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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:CPSF6-ETHE1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CPSF6-ETHE1
FusionPDB ID: 19153
FusionGDB2.0 ID: 19153
HgeneTgene
Gene symbol

CPSF6

ETHE1

Gene ID

11052

23474

Gene namecleavage and polyadenylation specific factor 6ETHE1 persulfide dioxygenase
SynonymsCFIM|CFIM68|CFIM72|HPBRII-4|HPBRII-7HSCO|YF13H12
Cytomap

12q15

19q13.31

Type of geneprotein-codingprotein-coding
Descriptioncleavage and polyadenylation specificity factor subunit 6CPSF 68 kDa subunitcleavage and polyadenylation specific factor 6, 68kDacleavage and polyadenylation specificity factor 68 kDa subunitcleavage factor Im complex 68 kDa subunitpre-mRNA cleavage persulfide dioxygenase ETHE1, mitochondrialethylmalonic encephalopathy 1hepatoma subtracted clone one proteinprotein ETHE1, mitochondrialsulfur dioxygenase ETHE1
Modification date2020031320200313
UniProtAcc

Q16630

Main function of 5'-partner protein: FUNCTION: Component of the cleavage factor Im (CFIm) complex that functions as an activator of the pre-mRNA 3'-end cleavage and polyadenylation processing required for the maturation of pre-mRNA into functional mRNAs (PubMed:9659921, PubMed:8626397, PubMed:14690600, PubMed:29276085). CFIm contributes to the recruitment of multiprotein complexes on specific sequences on the pre-mRNA 3'-end, so called cleavage and polyadenylation signals (pA signals) (PubMed:9659921, PubMed:8626397, PubMed:14690600). Most pre-mRNAs contain multiple pA signals, resulting in alternative cleavage and polyadenylation (APA) producing mRNAs with variable 3'-end formation (PubMed:23187700, PubMed:29276085). The CFIm complex acts as a key regulator of cleavage and polyadenylation site choice during APA through its binding to 5'-UGUA-3' elements localized in the 3'-untranslated region (UTR) for a huge number of pre-mRNAs (PubMed:20695905, PubMed:29276085). CPSF6 enhances NUDT21/CPSF5 binding to 5'-UGUA-3' elements localized upstream of pA signals and promotes RNA looping, and hence activates directly the mRNA 3'-processing machinery (PubMed:15169763, PubMed:29276085, PubMed:21295486). Plays a role in mRNA export (PubMed:19864460). {ECO:0000269|PubMed:14690600, ECO:0000269|PubMed:15169763, ECO:0000269|PubMed:19864460, ECO:0000269|PubMed:20695905, ECO:0000269|PubMed:21295486, ECO:0000269|PubMed:23187700, ECO:0000269|PubMed:29276085, ECO:0000269|PubMed:8626397, ECO:0000269|PubMed:9659921}.; FUNCTION: (Microbial infection) Binds HIV-1 capsid-nucleocapsid (HIV-1 CA-NC) complexes and might thereby promote the integration of the virus in the nucleus of dividing cells (in vitro). {ECO:0000269|PubMed:24130490}.

O95571

Main function of 5'-partner protein: FUNCTION: Sulfur dioxygenase that plays an essential role in hydrogen sulfide catabolism in the mitochondrial matrix. Hydrogen sulfide (H(2)S) is first oxidized by SQRDL, giving rise to cysteine persulfide residues. ETHE1 consumes molecular oxygen to catalyze the oxidation of the persulfide, once it has been transferred to a thiophilic acceptor, such as glutathione (R-SSH). Plays an important role in metabolic homeostasis in mitochondria by metabolizing hydrogen sulfide and preventing the accumulation of supraphysiological H(2)S levels that have toxic effects, due to the inhibition of cytochrome c oxidase. First described as a protein that can shuttle between the nucleus and the cytoplasm and suppress p53-induced apoptosis by sequestering the transcription factor RELA/NFKB3 in the cytoplasm and preventing its accumulation in the nucleus (PubMed:12398897). {ECO:0000269|PubMed:12398897, ECO:0000269|PubMed:14732903, ECO:0000269|PubMed:19136963, ECO:0000269|PubMed:23144459}.
Ensembl transtripts involved in fusion geneENST idsENST00000550987, ENST00000266679, 
ENST00000435070, ENST00000456847, 
ENST00000551516, 
ENST00000292147, 
ENST00000600651, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score69 X 12 X 19=1573211 X 2 X 7=154
# samples 7112
** MAII scorelog2(71/15732*10)=-4.46973925655087
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/154*10)=-0.359895945086383
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CPSF6 [Title/Abstract] AND ETHE1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CPSF6 [Title/Abstract] AND ETHE1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CPSF6(69633486)-ETHE1(44015718), # samples:2
Anticipated loss of major functional domain due to fusion event.CPSF6-ETHE1 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.
CPSF6-ETHE1 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
HgeneCPSF6

