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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:PDGFRA-USP8

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PDGFRA-USP8
FusionPDB ID: 63857
FusionGDB2.0 ID: 63857
HgeneTgene
Gene symbol

PDGFRA

USP8

Gene ID

5156

9101

Gene nameplatelet derived growth factor receptor alphaubiquitin specific peptidase 8
SynonymsCD140A|PDGFR-2|PDGFR2HumORF8|PITA4|SPG59|UBPY
Cytomap

4q12

15q21.2

Type of geneprotein-codingprotein-coding
Descriptionplatelet-derived growth factor receptor alphaCD140 antigen-like family member ACD140a antigenPDGF-R-alphaalpha-type platelet-derived growth factor receptorplatelet-derived growth factor receptor 2platelet-derived growth factor receptor, alpha polypeubiquitin carboxyl-terminal hydrolase 8deubiquitinating enzyme 8ubiquitin isopeptidase Yubiquitin thiolesterase 8ubiquitin-specific-processing protease 8
Modification date2020032920200322
UniProtAcc

P16234

Main function of 5'-partner protein: FUNCTION: Tyrosine-protein kinase that acts as a cell-surface receptor for PDGFA, PDGFB and PDGFC and plays an essential role in the regulation of embryonic development, cell proliferation, survival and chemotaxis. Depending on the context, promotes or inhibits cell proliferation and cell migration. Plays an important role in the differentiation of bone marrow-derived mesenchymal stem cells. Required for normal skeleton development and cephalic closure during embryonic development. Required for normal development of the mucosa lining the gastrointestinal tract, and for recruitment of mesenchymal cells and normal development of intestinal villi. Plays a role in cell migration and chemotaxis in wound healing. Plays a role in platelet activation, secretion of agonists from platelet granules, and in thrombin-induced platelet aggregation. Binding of its cognate ligands - homodimeric PDGFA, homodimeric PDGFB, heterodimers formed by PDGFA and PDGFB or homodimeric PDGFC -leads to the activation of several signaling cascades; the response depends on the nature of the bound ligand and is modulated by the formation of heterodimers between PDGFRA and PDGFRB. Phosphorylates PIK3R1, PLCG1, and PTPN11. Activation of PLCG1 leads to the production of the cellular signaling molecules diacylglycerol and inositol 1,4,5-trisphosphate, mobilization of cytosolic Ca(2+) and the activation of protein kinase C. Phosphorylates PIK3R1, the regulatory subunit of phosphatidylinositol 3-kinase, and thereby mediates activation of the AKT1 signaling pathway. Mediates activation of HRAS and of the MAP kinases MAPK1/ERK2 and/or MAPK3/ERK1. Promotes activation of STAT family members STAT1, STAT3 and STAT5A and/or STAT5B. Receptor signaling is down-regulated by protein phosphatases that dephosphorylate the receptor and its down-stream effectors, and by rapid internalization of the activated receptor. {ECO:0000269|PubMed:10734113, ECO:0000269|PubMed:10947961, ECO:0000269|PubMed:11297552, ECO:0000269|PubMed:12522257, ECO:0000269|PubMed:1646396, ECO:0000269|PubMed:17087943, ECO:0000269|PubMed:1709159, ECO:0000269|PubMed:17141222, ECO:0000269|PubMed:20972453, ECO:0000269|PubMed:21224473, ECO:0000269|PubMed:21596750, ECO:0000269|PubMed:2554309, ECO:0000269|PubMed:8188664, ECO:0000269|PubMed:8760137, ECO:0000269|PubMed:8943348}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000257290, ENST00000508170, 
ENST00000558892, ENST00000307179, 
ENST00000396444, ENST00000425032, 
ENST00000433963, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 7 X 6=42010 X 7 X 3=210
# samples 1110
** MAII scorelog2(11/420*10)=-1.93288580414146
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/210*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PDGFRA [Title/Abstract] AND USP8 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PDGFRA [Title/Abstract] AND USP8 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PDGFRA(55156721)-USP8(50751197), # samples:2
Anticipated loss of major functional domain due to fusion event.PDGFRA-USP8 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.
PDGFRA-USP8 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.
PDGFRA-USP8 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.
PDGFRA-USP8 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
HgenePDGFRA

