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 | Fusion Gene Summary |
| Fusion Gene ORF analysis |
| Fusion Genomic Features |
| Fusion Protein Features |
| Fusion Gene Sequence |
| Fusion Gene PPI analysis |
| Related Drugs |
| Related Diseases |
Fusion gene:NIPBL-MAPRE1 (FusionGDB2 ID:HG25836TG22919) |
Fusion Gene Summary for NIPBL-MAPRE1 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: NIPBL-MAPRE1 | Fusion gene ID: hg25836tg22919 | Hgene | Tgene | Gene symbol | NIPBL | MAPRE1 | Gene ID | 25836 | 22919 |
| Gene name | NIPBL cohesin loading factor | microtubule associated protein RP/EB family member 1 | |
| Synonyms | CDLS|CDLS1|IDN3|IDN3-B|Scc2 | EB1 | |
| Cytomap | ('NIPBL')('MAPRE1') 5p13.2 | 20q11.21 | |
| Type of gene | protein-coding | protein-coding | |
| Description | nipped-B-like proteinNipped-B homologSCC2 homologdelanginsister chromatid cohesion 2 homolog | microtubule-associated protein RP/EB family member 1APC-binding protein EB1adenomatous polyposis coli-binding protein EB1end-binding protein 1 | |
| Modification date | 20200313 | 20200313 | |
| UniProtAcc | . | Q15691 | |
| Ensembl transtripts involved in fusion gene | ENST00000282516, ENST00000448238, ENST00000504430, | ||
| Fusion gene scores | * DoF score | 26 X 13 X 16=5408 | 8 X 10 X 5=400 |
| # samples | 43 | 9 | |
| ** MAII score | log2(43/5408*10)=-3.65268658669272 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(9/400*10)=-2.15200309344505 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: NIPBL [Title/Abstract] AND MAPRE1 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint | NIPBL(36877280)-MAPRE1(31413731), # samples:3 | ||
| Anticipated loss of major functional domain due to fusion event. | |||
| * 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 | NIPBL | GO:0000122 | negative regulation of transcription by RNA polymerase II | 18854353 |
| Hgene | NIPBL | GO:0031065 | positive regulation of histone deacetylation | 18854353 |
| Hgene | NIPBL | GO:0045892 | negative regulation of transcription, DNA-templated | 18854353 |
| Hgene | NIPBL | GO:0071921 | cohesin loading | 22628566 |
| Tgene | MAPRE1 | GO:0031115 | negative regulation of microtubule polymerization | 11943150 |
| Tgene | MAPRE1 | GO:0035372 | protein localization to microtubule | 19632184|21820309 |
| 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 | LUSC | TCGA-77-8153-01A | NIPBL | chr5 | 36877280 | - | MAPRE1 | chr20 | 31413731 | + |
| ChimerDB4 | LUSC | TCGA-77-8153-01A | NIPBL | chr5 | 36877280 | + | MAPRE1 | chr20 | 31413731 | + |
| ChimerDB4 | LUSC | TCGA-77-8153 | NIPBL | chr5 | 36877280 | + | MAPRE1 | chr20 | 31413731 | + |
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Fusion Gene ORF analysis for NIPBL-MAPRE1 |
| 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 |
| 5UTR-5UTR | ENST00000282516 | ENST00000375571 | NIPBL | chr5 | 36877280 | + | MAPRE1 | chr20 | 31413731 | + |
| 5UTR-5UTR | ENST00000448238 | ENST00000375571 | NIPBL | chr5 | 36877280 | + | MAPRE1 | chr20 | 31413731 | + |
| intron-5UTR | ENST00000504430 | ENST00000375571 | NIPBL | chr5 | 36877280 | + | MAPRE1 | chr20 | 31413731 | + |
| ORFfinder result based on the fusion transcript sequence of in-frame fusion genes. |
| 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) |
| 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 |
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Fusion Genomic Features for NIPBL-MAPRE1 |
| FusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints. |
| Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
| NIPBL | chr5 | 36877280 | + | MAPRE1 | chr20 | 31413730 | + | 3.91E-11 | 1 |
| NIPBL | chr5 | 36877280 | + | MAPRE1 | chr20 | 31413730 | + | 3.91E-11 | 1 |
