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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:FNIP1-NCOR1 (FusionGDB2 ID:30955) |
Fusion Gene Summary for FNIP1-NCOR1 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: FNIP1-NCOR1 | Fusion gene ID: 30955 | Hgene | Tgene | Gene symbol | FNIP1 | NCOR1 | Gene ID | 96459 | 9611 |
| Gene name | folliculin interacting protein 1 | nuclear receptor corepressor 1 | |
| Synonyms | - | N-CoR|N-CoR1|PPP1R109|TRAC1|hN-CoR | |
| Cytomap | 5q31.1 | 17p12-p11.2 | |
| Type of gene | protein-coding | protein-coding | |
| Description | folliculin-interacting protein 1 | nuclear receptor corepressor 1protein phosphatase 1, regulatory subunit 109thyroid hormone- and retinoic acid receptor-associated corepressor 1 | |
| Modification date | 20200327 | 20200313 | |
| UniProtAcc | Q8TF40 | O75376 | |
| Ensembl transtripts involved in fusion gene | ENST00000307954, ENST00000307968, ENST00000510461, ENST00000511848, | ENST00000395848, ENST00000583226, ENST00000268712, ENST00000395851, ENST00000395857, | |
| Fusion gene scores | * DoF score | 15 X 11 X 10=1650 | 14 X 14 X 6=1176 |
| # samples | 18 | 14 | |
| ** MAII score | log2(18/1650*10)=-3.1963972128035 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(14/1176*10)=-3.0703893278914 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: FNIP1 [Title/Abstract] AND NCOR1 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint | FNIP1(131080257)-NCOR1(15952302), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | FNIP1-NCOR1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. FNIP1-NCOR1 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF. FNIP1-NCOR1 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF. FNIP1-NCOR1 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor 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 |
| Hgene | FNIP1 | GO:0000122 | negative regulation of transcription by RNA polymerase II | 21209915 |
| Hgene | FNIP1 | GO:0001932 | regulation of protein phosphorylation | 18663353 |
| Hgene | FNIP1 | GO:0031334 | positive regulation of protein complex assembly | 25126726 |
| Hgene | FNIP1 | GO:0033138 | positive regulation of peptidyl-serine phosphorylation | 19914239 |
| Tgene | NCOR1 | GO:0046329 | negative regulation of JNK cascade | 11931768 |
| Fusion gene breakpoints across FNIP1 (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 NCOR1 (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
| 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-EQ-A4SO-01A | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
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Fusion Gene ORF analysis for FNIP1-NCOR1 |
| 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 |
| 5CDS-intron | ENST00000307954 | ENST00000395848 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| 5CDS-intron | ENST00000307954 | ENST00000583226 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| 5CDS-intron | ENST00000307968 | ENST00000395848 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| 5CDS-intron | ENST00000307968 | ENST00000583226 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| 5CDS-intron | ENST00000510461 | ENST00000395848 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| 5CDS-intron | ENST00000510461 | ENST00000583226 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| 5CDS-intron | ENST00000511848 | ENST00000395848 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| 5CDS-intron | ENST00000511848 | ENST00000583226 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000307954 | ENST00000268712 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000307954 | ENST00000395851 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000307954 | ENST00000395857 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000307968 | ENST00000268712 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000307968 | ENST00000395851 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000307968 | ENST00000395857 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000510461 | ENST00000268712 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000510461 | ENST00000395851 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000510461 | ENST00000395857 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000511848 | ENST00000268712 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000511848 | ENST00000395851 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| Frame-shift | ENST00000511848 | ENST00000395857 | FNIP1 | chr5 | 131080257 | - | NCOR1 | chr17 | 15952302 | - |
| 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 FNIP1-NCOR1 |
| 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) |
| Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page. |
| 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 FNIP1-NCOR1 |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:131080257/:15952302) - 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 |
| FNIP1 | NCOR1 |
| FUNCTION: Binding partner of the GTPase-activating protein FLCN: involved in the cellular response to amino acid availability by regulating the mTORC1 signaling cascade controlling the MiT/TFE factors TFEB and TFE3 (PubMed:17028174, PubMed:18663353, PubMed:24081491). In low-amino acid conditions, component of the lysosomal folliculin complex (LFC) on the membrane of lysosomes, which inhibits the GTPase-activating activity of FLCN, thereby inactivating mTORC1 and promoting nuclear translocation of TFEB and TFE3 (By similarity). Upon amino acid restimulation, disassembly of the LFC complex liberates the GTPase-activating activity of FLCN, leading to activation of mTORC1 and subsequent cytoplasmic retention of TFEB and TFE3 (By similarity). Required to promote FLCN recruitment to lysosomes and interaction with Rag GTPases (PubMed:24081491). Together with FLCN, regulates autophagy: following phosphorylation by ULK1, interacts with GABARAP and promotes autophagy (PubMed:25126726). In addition to its role in mTORC1 signaling, also acts as a co-chaperone of HSP90AA1/Hsp90: following gradual phosphorylation by CK2, inhibits the ATPase activity of HSP90AA1/Hsp90, leading to activate both kinase and non-kinase client proteins of HSP90AA1/Hsp90 (PubMed:27353360, PubMed:30699359). Acts as a scaffold to load client protein FLCN onto HSP90AA1/Hsp90 (PubMed:27353360). Competes with the activating co-chaperone AHSA1 for binding to HSP90AA1, thereby providing a reciprocal regulatory mechanism for chaperoning of client proteins (PubMed:27353360). Required for B-cell development (By similarity). {ECO:0000250|UniProtKB:Q68FD7, ECO:0000250|UniProtKB:Q9P278, ECO:0000269|PubMed:17028174, ECO:0000269|PubMed:18663353, ECO:0000269|PubMed:24081491, ECO:0000269|PubMed:25126726, ECO:0000269|PubMed:27353360, ECO:0000269|PubMed:30699359}. | FUNCTION: Mediates transcriptional repression by certain nuclear receptors (PubMed:20812024). Part of a complex which promotes histone deacetylation and the formation of repressive chromatin structures which may impede the access of basal transcription factors. Participates in the transcriptional repressor activity produced by BCL6. Recruited by ZBTB7A to the androgen response elements/ARE on target genes, negatively regulates androgen receptor signaling and androgen-induced cell proliferation (PubMed:20812024). Mediates the NR1D1-dependent repression and circadian regulation of TSHB expression (By similarity). The NCOR1-HDAC3 complex regulates the circadian expression of the core clock gene ARTNL/BMAL1 and the genes involved in lipid metabolism in the liver (By similarity). {ECO:0000250|UniProtKB:Q60974, ECO:0000269|PubMed:14527417, ECO:0000269|PubMed:20812024}. |
| 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 FNIP1-NCOR1 |
| 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 FNIP1-NCOR1 |
| 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 FNIP1-NCOR1 |
| 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 FNIP1-NCOR1 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
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