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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:PPARD-WDR27 (FusionGDB2 ID:66919)

Fusion Gene Summary for PPARD-WDR27

check button Fusion gene summary
Fusion gene informationFusion gene name: PPARD-WDR27
Fusion gene ID: 66919
HgeneTgene
Gene symbol

PPARD

WDR27

Gene ID

5467

253769

Gene nameperoxisome proliferator activated receptor deltaWD repeat domain 27
SynonymsFAAR|NR1C2|NUC1|NUCI|NUCII|PPARB-
Cytomap

6p21.31

6q27

Type of geneprotein-codingprotein-coding
Descriptionperoxisome proliferator-activated receptor deltaPPAR-betaPPAR-deltaPPARD/MYO1D fusionnuclear hormone receptor 1nuclear receptor subfamily 1 group C member 2peroxisome proliferator-activated receptor betaWD repeat-containing protein 27
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000444397, ENST00000360694, 
ENST00000418635, ENST00000448077, 
ENST00000337400, ENST00000311565, 
ENST00000540939, 
ENST00000448612, 
ENST00000423258, ENST00000333572, 
ENST00000546525, ENST00000420344, 
Fusion gene scores* DoF score13 X 7 X 8=72811 X 7 X 5=385
# samples 1411
** MAII scorelog2(14/728*10)=-2.37851162325373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/385*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PPARD [Title/Abstract] AND WDR27 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPPARD(35314927)-WDR27(170002417), # samples:3
Anticipated loss of major functional domain due to fusion event.PPARD-WDR27 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
PPARD-WDR27 seems lost the major protein functional domain in Hgene 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
HgenePPARD

GO:0045893

positive regulation of transcription, DNA-templated

12955147


check buttonFusion gene breakpoints across PPARD (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 WDR27 (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
ChimerDB4PRADTCGA-EJ-5498-01APPARDchr6

35314927

+WDR27chr6

170002417

-
ChimerDB4PRADTCGA-EJ-5498PPARDchr6

35314927

+WDR27chr6

170002417

-
ChimerDB4PRADTCGA-EJ-5498-01APPARDchr6

35314927

-WDR27chr6

170002417

-


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Fusion Gene ORF analysis for PPARD-WDR27

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-3CDSENST00000444397ENST00000448612PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000444397ENST00000423258PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000444397ENST00000333572PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-5UTRENST00000444397ENST00000546525PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-intronENST00000444397ENST00000420344PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000360694ENST00000448612PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000360694ENST00000423258PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000360694ENST00000333572PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-5UTRENST00000360694ENST00000546525PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-intronENST00000360694ENST00000420344PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000418635ENST00000448612PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000418635ENST00000423258PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000418635ENST00000333572PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-5UTRENST00000418635ENST00000546525PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-intronENST00000418635ENST00000420344PPARDchr6

35314927

+WDR27chr6

170002417

-
Frame-shiftENST00000448077ENST00000448612PPARDchr6

35314927

+WDR27chr6

170002417

-
Frame-shiftENST00000448077ENST00000423258PPARDchr6

35314927

+WDR27chr6

170002417

-
Frame-shiftENST00000448077ENST00000333572PPARDchr6

35314927

+WDR27chr6

170002417

-
5CDS-5UTRENST00000448077ENST00000546525PPARDchr6

35314927

+WDR27chr6

170002417

-
5CDS-intronENST00000448077ENST00000420344PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000337400ENST00000448612PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000337400ENST00000423258PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000337400ENST00000333572PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-5UTRENST00000337400ENST00000546525PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-intronENST00000337400ENST00000420344PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000311565ENST00000448612PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000311565ENST00000423258PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-3CDSENST00000311565ENST00000333572PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-5UTRENST00000311565ENST00000546525PPARDchr6

35314927

+WDR27chr6

170002417

-
5UTR-intronENST00000311565ENST00000420344PPARDchr6

35314927

+WDR27chr6

170002417

-
intron-3CDSENST00000540939ENST00000448612PPARDchr6

35314927

+WDR27chr6

170002417

-
intron-3CDSENST00000540939ENST00000423258PPARDchr6

35314927

+WDR27chr6

170002417

-
intron-3CDSENST00000540939ENST00000333572PPARDchr6

35314927

+WDR27chr6

170002417

-
intron-5UTRENST00000540939ENST00000546525PPARDchr6

35314927

+WDR27chr6

170002417

-
intron-intronENST00000540939ENST00000420344PPARDchr6

35314927

+WDR27chr6

170002417

-

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 PPARD-WDR27


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 PPARD-WDR27


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
..
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: 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.

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 PPARD-WDR27


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 PPARD-WDR27


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 PPARD-WDR27


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 PPARD-WDR27


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePPARDC0007114Malignant neoplasm of skin2CTD_human
HgenePPARDC0028754Obesity2CTD_human
HgenePPARDC0037286Skin Neoplasms2CTD_human
HgenePPARDC0400966Non-alcoholic Fatty Liver Disease2CTD_human
HgenePPARDC3241937Nonalcoholic Steatohepatitis2CTD_human
HgenePPARDC4721453Peripheral Nervous System Diseases2CTD_human
HgenePPARDC0005586Bipolar Disorder1PSYGENET
HgenePPARDC0015695Fatty Liver1CTD_human
HgenePPARDC0018800Cardiomegaly1CTD_human
HgenePPARDC0023896Alcoholic Liver Diseases1CTD_human
HgenePPARDC0025202melanoma1CTD_human
HgenePPARDC0033141Cardiomyopathies, Primary1CTD_human
HgenePPARDC0036529Myocardial Diseases, Secondary1CTD_human
HgenePPARDC0043094Weight Gain1CTD_human
HgenePPARDC0878544Cardiomyopathies1CTD_human
HgenePPARDC1383860Cardiac Hypertrophy1CTD_human
HgenePPARDC2711227Steatohepatitis1CTD_human