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Fusion Protein:CPSF6-EZH2 |
Fusion Protein Summary |
Fusion gene summary |
Fusion partner gene information | Fusion gene name: CPSF6-EZH2 | FusionPDB ID: 19155 | FusionGDB2.0 ID: 19155 | Hgene | Tgene | Gene symbol | CPSF6 | EZH2 | Gene ID | 11052 | 2146 |
Gene name | cleavage and polyadenylation specific factor 6 | enhancer of zeste 2 polycomb repressive complex 2 subunit | |
Synonyms | CFIM|CFIM68|CFIM72|HPBRII-4|HPBRII-7 | ENX-1|ENX1|EZH2b|KMT6|KMT6A|WVS|WVS2 | |
Cytomap | 12q15 | 7q36.1 | |
Type of gene | protein-coding | protein-coding | |
Description | cleavage 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 | histone-lysine N-methyltransferase EZH2enhancer of zeste homolog 2lysine N-methyltransferase 6 | |
Modification date | 20200313 | 20200329 | |
UniProtAcc | Q16630 | Q15910 | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000266679, ENST00000435070, ENST00000456847, ENST00000551516, ENST00000550987, | ENST00000320356, ENST00000350995, ENST00000460911, ENST00000476773, ENST00000478654, ENST00000483967, ENST00000541220, ENST00000536783, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 69 X 12 X 19=15732 | 10 X 7 X 5=350 |
# samples | 71 | 9 | |
** MAII score | log2(71/15732*10)=-4.46973925655087 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(9/350*10)=-1.95935801550265 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: CPSF6 [Title/Abstract] AND EZH2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | CPSF6(69656342)-EZH2(148512638), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | CPSF6-EZH2 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-EZH2 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-EZH2 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. CPSF6-EZH2 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) |
Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | CPSF6 | GO:0006397 | mRNA processing | 14690600 |
Hgene | CPSF6 | GO:0051262 | protein tetramerization | 20695905 |
Hgene | CPSF6 | GO:0051290 | protein heterotetramerization | 23187700 |
Hgene | CPSF6 | GO:1990120 | messenger ribonucleoprotein complex assembly | 29276085 |
Tgene | EZH2 | GO:0000122 | negative regulation of transcription by RNA polymerase II | 20154697 |
Tgene | EZH2 | GO:0010718 | positive regulation of epithelial to mesenchymal transition | 20154697 |
Tgene | EZH2 | GO:0043406 | positive regulation of MAP kinase activity | 20154697 |
Tgene | EZH2 | GO:0043547 | positive regulation of GTPase activity | 20154697 |
Tgene | EZH2 | GO:0045814 | negative regulation of gene expression, epigenetic | 20154697 |
Tgene | EZH2 | GO:0070734 | histone H3-K27 methylation | 24474760 |
Tgene | EZH2 | GO:0071902 | positive regulation of protein serine/threonine kinase activity | 20154697 |
Fusion 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. |
Fusion gene breakpoints across EZH2 (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
Fusion gene information from FusionGDB2.0. |
Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | HNSC | TCGA-CR-6467 | CPSF6 | chr12 | 69656342 | + | EZH2 | chr7 | 148512638 | - |
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Fusion ORF Analysis |
Fusion information from ORFfinder translation from full-length transcript sequence from FusionPDB. |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000551516 | CPSF6 | chr12 | 69656342 | + | ENST00000478654 | EZH2 | chr7 | 148512638 | - | 1059 | 172 | 5 | 796 | 263 |
ENST00000551516 | CPSF6 | chr12 | 69656342 | + | ENST00000460911 | EZH2 | chr7 | 148512638 | - | 1184 | 172 | 5 | 922 | 305 |
ENST00000551516 | CPSF6 | chr12 | 69656342 | + | ENST00000350995 | EZH2 | chr7 | 148512638 | - | 1184 | 172 | 5 | 922 | 305 |
ENST00000551516 | CPSF6 | chr12 | 69656342 | + | ENST00000320356 | EZH2 | chr7 | 148512638 | - | 1184 | 172 | 5 | 922 | 305 |
ENST00000551516 | CPSF6 | chr12 | 69656342 | + | ENST00000541220 | EZH2 | chr7 | 148512638 | - | 1058 | 172 | 5 | 796 | 263 |
