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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:PSMD12-PRKCA

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PSMD12-PRKCA
FusionPDB ID: 69652
FusionGDB2.0 ID: 69652
HgeneTgene
Gene symbol

PSMD12

PRKCA

Gene ID

5718

5578

Gene nameproteasome 26S subunit, non-ATPase 12protein kinase C alpha
SynonymsRpn5|STISS|p55AAG6|PKC-alpha|PKCA|PKCI+/-|PKCalpha|PRKACA
Cytomap

17q24.2

17q24.2

Type of geneprotein-codingprotein-coding
Description26S proteasome non-ATPase regulatory subunit 1226S proteasome regulatory subunit RPN526S proteasome regulatory subunit p55proteasome (prosome, macropain) 26S subunit, non-ATPase, 12protein kinase C alpha typePKC-Aaging-associated gene 6
Modification date2020031320200327
UniProtAcc.

PICK1

Main function of 5'-partner protein: 415
Ensembl transtripts involved in fusion geneENST idsENST00000356126, ENST00000357146, 
ENST00000581618, 
ENST00000583361, 
ENST00000413366, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 3=10826 X 21 X 9=4914
# samples 929
** MAII scorelog2(9/108*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(29/4914*10)=-4.08277305234723
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PSMD12 [Title/Abstract] AND PRKCA [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PSMD12 [Title/Abstract] AND PRKCA [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PSMD12(65340722)-PRKCA(64492319), # samples:2
Anticipated loss of major functional domain due to fusion event.PSMD12-PRKCA 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.
PSMD12-PRKCA 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.
PSMD12-PRKCA 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.
PSMD12-PRKCA 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.
PSMD12-PRKCA seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PSMD12-PRKCA seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PSMD12-PRKCA seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PSMD12-PRKCA seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
PSMD12-PRKCA seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
PSMD12-PRKCA seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PSMD12-PRKCA seems lost the major protein functional domain in Tgene 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
TgenePRKCA

GO:0006468

protein phosphorylation

10770950

TgenePRKCA

GO:0035408

histone H3-T6 phosphorylation

20228790

TgenePRKCA

GO:0043536

positive regulation of blood vessel endothelial cell migration

20011604

TgenePRKCA

GO:0090330

regulation of platelet aggregation

12724315



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/chr17:65340722/chr17:64492319)
- 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 PSMD12 (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 PRKCA (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)
ENST00000356126PSMD12chr1765340722-ENST00000413366PRKCAchr1764637473+96281191182921967
ENST00000357146PSMD12chr1765340722-ENST00000413366PRKCAchr1764637473+95461109862839917

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
ENST00000356126ENST00000413366PSMD12chr1765340722-PRKCAchr1764637473+0.0002485360.9997515
ENST00000357146ENST00000413366PSMD12chr1765340722-PRKCAchr1764637473+0.0003167940.99968326

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 PSMD12-PRKCA

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PSMD12chr1765340722PRKCAchr17646374731109341KRWKDLKNRVVEHDPRSKHKFKIHTY
PSMD12chr1765340722PRKCAchr17646374731191391KRWKDLKNRVVEHDPRSKHKFKIHTY

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Potential FusionNeoAntigen Information of PSMD12-PRKCA 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.
PSMD12-PRKCA_65340722_64637473.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)
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B18:01VEHDPRSKH0.94110.88371019
PSMD12-PRKCAchr1765340722chr17646374731191HLA-A03:12RVVEHDPRSK0.99060.5204818
PSMD12-PRKCAchr1765340722chr17646374731191HLA-A30:08RVVEHDPRSK0.9850.7438818
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B39:01EHDPRSKHKF0.96820.77921121
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B38:01EHDPRSKHKF0.95920.89081121
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B38:02EHDPRSKHKF0.9410.89331121
PSMD12-PRKCAchr1765340722chr17646374731191HLA-A74:03RVVEHDPRSK0.85720.5415818
PSMD12-PRKCAchr1765340722chr17646374731191HLA-A74:09RVVEHDPRSK0.85720.5415818
PSMD12-PRKCAchr1765340722chr17646374731191HLA-A74:11RVVEHDPRSK0.85720.5415818
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B44:03VEHDPRSKHKF0.99940.84741021
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B38:01VEHDPRSKHKF0.98150.93261021
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B38:01EHDPRSKHKFK0.89580.80221122
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B38:02EHDPRSKHKFK0.88180.82191122
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B39:12EHDPRSKHKF0.95170.79331121
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B39:05EHDPRSKHKF0.93260.74891121
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B14:03EHDPRSKHKF0.92650.60271121
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B18:05VEHDPRSKH0.94110.88371019
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B18:06VEHDPRSKH0.92080.89131019
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B18:11VEHDPRSKH0.66320.88381019
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B15:53VEHDPRSKH0.01350.86191019
PSMD12-PRKCAchr1765340722chr17646374731191HLA-C18:01EHDPRSKHKF0.99790.78731121
PSMD12-PRKCAchr1765340722chr17646374731191HLA-A30:01RVVEHDPRSK0.9840.8683818
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B39:31EHDPRSKHKF0.96780.78011121
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B38:05EHDPRSKHKF0.95920.89081121
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B39:11EHDPRSKHKF0.94390.57591121
PSMD12-PRKCAchr1765340722chr17646374731191HLA-A74:01RVVEHDPRSK0.85720.5415818
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B15:53VEHDPRSKHKF0.99950.76851021
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B44:13VEHDPRSKHKF0.99940.84741021
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B44:26VEHDPRSKHKF0.99940.84741021
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B44:07VEHDPRSKHKF0.99940.84741021
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B38:05VEHDPRSKHKF0.98150.93261021
PSMD12-PRKCAchr1765340722chr17646374731191HLA-B38:05EHDPRSKHKFK0.89580.80221122

