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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:EEF2-MAP2K2 (FusionGDB2 ID:25212)

Fusion Gene Summary for EEF2-MAP2K2

check button Fusion gene summary
Fusion gene informationFusion gene name: EEF2-MAP2K2
Fusion gene ID: 25212
HgeneTgene
Gene symbol

EEF2

MAP2K2

Gene ID

1938

5605

Gene nameeukaryotic translation elongation factor 2mitogen-activated protein kinase kinase 2
SynonymsEEF-2|EF-2|EF2|SCA26CFC4|MAPKK2|MEK2|MKK2|PRKMK2
Cytomap

19p13.3

19p13.3

Type of geneprotein-codingprotein-coding
Descriptionelongation factor 2epididymis secretory sperm binding proteinpolypeptidyl-tRNA translocasedual specificity mitogen-activated protein kinase kinase 2ERK activator kinase 2MAP kinase kinase 2MAPK/ERK kinase 2mitogen-activated protein kinase kinase 2, p45
Modification date2020031320200327
UniProtAcc

P13639

P36507

Ensembl transtripts involved in fusion geneENST00000309311, ENST00000600720, 
ENST00000262948, ENST00000394867, 
ENST00000599345, 
Fusion gene scores* DoF score44 X 37 X 16=260486 X 7 X 5=210
# samples 569
** MAII scorelog2(56/26048*10)=-5.53960196732128
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/210*10)=-1.22239242133645
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: EEF2 [Title/Abstract] AND MAP2K2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointEEF2(3985375)-MAP2K2(4090706), # 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
TgeneMAP2K2

GO:0036289

peptidyl-serine autophosphorylation

8388392

TgeneMAP2K2

GO:0071902

positive regulation of protein serine/threonine kinase activity

8388392


check buttonFusion gene breakpoints across EEF2 (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 MAP2K2 (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-Cancer235NEEF2chr19

3985375

-MAP2K2chr19

4090706

-


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Fusion Gene ORF analysis for EEF2-MAP2K2

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
In-frameENST00000309311ENST00000262948EEF2chr19

3985375

-MAP2K2chr19

4090706

-
In-frameENST00000309311ENST00000394867EEF2chr19

3985375

-MAP2K2chr19

4090706

-
5CDS-intronENST00000309311ENST00000599345EEF2chr19

3985375

-MAP2K2chr19

4090706

-
intron-3CDSENST00000600720ENST00000262948EEF2chr19

3985375

-MAP2K2chr19

4090706

-
intron-3CDSENST00000600720ENST00000394867EEF2chr19

3985375

-MAP2K2chr19

4090706

-
intron-intronENST00000600720ENST00000599345EEF2chr19

3985375

-MAP2K2chr19

4090706

-

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)
ENST00000309311EEF2chr193985375-ENST00000262948MAP2K2chr194090706-480923522117
ENST00000309311EEF2chr193985375-ENST00000394867MAP2K2chr194090706-468923522117

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
ENST00000309311ENST00000262948EEF2chr193985375-MAP2K2chr194090706-0.76844530.23155466
ENST00000309311ENST00000394867EEF2chr193985375-MAP2K2chr194090706-0.739273370.26072663

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Fusion Genomic Features for EEF2-MAP2K2


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 EEF2-MAP2K2


check button Go to

FGviewer for the breakpoints of chr19:3985375-chr19:4090706

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
EEF2

P13639

MAP2K2

P36507

FUNCTION: Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post-translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome.FUNCTION: Catalyzes the concomitant phosphorylation of a threonine and a tyrosine residue in a Thr-Glu-Tyr sequence located in MAP kinases. Activates the ERK1 and ERK2 MAP kinases (By similarity). Activates BRAF in a KSR1 or KSR2-dependent manner; by binding to KSR1 or KSR2 releases the inhibitory intramolecular interaction between KSR1 or KSR2 protein kinase and N-terminal domains which promotes KSR1 or KSR2-BRAF dimerization and BRAF activation (PubMed:29433126). {ECO:0000250|UniProtKB:Q63932, ECO:0000269|PubMed:29433126}.