ENST00000551516 | CPSF6 | chr12 | 69656342 | + | ENST00000476773 | EZH2 | chr7 | 148512638 | - | 961 | 172 | 5 | 796 | 263 |
ENST00000551516 | CPSF6 | chr12 | 69656342 | + | ENST00000483967 | EZH2 | chr7 | 148512638 | - | 1044 | 172 | 5 | 922 | 305 |
DeepORF 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. |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000551516 | ENST00000478654 | CPSF6 | chr12 | 69656342 | + | EZH2 | chr7 | 148512638 | - | 0.004534836 | 0.9954652 |
ENST00000551516 | ENST00000460911 | CPSF6 | chr12 | 69656342 | + | EZH2 | chr7 | 148512638 | - | 0.002138256 | 0.9978618 |
ENST00000551516 | ENST00000350995 | CPSF6 | chr12 | 69656342 | + | EZH2 | chr7 | 148512638 | - | 0.002138256 | 0.9978618 |
ENST00000551516 | ENST00000320356 | CPSF6 | chr12 | 69656342 | + | EZH2 | chr7 | 148512638 | - | 0.002138256 | 0.9978618 |
ENST00000551516 | ENST00000541220 | CPSF6 | chr12 | 69656342 | + | EZH2 | chr7 | 148512638 | - | 0.004560874 | 0.9954391 |
ENST00000551516 | ENST00000476773 | CPSF6 | chr12 | 69656342 | + | EZH2 | chr7 | 148512638 | - | 0.00589475 | 0.9941052 |
ENST00000551516 | ENST00000483967 | CPSF6 | chr12 | 69656342 | + | EZH2 | chr7 | 148512638 | - | 0.003241127 | 0.9967589 |
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Fusion Amino Acid Sequences |
For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >19155_19155_1_CPSF6-EZH2_CPSF6_chr12_69656342_ENST00000551516_EZH2_chr7_148512638_ENST00000320356_length(amino acids)=305AA_BP=55 MADGVDHIDIYADVGEEFNQEAEYEREAENERGTGIVTETVTESVTESANIVIVRRLWAAHCRKIQLKKDGSSNHVYNYQPCDHPRQPCD SSCPCVIAQNFCEKFCQCSSECQNRFPGCRCKAQCNTKQCPCYLAVRECDPDLCLTCGAADHWDSKNVSCKNCSIQRGSKKHLLLAPSDV AGWGIFIKDPVQKNEFISEYCGEIISQDEADRRGKVYDKYMCSFLFNLNNDFVVDATRKGNKIRFANHSVNPNCYAKVMMVNGDHRIGIF -------------------------------------------------------------- >19155_19155_2_CPSF6-EZH2_CPSF6_chr12_69656342_ENST00000551516_EZH2_chr7_148512638_ENST00000350995_length(amino acids)=305AA_BP=55 MADGVDHIDIYADVGEEFNQEAEYEREAENERGTGIVTETVTESVTESANIVIVRRLWAAHCRKIQLKKDGSSNHVYNYQPCDHPRQPCD SSCPCVIAQNFCEKFCQCSSECQNRFPGCRCKAQCNTKQCPCYLAVRECDPDLCLTCGAADHWDSKNVSCKNCSIQRGSKKHLLLAPSDV AGWGIFIKDPVQKNEFISEYCGEIISQDEADRRGKVYDKYMCSFLFNLNNDFVVDATRKGNKIRFANHSVNPNCYAKVMMVNGDHRIGIF -------------------------------------------------------------- >19155_19155_3_CPSF6-EZH2_CPSF6_chr12_69656342_ENST00000551516_EZH2_chr7_148512638_ENST00000460911_length(amino acids)=305AA_BP=55 MADGVDHIDIYADVGEEFNQEAEYEREAENERGTGIVTETVTESVTESANIVIVRRLWAAHCRKIQLKKDGSSNHVYNYQPCDHPRQPCD SSCPCVIAQNFCEKFCQCSSECQNRFPGCRCKAQCNTKQCPCYLAVRECDPDLCLTCGAADHWDSKNVSCKNCSIQRGSKKHLLLAPSDV AGWGIFIKDPVQKNEFISEYCGEIISQDEADRRGKVYDKYMCSFLFNLNNDFVVDATRKGNKIRFANHSVNPNCYAKVMMVNGDHRIGIF -------------------------------------------------------------- >19155_19155_4_CPSF6-EZH2_CPSF6_chr12_69656342_ENST00000551516_EZH2_chr7_148512638_ENST00000476773_length(amino acids)=263AA_BP=55 MADGVDHIDIYADVGEEFNQEAEYEREAENERGTGIVTETVTESVTESANIVIVRRLWAAHCRKIQLKKGQNRFPGCRCKAQCNTKQCPC YLAVRECDPDLCLTCGAADHWDSKNVSCKNCSIQRGSKKHLLLAPSDVAGWGIFIKDPVQKNEFISEYCGEIISQDEADRRGKVYDKYMC -------------------------------------------------------------- >19155_19155_5_CPSF6-EZH2_CPSF6_chr12_69656342_ENST00000551516_EZH2_chr7_148512638_ENST00000478654_length(amino acids)=263AA_BP=55 MADGVDHIDIYADVGEEFNQEAEYEREAENERGTGIVTETVTESVTESANIVIVRRLWAAHCRKIQLKKGQNRFPGCRCKAQCNTKQCPC YLAVRECDPDLCLTCGAADHWDSKNVSCKNCSIQRGSKKHLLLAPSDVAGWGIFIKDPVQKNEFISEYCGEIISQDEADRRGKVYDKYMC -------------------------------------------------------------- >19155_19155_6_CPSF6-EZH2_CPSF6_chr12_69656342_ENST00000551516_EZH2_chr7_148512638_ENST00000483967_length(amino acids)=305AA_BP=55 MADGVDHIDIYADVGEEFNQEAEYEREAENERGTGIVTETVTESVTESANIVIVRRLWAAHCRKIQLKKDGSSNHVYNYQPCDHPRQPCD SSCPCVIAQNFCEKFCQCSSECQNRFPGCRCKAQCNTKQCPCYLAVRECDPDLCLTCGAADHWDSKNVSCKNCSIQRGSKKHLLLAPSDV AGWGIFIKDPVQKNEFISEYCGEIISQDEADRRGKVYDKYMCSFLFNLNNDFVVDATRKGNKIRFANHSVNPNCYAKVMMVNGDHRIGIF -------------------------------------------------------------- >19155_19155_7_CPSF6-EZH2_CPSF6_chr12_69656342_ENST00000551516_EZH2_chr7_148512638_ENST00000541220_length(amino acids)=263AA_BP=55 MADGVDHIDIYADVGEEFNQEAEYEREAENERGTGIVTETVTESVTESANIVIVRRLWAAHCRKIQLKKGQNRFPGCRCKAQCNTKQCPC YLAVRECDPDLCLTCGAADHWDSKNVSCKNCSIQRGSKKHLLLAPSDVAGWGIFIKDPVQKNEFISEYCGEIISQDEADRRGKVYDKYMC -------------------------------------------------------------- |
