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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:PPARG-PAX8 (FusionGDB2 ID:66926)

Fusion Gene Summary for PPARG-PAX8

check button Fusion gene summary
Fusion gene informationFusion gene name: PPARG-PAX8
Fusion gene ID: 66926
HgeneTgene
Gene symbol

PPARG

PAX8

Gene ID

5468

7849

Gene nameperoxisome proliferator activated receptor gammapaired box 8
SynonymsCIMT1|GLM1|NR1C3|PPARG1|PPARG2|PPARgamma-
Cytomap

3p25.2

2q14.1

Type of geneprotein-codingprotein-coding
Descriptionperoxisome proliferator-activated receptor gammaPPAR-gammanuclear receptor subfamily 1 group C member 3peroxisome proliferator-activated nuclear receptor gamma variant 1paired box protein Pax-8paired domain gene 8
Modification date2020032920200313
UniProtAcc.

Q06710

Ensembl transtripts involved in fusion geneENST00000397010, ENST00000309576, 
ENST00000397015, ENST00000397012, 
ENST00000397026, ENST00000397000, 
ENST00000539812, ENST00000287820, 
ENST00000348715, ENST00000397647, 
ENST00000263335, ENST00000429538, 
ENST00000263334, 
Fusion gene scores* DoF score7 X 9 X 5=3155 X 6 X 4=120
# samples 138
** MAII scorelog2(13/315*10)=-1.27684020535882
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/120*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PPARG [Title/Abstract] AND PAX8 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPAX8(113992971)-PPARG(12421203), # samples:12
PPARG(12353952)-PAX8(113984833), # samples:13
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
HgenePPARG

GO:0000122

negative regulation of transcription by RNA polymerase II

12700342

HgenePPARG

GO:0006919

activation of cysteine-type endopeptidase activity involved in apoptotic process

18293083

HgenePPARG

GO:0007165

signal transduction

9568716

HgenePPARG

GO:0010742

macrophage derived foam cell differentiation

26504087

HgenePPARG

GO:0010745

negative regulation of macrophage derived foam cell differentiation

19114110

HgenePPARG

GO:0010871

negative regulation of receptor biosynthetic process

12700342

HgenePPARG

GO:0010887

negative regulation of cholesterol storage

19114110

HgenePPARG

GO:0010891

negative regulation of sequestering of triglyceride

12700342

HgenePPARG

GO:0016525

negative regulation of angiogenesis

28566713

HgenePPARG

GO:0030224

monocyte differentiation

9568716

HgenePPARG

GO:0032526

response to retinoic acid

16239304

HgenePPARG

GO:0042953

lipoprotein transport

9568716

HgenePPARG

GO:0043537

negative regulation of blood vessel endothelial cell migration

28566713

HgenePPARG

GO:0045713

low-density lipoprotein particle receptor biosynthetic process

9568716

HgenePPARG

GO:0045944

positive regulation of transcription by RNA polymerase II

9568715|12700342|16239304|17611579

HgenePPARG

GO:0048469

cell maturation

9568716

HgenePPARG

GO:0048662

negative regulation of smooth muscle cell proliferation

20622039

HgenePPARG

GO:0051091

positive regulation of DNA-binding transcription factor activity

18293083

HgenePPARG

GO:0061614

pri-miRNA transcription by RNA polymerase II

28566713

HgenePPARG

GO:0071404

cellular response to low-density lipoprotein particle stimulus

9568716

HgenePPARG

GO:1904706

negative regulation of vascular smooth muscle cell proliferation

28522568

TgenePAX8

GO:0006351

transcription, DNA-templated

9590296

TgenePAX8

GO:0045893

positive regulation of transcription, DNA-templated

9388203|15356023|15961562

TgenePAX8

GO:0045944

positive regulation of transcription by RNA polymerase II

9388203

TgenePAX8

GO:0071371

cellular response to gonadotropin stimulus

15961562


check buttonFusion gene breakpoints across PPARG (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 PAX8 (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
ChimerDB4THCATCGA-BJ-A0YZ-01APPARGchr3