GO:0006397

mRNA processing

14690600

HgeneCPSF6

GO:0051262

protein tetramerization

20695905

HgeneCPSF6

GO:0051290

protein heterotetramerization

23187700

HgeneCPSF6

GO:1990120

messenger ribonucleoprotein complex assembly

29276085

TgeneETHE1

GO:0006749

glutathione metabolic process

23144459

TgeneETHE1

GO:0070813

hydrogen sulfide metabolic process

23144459



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/chr12:69633486/chr19:44015718)
- 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 CPSF6 (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 ETHE1 (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)
ENST00000435070CPSF6chr1269633486+ENST00000292147ETHE1chr1944015718-691170110559149
ENST00000435070CPSF6chr1269633486+ENST00000600651ETHE1chr1944015718-823170110577155
ENST00000456847CPSF6chr1269633486+ENST00000292147ETHE1chr1944015718-62810747496149
ENST00000456847CPSF6chr1269633486+ENST00000600651ETHE1chr1944015718-76010747514155
ENST00000266679CPSF6chr1269633486+ENST00000292147ETHE1chr1944015718-6129131480149
ENST00000266679CPSF6chr1269633486+ENST00000600651ETHE1chr1944015718-7449131498155
ENST00000551516CPSF6chr1269633486+ENST00000292147ETHE1chr1944015718-586655454149
ENST00000551516CPSF6chr1269633486+ENST00000600651ETHE1chr1944015718-718655472155

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
ENST00000435070ENST00000292147CPSF6chr1269633486+ETHE1chr1944015718-0.0119135740.98808646
ENST00000435070ENST00000600651CPSF6chr1269633486+ETHE1chr1944015718-0.0133867780.9866132
ENST00000456847ENST00000292147CPSF6chr1269633486+ETHE1chr1944015718-0.0112824990.98871756
ENST00000456847ENST00000600651CPSF6chr1269633486+ETHE1chr1944015718-0.0146510940.9853489
ENST00000266679ENST00000292147CPSF6chr1269633486+ETHE1chr1944015718-0.0099591440.99004084
ENST00000266679ENST00000600651CPSF6chr1269633486+ETHE1chr1944015718-0.0172760580.9827239
ENST00000551516ENST00000292147CPSF6chr1269633486+ETHE1chr1944015718-0.0123364940.98766345
ENST00000551516ENST00000600651CPSF6chr1269633486+ETHE1chr1944015718-0.0265373480.97346264

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 CPSF6-ETHE1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CPSF6chr1269633486ETHE1chr194401571810719HIDIYADVGEEFNQALETRASPGHTP
CPSF6chr1269633486ETHE1chr194401571817019HIDIYADVGEEFNQALETRASPGHTP
CPSF6chr1269633486ETHE1chr19440157186519HIDIYADVGEEFNQALETRASPGHTP
CPSF6chr1269633486ETHE1chr19440157189119HIDIYADVGEEFNQALETRASPGHTP

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Potential FusionNeoAntigen Information of CPSF6-ETHE1 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.
CPSF6-ETHE1_69633486_44015718.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)
CPSF6-ETHE1chr1269633486chr194401571891HLA-B39:13GEEFNQAL0.9680.9273816
CPSF6-ETHE1chr1269633486chr194401571891HLA-B45:01EEFNQALET0.99430.9548918
CPSF6-ETHE1chr1269633486chr194401571891HLA-B50:02EEFNQALET0.98440.6268918
CPSF6-ETHE1chr1269633486chr194401571891HLA-B18:01EEFNQALET0.75320.8865918
CPSF6-ETHE1chr1269633486chr194401571891HLA-B45:01EEFNQALETRA0.99990.9644920
CPSF6-ETHE1chr1269633486chr194401571891HLA-B50:02EEFNQALETRA0.9990.7642920
CPSF6-ETHE1chr1269633486chr194401571891HLA-B39:08GEEFNQAL0.97580.7946816
CPSF6-ETHE1chr1269633486chr194401571891HLA-C05:09VGEEFNQAL0.99980.9217716
CPSF6-ETHE1chr1269633486chr194401571891HLA-C08:15VGEEFNQAL0.99970.938716
CPSF6-ETHE1chr1269633486chr194401571891HLA-C08:04VGEEFNQAL0.91140.8954716
CPSF6-ETHE1chr1269633486chr194401571891HLA-C08:13VGEEFNQAL0.91140.8954716
CPSF6-ETHE1chr1269633486chr194401571891HLA-C08:03VGEEFNQAL0.73840.9751716
CPSF6-ETHE1chr1269633486chr194401571891HLA-B40:04GEEFNQAL0.99970.669816
CPSF6-ETHE1chr1269633486chr194401571891HLA-B41:03GEEFNQAL0.95090.5295816
CPSF6-ETHE1chr1269633486chr194401571891HLA-C05:01VGEEFNQAL0.99980.9217716
CPSF6-ETHE1chr1269633486chr194401571891HLA-C01:03VGEEFNQAL0.99970.8541716
CPSF6-ETHE1chr1269633486chr194401571891HLA-C04:03VGEEFNQAL0.99970.7922716
CPSF6-ETHE1chr1269633486chr194401571891HLA-C08:02VGEEFNQAL0.99970.938716
CPSF6-ETHE1chr1269633486chr194401571891HLA-B18:05EEFNQALET0.75320.8865918
CPSF6-ETHE1chr1269633486chr194401571891HLA-C08:01VGEEFNQAL0.73840.9751716
CPSF6-ETHE1chr1269633486chr194401571891HLA-B18:06EEFNQALET0.7230.909918
CPSF6-ETHE1chr1269633486chr194401571891HLA-B18:03EEFNQALET0.70080.8795918
CPSF6-ETHE1chr1269633486chr194401571891HLA-B18:11EEFNQALET0.55840.8165918
CPSF6-ETHE1chr1269633486chr194401571891HLA-B07:13VGEEFNQAL0.03820.6711716

