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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:MAP2K2-DAPK3 (FusionGDB2 ID:HG5605TG1613)

Fusion Gene Summary for MAP2K2-DAPK3

check button Fusion gene summary
Fusion gene informationFusion gene name: MAP2K2-DAPK3
Fusion gene ID: hg5605tg1613
HgeneTgene
Gene symbol

MAP2K2

DAPK3

Gene ID

5605

1613

Gene namemitogen-activated protein kinase kinase 2death associated protein kinase 3
SynonymsCFC4|MAPKK2|MEK2|MKK2|PRKMK2DLK|ZIP|ZIPK
Cytomap('MAP2K2')('DAPK3')

19p13.3

19p13.3

Type of geneprotein-codingprotein-coding
Descriptiondual specificity mitogen-activated protein kinase kinase 2ERK activator kinase 2MAP kinase kinase 2MAPK/ERK kinase 2mitogen-activated protein kinase kinase 2, p45death-associated protein kinase 3DAP kinase 3DAP-like kinaseMYPT1 kinaseZIP-kinasezipper-interacting protein kinase
Modification date2020032720200329
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000262948, ENST00000394867, 
ENST00000599345, 
Fusion gene scores* DoF score10 X 6 X 6=3604 X 4 X 3=48
# samples 104
** MAII scorelog2(10/360*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MAP2K2 [Title/Abstract] AND DAPK3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMAP2K2(4123781)-DAPK3(3969827), # 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
HgeneMAP2K2

GO:0036289

peptidyl-serine autophosphorylation

8388392

HgeneMAP2K2

GO:0071902

positive regulation of protein serine/threonine kinase activity

8388392

TgeneDAPK3

GO:0006468

protein phosphorylation

10356987

TgeneDAPK3

GO:0006915

apoptotic process

10580117

TgeneDAPK3

GO:0017148

negative regulation of translation

18995835

TgeneDAPK3

GO:0035556

intracellular signal transduction

10356987

TgeneDAPK3

GO:0043065

positive regulation of apoptotic process

21487036

TgeneDAPK3

GO:0046777

protein autophosphorylation

18239682

TgeneDAPK3

GO:0051893

regulation of focal adhesion assembly

23454120

TgeneDAPK3

GO:0071346

cellular response to interferon-gamma

18995835

TgeneDAPK3

GO:2000249

regulation of actin cytoskeleton reorganization

23454120



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-BR-4187-01AMAP2K2chr19

4123781

-DAPK3chr19

3969827

-


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Fusion Gene ORF analysis for MAP2K2-DAPK3

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
5CDS-5UTRENST00000262948ENST00000301264MAP2K2chr19

4123781

-DAPK3chr19

3969827

-
5CDS-5UTRENST00000262948ENST00000545797MAP2K2chr19

4123781

-DAPK3chr19

3969827

-
5UTR-5UTRENST00000394867ENST00000301264MAP2K2chr19

4123781

-DAPK3chr19

3969827

-
5UTR-5UTRENST00000394867ENST00000545797MAP2K2chr19

4123781

-DAPK3chr19

3969827

-
5UTR-5UTRENST00000599345ENST00000301264MAP2K2chr19

4123781

-DAPK3chr19

3969827

-
5UTR-5UTRENST00000599345ENST00000545797MAP2K2chr19

4123781

-DAPK3chr19

3969827

-

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 MAP2K2-DAPK3


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 MAP2K2-DAPK3


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/:4123781/:3969827)
- 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 MAP2K2-DAPK3


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 MAP2K2-DAPK3


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 MAP2K2-DAPK3


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 MAP2K2-DAPK3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMAP2K2C1275081Cardio-facio-cutaneous syndrome13CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneMAP2K2C3809007CARDIOFACIOCUTANEOUS SYNDROME 47GENOMICS_ENGLAND;UNIPROT
HgeneMAP2K2C0028326Noonan Syndrome4CLINGEN;CTD_human
HgeneMAP2K2C0010606Adenoid Cystic Carcinoma1CTD_human
HgeneMAP2K2C0025202melanoma1CGI;CTD_human
HgeneMAP2K2C0041409Turner Syndrome, Male1CTD_human
HgeneMAP2K2C0553586Cafe-au-lait macules with pulmonary stenosis1ORPHANET
HgeneMAP2K2C0587248Costello syndrome (disorder)1CLINGEN;CTD_human
HgeneMAP2K2C1527404Female Pseudo-Turner Syndrome1CTD_human
HgeneMAP2K2C2931482Neurofibromatosis-Noonan syndrome1ORPHANET
HgeneMAP2K2C4551602Noonan Syndrome 11CTD_human