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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:PPM1G-FOXO3 (FusionGDB2 ID:HG5496TG2309)

Fusion Gene Summary for PPM1G-FOXO3

check button Fusion gene summary
Fusion gene informationFusion gene name: PPM1G-FOXO3
Fusion gene ID: hg5496tg2309
HgeneTgene
Gene symbol

PPM1G

FOXO3

Gene ID

5496

2309

Gene nameprotein phosphatase, Mg2+/Mn2+ dependent 1Gforkhead box O3
SynonymsPP2CG|PP2CGAMMA|PPP2CGAF6q21|FKHRL1|FKHRL1P2|FOXO2|FOXO3A
Cytomap('PPM1G')('FOXO3')

2p23.3

6q21

Type of geneprotein-codingprotein-coding
Descriptionprotein phosphatase 1GPP2C-gammaprotein phosphatase 1Cprotein phosphatase 1G (formerly 2C), magnesium-dependent, gamma isoformprotein phosphatase 2, catalytic subunit, gamma isoformprotein phosphatase 2C gamma isoformprotein phosphatase 2C isoform gforkhead box protein O3forkhead box O3Aforkhead homolog (rhabdomyosarcoma) like 1forkhead in rhabdomyosarcoma-like 1forkhead, Drosophila, homolog of, in rhabdomyosarcoma-like 1
Modification date2020031320200329
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000344034, ENST00000350803, 
Fusion gene scores* DoF score14 X 12 X 5=84010 X 7 X 6=420
# samples 1710
** MAII scorelog2(17/840*10)=-2.30485458152842
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/420*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PPM1G [Title/Abstract] AND FOXO3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPPM1G(27604640)-FOXO3(108915984), # 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
HgenePPM1G

GO:0035970

peptidyl-threonine dephosphorylation

20801214

TgeneFOXO3

GO:0000122

negative regulation of transcription by RNA polymerase II

20371612

TgeneFOXO3

GO:0006417

regulation of translation

21329882

TgeneFOXO3

GO:0043065

positive regulation of apoptotic process

20371612

TgeneFOXO3

GO:0045648

positive regulation of erythrocyte differentiation

14734530

TgeneFOXO3

GO:0045893

positive regulation of transcription, DNA-templated

10102273|15084260

TgeneFOXO3

GO:0045944

positive regulation of transcription by RNA polymerase II

10102273|14734530



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/ABE149668PPM1Gchr2

27604640

+FOXO3chr6

108915984

+


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Fusion Gene ORF analysis for PPM1G-FOXO3

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-intronENST00000344034ENST00000343882PPM1Gchr2

27604640

+FOXO3chr6

108915984

+
intron-intronENST00000344034ENST00000406360PPM1Gchr2

27604640

+FOXO3chr6

108915984

+
intron-intronENST00000344034ENST00000540898PPM1Gchr2

27604640

+FOXO3chr6

108915984

+
intron-intronENST00000350803ENST00000343882PPM1Gchr2

27604640

+FOXO3chr6

108915984

+
intron-intronENST00000350803ENST00000406360PPM1Gchr2

27604640

+FOXO3chr6

108915984

+
intron-intronENST00000350803ENST00000540898PPM1Gchr2

27604640

+FOXO3chr6

108915984

+

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 PPM1G-FOXO3


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)


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Fusion Protein Features for PPM1G-FOXO3


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/:27604640/:108915984)
- 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
..
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}.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 PPM1G-FOXO3


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 PPM1G-FOXO3


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 PPM1G-FOXO3


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 PPM1G-FOXO3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePPM1GC0001956Alcohol Use Disorder1PSYGENET
TgeneC0002152Alloxan Diabetes2CTD_human
TgeneC0011853Diabetes Mellitus, Experimental2CTD_human
TgeneC0038433Streptozotocin Diabetes2CTD_human
TgeneC0007131Non-Small Cell Lung Carcinoma1CTD_human
TgeneC0010606Adenoid Cystic Carcinoma1CTD_human
TgeneC0014072Experimental Autoimmune Encephalomyelitis1CTD_human
TgeneC0024117Chronic Obstructive Airway Disease1CTD_human
TgeneC0028754Obesity1CTD_human
TgeneC0152013Adenocarcinoma of lung (disorder)1CTD_human
TgeneC1527303Chronic Airflow Obstruction1CTD_human