12353952

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-DE-A4M9-01APPARGchr3

12353952

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-EM-A3AJ-01APPARGchr3

12353952

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-EM-A3AJPPARGchr3

12353952

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-EM-A3AJPPARGchr3

12353952

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-BJ-A0YZPPARGchr3

12353952

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-BJ-A0YZPPARGchr3

12353952

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-EM-A3AJ-01APPARGchr3

12353952

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-DE-A4M9-01APPARGchr3

12353952

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-DE-A4M9-01APPARGchr3

12329519

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-DE-A4M9-01APPARGchr3

12329174

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-BJ-A0YZ-01APPARGchr3

12353952

+PAX8chr2

113984833

-
ChimerDB4THCATCGA-BJ-A0YZ-01APPARGchr3

12353952

-PAX8chr2

113984833

-
ChimerDB4THCATCGA-DE-A4M9-01APPARGchr3

12353952

-PAX8chr2

113984833

-
ChimerDB4THCATCGA-EM-A3AJ-01APPARGchr3

12353952

-PAX8chr2

113984833

-


Top

Fusion Gene ORF analysis for PPARG-PAX8

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-3CDSENST00000397010ENST00000348715PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397010ENST00000397647PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397010ENST00000263335PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397010ENST00000429538PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397010ENST00000263334PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-3CDSENST00000309576ENST00000348715PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000309576ENST00000397647PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000309576ENST00000263335PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000309576ENST00000429538PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000309576ENST00000263334PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-3CDSENST00000397015ENST00000348715PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-intronENST00000397015ENST00000397647PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-intronENST00000397015ENST00000263335PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-intronENST00000397015ENST00000429538PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-intronENST00000397015ENST00000263334PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-3CDSENST00000397012ENST00000348715PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397012ENST00000397647PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397012ENST00000263335PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397012ENST00000429538PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397012ENST00000263334PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-3CDSENST00000397026ENST00000348715PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397026ENST00000397647PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397026ENST00000263335PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397026ENST00000429538PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397026ENST00000263334PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-3CDSENST00000397000ENST00000348715PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397000ENST00000397647PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397000ENST00000263335PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397000ENST00000429538PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000397000ENST00000263334PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-3CDSENST00000539812ENST00000348715PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000539812ENST00000397647PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000539812ENST00000263335PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000539812ENST00000429538PPARGchr3

12353952

+PAX8chr2

113984833

-
5UTR-intronENST00000539812ENST00000263334PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-3CDSENST00000287820ENST00000348715PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000397647PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000263335PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000429538PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000263334PPARGchr3

12353952

+PAX8chr2

113984833

-
intron-3CDSENST00000397010ENST00000348715PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397010ENST00000397647PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397010ENST00000263335PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397010ENST00000429538PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397010ENST00000263334PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-3CDSENST00000309576ENST00000348715PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-intronENST00000309576ENST00000397647PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-intronENST00000309576ENST00000263335PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-intronENST00000309576ENST00000429538PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-intronENST00000309576ENST00000263334PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-3CDSENST00000397015ENST00000348715PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-intronENST00000397015ENST00000397647PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-intronENST00000397015ENST00000263335PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-intronENST00000397015ENST00000429538PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-intronENST00000397015ENST00000263334PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-3CDSENST00000397012ENST00000348715PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397012ENST00000397647PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397012ENST00000263335PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397012ENST00000429538PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397012ENST00000263334PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-3CDSENST00000397026ENST00000348715PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397026ENST00000397647PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397026ENST00000263335PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397026ENST00000429538PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397026ENST00000263334PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-3CDSENST00000397000ENST00000348715PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397000ENST00000397647PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397000ENST00000263335PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397000ENST00000429538PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000397000ENST00000263334PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-3CDSENST00000539812ENST00000348715PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000539812ENST00000397647PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000539812ENST00000263335PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000539812ENST00000429538PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000539812ENST00000263334PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-3CDSENST00000287820ENST00000348715PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000397647PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000263335PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000429538PPARGchr3

12329519

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000263334PPARGchr3

12329519

+PAX8chr2

113984833

-
5UTR-3CDSENST00000397010ENST00000348715PPARGchr3

12329174

+PAX8chr2

113984833

-
5UTR-intronENST00000397010ENST00000397647PPARGchr3

12329174

+PAX8chr2

113984833

-
5UTR-intronENST00000397010ENST00000263335PPARGchr3

12329174

+PAX8chr2

113984833

-
5UTR-intronENST00000397010ENST00000429538PPARGchr3

12329174

+PAX8chr2

113984833

-
5UTR-intronENST00000397010ENST00000263334PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-3CDSENST00000309576ENST00000348715PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000309576ENST00000397647PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000309576ENST00000263335PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000309576ENST00000429538PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000309576ENST00000263334PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-3CDSENST00000397015ENST00000348715PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397015ENST00000397647PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397015ENST00000263335PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397015ENST00000429538PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397015ENST00000263334PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-3CDSENST00000397012ENST00000348715PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397012ENST00000397647PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397012ENST00000263335PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397012ENST00000429538PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397012ENST00000263334PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-3CDSENST00000397026ENST00000348715PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397026ENST00000397647PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397026ENST00000263335PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397026ENST00000429538PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397026ENST00000263334PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-3CDSENST00000397000ENST00000348715PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397000ENST00000397647PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397000ENST00000263335PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397000ENST00000429538PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000397000ENST00000263334PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-3CDSENST00000539812ENST00000348715PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000539812ENST00000397647PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000539812ENST00000263335PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000539812ENST00000429538PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000539812ENST00000263334PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-3CDSENST00000287820ENST00000348715PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000397647PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000263335PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000429538PPARGchr3