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Fusion Protein Functional Features |
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/chr7:148512638) - 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. |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
CPSF6 | EZH2 |
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}. | FUNCTION: Polycomb group (PcG) protein. Catalytic subunit of the PRC2/EED-EZH2 complex, which methylates 'Lys-9' (H3K9me) and 'Lys-27' (H3K27me) of histone H3, leading to transcriptional repression of the affected target gene. Able to mono-, di- and trimethylate 'Lys-27' of histone H3 to form H3K27me1, H3K27me2 and H3K27me3, respectively. Displays a preference for substrates with less methylation, loses activity when progressively more methyl groups are incorporated into H3K27, H3K27me0 > H3K27me1 > H3K27me2 (PubMed:22323599, PubMed:30923826). Compared to EZH1-containing complexes, it is more abundant in embryonic stem cells and plays a major role in forming H3K27me3, which is required for embryonic stem cell identity and proper differentiation. The PRC2/EED-EZH2 complex may also serve as a recruiting platform for DNA methyltransferases, thereby linking two epigenetic repression systems. Genes repressed by the PRC2/EED-EZH2 complex include HOXC8, HOXA9, MYT1, CDKN2A and retinoic acid target genes. EZH2 can also methylate non-histone proteins such as the transcription factor GATA4 and the nuclear receptor RORA. Regulates the circadian clock via histone methylation at the promoter of the circadian genes. Essential for the CRY1/2-mediated repression of the transcriptional activation of PER1/2 by the CLOCK-ARNTL/BMAL1 heterodimer; involved in the di and trimethylation of 'Lys-27' of histone H3 on PER1/2 promoters which is necessary for the CRY1/2 proteins to inhibit transcription. {ECO:0000269|PubMed:14532106, ECO:0000269|PubMed:15225548, ECO:0000269|PubMed:15231737, ECO:0000269|PubMed:15385962, ECO:0000269|PubMed:16179254, ECO:0000269|PubMed:16357870, ECO:0000269|PubMed:16618801, ECO:0000269|PubMed:16717091, ECO:0000269|PubMed:16936726, ECO:0000269|PubMed:17210787, ECO:0000269|PubMed:17344414, ECO:0000269|PubMed:18285464, ECO:0000269|PubMed:19026781, ECO:0000269|PubMed:20935635, ECO:0000269|PubMed:22323599, ECO:0000269|PubMed:23063525, ECO:0000269|PubMed:24474760, ECO:0000269|PubMed:30923826}. |
Retention 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, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at * Minus value of BPloci means that the break pointn is located before the CDS. |
- Retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000266679 | + | 10 | 11 | 208_398 | 590.0 | 701.3333333333334 | Compositional bias | Note=Pro-rich |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000266679 | + | 10 | 11 | 490_551 | 590.0 | 701.3333333333334 | Compositional bias | Note=Arg-rich |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000435070 | + | 9 | 10 | 208_398 | 553.0 | 2111.0 | Compositional bias | Note=Pro-rich |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000435070 | + | 9 | 10 | 490_551 | 553.0 | 2111.0 | Compositional bias | Note=Arg-rich |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000266679 | + | 10 | 11 | 202_206 | 590.0 | 701.3333333333334 | Motif | GAR |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000435070 | + | 9 | 10 | 202_206 | 553.0 | 2111.0 | Motif | GAR |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000266679 | + | 10 | 11 | 