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Potential FusionNeoAntigen Information of PSMD12-PRKCA 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.
PSMD12-PRKCA_65340722_64637473.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)
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0103KRWKDLKNRVVEHDP015
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0301NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0301KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0303NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0303KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0305NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0307NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0307KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0310NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0313NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0313KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0315NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0315KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0318NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0318KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0320NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0320KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0320LKNRVVEHDPRSKHK520
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0322NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0322KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0324NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0324KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0326NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0326KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0328NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0328KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0330NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0330KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0332NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0332KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0334NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0334KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0336NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0336KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0340NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0344NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0344KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0346NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0346KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0348NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0348KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0350NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0350KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0352NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0352KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0354NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0354KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0806WKDLKNRVVEHDPRS217
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-0806RWKDLKNRVVEHDPR116
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-1107NRVVEHDPRSKHKFK722
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-1107KNRVVEHDPRSKHKF621
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-1601KRWKDLKNRVVEHDP015
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-1603KRWKDLKNRVVEHDP015
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-1604KRWKDLKNRVVEHDP015
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-1608KRWKDLKNRVVEHDP015
PSMD12-PRKCAchr1765340722chr17646374731191DRB1-1609KRWKDLKNRVVEHDP015

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Fusion breakpoint peptide structures of PSMD12-PRKCA

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
4462KNRVVEHDPRSKHKPSMD12PRKCAchr1765340722chr17646374731191

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PSMD12-PRKCA

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-B14:023BVN4462KNRVVEHDPRSKHK-5.6364-5.6364
HLA-A24:025HGA4462KNRVVEHDPRSKHK-9.18993-9.18993

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Vaccine Design for the FusionNeoAntigens of PSMD12-PRKCA

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
PSMD12-PRKCAchr1765340722chr17646374731019VEHDPRSKHGTTGAACATGACCCCAGGAGCAAGCAC
PSMD12-PRKCAchr1765340722chr17646374731021VEHDPRSKHKFGTTGAACATGACCCCAGGAGCAAGCACAAGTTC
PSMD12-PRKCAchr1765340722chr17646374731121EHDPRSKHKFGAACATGACCCCAGGAGCAAGCACAAGTTC
PSMD12-PRKCAchr1765340722chr17646374731122EHDPRSKHKFKGAACATGACCCCAGGAGCAAGCACAAGTTCAAA
PSMD12-PRKCAchr1765340722chr1764637473818RVVEHDPRSKAGAGTTGTTGAACATGACCCCAGGAGCAAG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PSMD12-PRKCAchr1765340722chr1764637473015KRWKDLKNRVVEHDPAAAAGGTGGAAAGACTTGAAGAACAGAGTTGTTGAACATGACCCC
PSMD12-PRKCAchr1765340722chr1764637473116RWKDLKNRVVEHDPRAGGTGGAAAGACTTGAAGAACAGAGTTGTTGAACATGACCCCAGG
PSMD12-PRKCAchr1765340722chr1764637473217WKDLKNRVVEHDPRSTGGAAAGACTTGAAGAACAGAGTTGTTGAACATGACCCCAGGAGC
PSMD12-PRKCAchr1765340722chr1764637473520LKNRVVEHDPRSKHKTTGAAGAACAGAGTTGTTGAACATGACCCCAGGAGCAAGCACAAG
PSMD12-PRKCAchr1765340722chr1764637473621KNRVVEHDPRSKHKFAAGAACAGAGTTGTTGAACATGACCCCAGGAGCAAGCACAAGTTC
PSMD12-PRKCAchr1765340722chr1764637473722NRVVEHDPRSKHKFKAACAGAGTTGTTGAACATGACCCCAGGAGCAAGCACAAGTTCAAA

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Information of the samples that have these potential fusion neoantigens of PSMD12-PRKCA

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
BRCAPSMD12-PRKCAchr1765340722ENST00000356126chr1764637473ENST00000413366TCGA-C8-A12P-01A

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Potential target of CAR-T therapy development for PSMD12-PRKCA

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 PSMD12-PRKCA

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 PSMD12-PRKCA

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