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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:MORC2-APOC3 (FusionGDB2 ID:54586)

Fusion Gene Summary for MORC2-APOC3

check button Fusion gene summary
Fusion gene informationFusion gene name: MORC2-APOC3
Fusion gene ID: 54586
HgeneTgene
Gene symbol

MORC2

APOC3

Gene ID

22880

345

Gene nameMORC family CW-type zinc finger 2apolipoprotein C3
SynonymsCMT2Z|ZCW3|ZCWCC1APOCIII
Cytomap

22q12.2

11q23.3

Type of geneprotein-codingprotein-coding
DescriptionATPase MORC2zinc finger CW-type coiled-coil domain protein 1apolipoprotein C-III
Modification date2020031320200313
UniProtAcc

Q9Y6X9

P02656

Ensembl transtripts involved in fusion geneENST00000215862, ENST00000397641, 
ENST00000469915, 
ENST00000227667, 
ENST00000375345, ENST00000470144, 
Fusion gene scores* DoF score2 X 3 X 3=184 X 3 X 3=36
# samples 34
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/36*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MORC2 [Title/Abstract] AND APOC3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMORC2(31328637)-APOC3(116703480), # samples:2
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
HgeneMORC2

GO:0006338

chromatin remodeling

23260667

HgeneMORC2

GO:0006974

cellular response to DNA damage stimulus

23260667

HgeneMORC2

GO:0045814

negative regulation of gene expression, epigenetic

28581500|29211708

HgeneMORC2

GO:0090309

positive regulation of methylation-dependent chromatin silencing

28581500|29211708

TgeneAPOC3

GO:0007186

G protein-coupled receptor signaling pathway

16443932

TgeneAPOC3

GO:0010897

negative regulation of triglyceride catabolic process

3973011|18635818

TgeneAPOC3

GO:0010903

negative regulation of very-low-density lipoprotein particle remodeling

3973011

TgeneAPOC3

GO:0010916

negative regulation of very-low-density lipoprotein particle clearance

1917954

TgeneAPOC3

GO:0019433

triglyceride catabolic process

11060345

TgeneAPOC3

GO:0032489

regulation of Cdc42 protein signal transduction

16443932

TgeneAPOC3

GO:0033344

cholesterol efflux

11162594|16443932

TgeneAPOC3

GO:0033700

phospholipid efflux

11162594

TgeneAPOC3

GO:0034382

chylomicron remnant clearance

4020294

TgeneAPOC3

GO:0045717

negative regulation of fatty acid biosynthetic process

11060345|18635818

TgeneAPOC3

GO:0045833

negative regulation of lipid metabolic process

182536

TgeneAPOC3

GO:0048261

negative regulation of receptor-mediated endocytosis

1917954

TgeneAPOC3

GO:0050995

negative regulation of lipid catabolic process

15576844

TgeneAPOC3

GO:0051005

negative regulation of lipoprotein lipase activity

3973011|11060345|18635818


check buttonFusion gene breakpoints across MORC2 (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 APOC3 (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-A4U2-01AMORC2chr22

31328637

-APOC3chr11

116703480

+
ChimerDB4LIHCTCGA-ZS-A9CE-01AMORC2chr22

31328637

-APOC3chr11

116703480

+


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Fusion Gene ORF analysis for MORC2-APOC3

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-3CDSENST00000215862ENST00000227667MORC2chr22

31328637

-APOC3chr11

116703480

+
intron-3CDSENST00000215862ENST00000375345MORC2chr22

31328637

-APOC3chr11

116703480

+
intron-3CDSENST00000397641ENST00000227667MORC2chr22

31328637

-APOC3chr11

116703480

+
intron-3CDSENST00000397641ENST00000375345MORC2chr22

31328637

-APOC3chr11

116703480

+
intron-3CDSENST00000469915ENST00000227667MORC2chr22

31328637

-APOC3chr11

116703480

+
intron-3CDSENST00000469915ENST00000375345MORC2chr22

31328637

-APOC3chr11

116703480

+
intron-intronENST00000215862ENST00000470144MORC2chr22

31328637

-APOC3chr11

116703480

+
intron-intronENST00000397641ENST00000470144MORC2chr22

31328637

-APOC3chr11

116703480

+
intron-intronENST00000469915ENST00000470144MORC2chr22

31328637

-APOC3chr11

116703480

+

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 MORC2-APOC3


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 MORC2-APOC3


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/:31328637/:116703480)
- 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
MORC2

Q9Y6X9

APOC3

P02656

FUNCTION: Essential for epigenetic silencing by the HUSH (human silencing hub) complex. Recruited by HUSH to target site in heterochromatin, the ATPase activity and homodimerization are critical for HUSH-mediated silencing (PubMed:28581500, PubMed:29440755). Represses germ cell-related genes and L1 retrotransposons in collaboration with SETDB1 and the HUSH complex, the silencing is dependent of repressive epigenetic modifications, such as H3K9me3 mark. Silencing events often occur within introns of transcriptionally active genes, and lead to the down-regulation of host gene expression (PubMed:29211708). During DNA damage response, regulates chromatin remodeling through ATP hydrolysis. Upon DNA damage, is phosphorylated by PAK1, both colocalize to chromatin and induce H2AX expression. ATPase activity is required and dependent of phosphorylation by PAK1 and presence of DNA (PubMed:23260667). Recruits histone deacetylases, such as HDAC4, to promoter regions, causing local histone H3 deacetylation and transcriptional repression of genes such as CA9 (PubMed:20225202, PubMed:20110259). Exhibits a cytosolic function in lipogenesis, adipogenic differentiation, and lipid homeostasis by increasing the activity of ACLY, possibly preventing its dephosphorylation (PubMed:24286864). {ECO:0000269|PubMed:20110259, ECO:0000269|PubMed:20225202, ECO:0000269|PubMed:23260667, ECO:0000269|PubMed:24286864, ECO:0000269|PubMed:28581500, ECO:0000269|PubMed:29211708, ECO:0000269|PubMed:29440755}.FUNCTION: Component of triglyceride-rich very low density lipoproteins (VLDL) and high density lipoproteins (HDL) in plasma (PubMed:18201179, PubMed:22510806). Plays a multifaceted role in triglyceride homeostasis (PubMed:18201179, PubMed:22510806). Intracellularly, promotes hepatic very low density lipoprotein 1 (VLDL1) assembly and secretion; extracellularly, attenuates hydrolysis and clearance of triglyceride-rich lipoproteins (TRLs) (PubMed:18201179, PubMed:22510806). Impairs the lipolysis of TRLs by inhibiting lipoprotein lipase and the hepatic uptake of TRLs by remnant receptors (PubMed:18201179, PubMed:22510806). Formed of several curved helices connected via semiflexible hinges, so that it can wrap tightly around the curved micelle surface and easily adapt to the different diameters of its natural binding partners (PubMed:18408013). {ECO:0000269|PubMed:18408013, ECO:0000303|PubMed:18201179, ECO:0000303|PubMed:22510806}.

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 MORC2-APOC3


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 MORC2-APOC3


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 MORC2-APOC3


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 MORC2-APOC3


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