GO:0008284

positive regulation of cell proliferation

10806482

HgenePDGFRA

GO:0010544

negative regulation of platelet activation

8188664

HgenePDGFRA

GO:0018108

peptidyl-tyrosine phosphorylation

1646396|2536956|8188664

HgenePDGFRA

GO:0030335

positive regulation of cell migration

17470632

HgenePDGFRA

GO:0034614

cellular response to reactive oxygen species

24190966

HgenePDGFRA

GO:0038091

positive regulation of cell proliferation by VEGF-activated platelet derived growth factor receptor signaling pathway

17470632

HgenePDGFRA

GO:0046777

protein autophosphorylation

1646396|2536956|8188664

HgenePDGFRA

GO:0048008

platelet-derived growth factor receptor signaling pathway

2536956|10806482

HgenePDGFRA

GO:0048146

positive regulation of fibroblast proliferation

10806482

TgeneUSP8

GO:0070536

protein K63-linked deubiquitination

16520378

TgeneUSP8

GO:0071108

protein K48-linked deubiquitination

16520378



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/chr4:55156721/chr15:50751197)
- 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 PDGFRA (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 USP8 (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)
ENST00000257290PDGFRAchr455156721+ENST00000307179USP8chr1550751197+7163345316364742103
ENST00000257290PDGFRAchr455156721+ENST00000433963USP8chr1550751197+8466345316364742103
ENST00000257290PDGFRAchr455156721+ENST00000396444USP8chr1550751197+8470345316364742103
ENST00000257290PDGFRAchr455156721+ENST00000425032USP8chr1550751197+6715345316363872074

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
ENST00000257290ENST00000307179PDGFRAchr455156721+USP8chr1550751197+0.0002158420.9997842
ENST00000257290ENST00000433963PDGFRAchr455156721+USP8chr1550751197+0.0001821680.9998179
ENST00000257290ENST00000396444PDGFRAchr455156721+USP8chr1550751197+0.0001867250.99981326
ENST00000257290ENST00000425032PDGFRAchr455156721+USP8chr1550751197+0.0003615070.99963844

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 PDGFRA-USP8

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PDGFRAchr455156721USP8chr155075119734531096VPEEEDLGKRNRHRYEEAEVRKKLEE

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Potential FusionNeoAntigen Information of PDGFRA-USP8 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.
PDGFRA-USP8_55156721_50751197.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)
PDGFRA-USP8chr455156721chr15507511973453HLA-B39:06HRYEEAEV0.99950.80181220
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:05HRYEEAEVR0.99810.83181221
PDGFRA-USP8chr455156721chr15507511973453HLA-B07:10RHRYEEAEV0.05770.57861120
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:05HRYEEAEVRK0.99930.851222
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:05RHRYEEAEVR0.97150.72921121
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:05HRYEEAEVRKK0.99880.78381223
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:14HRYEEAEVR0.99790.7761221
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:03HRYEEAEVR0.86910.8551221
PDGFRA-USP8chr455156721chr15507511973453HLA-B73:01HRYEEAEVR0.82980.82421221
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:14HRYEEAEVRK0.99850.76121222
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:03HRYEEAEVRK0.98950.86711222
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:14RHRYEEAEVR0.97380.70061121
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:03RHRYEEAEVR0.58740.74791121
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:14HRYEEAEVRKK0.99850.73061223
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:03HRYEEAEVRKK0.97980.80011223
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:08HRYEEAEVR0.9980.76241221
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:10HRYEEAEVR0.99630.85171221
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:10HRYEEAEVRK0.99860.86691222
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:10RHRYEEAEVR0.97230.79331121
PDGFRA-USP8chr455156721chr15507511973453HLA-B27:10HRYEEAEVRKK0.99820.85271223