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Potential FusionNeoAntigen Information of CPSF6-ETHE1 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.
CPSF6-ETHE1_69633486_44015718.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)
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0310HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0338HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0342HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0901GEEFNQALETRASPG823
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0901VGEEFNQALETRASP722
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0901DVGEEFNQALETRAS621
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0902GEEFNQALETRASPG823
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0902VGEEFNQALETRASP722
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0903GEEFNQALETRASPG823
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0903VGEEFNQALETRASP722
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0904GEEFNQALETRASPG823
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0904VGEEFNQALETRASP722
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0905GEEFNQALETRASPG823
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0905VGEEFNQALETRASP722
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0907GEEFNQALETRASPG823
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0907VGEEFNQALETRASP722
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0908GEEFNQALETRASPG823
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0908VGEEFNQALETRASP722
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0909GEEFNQALETRASPG823
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0909VGEEFNQALETRASP722
CPSF6-ETHE1chr1269633486chr194401571891DRB1-0909DVGEEFNQALETRAS621
CPSF6-ETHE1chr1269633486chr194401571891DRB1-1476HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB1-1479HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB1-1525HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0101HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0101IDIYADVGEEFNQAL116
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0104HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0104IDIYADVGEEFNQAL116
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0105HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0105IDIYADVGEEFNQAL116
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0108HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0108IDIYADVGEEFNQAL116
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0109HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0111HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0111IDIYADVGEEFNQAL116
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0112HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0112IDIYADVGEEFNQAL116
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0113HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0113IDIYADVGEEFNQAL116
CPSF6-ETHE1chr1269633486chr194401571891DRB3-0114HIDIYADVGEEFNQA015
CPSF6-ETHE1chr1269633486chr194401571891DRB5-0112GEEFNQALETRASPG823

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Fusion breakpoint peptide structures of CPSF6-ETHE1

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
1453DVGEEFNQALETRACPSF6ETHE1chr1269633486chr194401571891

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CPSF6-ETHE1

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-B57:032BVO1453DVGEEFNQALETRA-5.71288-5.71288
HLA-B52:013W391453DVGEEFNQALETRA-3.19796-3.19796
HLA-B44:053DX81453DVGEEFNQALETRA-3.21962-3.21962
HLA-A02:016TDR1453DVGEEFNQALETRA-1.80057-1.80057

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Vaccine Design for the FusionNeoAntigens of CPSF6-ETHE1

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
CPSF6-ETHE1chr1269633486chr1944015718716VGEEFNQALGGCGAAGAGTTCAACCAGGCGTTGGAG
CPSF6-ETHE1chr1269633486chr1944015718816GEEFNQALGAAGAGTTCAACCAGGCGTTGGAG
CPSF6-ETHE1chr1269633486chr1944015718918EEFNQALETGAGTTCAACCAGGCGTTGGAGACCAGG
CPSF6-ETHE1chr1269633486chr1944015718920EEFNQALETRAGAGTTCAACCAGGCGTTGGAGACCAGGGCCAGC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CPSF6-ETHE1chr1269633486chr1944015718015HIDIYADVGEEFNQAATAGACATTTACGCGGATGTCGGCGAAGAGTTCAACCAGGCGTTG
CPSF6-ETHE1chr1269633486chr1944015718116IDIYADVGEEFNQALGACATTTACGCGGATGTCGGCGAAGAGTTCAACCAGGCGTTGGAG
CPSF6-ETHE1chr1269633486chr1944015718621DVGEEFNQALETRASGTCGGCGAAGAGTTCAACCAGGCGTTGGAGACCAGGGCCAGCCCT
CPSF6-ETHE1chr1269633486chr1944015718722VGEEFNQALETRASPGGCGAAGAGTTCAACCAGGCGTTGGAGACCAGGGCCAGCCCTGGC
CPSF6-ETHE1chr1269633486chr1944015718823GEEFNQALETRASPGGAAGAGTTCAACCAGGCGTTGGAGACCAGGGCCAGCCCTGGCCAC

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Information of the samples that have these potential fusion neoantigens of CPSF6-ETHE1

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
STADCPSF6-ETHE1chr1269633486ENST00000266679chr1944015718ENST00000292147TCGA-FP-A8CX

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Potential target of CAR-T therapy development for CPSF6-ETHE1

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 CPSF6-ETHE1

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 CPSF6-ETHE1

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