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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:APOC2-NOXRED1 (FusionGDB2 ID:5559)

Fusion Gene Summary for APOC2-NOXRED1

check button Fusion gene summary
Fusion gene informationFusion gene name: APOC2-NOXRED1
Fusion gene ID: 5559
HgeneTgene
Gene symbol

APOC2

NOXRED1

Gene ID

344

122945

Gene nameapolipoprotein C2NADP dependent oxidoreductase domain containing 1
SynonymsAPO-CII|APOC-IIC14orf148
Cytomap

19q13.32

14q24.3

Type of geneprotein-codingprotein-coding
Descriptionapolipoprotein C-IINADP-dependent oxidoreductase domain-containing protein 1pyrroline-5-carboxylate reductase-like protein C14orf148
Modification date2020031320200313
UniProtAcc

P02655

Q6NXP6

Ensembl transtripts involved in fusion geneENST00000252490, ENST00000591597, 
ENST00000592257, ENST00000585786, 
ENST00000590360, 
ENST00000380835, 
ENST00000298358, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 2=8
# samples 12
** MAII scorelog2(1/1*10)=3.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: APOC2 [Title/Abstract] AND NOXRED1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointAPOC2(45449332)-NOXRED1(77872478), # 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
HgeneAPOC2

GO:0010518

positive regulation of phospholipase activity

10727238

HgeneAPOC2

GO:0010898

positive regulation of triglyceride catabolic process

10727238

HgeneAPOC2

GO:0010916

negative regulation of very-low-density lipoprotein particle clearance

1917954

HgeneAPOC2

GO:0033344

cholesterol efflux

11162594

HgeneAPOC2

GO:0033700

phospholipid efflux

11162594

HgeneAPOC2

GO:0034382

chylomicron remnant clearance

4020294

HgeneAPOC2

GO:0045723

positive regulation of fatty acid biosynthetic process

10727238

HgeneAPOC2

GO:0045833

negative regulation of lipid metabolic process

182536

HgeneAPOC2

GO:0048261

negative regulation of receptor-mediated endocytosis

1917954

HgeneAPOC2

GO:0051006

positive regulation of lipoprotein lipase activity

10727238|15878877

HgeneAPOC2

GO:0060697

positive regulation of phospholipid catabolic process

10727238


check buttonFusion gene breakpoints across APOC2 (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 NOXRED1 (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
ChimerDB4LIHCTCGA-NI-A4U2APOC2chr19

45449332

+NOXRED1chr14

77872478

-


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Fusion Gene ORF analysis for APOC2-NOXRED1

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-3CDSENST00000252490ENST00000380835APOC2chr19

45449332

+NOXRED1chr14

77872478

-
5UTR-3CDSENST00000591597ENST00000380835APOC2chr19

45449332

+NOXRED1chr14

77872478

-
5UTR-3CDSENST00000592257ENST00000380835APOC2chr19

45449332

+NOXRED1chr14

77872478

-
5UTR-intronENST00000252490ENST00000298358APOC2chr19

45449332

+NOXRED1chr14

77872478

-
5UTR-intronENST00000591597ENST00000298358APOC2chr19

45449332

+NOXRED1chr14

77872478

-
5UTR-intronENST00000592257ENST00000298358APOC2chr19

45449332

+NOXRED1chr14

77872478

-
intron-3CDSENST00000585786ENST00000380835APOC2chr19

45449332

+NOXRED1chr14

77872478

-
intron-3CDSENST00000590360ENST00000380835APOC2chr19

45449332

+NOXRED1chr14

77872478

-
intron-intronENST00000585786ENST00000298358APOC2chr19

45449332

+NOXRED1chr14

77872478

-
intron-intronENST00000590360ENST00000298358APOC2chr19

45449332

+NOXRED1chr14

77872478

-

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 APOC2-NOXRED1


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 APOC2-NOXRED1


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/:45449332/:77872478)
- 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
APOC2

P02655

NOXRED1

Q6NXP6

FUNCTION: Component of chylomicrons, very low-density lipoproteins (VLDL), low-density lipoproteins (LDL), and high-density lipoproteins (HDL) in plasma. Plays an important role in lipoprotein metabolism as an activator of lipoprotein lipase. Both proapolipoprotein C-II and apolipoprotein C-II can activate lipoprotein lipase. In normolipidemic individuals, it is mainly distributed in the HDL, whereas in hypertriglyceridemic individuals, predominantly found in the VLDL and LDL. {ECO:0000269|PubMed:2209608, ECO:0000303|PubMed:22304839}.FUNCTION: Probable oxidoreductase. {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 APOC2-NOXRED1


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 APOC2-NOXRED1


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 APOC2-NOXRED1


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 APOC2-NOXRED1


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