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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:PLEK-IER3

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PLEK-IER3
FusionPDB ID: 66339
FusionGDB2.0 ID: 66339
HgeneTgene
Gene symbol

PLEK

IER3

Gene ID

5341

8870

Gene namepleckstrinimmediate early response 3
SynonymsP47DIF-2|DIF2|GLY96|IEX-1|IEX-1L|IEX1|PRG1
Cytomap

2p14

6p21.33

Type of geneprotein-codingprotein-coding
Descriptionpleckstrinplatelet 47 kDa proteinradiation-inducible immediate-early gene IEX-1PACAP-responsive gene 1 proteinanti-death proteindifferentiation-dependent gene 2 proteinexpressed in pancreatic carcinomagly96, mouse, homolog ofimmediate early protein GLY96immediate early response 3
Modification date2020031320200313
UniProtAcc.

Q9Y5U9

Ensembl transtripts involved in fusion geneENST idsENST00000234313, ENST00000383560, 
ENST00000400509, ENST00000416336, 
ENST00000416884, ENST00000429592, 
ENST00000435856, ENST00000436988, 
ENST00000439190, ENST00000446599, 
ENST00000450236, ENST00000259874, 
ENST00000376377, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score4 X 4 X 2=324 X 3 X 2=24
# samples 44
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/24*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: PLEK [Title/Abstract] AND IER3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PLEK(68592525)-IER3(30711973), # samples:1
Anticipated loss of major functional domain due to fusion event.PLEK-IER3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
PLEK-IER3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
PLEK-IER3 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
PLEK-IER3 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* 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
HgenePLEK

GO:0007229

integrin-mediated signaling pathway

10995449

HgenePLEK

GO:0010920

negative regulation of inositol phosphate biosynthetic process

7559487|7782310

HgenePLEK

GO:0010925

positive regulation of inositol-polyphosphate 5-phosphatase activity

8999861

HgenePLEK

GO:0030030

cell projection organization

9060471

HgenePLEK

GO:0030836

positive regulation of actin filament depolymerization

10497244

HgenePLEK

GO:0030845

phospholipase C-inhibiting G protein-coupled receptor signaling pathway

7782310

HgenePLEK

GO:0030866

cortical actin cytoskeleton organization

10497244

HgenePLEK

GO:0031529

ruffle organization

10497244

HgenePLEK

GO:0031532

actin cytoskeleton reorganization

10497244

HgenePLEK

GO:0032233

positive regulation of actin filament bundle assembly

10497244

HgenePLEK

GO:0045744

negative regulation of G protein-coupled receptor signaling pathway

7782310

HgenePLEK

GO:0046488

phosphatidylinositol metabolic process

7559487

HgenePLEK

GO:0060305

regulation of cell diameter

10995449

HgenePLEK

GO:0070493

thrombin-activated receptor signaling pathway

7782310


check buttonFusion gene breakpoints across PLEK (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across IER3 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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-CancerERR315404PLEKchr2

68592525

+IER3chr6

30711973

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000234313PLEKchr268592525+ENST00000376377IER3chr630711973-1219221143481112

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
ENST00000234313ENST00000376377PLEKchr268592525+IER3chr630711973-0.0842184050.9157816

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>66339_66339_1_PLEK-IER3_PLEK_chr2_68592525_ENST00000234313_IER3_chr6_30711973_ENST00000376377_length(amino acids)=112AA_BP=26
MRVTFASACPASMEPKRIREGYLVKKVRRQLPVEEPNPAKRLLFLLLTIVFCQILMAEEGVPAPLPPEDAPNAASLAPTPVSAVLEPFNL

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

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Fusion Protein Functional Features


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/chr2:68592525/chr6:30711973)
- 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
.IER3

Q9Y5U9

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Regulator of endoplasmic reticulum secretion that acts as a key determinant of brain size (PubMed:33122427). Required for secretion of extracellular matrix proteins (PubMed:33122427). Required for correct brain development by depositing sufficient extracellular matrix proteins for tissue integrity and the proliferation of neural progenitors (PubMed:33122427). Acts as a regulator of the unfolded protein response (UPR) (By similarity). {ECO:0000250|UniProtKB:Q9CR20, ECO:0000269|PubMed:33122427}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneIER3chr2:68592525chr6:30711973ENST0000025987402100_15670.0157.0Topological domainExtracellular
TgeneIER3chr2:68592525chr6:30711973ENST0000038356002100_1560157.0Topological domainExtracellular
TgeneIER3chr2:68592525chr6:30711973ENST00000383560021_820157.0Topological domainCytoplasmic
TgeneIER3chr2:68592525chr6:30711973ENST0000041688402100_1560157.0Topological domainExtracellular
TgeneIER3chr2:68592525chr6:30711973ENST00000416884021_820157.0Topological domainCytoplasmic
TgeneIER3chr2:68592525chr6:30711973ENST0000043585602100_1560157.0Topological domainExtracellular
TgeneIER3chr2:68592525chr6:30711973ENST00000435856021_820157.0Topological domainCytoplasmic
TgeneIER3chr2:68592525chr6:30711973ENST0000043919002100_1560157.0Topological domainExtracellular
TgeneIER3chr2:68592525chr6:30711973ENST00000439190021_820157.0Topological domainCytoplasmic
TgeneIER3chr2:68592525chr6:30711973ENST0000045023602100_1560157.0Topological domainExtracellular
TgeneIER3chr2:68592525chr6:30711973ENST00000450236021_820157.0Topological domainCytoplasmic
TgeneIER3chr2:68592525chr6:30711973ENST000002598740283_9970.0157.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneIER3chr2:68592525chr6:30711973ENST000003835600283_990157.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneIER3chr2:68592525chr6:30711973ENST000004168840283_990157.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneIER3chr2:68592525chr6:30711973ENST000004358560283_990157.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneIER3chr2:68592525chr6:30711973ENST000004391900283_990157.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneIER3chr2:68592525chr6:30711973ENST000004502360283_990157.0TransmembraneHelical%3B Signal-anchor for type II membrane protein

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgenePLEKchr2:68592525chr6:30711973ENST00000234313+19136_22114.0351.0DomainDEP
HgenePLEKchr2:68592525chr6:30711973ENST00000234313+19244_34714.0351.0DomainPH 2
HgenePLEKchr2:68592525chr6:30711973ENST00000234313+194_10114.0351.0DomainPH 1
TgeneIER3chr2:68592525chr6:30711973ENST00000259874021_8270.0157.0Topological domainCytoplasmic


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
PLEK
IER3


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to PLEK-IER3


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to PLEK-IER3


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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