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Potential FusionNeoAntigen Information of PDGFRA-USP8 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.
PDGFRA-USP8_55156721_50751197.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)
PDGFRA-USP8chr455156721chr15507511973453DRB1-1102EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1116EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1121EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1121EEEDLGKRNRHRYEE217
PDGFRA-USP8chr455156721chr15507511973453DRB1-1136EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1155EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1165EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1170EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1170EEEDLGKRNRHRYEE217
PDGFRA-USP8chr455156721chr15507511973453DRB1-1301EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1304EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1315EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1315EEEDLGKRNRHRYEE217
PDGFRA-USP8chr455156721chr15507511973453DRB1-1317EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1320EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1322EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1327EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1335EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1343EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1343EEEDLGKRNRHRYEE217
PDGFRA-USP8chr455156721chr15507511973453DRB1-1351EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1352EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1357EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1357EEEDLGKRNRHRYEE217
PDGFRA-USP8chr455156721chr15507511973453DRB1-1359EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1364EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1368EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1369EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1378EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1379EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1380EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1383EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1387EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1391EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1392EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1393EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB1-1398EEDLGKRNRHRYEEA318
PDGFRA-USP8chr455156721chr15507511973453DRB5-0101RHRYEEAEVRKKLEE1126
PDGFRA-USP8chr455156721chr15507511973453DRB5-0101NRHRYEEAEVRKKLE1025
PDGFRA-USP8chr455156721chr15507511973453DRB5-0102RHRYEEAEVRKKLEE1126
PDGFRA-USP8chr455156721chr15507511973453DRB5-0103RHRYEEAEVRKKLEE1126
PDGFRA-USP8chr455156721chr15507511973453DRB5-0104RHRYEEAEVRKKLEE1126
PDGFRA-USP8chr455156721chr15507511973453DRB5-0104NRHRYEEAEVRKKLE1025
PDGFRA-USP8chr455156721chr15507511973453DRB5-0105RHRYEEAEVRKKLEE1126
PDGFRA-USP8chr455156721chr15507511973453DRB5-0105NRHRYEEAEVRKKLE1025
PDGFRA-USP8chr455156721chr15507511973453DRB5-0108NRHRYEEAEVRKKLEE1126
PDGFRA-USP8chr455156721chr15507511973453DRB5-0111RHRYEEAEVRKKLEE1126
PDGFRA-USP8chr455156721chr15507511973453DRB5-0112RHRYEEAEVRKKLEE1126
PDGFRA-USP8chr455156721chr15507511973453DRB5-0112NRHRYEEAEVRKKLE1025
PDGFRA-USP8chr455156721chr15507511973453DRB5-0112RNRHRYEEAEVRKKL924
PDGFRA-USP8chr455156721chr15507511973453DRB5-0113RHRYEEAEVRKKLEE1126
PDGFRA-USP8chr455156721chr15507511973453DRB5-0113NRHRYEEAEVRKKLE1025
PDGFRA-USP8chr455156721chr15507511973453DRB5-0114RHRYEEAEVRKKLEE1126
PDGFRA-USP8chr455156721chr15507511973453DRB5-0114NRHRYEEAEVRKKLE1025

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Fusion breakpoint peptide structures of PDGFRA-USP8

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
5010LGKRNRHRYEEAEVPDGFRAUSP8chr455156721chr15507511973453

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PDGFRA-USP8

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-B14:023BVN5010LGKRNRHRYEEAEV-7.9962-8.1096
HLA-B14:023BVN5010LGKRNRHRYEEAEV-5.70842-6.74372
HLA-B52:013W395010LGKRNRHRYEEAEV-6.83737-6.95077
HLA-B52:013W395010LGKRNRHRYEEAEV-4.4836-5.5189
HLA-A11:014UQ25010LGKRNRHRYEEAEV-10.0067-10.1201
HLA-A11:014UQ25010LGKRNRHRYEEAEV-9.03915-10.0745
HLA-A24:025HGA5010LGKRNRHRYEEAEV-6.56204-6.67544
HLA-A24:025HGA5010LGKRNRHRYEEAEV-5.42271-6.45801
HLA-B44:053DX85010LGKRNRHRYEEAEV-7.85648-8.89178
HLA-B44:053DX85010LGKRNRHRYEEAEV-5.3978-5.5112
HLA-A02:016TDR5010LGKRNRHRYEEAEV-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of PDGFRA-USP8

