances cisplatin-mediated apoptosis, when overexpressed. {ECO:0000269|PubMed:11162647}.
Ensembl transtripts involved in fusion geneENST idsENST00000367770, ENST00000367771, 
ENST00000367772, ENST00000470238, 
ENST00000506641, ENST00000320895, 
ENST00000320927, ENST00000507807, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score4 X 3 X 5=6015 X 11 X 8=1320
# samples 517
** MAII scorelog2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(17/1320*10)=-2.95693127810811
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SCYL3 [Title/Abstract] AND CLPTM1L [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SCYL3 [Title/Abstract] AND CLPTM1L [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SCYL3(169857817)-CLPTM1L(1325931), # samples:3
Anticipated loss of major functional domain due to fusion event.SCYL3-CLPTM1L 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.
SCYL3-CLPTM1L 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.
SCYL3-CLPTM1L seems lost the major protein functional domain in Hgene partner, which is a kinase 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


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/chr1:169857817/chr5:1325931)
- 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 SCYL3 (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 CLPTM1L (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)
ENST00000367770SCYL3chr1169857817-ENST00000320895CLPTM1Lchr51325931-137521348749233
ENST00000367770SCYL3chr1169857817-ENST00000507807CLPTM1Lchr51325931-136621348749233
ENST00000367770SCYL3chr1169857817-ENST00000320927CLPTM1Lchr51325931-125121348749233

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
ENST00000367770ENST00000320895SCYL3chr1169857817-CLPTM1Lchr51325931-0.0028392850.9971608
ENST00000367770ENST00000507807SCYL3chr1169857817-CLPTM1Lchr51325931-0.0028414090.99715865
ENST00000367770ENST00000320927SCYL3chr1169857817-CLPTM1Lchr51325931-0.0028150450.99718493

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 SCYL3-CLPTM1L

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SCYL3chr1169857817CLPTM1Lchr5132593121355KRENEDKVNKAAKLWKVKKALKMTIF

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Potential FusionNeoAntigen Information of SCYL3-CLPTM1L 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.
SCYL3-CLPTM1L_169857817_1325931.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)
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B57:01KVNKAAKLW0.99920.9805615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B58:02KVNKAAKLW0.99810.9605615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B58:01KVNKAAKLW0.99790.9417615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A30:08KAAKLWKVK0.99420.7152918
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B57:03KVNKAAKLW0.99380.985615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B15:17KVNKAAKLW0.98940.9016615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B15:16KVNKAAKLW0.98850.7187615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A30:08AAKLWKVKK0.97710.88451019
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B14:02DKVNKAAKL0.96540.5257514
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B14:01DKVNKAAKL0.96540.5257514
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A32:13KVNKAAKLW0.96060.9373615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B14:02NKAAKLWKV0.95370.8141817
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B14:01NKAAKLWKV0.95370.8141817
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A02:11KLWKVKKAL0.78280.67441221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A02:04KLWKVKKAL0.75360.69681221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A02:67KLWKVKKAL0.75290.64051221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A02:24KLWKVKKAL0.75290.64051221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A02:30KLWKVKKAL0.75290.64051221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A02:29KLWKVKKAL0.58670.63961221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A02:20KLWKVKKAL0.55480.64341221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A32:13KLWKVKKAL0.50210.9221221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B15:37DKVNKAAKL0.35870.5449514
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B13:01KLWKVKKAL0.00880.96421221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B13:02KLWKVKKAL0.00780.72491221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A30:08KVNKAAKLWK0.99810.5949616
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A74:09KLWKVKKALK0.97560.50481222
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A74:11KLWKVKKALK0.97560.50481222
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A74:03KLWKVKKALK0.97560.50481222
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A02:01KLWKVKKAL0.75290.64051221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B15:04KLWKVKKAL0.46550.85191221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B14:03DKVNKAAKL0.16750.8006514
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B57:10KVNKAAKLW0.99920.9805615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B57:04KVNKAAKLW0.99760.7258615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B58:06KVNKAAKLW0.99590.8073615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A30:01KAAKLWKVK0.99480.8905918
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A32:01KVNKAAKLW0.99390.9339615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A30:01AAKLWKVKK0.97950.95311019
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B57:02KVNKAAKLW0.97580.9074615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B15:13KVNKAAKLW0.92030.6289615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A32:01KLWKVKKAL0.88690.95681221
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-B15:24KVNKAAKLW0.71150.891615
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A30:01KVNKAAKLWK0.99820.7613616
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A30:01KAAKLWKVKK0.99020.879919
SCYL3-CLPTM1Lchr1169857817chr51325931213HLA-A74:01KLWKVKKALK0.97560.50481222

