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Fusion Protein:CEP85L-HDAC2 |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: CEP85L-HDAC2 | FusionPDB ID: 15913 | FusionGDB2.0 ID: 15913 | Hgene | Tgene | Gene symbol | CEP85L | HDAC2 | Gene ID | 387119 | 3066 |
| Gene name | centrosomal protein 85 like | histone deacetylase 2 | |
| Synonyms | C6orf204|NY-BR-15|bA57K17.2 | HD2|KDAC2|RPD3|YAF1 | |
| Cytomap | 6q22.31 | 6q21 | |
| Type of gene | protein-coding | protein-coding | |
| Description | centrosomal protein of 85 kDa-likecentrosomal protein 85kDa-likeserologically defined breast cancer antigen NY-BR-15 | histone deacetylase 2YY1-associated factor 1transcriptional regulator homolog RPD3 | |
| Modification date | 20200313 | 20200322 | |
| UniProtAcc | Q5SZL2 | Q92769 | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000368488, ENST00000368491, ENST00000392500, ENST00000419517, ENST00000360290, ENST00000472713, | ENST00000368632, ENST00000519108, ENST00000398283, ENST00000519065, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 10 X 10 X 6=600 | 6 X 5 X 2=60 |
| # samples | 11 | 6 | |
| ** MAII score | log2(11/600*10)=-2.44745897697122 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(6/60*10)=0 | |
| Context (manual curation of fusion genes in FusionPDB) | PubMed: CEP85L [Title/Abstract] AND HDAC2 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | CEP85L(118953616)-HDAC2(114281182), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | CEP85L-HDAC2 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. CEP85L-HDAC2 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. CEP85L-HDAC2 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. CEP85L-HDAC2 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. CEP85L-HDAC2 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF. CEP85L-HDAC2 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. CEP85L-HDAC2 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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) |
| 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 |
| Fusion gene breakpoints across CEP85L (5'-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 breakpoints across HDAC2 (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 | STAD | TCGA-IN-7808-01A | CEP85L | chr6 | 118953616 | - | HDAC2 | chr6 | 114281182 | - |
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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) |
| ENST00000368491 | CEP85L | chr6 | 118953616 | - | ENST00000519065 | HDAC2 | chr6 | 114281182 | - | 10299 | 854 | 511 | 2268 | 585 |
| ENST00000368491 | CEP85L | chr6 | 118953616 | - | ENST00000398283 | HDAC2 | chr6 | 114281182 | - | 7171 | 854 | 511 | 2268 | 585 |
| ENST00000419517 | CEP85L | chr6 | 118953616 | - | ENST00000519065 | HDAC2 | chr6 | 114281182 | - | 10265 | 820 | 477 | 2234 | 585 |
| ENST00000419517 | CEP85L | chr6 | 118953616 | - | ENST00000398283 | HDAC2 | chr6 | 114281182 | - | 7137 | 820 | 477 | 2234 | 585 |
| 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 |
| ENST00000368491 | ENST00000519065 | CEP85L | chr6 | 118953616 | - | HDAC2 | chr6 | 114281182 | - | 0.000125297 | 0.9998747 |
| ENST00000368491 | ENST00000398283 | CEP85L | chr6 | 118953616 | - | HDAC2 | chr6 | 114281182 | - | 0.000150607 | 0.9998493 |
| ENST00000419517 | ENST00000519065 | CEP85L | chr6 | 118953616 | - | HDAC2 | chr6 | 114281182 | - | 0.000125921 | 0.9998741 |
| ENST00000419517 | ENST00000398283 | CEP85L | chr6 | 118953616 | - | HDAC2 | chr6 | 114281182 | - | 0.000153877 | 0.9998461 |
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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 >15913_15913_1_CEP85L-HDAC2_CEP85L_chr6_118953616_ENST00000368491_HDAC2_chr6_114281182_ENST00000398283_length(amino acids)=585AA_BP=114 MPVSPRPTLRASFRRRRSRRTDVRSRASLAHPALSPAMWGRFLAPEASGRDSPGGARSFPAGPDYSSAWLPANESLWQATTVPSNHRNNH IRRHSIASDSGDTGIGTSCSDSVEGDIGNYYYGQGHPMKPHRIRMTHNLLLNYGLYRKMEIYRPHKATAEEMTKYHSDEYIKFLRSIRPD NMSEYSKQMQRFNVGEDCPVFDGLFEFCQLSTGGSVAGAVKLNRQQTDMAVNWAGGLHHAKKSEASGFCYVNDIVLAILELLKYHQRVLY IDIDIHHGDGVEEAFYTTDRVMTVSFHKYGEYFPGTGDLRDIGAGKGKYYAVNFPMRDGIDDESYGQIFKPIISKVMEMYQPSAVVLQCG ADSLSGDRLGCFNLTVKGHAKCVEVVKTFNLPLLMLGGGGYTIRNVARCWTYETAVALDCEIPNELPYNDYFEYFGPDFKLHISPSNMTN QNTPEYMEKIKQRLFENLRMLPHAPGVQMQAIPEDAVHEDSGDEDGEDPDKRISIRASDKRIACDEEFSDSEDEGEGGRRNVADHKKGAK -------------------------------------------------------------- >15913_15913_2_CEP85L-HDAC2_CEP85L_chr6_118953616_ENST00000368491_HDAC2_chr6_114281182_ENST00000519065_length(amino acids)=585AA_BP=114 MPVSPRPTLRASFRRRRSRRTDVRSRASLAHPALSPAMWGRFLAPEASGRDSPGGARSFPAGPDYSSAWLPANESLWQATTVPSNHRNNH IRRHSIASDSGDTGIGTSCSDSVEGDIGNYYYGQGHPMKPHRIRMTHNLLLNYGLYRKMEIYRPHKATAEEMTKYHSDEYIKFLRSIRPD NMSEYSKQMQRFNVGEDCPVFDGLFEFCQLSTGGSVAGAVKLNRQQTDMAVNWAGGLHHAKKSEASGFCYVNDIVLAILELLKYHQRVLY IDIDIHHGDGVEEAFYTTDRVMTVSFHKYGEYFPGTGDLRDIGAGKGKYYAVNFPMRDGIDDESYGQIFKPIISKVMEMYQPSAVVLQCG ADSLSGDRLGCFNLTVKGHAKCVEVVKTFNLPLLMLGGGGYTIRNVARCWTYETAVALDCEIPNELPYNDYFEYFGPDFKLHISPSNMTN QNTPEYMEKIKQRLFENLRMLPHAPGVQMQAIPEDAVHEDSGDEDGEDPDKRISIRASDKRIACDEEFSDSEDEGEGGRRNVADHKKGAK -------------------------------------------------------------- >15913_15913_3_CEP85L-HDAC2_CEP85L_chr6_118953616_ENST00000419517_HDAC2_chr6_114281182_ENST00000398283_length(amino acids)=585AA_BP=114 MPVSPRPTLRASFRRRRSRRTDVRSRASLAHPALSPAMWGRFLAPEASGRDSPGGARSFPAGPDYSSAWLPANESLWQATTVPSNHRNNH IRRHSIASDSGDTGIGTSCSDSVEGDIGNYYYGQGHPMKPHRIRMTHNLLLNYGLYRKMEIYRPHKATAEEMTKYHSDEYIKFLRSIRPD NMSEYSKQMQRFNVGEDCPVFDGLFEFCQLSTGGSVAGAVKLNRQQTDMAVNWAGGLHHAKKSEASGFCYVNDIVLAILELLKYHQRVLY IDIDIHHGDGVEEAFYTTDRVMTVSFHKYGEYFPGTGDLRDIGAGKGKYYAVNFPMRDGIDDESYGQIFKPIISKVMEMYQPSAVVLQCG ADSLSGDRLGCFNLTVKGHAKCVEVVKTFNLPLLMLGGGGYTIRNVARCWTYETAVALDCEIPNELPYNDYFEYFGPDFKLHISPSNMTN QNTPEYMEKIKQRLFENLRMLPHAPGVQMQAIPEDAVHEDSGDEDGEDPDKRISIRASDKRIACDEEFSDSEDEGEGGRRNVADHKKGAK -------------------------------------------------------------- >15913_15913_4_CEP85L-HDAC2_CEP85L_chr6_118953616_ENST00000419517_HDAC2_chr6_114281182_ENST00000519065_length(amino acids)=585AA_BP=114 MPVSPRPTLRASFRRRRSRRTDVRSRASLAHPALSPAMWGRFLAPEASGRDSPGGARSFPAGPDYSSAWLPANESLWQATTVPSNHRNNH IRRHSIASDSGDTGIGTSCSDSVEGDIGNYYYGQGHPMKPHRIRMTHNLLLNYGLYRKMEIYRPHKATAEEMTKYHSDEYIKFLRSIRPD NMSEYSKQMQRFNVGEDCPVFDGLFEFCQLSTGGSVAGAVKLNRQQTDMAVNWAGGLHHAKKSEASGFCYVNDIVLAILELLKYHQRVLY IDIDIHHGDGVEEAFYTTDRVMTVSFHKYGEYFPGTGDLRDIGAGKGKYYAVNFPMRDGIDDESYGQIFKPIISKVMEMYQPSAVVLQCG ADSLSGDRLGCFNLTVKGHAKCVEVVKTFNLPLLMLGGGGYTIRNVARCWTYETAVALDCEIPNELPYNDYFEYFGPDFKLHISPSNMTN QNTPEYMEKIKQRLFENLRMLPHAPGVQMQAIPEDAVHEDSGDEDGEDPDKRISIRASDKRIACDEEFSDSEDEGEGGRRNVADHKKGAK -------------------------------------------------------------- |
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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/chr6:118953616/chr6:114281182) - 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. |
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| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| CEP85L | HDAC2 |
| FUNCTION: Plays an essential role in neuronal cell migration. {ECO:0000269|PubMed:32097630}. | FUNCTION: Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Forms transcriptional repressor complexes by associating with MAD, SIN3, YY1 and N-COR. Interacts in the late S-phase of DNA-replication with DNMT1 in the other transcriptional repressor complex composed of DNMT1, DMAP1, PCNA, CAF1. Deacetylates TSHZ3 and regulates its transcriptional repressor activity. Component of a RCOR/GFI/KDM1A/HDAC complex that suppresses, via histone deacetylase (HDAC) recruitment, a number of genes implicated in multilineage blood cell development. May be involved in the transcriptional repression of circadian target genes, such as PER1, mediated by CRY1 through histone deacetylation. Involved in MTA1-mediated transcriptional corepression of TFF1 and CDKN1A. {ECO:0000269|PubMed:19343227, ECO:0000269|PubMed:21965678}. |
| 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 |
| Tgene | HDAC2 | chr6:118953616 | chr6:114281182 | ENST00000519065 | 0 | 14 | 300_303 | 17.333333333333332 | 489.0 | Compositional bias | Note=Poly-Gly |
| - 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 |
| Hgene | CEP85L | chr6:118953616 | chr6:114281182 | ENST00000360290 | - | 2 | 6 | 439_682 | 0 | 395.0 | Coiled coil | Ontology_term=ECO:0000255 |
| Hgene | CEP85L | chr6:118953616 | chr6:114281182 | ENST00000368488 | - | 3 | 14 | 439_682 | 80.33333333333333 | 809.0 | Coiled coil | Ontology_term=ECO:0000255 |
| Hgene | CEP85L | chr6:118953616 | chr6:114281182 | ENST00000368491 | - | 2 | 13 | 439_682 | 77.33333333333333 | 806.0 | Coiled coil | Ontology_term=ECO:0000255 |
| Hgene | CEP85L | chr6:118953616 | chr6:114281182 | ENST00000392500 | - | 4 | 8 | 439_682 | 80.33333333333333 | 500.0 | Coiled coil | Ontology_term=ECO:0000255 |
| Hgene | CEP85L | chr6:118953616 | chr6:114281182 | ENST00000419517 | - | 2 | 6 | 439_682 | 77.33333333333333 | 497.0 | Coiled coil | Ontology_term=ECO:0000255 |
| Tgene | HDAC2 | chr6:118953616 | chr6:114281182 | ENST00000519065 | 0 | 14 | 9_322 | 17.333333333333332 | 489.0 | Region | Note=Histone deacetylase |
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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 |
| CEP85L | |
| HDAC2 |
| - 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 |
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Related Drugs to CEP85L-HDAC2 |
| 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 CEP85L-HDAC2 |
| 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 |
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