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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:NEU4-NOC4L (FusionGDB2 ID:58643)

Fusion Gene Summary for NEU4-NOC4L

check button Fusion gene summary
Fusion gene informationFusion gene name: NEU4-NOC4L
Fusion gene ID: 58643
HgeneTgene
Gene symbol

NEU4

NOC4L

Gene ID

129807

79050

Gene nameneuraminidase 4nucleolar complex associated 4 homolog
Synonyms-NET49|NOC4|UTP19
Cytomap

2q37.3

12q24.33

Type of geneprotein-codingprotein-coding
Descriptionsialidase-4N-acetyl-alpha-neuraminidase 4neuraminidase 4 (sialidase)nucleolar complex protein 4 homologNOC4 protein homologNOC4-like proteinnucleolar complex-associated protein 4-like protein
Modification date2020031320200313
UniProtAcc

Q8WWR8

Q9BVI4

Ensembl transtripts involved in fusion geneENST00000405370, ENST00000407683, 
ENST00000325935, ENST00000391969, 
ENST00000404257, 
ENST00000330579, 
ENST00000538784, ENST00000535343, 
Fusion gene scores* DoF score1 X 1 X 1=136 X 4 X 20=2880
# samples 141
** MAII scorelog2(1/1*10)=3.32192809488736log2(41/2880*10)=-2.81237299682423
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NEU4 [Title/Abstract] AND NOC4L [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNEU4(242750369)-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
HgeneNEU4

GO:0006516

glycoprotein catabolic process

15213228

HgeneNEU4

GO:0006689

ganglioside catabolic process

15213228

HgeneNEU4

GO:0009313

oligosaccharide catabolic process

15213228


check buttonFusion gene breakpoints across NEU4 (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 NOC4L (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
ChimerDB4Non-CancerTCGA-BR-7851-11ANEU4chr2

242750369

+NOC4Lchr12

132635526

+


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Fusion Gene ORF analysis for NEU4-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-3CDSENST00000405370ENST00000330579NEU4chr2

242750369

+NOC4Lchr12

132635526

+
5UTR-3CDSENST00000407683ENST00000330579NEU4chr2

242750369

+NOC4Lchr12

132635526

+
5UTR-5UTRENST00000405370ENST00000538784NEU4chr2

242750369

+NOC4Lchr12

132635526

+
5UTR-5UTRENST00000407683ENST00000538784NEU4chr2

242750369

+NOC4Lchr12

132635526

+
5UTR-intronENST00000405370ENST00000535343NEU4chr2

242750369

+NOC4Lchr12

132635526

+
5UTR-intronENST00000407683ENST00000535343NEU4chr2

242750369

+NOC4Lchr12

132635526

+
intron-3CDSENST00000325935ENST00000330579NEU4chr2

242750369

+NOC4Lchr12

132635526

+
intron-3CDSENST00000391969ENST00000330579NEU4chr2

242750369

+NOC4Lchr12

132635526

+
intron-3CDSENST00000404257ENST00000330579NEU4chr2

242750369

+NOC4Lchr12

132635526

+
intron-5UTRENST00000325935ENST00000538784NEU4chr2

242750369

+NOC4Lchr12

132635526

+
intron-5UTRENST00000391969ENST00000538784NEU4chr2

242750369

+NOC4Lchr12

132635526

+
intron-5UTRENST00000404257ENST00000538784NEU4chr2

242750369

+NOC4Lchr12

132635526

+
intron-intronENST00000325935ENST00000535343NEU4chr2

242750369

+NOC4Lchr12

132635526

+
intron-intronENST00000391969ENST00000535343NEU4chr2

242750369

+NOC4Lchr12

132635526

+
intron-intronENST00000404257ENST00000535343NEU4chr2

242750369

+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 NEU4-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)
NEU4chr2242750369+NOC4Lchr12132635525+0.148253780.8517462
NEU4chr2242750369+NOC4Lchr12132635525+0.148253780.8517462

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.
genomic feature of top 1%

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Fusion Protein Features for NEU4-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/:242750369/: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
NEU4

Q8WWR8

NOC4L

Q9BVI4

FUNCTION: Exo-alpha-sialidase that catalyzes the hydrolytic cleavage of the terminal sialic acid (N-acetylneuraminic acid, Neu5Ac) of a glycan moiety in the catabolism of glycolipids, glycoproteins and oligosacharides. Efficiently hydrolyzes gangliosides including alpha-(2->3)-sialylated GD1a and GM3 and alpha-(2->8)-sialylated GD3 (PubMed:15847605, PubMed:21521691, PubMed:15213228). Hydrolyzes poly-alpha-(2->8)-sialylated neural cell adhesion molecule NCAM1 likely at growth cones, suppressing neurite outgrowth in hippocampal neurons (By similarity). May desialylate sialyl Lewis A and X antigens at the cell surface, down-regulating these glycan epitopes recognized by SELE/E selectin in the initiation of cell adhesion and extravasation (PubMed:21521691). Has sialidase activity toward mucin, fetuin and sialyllactose (PubMed:15847605). {ECO:0000250|UniProtKB:Q8BZL1, ECO:0000269|PubMed:15213228, ECO:0000269|PubMed:15847605, ECO:0000269|PubMed:21521691}.

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 NEU4-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 NEU4-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 NEU4-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 NEU4-NOC4L


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