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
HgeneEEF2chr19:3985375chr19:4090706ENST00000309311-11517_3621.0859.0Domaintr-type G
HgeneEEF2chr19:3985375chr19:4090706ENST00000309311-115104_1081.0859.0Nucleotide bindingGTP
HgeneEEF2chr19:3985375chr19:4090706ENST00000309311-115158_1611.0859.0Nucleotide bindingGTP
HgeneEEF2chr19:3985375chr19:4090706ENST00000309311-11526_331.0859.0Nucleotide bindingGTP
TgeneMAP2K2chr19:3985375chr19:4090706ENST00000262948911266_315364.0401.0Compositional biasNote=Pro-rich
TgeneMAP2K2chr19:3985375chr19:4090706ENST0000026294891172_369364.0401.0DomainProtein kinase
TgeneMAP2K2chr19:3985375chr19:4090706ENST0000026294891178_86364.0401.0Nucleotide bindingATP


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Fusion Gene Sequence for EEF2-MAP2K2


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.
>In-frame_ENST00000309311_ENST00000262948_235N_EEF2_chr19_3985375_-_MAP2K2_chr19_4090706_length(transcript)=480nt_BP=92nt
AGCGTTCTCTTCCGCCGTCGTCGCCGCCATCCTCGGCGCGACTCGCTTCTTTCGGTTCTACCTGGGAGAATCCACCGCCATCCGCCACCA
TGAACCACACCTTCATCAAGCGGTCCGAGGTGGAAGAAGTGGATTTTGCCGGCTGGTTGTGTAAAACCCTGCGGCTGAACCAGCCCGGCA
CACCCACGCGCACCGCCGTGTGACAGTGGCCGGGCTCCCTGCGTCCCGCTGGTGACCTGCCCACCGTCCCTGTCCATGCCCCGCCCTTCC
AGCTGAGGACAGGCTGGCGCCTCCACCCACCCTCCTGCCTCACCCCTGCGGAGAGCACCGTGGCGGGGCGACAGCGCATGCAGGAACGGG
GGTCTCCTCTCCTGCCCGTCCTGGCCGGGGTGCCTCTGGGGACGGGCGACGCTGCTGTGTGTGGTCTCAGAGGCTCTGCTTCCTTAGGTT

>In-frame_ENST00000309311_ENST00000262948_235N_EEF2_chr19_3985375_-_MAP2K2_chr19_4090706_length(amino acids)=117AA_start in transcript=352_stop in transcript=2
MHALSPRHGALRRGEAGGWVEAPACPQLEGRGMDRDGGQVTSGTQGARPLSHGGARGCAGLVQPQGFTQPAGKIHFFHLGPLDEGVVHGG

--------------------------------------------------------------
>In-frame_ENST00000309311_ENST00000394867_235N_EEF2_chr19_3985375_-_MAP2K2_chr19_4090706_length(transcript)=468nt_BP=92nt
AGCGTTCTCTTCCGCCGTCGTCGCCGCCATCCTCGGCGCGACTCGCTTCTTTCGGTTCTACCTGGGAGAATCCACCGCCATCCGCCACCA
TGAACCACACCTTCATCAAGCGGTCCGAGGTGGAAGAAGTGGATTTTGCCGGCTGGTTGTGTAAAACCCTGCGGCTGAACCAGCCCGGCA
CACCCACGCGCACCGCCGTGTGACAGTGGCCGGGCTCCCTGCGTCCCGCTGGTGACCTGCCCACCGTCCCTGTCCATGCCCCGCCCTTCC
AGCTGAGGACAGGCTGGCGCCTCCACCCACCCTCCTGCCTCACCCCTGCGGAGAGCACCGTGGCGGGGCGACAGCGCATGCAGGAACGGG
GGTCTCCTCTCCTGCCCGTCCTGGCCGGGGTGCCTCTGGGGACGGGCGACGCTGCTGTGTGTGGTCTCAGAGGCTCTGCTTCCTTAGGTT

>In-frame_ENST00000309311_ENST00000394867_235N_EEF2_chr19_3985375_-_MAP2K2_chr19_4090706_length(amino acids)=117AA_start in transcript=352_stop in transcript=2
MHALSPRHGALRRGEAGGWVEAPACPQLEGRGMDRDGGQVTSGTQGARPLSHGGARGCAGLVQPQGFTQPAGKIHFFHLGPLDEGVVHGG

--------------------------------------------------------------

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Fusion Gene PPI Analysis for EEF2-MAP2K2


