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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:PPIC-TRPM7

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PPIC-TRPM7
FusionPDB ID: 67529
FusionGDB2.0 ID: 67529
HgeneTgene
Gene symbol

PPIC

TRPM7

Gene ID

5480

54822

Gene namepeptidylprolyl isomerase Ctransient receptor potential cation channel subfamily M member 7
SynonymsCYPCALSPDC|CHAK|CHAK1|LTRPC7|LTrpC-7|TRP-PLIK
Cytomap

5q23.2

15q21.2

Type of geneprotein-codingprotein-coding
Descriptionpeptidyl-prolyl cis-trans isomerase CPPIase Ccyclophilin Cparvulinrotamase Ctransient receptor potential cation channel subfamily M member 7LTRPC ion channel family member 7channel-kinase 1long transient receptor potential channel 7transient receptor potential-phospholipase C-interacting kinase
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000306442, ENST00000561443, 
ENST00000313478, ENST00000560955, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 3 X 2=1813 X 16 X 5=1040
# samples 315
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(15/1040*10)=-2.79354912253257
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PPIC [Title/Abstract] AND TRPM7 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PPIC [Title/Abstract] AND TRPM7 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PPIC(122365000)-TRPM7(50905026), # samples:1
Anticipated loss of major functional domain due to fusion event.PPIC-TRPM7 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.
PPIC-TRPM7 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.
PPIC-TRPM7 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.
PPIC-TRPM7 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
HgenePPIC

GO:0000413

protein peptidyl-prolyl isomerization

20676357



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/chr5:122365000/chr15:50905026)
- 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 PPIC (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 TRPM7 (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)
ENST00000306442PPICchr5122365000-ENST00000560955TRPM7chr1550905026-555734710141711356
ENST00000306442PPICchr5122365000-ENST00000313478TRPM7chr1550905026-555834710141741357

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
ENST00000306442ENST00000560955PPICchr5122365000-TRPM7chr1550905026-0.0001579780.99984205
ENST00000306442ENST00000313478PPICchr5122365000-TRPM7chr1550905026-0.000114640.9998853

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 PPIC-TRPM7

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PPICchr5122365000TRPM7chr155090502634782KTVENFVALATGEIDTVMEEGKKKRT

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Potential FusionNeoAntigen Information of PPIC-TRPM7 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.
PPIC-TRPM7_122365000_50905026.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)
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:22ALATGEIDTV0.99720.7448717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:27ALATGEIDTV0.99420.7595717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:13ALATGEIDTV0.99340.8144717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:30ALATGEIDTV0.99090.6948717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:67ALATGEIDTV0.99090.6948717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:60ALATGEIDTV0.99090.6991717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:24ALATGEIDTV0.99090.6948717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:16ALATGEIDTV0.98960.6911717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:38ALATGEIDTV0.98120.8196717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:19ALATGEIDTV0.97470.5963717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:35ALATGEIDTV0.90840.7281717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:29ALATGEIDTV0.88340.7061717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:20ALATGEIDTV0.86820.7014717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:02ALATGEIDTV0.99730.6451717
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:01ALATGEIDTV0.99090.6948717
PPIC-TRPM7chr5122365000chr1550905026347HLA-B51:05LATGEIDTV0.75930.5556817
PPIC-TRPM7chr5122365000chr1550905026347HLA-A02:03ALATGEIDTV0.99730.7707717

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Potential FusionNeoAntigen Information of PPIC-TRPM7 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.
PPIC-TRPM7_122365000_50905026.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)
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0101VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0101TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0105VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0105TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0107VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0107TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0109VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0111VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0111TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0113VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0113TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0115VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0115TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0117VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0117TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0117KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0119VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0119TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0121VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0121TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0125VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0125TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0127VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0127TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0129VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0129TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0129KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0131VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0131TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0447VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0447TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0469TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0469VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0482TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0482VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0482KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0807TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0807VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0807KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0819VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0819TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0819KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0825TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0825VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0825KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0832TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0832VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0834TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0834VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0834KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0905TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-0905VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1001TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1001VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1003TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1003VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1216TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1216VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1216KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1216ENFVALATGEIDTVM318
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1222VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1222TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1222KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-13100TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-13100VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1346TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1346VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1446VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1446TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1448VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1448TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1527VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1527TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1534VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1534TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1601TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1601VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1601KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1601ENFVALATGEIDTVM318
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1602VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1602TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1602KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1603TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1603VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1603KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1603ENFVALATGEIDTVM318
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1604VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1604TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1604KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1605VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1605TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1607VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1607TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1608TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1608VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1608KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1608ENFVALATGEIDTVM318
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1609VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1609TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1609KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1609ENFVALATGEIDTVM318
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1610VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1610TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1610KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1611VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1611TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1611KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1612VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1612TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1612KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1614VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1614TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1614KTVENFVALATGEID015
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1616VENFVALATGEIDTV217
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1616TVENFVALATGEIDT116
PPIC-TRPM7chr5122365000chr1550905026347DRB1-1616KTVENFVALATGEID015

