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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:EGFL7-NOC4L (FusionGDB2 ID:HG51162TG79050)

Fusion Gene Summary for EGFL7-NOC4L

check button Fusion gene summary
Fusion gene informationFusion gene name: EGFL7-NOC4L
Fusion gene ID: hg51162tg79050
HgeneTgene
Gene symbol

EGFL7

NOC4L

Gene ID

51162

79050

Gene nameEGF like domain multiple 7nucleolar complex associated 4 homolog
SynonymsNEU1|VE-STATIN|ZNEU1NET49|NOC4|UTP19
Cytomap('EGFL7')('NOC4L')

9q34.3

12q24.33

Type of geneprotein-codingprotein-coding
Descriptionepidermal growth factor-like protein 7EGF-like protein 7NOTCH4-like proteinmultiple EGF-like domains protein 7multiple epidermal growth factor-like domains protein 7vascular endothelial statinnucleolar complex protein 4 homologNOC4 protein homologNOC4-like proteinnucleolar complex-associated protein 4-like protein
Modification date2020031320200313
UniProtAcc.

Q9BVI4

Ensembl transtripts involved in fusion geneENST00000308874, ENST00000371699, 
ENST00000406555, ENST00000371698, 
ENST00000492002, 
Fusion gene scores* DoF score4 X 2 X 2=1636 X 4 X 20=2880
# samples 441
** MAII scorelog2(4/16*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(41/2880*10)=-2.81237299682423
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: EGFL7 [Title/Abstract] AND NOC4L [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointEGFL7(139559237)-NOC4L(132635526), # 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


check button Fusion gene information
* 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
ChimerDB4STADTCGA-FP-8210-01AEGFL7chr9

139559237

+NOC4Lchr12

132635526

+


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Fusion Gene ORF analysis for EGFL7-NOC4L

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
5UTR-3CDSENST00000308874ENST00000330579EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
5UTR-3CDSENST00000371699ENST00000330579EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
5UTR-3CDSENST00000406555ENST00000330579EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
5UTR-5UTRENST00000308874ENST00000538784EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
5UTR-5UTRENST00000371699ENST00000538784EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
5UTR-5UTRENST00000406555ENST00000538784EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
5UTR-intronENST00000308874ENST00000535343EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
5UTR-intronENST00000371699ENST00000535343EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
5UTR-intronENST00000406555ENST00000535343EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
intron-3CDSENST00000371698ENST00000330579EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
intron-3CDSENST00000492002ENST00000330579EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
intron-5UTRENST00000371698ENST00000538784EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
intron-5UTRENST00000492002ENST00000538784EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
intron-intronENST00000371698ENST00000535343EGFL7chr9

139559237

+NOC4Lchr12

132635526

+
intron-intronENST00000492002ENST00000535343EGFL7chr9

139559237

+NOC4Lchr12

132635526

+

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 EGFL7-NOC4L


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)
EGFL7chr9139559237+NOC4Lchr12132635525+0.54937290.4506271
EGFL7chr9139559237+NOC4Lchr12132635525+0.54937290.4506271


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.
genomic feature of top 1%

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Fusion Protein Features for EGFL7-NOC4L


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/:139559237/:132635526)
- 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
.NOC4L

Q9BVI4

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}.

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 EGFL7-NOC4L


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 EGFL7-NOC4L


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 EGFL7-NOC4L


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 EGFL7-NOC4L


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