358_551 | 590.0 | 701.3333333333334 | Region | (Microbial infection) Binds to HIV-1 capsid protein p24 (CA) |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000266679 | + | 10 | 11 | 404_551 | 590.0 | 701.3333333333334 | Region | Sufficient for nuclear speckle localization |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000266679 | + | 10 | 11 | 405_551 | 590.0 | 701.3333333333334 | Region | Necessary for RNA-binding |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000266679 | + | 10 | 11 | 510_551 | 590.0 | 701.3333333333334 | Region | Sufficient for nuclear targeting |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000266679 | + | 10 | 11 | 81_161 | 590.0 | 701.3333333333334 | Region | Necessary for nuclear paraspeckles localization |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000435070 | + | 9 | 10 | 358_551 | 553.0 | 2111.0 | Region | (Microbial infection) Binds to HIV-1 capsid protein p24 (CA) |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000435070 | + | 9 | 10 | 404_551 | 553.0 | 2111.0 | Region | Sufficient for nuclear speckle localization |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000435070 | + | 9 | 10 | 405_551 | 553.0 | 2111.0 | Region | Necessary for RNA-binding |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000435070 | + | 9 | 10 | 510_551 | 553.0 | 2111.0 | Region | Sufficient for nuclear targeting |
Hgene | CPSF6 | chr12:69656342 | chr7:148512638 | ENST00000435070 | + | 9 | 10 | 81_161 | 553.0 | 2111.0 | Region | Necessary for nuclear paraspeckles localization |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000320356 | 11 | 20 | 523_605 | 501.6666666666667 | 752.0 | Compositional bias | Note=Cys-rich | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000350995 | 10 | 19 | 523_605 | 457.6666666666667 | 708.0 | Compositional bias | Note=Cys-rich | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000460911 | 11 | 20 | 523_605 | 496.6666666666667 | 747.0 | Compositional bias | Note=Cys-rich | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000476773 | 11 | 19 | 523_605 | 487.6666666666667 | 696.0 | Compositional bias | Note=Cys-rich | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000478654 | 12 | 20 | 523_605 | 487.6666666666667 | 696.0 | Compositional bias | Note=Cys-rich | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000483967 | 11 | 20 | 523_605 | 487.6666666666667 | 738.0 | Compositional bias | Note=Cys-rich | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000541220 | 11 | 19 | 523_605 | 487.6666666666667 | 696.0 | Compositional bias | Note=Cys-rich | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000320356 | 11 | 20 | 503_605 | 501.6666666666667 | 752.0 | Domain | CXC | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000320356 | 11 | 20 | 612_727 | 501.6666666666667 | 752.0 | Domain | SET | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000350995 | 10 | 19 | 503_605 | 457.6666666666667 | 708.0 | Domain | CXC | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000350995 | 10 | 19 | 612_727 | 457.6666666666667 | 708.0 | Domain | SET | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000460911 | 11 | 20 | 503_605 | 496.6666666666667 | 747.0 | Domain | CXC | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000460911 | 11 | 20 | 612_727 | 496.6666666666667 | 747.0 | Domain | SET | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000476773 | 11 | 19 | 503_605 | 487.6666666666667 | 696.0 | Domain | CXC | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000476773 | 11 | 19 | 612_727 | 487.6666666666667 | 696.0 | Domain | SET | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000478654 | 12 | 20 | 503_605 | 487.6666666666667 | 696.0 | Domain | CXC | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000478654 | 12 | 20 | 612_727 | 487.6666666666667 | 696.0 | Domain | SET | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000483967 | 11 | 20 | 503_605 | 487.6666666666667 | 738.0 | Domain | CXC | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000483967 | 11 | 20 | 612_727 | 487.6666666666667 | 738.0 | Domain | SET | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000541220 | 11 | 19 | 503_605 | 487.6666666666667 | 696.0 | Domain | CXC | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000541220 | 11 | 19 | 612_727 | 487.6666666666667 | 696.0 | Domain | SET |
