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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-CDK13

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CPSF6-CDK13
FusionPDB ID: 19142
FusionGDB2.0 ID: 19142
HgeneTgene
Gene symbol

CPSF6

CDK13

Gene ID

11052

8621

Gene namecleavage and polyadenylation specific factor 6cyclin dependent kinase 13
SynonymsCFIM|CFIM68|CFIM72|HPBRII-4|HPBRII-7CDC2L|CDC2L5|CHDFIDD|CHED|hCDK13
Cytomap

12q15

7p14.1

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 cyclin-dependent kinase 13CDC2-related protein kinase 5cell division cycle 2-like protein kinase 5cell division protein kinase 13cholinesterase-related cell division controller
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}.

Q14004

Main function of 5'-partner protein: FUNCTION: Cyclin-dependent kinase which displays CTD kinase activity and is required for RNA splicing. Has CTD kinase activity by hyperphosphorylating the C-terminal heptapeptide repeat domain (CTD) of the largest RNA polymerase II subunit RPB1, thereby acting as a key regulator of transcription elongation. Required for RNA splicing, probably by phosphorylating SRSF1/SF2. Required during hematopoiesis. In case of infection by HIV-1 virus, interacts with HIV-1 Tat protein acetylated at 'Lys-50' and 'Lys-51', thereby increasing HIV-1 mRNA splicing and promoting the production of the doubly spliced HIV-1 protein Nef. {ECO:0000269|PubMed:16721827, ECO:0000269|PubMed:1731328, ECO:0000269|PubMed:18480452, ECO:0000269|PubMed:20952539}.
Ensembl transtripts involved in fusion geneENST idsENST00000266679, ENST00000435070, 
ENST00000456847, ENST00000551516, 
ENST00000550987, 
ENST00000181839, 
ENST00000340829, ENST00000484589, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score69 X 12 X 19=157325 X 6 X 2=60
# samples 716
** MAII scorelog2(71/15732*10)=-4.46973925655087
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/60*10)=0
Fusion gene context

PubMed: CPSF6 [Title/Abstract] AND CDK13 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CPSF6 [Title/Abstract] AND CDK13 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CPSF6(69656342)-CDK13(40027198), # samples:1
Anticipated loss of major functional domain due to fusion event.CPSF6-CDK13 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-CDK13 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

TgeneCDK13

GO:0070816

phosphorylation of RNA polymerase II C-terminal domain

20952539



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/chr12:69656342/chr7:40027198)
- 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 CDK13 (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)
ENST00000551516CPSF6chr1269656342+ENST00000181839CDK13chr740027198+5654172534991164
ENST00000551516CPSF6chr1269656342+ENST00000340829CDK13chr740027198+3895172533191104

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
ENST00000551516ENST00000181839CPSF6chr1269656342+CDK13chr740027198+0.0001807560.9998192
ENST00000551516ENST00000340829CPSF6chr1269656342+CDK13chr740027198+0.0005141250.99948585

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-CDK13

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CPSF6chr1269656342CDK13chr74002719817255ESVTESANIVIVRRRSGKSRSRSPYS
CPSF6chr1269656342CDK13chr74002719817261ANIVIVRRRSGKSRSRSPYSSRHSRS
CPSF6chr1269656342CDK13chr74002719817271GKSRSRSPYSSRHSRSRSRHRLSRSR

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Potential FusionNeoAntigen Information of CPSF6-CDK13 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-CDK13_69656342_40027198.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-CDK13chr1269656342chr740027198172HLA-A30:08RSPYSSRHSR0.97720.7658515
CPSF6-CDK13chr1269656342chr740027198172HLA-A74:03RSPYSSRHSR0.97660.5027515
CPSF6-CDK13chr1269656342chr740027198172HLA-A74:09RSPYSSRHSR0.97660.5027515
CPSF6-CDK13chr1269656342chr740027198172HLA-A74:11RSPYSSRHSR0.97660.5027515
CPSF6-CDK13chr1269656342chr740027198172HLA-B27:05SRSPYSSRHSR0.99970.8122415
CPSF6-CDK13chr1269656342chr740027198172HLA-B27:14SRSPYSSRHSR0.99970.7821415
CPSF6-CDK13chr1269656342chr740027198172HLA-B27:10SRHSRSRSR0.98220.91751019
CPSF6-CDK13chr1269656342chr740027198172HLA-A30:01RSPYSSRHSR0.98290.8957515
CPSF6-CDK13chr1269656342chr740027198172HLA-A74:01RSPYSSRHSR0.97660.5027515
CPSF6-CDK13chr1269656342chr740027198172HLA-B27:10SRSPYSSRHSR0.99950.8633415

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Potential FusionNeoAntigen Information of CPSF6-CDK13 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-CDK13_69656342_40027198.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-CDK13chr1269656342chr740027198172DRB1-1186RSPYSSRHSRSRSRH520
CPSF6-CDK13chr1269656342chr740027198172DRB1-1316RSPYSSRHSRSRSRH520
CPSF6-CDK13chr1269656342chr740027198172DRB5-0103RSPYSSRHSRSRSRH520

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Fusion breakpoint peptide structures of CPSF6-CDK13

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
8908SPYSSRHSRSRSRHCPSF6CDK13chr1269656342chr740027198172

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CPSF6-CDK13

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-B14:023BVN8908SPYSSRHSRSRSRH-5.68384-5.79564
HLA-B14:023BVN8908SPYSSRHSRSRSRH-3.56904-4.61214
HLA-B52:013W398908SPYSSRHSRSRSRH-6.63523-6.74703
HLA-B52:013W398908SPYSSRHSRSRSRH-5.62878-6.67188
HLA-A11:014UQ28908SPYSSRHSRSRSRH-5.4101-6.4532
HLA-A11:014UQ28908SPYSSRHSRSRSRH-4.27122-4.38302
HLA-A24:025HGA8908SPYSSRHSRSRSRH-9.1657-10.2088
HLA-A24:025HGA8908SPYSSRHSRSRSRH-4.66063-4.77243
HLA-B44:053DX88908SPYSSRHSRSRSRH-5.55787-6.60097
HLA-B44:053DX88908SPYSSRHSRSRSRH-4.40408-4.51588

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Vaccine Design for the FusionNeoAntigens of CPSF6-CDK13

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-CDK13chr1269656342chr7400271981019SRHSRSRSRCGTTAGAAGACGGTCTGGAAAATCCCG
CPSF6-CDK13chr1269656342chr740027198415SRSPYSSRHSRGAGCGCGAATATCGTCATCGTTAGAAGACGGTC
CPSF6-CDK13chr1269656342chr740027198515RSPYSSRHSRCGCGAATATCGTCATCGTTAGAAGACGGTC

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-CDK13chr1269656342chr740027198520RSPYSSRHSRSRSRHCGCGAATATCGTCATCGTTAGAAGACGGTCTGGAAAATCCCGAAG

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Information of the samples that have these potential fusion neoantigens of CPSF6-CDK13

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-CDK13chr1269656342ENST00000551516chr740027198ENST00000181839TCGA-D7-8574-01A

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Potential target of CAR-T therapy development for CPSF6-CDK13

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-CDK13

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-CDK13

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