| NIPBL | chr5 | 36877280 | + | MAPRE1 | chr20 | 31413730 | + | 3.91E-11 | 1 |
| NIPBL | chr5 | 36877280 | + | MAPRE1 | chr20 | 31413730 | + | 3.91E-11 | 1 |
| Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page. |
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Fusion Protein Features for NIPBL-MAPRE1 |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:36877280/:31413731) - 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 |
| . | MAPRE1 |
| FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. | FUNCTION: Plus-end tracking protein (+TIP) that binds to the plus-end of microtubules and regulates the dynamics of the microtubule cytoskeleton (PubMed:12388762, PubMed:16109370, PubMed:19632184, PubMed:21646404, PubMed:23001180, PubMed:28726242, PubMed:28814570, PubMed:34608293). Promotes cytoplasmic microtubule nucleation and elongation (PubMed:12388762, PubMed:16109370, PubMed:19632184, PubMed:21646404, PubMed:28726242, PubMed:28814570). Involved in mitotic spindle positioning by stabilizing microtubules and promoting dynamic connection between astral microtubules and the cortex during mitotic chromosome segregation (PubMed:12388762, PubMed:34608293). Also acts as a regulator of minus-end microtubule organization: interacts with the complex formed by AKAP9 and PDE4DIP, leading to recruit CAMSAP2 to the Golgi apparatus, thereby tethering non-centrosomal minus-end microtubules to the Golgi, an important step for polarized cell movement (PubMed:28814570). Promotes elongation of CAMSAP2-decorated microtubule stretches on the minus-end of microtubules (PubMed:28814570). Acts as a regulator of autophagosome transport via interaction with CAMSAP2 (PubMed:28726242). May play a role in cell migration (By similarity). {ECO:0000250|UniProtKB:Q61166, ECO:0000269|PubMed:12388762, ECO:0000269|PubMed:16109370, ECO:0000269|PubMed:19632184, ECO:0000269|PubMed:21646404, ECO:0000269|PubMed:23001180, ECO:0000269|PubMed:28726242, ECO:0000269|PubMed:28814570, ECO:0000269|PubMed:34608293}. |
| 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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Fusion Gene Sequence for NIPBL-MAPRE1 |
| For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
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Fusion Gene PPI Analysis for NIPBL-MAPRE1 |
| 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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Related Drugs for NIPBL-MAPRE1 |
| Drugs targeting genes involved in this fusion gene. (DrugBank Version 5.1.8 2021-05-08) |
| Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Related Diseases for NIPBL-MAPRE1 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | NIPBL | C4551851 | Cornelia de Lange Syndrome 1 | 16 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
| Hgene | NIPBL | C0270972 | Cornelia De Lange Syndrome | 8 | CLINGEN;CTD_human |
| Hgene | NIPBL | C1802395 | Congenital muscular hypertrophy-cerebral syndrome | 3 | CTD_human |
| Hgene | NIPBL | C1853099 | Cornelia de Lange Syndrome 3 | 3 | CTD_human |
| Hgene | NIPBL | C0005941 | Bone Diseases, Developmental | 1 | CTD_human |
| Hgene | NIPBL | C0018798 | Congenital Heart Defects | 1 | CTD_human |
| Hgene | NIPBL | C0155536 | Paracousis | 1 | CTD_human |
| Hgene | NIPBL | C0260662 | Hearing problem | 1 | CTD_human |
| Hgene | NIPBL | C0376634 | Craniofacial Abnormalities | 1 | CTD_human |
| Hgene | NIPBL | C0877848 | Distorted hearing | 1 | CTD_human |
| Hgene | NIPBL | C1510450 | Dysacusis | 1 | CTD_human |
| Hgene | NIPBL | C2750805 | Chromosome 5p13 Duplication Syndrome | 1 | ORPHANET |
| Tgene | C0043094 | Weight Gain | 1 | CTD_human | |
| Tgene | C0151744 | Myocardial Ischemia | 1 | CTD_human |
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