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Potential FusionNeoAntigen Information of SCYL3-CLPTM1L 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.
SCYL3-CLPTM1L_169857817_1325931.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)
SCYL3-CLPTM1Lchr1169857817chr51325931213DRB1-0103AAKLWKVKKALKMTI1025
SCYL3-CLPTM1Lchr1169857817chr51325931213DRB1-0103AKLWKVKKALKMTIF1126
SCYL3-CLPTM1Lchr1169857817chr51325931213DRB1-1467AAKLWKVKKALKMTI1025
SCYL3-CLPTM1Lchr1169857817chr51325931213DRB1-1498AAKLWKVKKALKMTI1025
SCYL3-CLPTM1Lchr1169857817chr51325931213DRB1-1498AKLWKVKKALKMTIF1126
SCYL3-CLPTM1Lchr1169857817chr51325931213DRB1-1498KAAKLWKVKKALKMT924

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Fusion breakpoint peptide structures of SCYL3-CLPTM1L

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
4687KVNKAAKLWKVKKASCYL3CLPTM1Lchr1169857817chr51325931213

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SCYL3-CLPTM1L

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-B14:023BVN4687KVNKAAKLWKVKKA-7.15543-7.26883
HLA-B14:023BVN4687KVNKAAKLWKVKKA-4.77435-5.80965
HLA-B52:013W394687KVNKAAKLWKVKKA-6.80875-6.92215
HLA-B52:013W394687KVNKAAKLWKVKKA-4.20386-5.23916
HLA-A11:014UQ24687KVNKAAKLWKVKKA-7.5194-8.5547
HLA-A11:014UQ24687KVNKAAKLWKVKKA-6.9601-7.0735
HLA-A24:025HGA4687KVNKAAKLWKVKKA-7.52403-7.63743
HLA-A24:025HGA4687KVNKAAKLWKVKKA-5.82433-6.85963
HLA-B27:056PYJ4687KVNKAAKLWKVKKA-3.28285-4.31815
HLA-B44:053DX84687KVNKAAKLWKVKKA-5.91172-6.94702
HLA-B44:053DX84687KVNKAAKLWKVKKA-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of SCYL3-CLPTM1L

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
SCYL3-CLPTM1Lchr1169857817chr513259311019AAKLWKVKKGCTGCCAAGCTGTGGAAAGTGAAGAAG
SCYL3-CLPTM1Lchr1169857817chr513259311221KLWKVKKALAAGCTGTGGAAAGTGAAGAAGGCATTG
SCYL3-CLPTM1Lchr1169857817chr513259311222KLWKVKKALKAAGCTGTGGAAAGTGAAGAAGGCATTGAAG
SCYL3-CLPTM1Lchr1169857817chr51325931514DKVNKAAKLGACAAGGTTAATAAAGCTGCCAAGCTG
SCYL3-CLPTM1Lchr1169857817chr51325931615KVNKAAKLWAAGGTTAATAAAGCTGCCAAGCTGTGG
SCYL3-CLPTM1Lchr1169857817chr51325931616KVNKAAKLWKAAGGTTAATAAAGCTGCCAAGCTGTGGAAA
SCYL3-CLPTM1Lchr1169857817chr51325931817NKAAKLWKVAATAAAGCTGCCAAGCTGTGGAAAGTG
SCYL3-CLPTM1Lchr1169857817chr51325931918KAAKLWKVKAAAGCTGCCAAGCTGTGGAAAGTGAAG
SCYL3-CLPTM1Lchr1169857817chr51325931919KAAKLWKVKKAAAGCTGCCAAGCTGTGGAAAGTGAAGAAG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SCYL3-CLPTM1Lchr1169857817chr513259311025AAKLWKVKKALKMTIGCTGCCAAGCTGTGGAAAGTGAAGAAGGCATTGAAGATGACTATT
SCYL3-CLPTM1Lchr1169857817chr513259311126AKLWKVKKALKMTIFGCCAAGCTGTGGAAAGTGAAGAAGGCATTGAAGATGACTATTTTT
SCYL3-CLPTM1Lchr1169857817chr51325931924KAAKLWKVKKALKMTAAAGCTGCCAAGCTGTGGAAAGTGAAGAAGGCATTGAAGATGACT

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Information of the samples that have these potential fusion neoantigens of SCYL3-CLPTM1L

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
SKCMSCYL3-CLPTM1Lchr1169857817ENST00000367770chr51325931ENST00000320895TCGA-EE-A20F-06A

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Potential target of CAR-T therapy development for SCYL3-CLPTM1L

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
TgeneCLPTM1Lchr1:169857817chr5:1325931ENST00000320895817403_4230539.0TransmembraneHelical
TgeneCLPTM1Lchr1:169857817chr5:1325931ENST00000320895817429_4490539.0TransmembraneHelical
TgeneCLPTM1Lchr1:169857817chr5:1325931ENST00000320927716325_3420503.0TransmembraneHelical
TgeneCLPTM1Lchr1:169857817chr5:1325931ENST00000320927716347_3640503.0TransmembraneHelical
TgeneCLPTM1Lchr1:169857817chr5:1325931ENST00000320927716403_4230503.0TransmembraneHelical
TgeneCLPTM1Lchr1:169857817chr5:1325931ENST00000320927716429_4490503.0TransmembraneHelical

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 SCYL3-CLPTM1L

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 SCYL3-CLPTM1L

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