- Not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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Fusion Protein-Protein Interaction |
Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in |
Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160) |
Gene | PPI interactors |
Protein-protein interactors based on sequence similarity (STRING) |
Gene | STRING network |
CPSF6 | |
EZH2 |
- Retained interactions in fusion protein (protein functional feature from UniProt). |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
- Lost interactions due to fusion (protein functional feature from UniProt). |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000320356 | 11 | 20 | 329_522 | 501.6666666666667 | 752.0 | CDYL | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000350995 | 10 | 19 | 329_522 | 457.6666666666667 | 708.0 | CDYL | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000460911 | 11 | 20 | 329_522 | 496.6666666666667 | 747.0 | CDYL | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000476773 | 11 | 19 | 329_522 | 487.6666666666667 | 696.0 | CDYL | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000478654 | 12 | 20 | 329_522 | 487.6666666666667 | 696.0 | CDYL | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000483967 | 11 | 20 | 329_522 | 487.6666666666667 | 738.0 | CDYL | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000541220 | 11 | 19 | 329_522 | 487.6666666666667 | 696.0 | CDYL | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000320356 | 11 | 20 | 1_340 | 501.6666666666667 | 752.0 | DNMT1%2C DNMT3A and DNMT3B | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000350995 | 10 | 19 | 1_340 | 457.6666666666667 | 708.0 | DNMT1%2C DNMT3A and DNMT3B | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000460911 | 11 | 20 | 1_340 | 496.6666666666667 | 747.0 | DNMT1%2C DNMT3A and DNMT3B | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000476773 | 11 | 19 | 1_340 | 487.6666666666667 | 696.0 | DNMT1%2C DNMT3A and DNMT3B | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000478654 | 12 | 20 | 1_340 | 487.6666666666667 | 696.0 | DNMT1%2C DNMT3A and DNMT3B | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000483967 | 11 | 20 | 1_340 | 487.6666666666667 | 738.0 | DNMT1%2C DNMT3A and DNMT3B | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000541220 | 11 | 19 | 1_340 | 487.6666666666667 | 696.0 | DNMT1%2C DNMT3A and DNMT3B | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000320356 | 11 | 20 | 39_68 | 501.6666666666667 | 752.0 | EED | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000350995 | 10 | 19 | 39_68 | 457.6666666666667 | 708.0 | EED | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000460911 | 11 | 20 | 39_68 | 496.6666666666667 | 747.0 | EED | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000476773 | 11 | 19 | 39_68 | 487.6666666666667 | 696.0 | EED | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000478654 | 12 | 20 | 39_68 | 487.6666666666667 | 696.0 | EED | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000483967 | 11 | 20 | 39_68 | 487.6666666666667 | 738.0 | EED | |
Tgene | EZH2 | chr12:69656342 | chr7:148512638 | ENST00000541220 | 11 | 19 | 39_68 | 487.6666666666667 | 696.0 | EED |
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Related Drugs to CPSF6-EZH2 |
Drugs used for this fusion-positive patient. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to CPSF6-EZH2 |
Diseases that have this fusion gene. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |