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Fusion gene ID: 8073 |
FusionGeneSummary for COPE_PLXNB1 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: COPE_PLXNB1 | Fusion gene ID: 8073 | Hgene | Tgene | Gene symbol | COPE | PLXNB1 | Gene ID | 11316 | 5364 |
| Gene name | coatomer protein complex subunit epsilon | plexin B1 | |
| Synonyms | epsilon-COP | PLEXIN-B1|PLXN5|SEP | |
| Cytomap | 19p13.11 | 3p21.31 | |
| Type of gene | protein-coding | protein-coding | |
| Description | coatomer subunit epsiloncoatomer epsilon subunitepsilon coat protein | plexin-B1plexin 5semaphorin receptor SEP | |
| Modification date | 20180523 | 20180523 | |
| UniProtAcc | O14579 | O43157 | |
| Ensembl transtripts involved in fusion gene | ENST00000262812, ENST00000349893, ENST00000600932, ENST00000598969, ENST00000351079, | ENST00000296440, ENST00000358459, ENST00000358536, ENST00000448774, ENST00000456774, ENST00000465117, | |
| Fusion gene scores | * DoF score | 5 X 5 X 3=75 | 6 X 6 X 3=108 |
| # samples | 5 | 5 | |
| ** MAII score | log2(5/75*10)=-0.584962500721156 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(5/108*10)=-1.11103131238874 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: COPE [Title/Abstract] AND PLXNB1 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Functional or gene categories assigned by FusionGDB annotation | |||
| * 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 |
| Tgene | PLXNB1 | GO:0007162 | negative regulation of cell adhesion | 15218527 |
| Tgene | PLXNB1 | GO:0008360 | regulation of cell shape | 19843518 |
| Tgene | PLXNB1 | GO:0051493 | regulation of cytoskeleton organization | 19843518 |
| Tgene | PLXNB1 | GO:0071526 | semaphorin-plexin signaling pathway | 15218527|19843518 |
| Fusion gene information from three resources (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * 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. |
| Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| ChiTaRS3.1 | AK126476 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| * LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
| Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
| ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| intron-intron | ENST00000262812 | ENST00000296440 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000262812 | ENST00000358459 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000262812 | ENST00000358536 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000262812 | ENST00000448774 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000262812 | ENST00000456774 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000262812 | ENST00000465117 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000349893 | ENST00000296440 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000349893 | ENST00000358459 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000349893 | ENST00000358536 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000349893 | ENST00000448774 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000349893 | ENST00000456774 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000349893 | ENST00000465117 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000600932 | ENST00000296440 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000600932 | ENST00000358459 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000600932 | ENST00000358536 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000600932 | ENST00000448774 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000600932 | ENST00000456774 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000600932 | ENST00000465117 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000598969 | ENST00000296440 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000598969 | ENST00000358459 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000598969 | ENST00000358536 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000598969 | ENST00000448774 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000598969 | ENST00000456774 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000598969 | ENST00000465117 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000351079 | ENST00000296440 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000351079 | ENST00000358459 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000351079 | ENST00000358536 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000351079 | ENST00000448774 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000351079 | ENST00000456774 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
| intron-intron | ENST00000351079 | ENST00000465117 | COPE | chr19 | 19010391 | - | PLXNB1 | chr3 | 48448371 | - |
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FusionProtFeatures for COPE_PLXNB1 |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| COPE | PLXNB1 |
| The coatomer is a cytosolic protein complex that bindsto dilysine motifs and reversibly associates with Golgi non-clathrin-coated vesicles, which further mediate biosyntheticprotein transport from the ER, via the Golgi up to the trans Golginetwork. The coatomer complex is required for budding from Golgimembranes, and is essential for the retrograde Golgi-to-ERtransport of dilysine-tagged proteins. In mammals, the coatomercan only be recruited by membranes associated with ADP-ribosylation factors (ARFs), which are small GTP-binding proteins;the complex also influences the Golgi structural integrity, aswell as the processing, activity, and endocytic recycling of LDLreceptors (By similarity). {ECO:0000250}. | Receptor for SEMA4D. Plays a role in RHOA activation andsubsequent changes of the actin cytoskeleton. Plays a role in axonguidance, invasive growth and cell migration.{ECO:0000269|PubMed:12196628, ECO:0000269|PubMed:12198496,ECO:0000269|PubMed:15210733, ECO:0000269|PubMed:19843518,ECO:0000269|PubMed:20877282, ECO:0000269|PubMed:21912513}. |
| 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. |
| - In-frame and 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 |
| - In-frame and 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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FusionGeneSequence for COPE_PLXNB1 |
| For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. (nt: nucleotides, aa: amino acids) |
| * Fusion amino acid sequences. |
| * Fusion transcript sequences (only coding sequence (CDS) region). |
| * Fusion transcript sequences (Full-length transcript). |
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FusionGenePPI for COPE_PLXNB1 |
| 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 (BIOGRID-3.4.160) |
| Hgene | Hgene's interactors | Tgene | Tgene's interactors |
| - Retained PPIs in in-frame fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost PPIs in in-frame fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
| - Retained PPIs, but lost function due to frame-shift fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for COPE_PLXNB1 |
| Drugs targeting genes involved in this fusion gene. (DrugBank Version 5.1.0 2018-04-02) |
| Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for COPE_PLXNB1 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Copyright 2018-Present -The University of Texas Health Science Center at Houston (UTHealth)
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