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
PDGFRA-USP8chr455156721chr15507511971120RHRYEEAEVACACAGATATGAAGAAGCTGAAGTCCG
PDGFRA-USP8chr455156721chr15507511971121RHRYEEAEVRACACAGATATGAAGAAGCTGAAGTCCGGAA
PDGFRA-USP8chr455156721chr15507511971220HRYEEAEVCAGATATGAAGAAGCTGAAGTCCG
PDGFRA-USP8chr455156721chr15507511971221HRYEEAEVRCAGATATGAAGAAGCTGAAGTCCGGAA
PDGFRA-USP8chr455156721chr15507511971222HRYEEAEVRKCAGATATGAAGAAGCTGAAGTCCGGAAAAA
PDGFRA-USP8chr455156721chr15507511971223HRYEEAEVRKKCAGATATGAAGAAGCTGAAGTCCGGAAAAAACT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PDGFRA-USP8chr455156721chr15507511971025NRHRYEEAEVRKKLECAGACACAGATATGAAGAAGCTGAAGTCCGGAAAAAACTTGAGGA
PDGFRA-USP8chr455156721chr15507511971126RHRYEEAEVRKKLEEACACAGATATGAAGAAGCTGAAGTCCGGAAAAAACTTGAGGAAAA
PDGFRA-USP8chr455156721chr1550751197217EEEDLGKRNRHRYEEGGAGGAGGACCTGGGCAAGAGGAACAGACACAGATATGAAGAAGC
PDGFRA-USP8chr455156721chr1550751197318EEDLGKRNRHRYEEAGGAGGACCTGGGCAAGAGGAACAGACACAGATATGAAGAAGCTGA
PDGFRA-USP8chr455156721chr1550751197924RNRHRYEEAEVRKKLGAACAGACACAGATATGAAGAAGCTGAAGTCCGGAAAAAACTTGA

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Information of the samples that have these potential fusion neoantigens of PDGFRA-USP8

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
SARCPDGFRA-USP8chr455156721ENST00000257290chr1550751197ENST00000307179TCGA-Z4-AAPG-01A

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Potential target of CAR-T therapy development for PDGFRA-USP8

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
HgenePDGFRAchr4:55156721chr15:50751197ENST00000257290+2223529_54910401090.0TransmembraneHelical

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 PDGFRA-USP8

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 PDGFRA-USP8

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
HgenePDGFRAC0238198Gastrointestinal Stromal Tumors10CGI;CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgenePDGFRAC3179349Gastrointestinal Stromal Sarcoma9CLINGEN;CTD_human;ORPHANET
HgenePDGFRAC0346421Chronic eosinophilic leukemia4ORPHANET
HgenePDGFRAC0206141Idiopathic Hypereosinophilic Syndrome3CTD_human;GENOMICS_ENGLAND
HgenePDGFRAC0006413Burkitt Lymphoma2ORPHANET
HgenePDGFRAC0206142Eosinophilic leukemia2CTD_human
HgenePDGFRAC0206143Loeffler's Endocarditis2CTD_human
HgenePDGFRAC1292769Precursor B-cell lymphoblastic leukemia2ORPHANET
HgenePDGFRAC1540912Hypereosinophilic syndrome2CGI;CTD_human
HgenePDGFRAC0008925Cleft Palate1CTD_human
HgenePDGFRAC0015923Fetal Alcohol Syndrome1PSYGENET
HgenePDGFRAC0018801Heart failure1CTD_human
HgenePDGFRAC0018802Congestive heart failure1CTD_human
HgenePDGFRAC0023212Left-Sided Heart Failure1CTD_human
HgenePDGFRAC0023893Liver Cirrhosis, Experimental1CTD_human
HgenePDGFRAC0024115Lung diseases1CTD_human
HgenePDGFRAC0025149Medulloblastoma1CTD_human
HgenePDGFRAC0035238Congenital abnormality of respiratory system1CTD_human
HgenePDGFRAC0038219Status Dysraphicus1CTD_human
HgenePDGFRAC0080178Spina Bifida1CTD_human
HgenePDGFRAC0205833Medullomyoblastoma1CTD_human
HgenePDGFRAC0206637Mesenchymal Chondrosarcoma1CTD_human
HgenePDGFRAC0235527Heart Failure, Right-Sided1CTD_human
HgenePDGFRAC0266508Rachischisis1CTD_human
HgenePDGFRAC0278510Childhood Medulloblastoma1CTD_human
HgenePDGFRAC0278876Adult Medulloblastoma1CTD_human
HgenePDGFRAC0376634Craniofacial Abnormalities1CTD_human
HgenePDGFRAC0751291Desmoplastic Medulloblastoma1CTD_human
HgenePDGFRAC1275668Melanotic medulloblastoma1CTD_human
HgenePDGFRAC1837218Cleft palate, isolated1CTD_human
HgenePDGFRAC1959583Myocardial Failure1CTD_human
HgenePDGFRAC1961112Heart Decompensation1CTD_human
HgenePDGFRAC2718076Fetal Mummification1CTD_human
HgenePDGFRAC2985290Fetal Alcohol Spectrum Disorders1PSYGENET
HgenePDGFRAC4545381Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement1ORPHANET