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 EEF2-MAP2K2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneEEF2P13639DB11823EsketamineInhibitorSmall moleculeApproved|Investigational
HgeneEEF2P13639DB11823EsketamineInhibitorSmall moleculeApproved|Investigational
HgeneEEF2P13639DB12688Moxetumomab PasudotoxInactivatorBiotechApproved|Investigational
HgeneEEF2P13639DB12688Moxetumomab PasudotoxInactivatorBiotechApproved|Investigational
TgeneMAP2K2P36507DB06616BosutinibInhibitorSmall moleculeApproved
TgeneMAP2K2P36507DB06616BosutinibInhibitorSmall moleculeApproved
TgeneMAP2K2P36507DB06616BosutinibInhibitorSmall moleculeApproved
TgeneMAP2K2P36507DB06616BosutinibInhibitorSmall moleculeApproved
TgeneMAP2K2P36507DB08911TrametinibAntagonist|InhibitorSmall moleculeApproved
TgeneMAP2K2P36507DB08911TrametinibAntagonist|InhibitorSmall moleculeApproved
TgeneMAP2K2P36507DB08911TrametinibAntagonist|InhibitorSmall moleculeApproved
TgeneMAP2K2P36507DB08911TrametinibAntagonist|InhibitorSmall moleculeApproved
TgeneMAP2K2P36507DB11689SelumetinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB11689SelumetinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB11689SelumetinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB11689SelumetinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB11967BinimetinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB11967BinimetinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB11967BinimetinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB11967BinimetinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB12010FostamatinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB12010FostamatinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB12010FostamatinibInhibitorSmall moleculeApproved|Investigational
TgeneMAP2K2P36507DB12010FostamatinibInhibitorSmall moleculeApproved|Investigational

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Related Diseases for EEF2-MAP2K2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneEEF2C0001418Adenocarcinoma1CTD_human
HgeneEEF2C0006142Malignant neoplasm of breast1CTD_human
HgeneEEF2C0007134Renal Cell Carcinoma1CTD_human
HgeneEEF2C0024121Lung Neoplasms1CTD_human
HgeneEEF2C0027626Neoplasm Invasiveness1CTD_human
HgeneEEF2C0027627Neoplasm Metastasis1CTD_human
HgeneEEF2C0029408Degenerative polyarthritis1CTD_human
HgeneEEF2C0086743Osteoarthrosis Deformans1CTD_human
HgeneEEF2C0205641Adenocarcinoma, Basal Cell1CTD_human
HgeneEEF2C0205642Adenocarcinoma, Oxyphilic1CTD_human
HgeneEEF2C0205643Carcinoma, Cribriform1CTD_human
HgeneEEF2C0205644Carcinoma, Granular Cell1CTD_human
HgeneEEF2C0205645Adenocarcinoma, Tubular1CTD_human
HgeneEEF2C0242379Malignant neoplasm of lung1CTD_human
HgeneEEF2C0279702Conventional (Clear Cell) Renal Cell Carcinoma1CTD_human
HgeneEEF2C0678222Breast Carcinoma1CTD_human
HgeneEEF2C1257931Mammary Neoplasms, Human1CTD_human
HgeneEEF2C1266042Chromophobe Renal Cell Carcinoma1CTD_human
HgeneEEF2C1266043Sarcomatoid Renal Cell Carcinoma1CTD_human
HgeneEEF2C1266044Collecting Duct Carcinoma of the Kidney1CTD_human
HgeneEEF2C1306837Papillary Renal Cell Carcinoma1CTD_human
HgeneEEF2C1458155Mammary Neoplasms1CTD_human
HgeneEEF2C1836395SPINOCEREBELLAR ATAXIA 261CTD_human;ORPHANET;UNIPROT
HgeneEEF2C4704874Mammary Carcinoma, Human1CTD_human
TgeneMAP2K2C1275081Cardio-facio-cutaneous syndrome13CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneMAP2K2C3809007CARDIOFACIOCUTANEOUS SYNDROME 47GENOMICS_ENGLAND;UNIPROT
TgeneMAP2K2C0028326Noonan Syndrome4CLINGEN;CTD_human
TgeneMAP2K2C0010606Adenoid Cystic Carcinoma1CTD_human
TgeneMAP2K2C0025202melanoma1CGI;CTD_human
TgeneMAP2K2C0041409Turner Syndrome, Male1CTD_human
TgeneMAP2K2C0553586Cafe-au-lait macules with pulmonary stenosis1ORPHANET
TgeneMAP2K2C0587248Costello syndrome (disorder)1CLINGEN;CTD_human
TgeneMAP2K2C1527404Female Pseudo-Turner Syndrome1CTD_human
TgeneMAP2K2C2931482Neurofibromatosis-Noonan syndrome1ORPHANET
TgeneMAP2K2C4551602Noonan Syndrome 11CTD_human