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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:MAP4K3-MPHOSPH8 (FusionGDB2 ID:51394)

Fusion Gene Summary for MAP4K3-MPHOSPH8

check button Fusion gene summary
Fusion gene informationFusion gene name: MAP4K3-MPHOSPH8
Fusion gene ID: 51394
HgeneTgene
Gene symbol

MAP4K3

MPHOSPH8

Gene ID

8491

54737

Gene namemitogen-activated protein kinase kinase kinase kinase 3M-phase phosphoprotein 8
SynonymsGLK|MAPKKKK3|MEKKK 3|MEKKK3|RAB8IPL1HSMPP8|TWA3|mpp8
Cytomap

2p22.1

13q12.11

Type of geneprotein-codingprotein-coding
Descriptionmitogen-activated protein kinase kinase kinase kinase 3MAPK/ERK kinase kinase kinase 3MEK kinase kinase 3germinal center kinase-like kinasegerminal center kinase-related protein kinaseM-phase phosphoprotein 8M-phase phosphoprotein, mppM-phase phosphoprotein, mpp8two hybrid-associated protein 3 with RanBPM
Modification date2020031320200313
UniProtAcc

Q8IVH8

Q99549

Ensembl transtripts involved in fusion geneENST00000263881, ENST00000341681, 
ENST00000437545, ENST00000536018, 
ENST00000474502, ENST00000484274, 
ENST00000496525, ENST00000361479, 
ENST00000414242, 
Fusion gene scores* DoF score9 X 6 X 7=37825 X 17 X 10=4250
# samples 1030
** MAII scorelog2(10/378*10)=-1.91838623444635
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(30/4250*10)=-3.82442843541655
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MAP4K3 [Title/Abstract] AND MPHOSPH8 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMAP4K3(39536601)-MPHOSPH8(20245345), # 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
HgeneMAP4K3

GO:0006468

protein phosphorylation

9275185

HgeneMAP4K3

GO:0009411

response to UV

9275185

HgeneMAP4K3

GO:0034612

response to tumor necrosis factor

9275185

HgeneMAP4K3

GO:0035556

intracellular signal transduction

9275185

TgeneMPHOSPH8

GO:0045814

negative regulation of gene expression, epigenetic

26022416|28581500|29211708

TgeneMPHOSPH8

GO:0090309

positive regulation of methylation-dependent chromatin silencing

28581500|29211708


check buttonFusion gene breakpoints across MAP4K3 (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 MPHOSPH8 (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-Cancer201NMAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+


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Fusion Gene ORF analysis for MAP4K3-MPHOSPH8

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-3UTRENST00000263881ENST00000496525MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5CDS-3UTRENST00000341681ENST00000496525MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5CDS-3UTRENST00000437545ENST00000496525MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5CDS-intronENST00000263881ENST00000361479MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5CDS-intronENST00000263881ENST00000414242MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5CDS-intronENST00000341681ENST00000361479MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5CDS-intronENST00000341681ENST00000414242MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5CDS-intronENST00000437545ENST00000361479MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5CDS-intronENST00000437545ENST00000414242MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5UTR-3UTRENST00000536018ENST00000496525MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5UTR-intronENST00000536018ENST00000361479MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
5UTR-intronENST00000536018ENST00000414242MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
intron-3UTRENST00000474502ENST00000496525MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
intron-3UTRENST00000484274ENST00000496525MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
intron-intronENST00000474502ENST00000361479MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
intron-intronENST00000474502ENST00000414242MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
intron-intronENST00000484274ENST00000361479MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+
intron-intronENST00000484274ENST00000414242MAP4K3chr2

39536601

-MPHOSPH8chr13

20245345

+

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 MAP4K3-MPHOSPH8


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.
genomic feature

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 MAP4K3-MPHOSPH8


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/:39536601/:20245345)
- 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
MAP4K3

Q8IVH8

MPHOSPH8

Q99549

FUNCTION: May play a role in the response to environmental stress. Appears to act upstream of the JUN N-terminal pathway. {ECO:0000269|PubMed:9275185}.FUNCTION: Heterochromatin component that specifically recognizes and binds methylated 'Lys-9' of histone H3 (H3K9me) and promotes recruitment of proteins that mediate epigenetic repression (PubMed:20871592, PubMed:26022416). Mediates recruitment of the HUSH complex to H3K9me3 sites: the HUSH complex is recruited to genomic loci rich in H3K9me3 and is required to maintain transcriptional silencing by promoting recruitment of SETDB1, a histone methyltransferase that mediates further deposition of H3K9me3, as well as MORC2 (PubMed:26022416, PubMed:28581500). Binds H3K9me and promotes DNA methylation by recruiting DNMT3A to target CpG sites; these can be situated within the coding region of the gene (PubMed:20871592). Mediates down-regulation of CDH1 expression (PubMed:20871592). Also represses L1 retrotransposons in collaboration with MORC2 and, probably, SETDB1, 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). The HUSH complex is also involved in the silencing of unintegrated retroviral DNA by being recruited by ZNF638: some part of the retroviral DNA formed immediately after infection remains unintegrated in the host genome and is transcriptionally repressed (PubMed:30487602). {ECO:0000269|PubMed:20871592, ECO:0000269|PubMed:26022416, ECO:0000269|PubMed:28581500, ECO:0000269|PubMed:29211708, ECO:0000269|PubMed:30487602}.

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 MAP4K3-MPHOSPH8


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 MAP4K3-MPHOSPH8


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 MAP4K3-MPHOSPH8


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 MAP4K3-MPHOSPH8


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