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Fusion breakpoint peptide structures of PPIC-TRPM7

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
9792VALATGEIDTVMEEPPICTRPM7chr5122365000chr1550905026347

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PPIC-TRPM7

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-B14:023BVN9792VALATGEIDTVMEE-7.9962-8.1096
HLA-B14:023BVN9792VALATGEIDTVMEE-5.70842-6.74372
HLA-B52:013W399792VALATGEIDTVMEE-6.83737-6.95077
HLA-B52:013W399792VALATGEIDTVMEE-4.4836-5.5189
HLA-A11:014UQ29792VALATGEIDTVMEE-10.0067-10.1201
HLA-A11:014UQ29792VALATGEIDTVMEE-9.03915-10.0745
HLA-A24:025HGA9792VALATGEIDTVMEE-6.56204-6.67544
HLA-A24:025HGA9792VALATGEIDTVMEE-5.42271-6.45801
HLA-B44:053DX89792VALATGEIDTVMEE-7.85648-8.89178
HLA-B44:053DX89792VALATGEIDTVMEE-5.3978-5.5112
HLA-A02:016TDR9792VALATGEIDTVMEE-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of PPIC-TRPM7

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
PPIC-TRPM7chr5122365000chr1550905026717ALATGEIDTVGCTCTAGCAACAGGAGAGATTGATACAGTT
PPIC-TRPM7chr5122365000chr1550905026817LATGEIDTVCTAGCAACAGGAGAGATTGATACAGTT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PPIC-TRPM7chr5122365000chr1550905026015KTVENFVALATGEIDAAGACAGTGGAAAATTTTGTTGCTCTAGCAACAGGAGAGATTGAT
PPIC-TRPM7chr5122365000chr1550905026116TVENFVALATGEIDTACAGTGGAAAATTTTGTTGCTCTAGCAACAGGAGAGATTGATACA
PPIC-TRPM7chr5122365000chr1550905026217VENFVALATGEIDTVGTGGAAAATTTTGTTGCTCTAGCAACAGGAGAGATTGATACAGTT
PPIC-TRPM7chr5122365000chr1550905026318ENFVALATGEIDTVMGAAAATTTTGTTGCTCTAGCAACAGGAGAGATTGATACAGTTATG

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Information of the samples that have these potential fusion neoantigens of PPIC-TRPM7

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
STADPPIC-TRPM7chr5122365000ENST00000306442chr1550905026ENST00000313478TCGA-HU-A4GH-01A

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Potential target of CAR-T therapy development for PPIC-TRPM7

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
TgeneTRPM7chr5:122365000chr15:50905026ENST0000031347814391036_105601866.0IntramembranePore-forming
TgeneTRPM7chr5:122365000chr15:50905026ENST0000031347814391075_109501866.0TransmembraneHelical
TgeneTRPM7chr5:122365000chr15:50905026ENST000003134781439756_77601866.0TransmembraneHelical
TgeneTRPM7chr5:122365000chr15:50905026ENST000003134781439856_87601866.0TransmembraneHelical
TgeneTRPM7chr5:122365000chr15:50905026ENST000003134781439919_93901866.0TransmembraneHelical
TgeneTRPM7chr5:122365000chr15:50905026ENST000003134781439963_98301866.0TransmembraneHelical
TgeneTRPM7chr5:122365000chr15:50905026ENST000003134781439996_101601866.0TransmembraneHelical

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 PPIC-TRPM7

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 PPIC-TRPM7

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