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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:NCOR1-FBLN5 (FusionGDB2 ID:57833)

Fusion Gene Summary for NCOR1-FBLN5

check button Fusion gene summary
Fusion gene informationFusion gene name: NCOR1-FBLN5
Fusion gene ID: 57833
HgeneTgene
Gene symbol

NCOR1

FBLN5

Gene ID

9611

10516

Gene namenuclear receptor corepressor 1fibulin 5
SynonymsN-CoR|N-CoR1|PPP1R109|TRAC1|hN-CoRADCL2|ARCL1A|ARMD3|DANCE|EVEC|FIBL-5|HNARMD|UP50
Cytomap

17p12-p11.2

14q32.12

Type of geneprotein-codingprotein-coding
Descriptionnuclear receptor corepressor 1protein phosphatase 1, regulatory subunit 109thyroid hormone- and retinoic acid receptor-associated corepressor 1fibulin-5developmental arteries and neural crest EGF-like proteinembryonic vascular EGF-like repeat-containing proteintestis tissue sperm-binding protein Li 75nurine p50 protein
Modification date2020031320200313
UniProtAcc

O75376

Q9UBX5

Ensembl transtripts involved in fusion geneENST00000268712, ENST00000395848, 
ENST00000395851, ENST00000395857, 
ENST00000583226, 
ENST00000267620, 
ENST00000342058, ENST00000556154, 
ENST00000556961, 
Fusion gene scores* DoF score30 X 30 X 13=1170011 X 8 X 7=616
# samples 3315
** MAII scorelog2(33/11700*10)=-5.14789869511231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/616*10)=-2.03796785019902
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NCOR1 [Title/Abstract] AND FBLN5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNCOR1(15935258)-FBLN5(92349986), # samples:1
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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneNCOR1

GO:0046329

negative regulation of JNK cascade

11931768

TgeneFBLN5

GO:0046903

secretion

20599547


check buttonFusion gene breakpoints across NCOR1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across FBLN5 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/AAF044209NCOR1chr17

15935258

-FBLN5chr14

92349986

+


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Fusion Gene ORF analysis for NCOR1-FBLN5

check button 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.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
intron-intronENST00000268712ENST00000267620NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000268712ENST00000342058NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000268712ENST00000556154NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000268712ENST00000556961NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395848ENST00000267620NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395848ENST00000342058NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395848ENST00000556154NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395848ENST00000556961NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395851ENST00000267620NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395851ENST00000342058NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395851ENST00000556154NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395851ENST00000556961NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395857ENST00000267620NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395857ENST00000342058NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395857ENST00000556154NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000395857ENST00000556961NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000583226ENST00000267620NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000583226ENST00000342058NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000583226ENST00000556154NCOR1chr17

15935258

-FBLN5chr14

92349986

+
intron-intronENST00000583226ENST00000556961NCOR1chr17

15935258

-FBLN5chr14

92349986

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF 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.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for NCOR1-FBLN5


check buttonFusionAI 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.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution 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.

check buttonDistribution 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 NCOR1-FBLN5


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:15935258/:92349986)
- 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.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NCOR1

O75376

FBLN5

Q9UBX5

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}.FUNCTION: Essential for elastic fiber formation, is involved in the assembly of continuous elastin (ELN) polymer and promotes the interaction of microfibrils and ELN (PubMed:18185537). Stabilizes and organizes elastic fibers in the skin, lung and vasculature (By similarity). Promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. Vascular ligand for integrin receptors which may play a role in vascular development and remodeling (PubMed:10428823). May act as an adapter that mediates the interaction between FBN1 and ELN (PubMed:17255108). {ECO:0000250|UniProtKB:Q9WVH9, ECO:0000269|PubMed:10428823, ECO:0000269|PubMed:17255108, ECO:0000269|PubMed:18185537}.

check buttonRetention 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

download page


* 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.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for NCOR1-FBLN5


check button 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 NCOR1-FBLN5


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for NCOR1-FBLN5


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for NCOR1-FBLN5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource