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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:PIAS3-REN (FusionGDB2 ID:64715)

Fusion Gene Summary for PIAS3-REN

check button Fusion gene summary
Fusion gene informationFusion gene name: PIAS3-REN
Fusion gene ID: 64715
HgeneTgene
Gene symbol

PIAS3

REN

Gene ID

10401

147040

Gene nameprotein inhibitor of activated STAT 3potassium channel tetramerization domain containing 11
SynonymsZMIZ5C17orf36|KCASH1|REN|REN/KCTD11
Cytomap

1q21.1

17p13.1

Type of geneprotein-codingprotein-coding
DescriptionE3 SUMO-protein ligase PIAS3E3 SUMO-protein transferase PIAS3protein inhibitor of activated STAT protein 3zinc finger, MIZ-type containing 5BTB/POZ domain-containing protein KCTD11RING-type E3 ubiquitin transferase subunit KCTD11potassium channel tetramerization domain-containing protein 11retinoic acid, EGF, NGF induced gene protein
Modification date2020031320200313
UniProtAcc.

REN

Ensembl transtripts involved in fusion geneENST00000369299, ENST00000393045, 
ENST00000369298, 
ENST00000367195, 
ENST00000272190, 
Fusion gene scores* DoF score5 X 6 X 3=903 X 1 X 3=9
# samples 64
** MAII scorelog2(6/90*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/9*10)=2.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: PIAS3 [Title/Abstract] AND REN [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPIAS3(145575404)-REN(204131291), # samples:3
Anticipated loss of major functional domain due to fusion event.PIAS3-REN seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PIAS3-REN seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
PIAS3-REN seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgenePIAS3

GO:0033234

negative regulation of protein sumoylation

24651376

HgenePIAS3

GO:0033235

positive regulation of protein sumoylation

17696781|21965678


check buttonFusion gene breakpoints across PIAS3 (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 REN (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
ChimerDB4OVTCGA-24-2024-01APIAS3chr1

145575404

-RENchr1

204131291

-
ChimerDB4OVTCGA-24-2024PIAS3chr1

145576102

+RENchr1

204131291

-
ChimerDB4OVTCGA-24-2024-01APIAS3chr1

145575404

+RENchr1

204131291

-
ChimerDB4OVTCGA-24-2024-01APIAS3chr1

145576102

+RENchr1

204131291

-
ChimerDB4OVTCGA-24-2024-01APIAS3chr1

145575404

-RENchr1

204131291

-


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Fusion Gene ORF analysis for PIAS3-REN

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
5UTR-3CDSENST00000369299ENST00000367195PIAS3chr1

145575404

-RENchr1

204131291

-
5UTR-3CDSENST00000369299ENST00000272190PIAS3chr1

145575404

-RENchr1

204131291

-
intron-3CDSENST00000393045ENST00000367195PIAS3chr1

145575404

-RENchr1

204131291

-
intron-3CDSENST00000393045ENST00000272190PIAS3chr1

145575404

-RENchr1

204131291

-
intron-3CDSENST00000369298ENST00000367195PIAS3chr1

145575404

-RENchr1

204131291

-
intron-3CDSENST00000369298ENST00000272190PIAS3chr1

145575404

-RENchr1

204131291

-
intron-3CDSENST00000369299ENST00000367195PIAS3chr1

145576102

+RENchr1

204131291

-
intron-3CDSENST00000369299ENST00000272190PIAS3chr1

145576102

+RENchr1

204131291

-
Frame-shiftENST00000393045ENST00000367195PIAS3chr1

145576102

+RENchr1

204131291

-
Frame-shiftENST00000393045ENST00000272190PIAS3chr1

145576102

+RENchr1

204131291

-
Frame-shiftENST00000369298ENST00000367195PIAS3chr1

145576102

+RENchr1

204131291

-
Frame-shiftENST00000369298ENST00000272190PIAS3chr1

145576102

+RENchr1

204131291

-

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 PIAS3-REN


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 PIAS3-REN


check button Go to

FGviewer for the breakpoints of :-:

.
- 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
.REN

REN

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.427

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 PIAS3-REN


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 PIAS3-REN


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 PIAS3-REN


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 PIAS3-REN


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePIAS3C0007873Uterine Cervical Neoplasm1CTD_human
HgenePIAS3C4048328cervical cancer1CTD_human
TgeneRENC0020538Hypertensive disease17CTD_human
TgeneRENC0011570Mental Depression5PSYGENET
TgeneRENC0011581Depressive disorder5PSYGENET
TgeneRENC0004775Bartter Disease3CTD_human
TgeneRENC0018801Heart failure3CTD_human
TgeneRENC0018802Congestive heart failure3CTD_human
TgeneRENC0020649Hypotension3CTD_human
TgeneRENC0022658Kidney Diseases3CTD_human
TgeneRENC0023212Left-Sided Heart Failure3CTD_human
TgeneRENC0041696Unipolar Depression3PSYGENET
TgeneRENC0235527Heart Failure, Right-Sided3CTD_human
TgeneRENC0266313Allanson Pantzar McLeod syndrome3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneRENC1959583Myocardial Failure3CTD_human
TgeneRENC1961112Heart Decompensation3CTD_human
TgeneRENC0001925Albuminuria2CTD_human
TgeneRENC0001969Alcoholic Intoxication2PSYGENET
TgeneRENC0001973Alcoholic Intoxication, Chronic2PSYGENET
TgeneRENC0018800Cardiomegaly2CTD_human
TgeneRENC0027720Nephrosis2CTD_human
TgeneRENC0033687Proteinuria2CTD_human
TgeneRENC0149721Left Ventricular Hypertrophy2CTD_human
TgeneRENC1383860Cardiac Hypertrophy2CTD_human
TgeneRENC2678367Renal Tubular Dysgenesis With Choanal Atresia And Athelia2ORPHANET
TgeneRENC0001787Osteoporosis, Age-Related1CTD_human
TgeneRENC0002152Alloxan Diabetes1CTD_human
TgeneRENC0002871Anemia1CTD_human
TgeneRENC0005586Bipolar Disorder1PSYGENET
TgeneRENC0011853Diabetes Mellitus, Experimental1CTD_human
TgeneRENC0013221Drug toxicity1CTD_human
TgeneRENC0015934Fetal Growth Retardation1CTD_human
TgeneRENC0016059Fibrosis1CTD_human
TgeneRENC0019080Hemorrhage1CTD_human
TgeneRENC0020540Malignant Hypertension1CTD_human
TgeneRENC0022116Ischemia1CTD_human
TgeneRENC0023890Liver Cirrhosis1CTD_human
TgeneRENC0027051Myocardial Infarction1CTD_human
TgeneRENC0029456Osteoporosis1CTD_human
TgeneRENC0029459Osteoporosis, Senile1CTD_human
TgeneRENC0030246Pustulosis of Palms and Soles1CTD_human
TgeneRENC0033860Psoriasis1CTD_human
TgeneRENC0038433Streptozotocin Diabetes1CTD_human
TgeneRENC0038587Substance Withdrawal Syndrome1CTD_human
TgeneRENC0041755Adverse reaction to drug1CTD_human
TgeneRENC0086189Drug Withdrawal Symptoms1CTD_human
TgeneRENC0087169Withdrawal Symptoms1CTD_human
TgeneRENC0221043Liddle Syndrome1CTD_human
TgeneRENC0239946Fibrosis, Liver1CTD_human
TgeneRENC0242528Azotemia1CTD_human
TgeneRENC0751406Post-Traumatic Osteoporosis1CTD_human
TgeneRENC1623038Cirrhosis1CTD_human
TgeneRENC2751310Hyperuricemic Nephropathy, Familial Juvenile 21CTD_human;GENOMICS_ENGLAND;UNIPROT