12329174

+PAX8chr2

113984833

-
intron-intronENST00000287820ENST00000263334PPARGchr3

12329174

+PAX8chr2

113984833

-
In-frameENST00000287820ENST00000263334PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000287820ENST00000263335PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000287820ENST00000348715PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000287820ENST00000397647PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000287820ENST00000429538PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000309576ENST00000263334PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000309576ENST00000263335PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000309576ENST00000348715PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000309576ENST00000397647PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000309576ENST00000429538PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397010ENST00000263334PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397010ENST00000263335PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397010ENST00000348715PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397010ENST00000397647PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397010ENST00000429538PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397012ENST00000263334PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397012ENST00000263335PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397012ENST00000348715PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397012ENST00000397647PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397012ENST00000429538PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397015ENST00000263334PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397015ENST00000263335PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397015ENST00000348715PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397015ENST00000397647PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397015ENST00000429538PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397026ENST00000263334PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397026ENST00000263335PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397026ENST00000348715PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397026ENST00000397647PPARGchr3

12458653

+PAX8chr2

113999303

-
In-frameENST00000397026ENST00000429538PPARGchr3

12458653

+PAX8chr2

113999303

-
intron-3CDSENST00000397000ENST00000263334PPARGchr3

12458653

+PAX8chr2

113999303

-
intron-3CDSENST00000397000ENST00000263335PPARGchr3

12458653

+PAX8chr2

113999303

-
intron-3CDSENST00000397000ENST00000348715PPARGchr3

12458653

+PAX8chr2

113999303

-
intron-3CDSENST00000397000ENST00000397647PPARGchr3

12458653

+PAX8chr2

113999303

-
intron-3CDSENST00000397000ENST00000429538PPARGchr3

12458653

+PAX8chr2

113999303

-
intron-3CDSENST00000539812ENST00000263334PPARGchr3

12458653

+PAX8chr2

113999303

-
intron-3CDSENST00000539812ENST00000263335PPARGchr3

12458653

+PAX8chr2

113999303

-
intron-3CDSENST00000539812ENST00000348715PPARGchr3

12458653

+PAX8chr2

113999303

-
intron-3CDSENST00000539812ENST00000397647PPARGchr3

12458653

+PAX8chr2

113999303

-
intron-3CDSENST00000539812ENST00000429538PPARGchr3

12458653

+PAX8chr2

113999303

-

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 PPARG-PAX8


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 PPARG-PAX8


check button Go to

FGviewer for the breakpoints of chr3:12458653-chr2:113999303

.
- 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
.PAX8

Q06710

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: Transcription factor for the thyroid-specific expression of the genes exclusively expressed in the thyroid cell type, maintaining the functional differentiation of such cells.

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 PPARG-PAX8


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 PPARG-PAX8


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 PPARG-PAX8


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 PPARG-PAX8


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePPARGC0011860Diabetes Mellitus, Non-Insulin-Dependent6CTD_human;GENOMICS_ENGLAND
HgenePPARGC0238463Papillary thyroid carcinoma4ORPHANET
HgenePPARGC0002152Alloxan Diabetes3CTD_human
HgenePPARGC0002395Alzheimer's Disease3CTD_human
HgenePPARGC0011265Presenile dementia3CTD_human
HgenePPARGC0011853Diabetes Mellitus, Experimental3CTD_human
HgenePPARGC0020538Hypertensive disease3CTD_human
HgenePPARGC0021655Insulin Resistance3CTD_human
HgenePPARGC0022660Kidney Failure, Acute3CTD_human
HgenePPARGC0028754Obesity3CTD_human;GENOMICS_ENGLAND;UNIPROT
HgenePPARGC0035126Reperfusion Injury3CTD_human
HgenePPARGC0038433Streptozotocin Diabetes3CTD_human
HgenePPARGC0276496Familial Alzheimer Disease (FAD)3CTD_human
HgenePPARGC0494463Alzheimer Disease, Late Onset3CTD_human
HgenePPARGC0546126Acute Confusional Senile Dementia3CTD_human
HgenePPARGC0750900Alzheimer's Disease, Focal Onset3CTD_human
HgenePPARGC0750901Alzheimer Disease, Early Onset3CTD_human
HgenePPARGC0920563Insulin Sensitivity3CTD_human
HgenePPARGC1565662Acute Kidney Insufficiency3CTD_human
HgenePPARGC1720861Familial Partial Lipodystrophy, Type 33CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgenePPARGC2609414Acute kidney injury3CTD_human
HgenePPARGC0021368Inflammation2CTD_human
HgenePPARGC0022116Ischemia2CTD_human
HgenePPARGC0024623Malignant neoplasm of stomach2CTD_human
HgenePPARGC0025202melanoma2CTD_human
HgenePPARGC0030297Pancreatic Neoplasm2CTD_human
HgenePPARGC0038356Stomach Neoplasms2CTD_human
HgenePPARGC0346647Malignant neoplasm of pancreas2CTD_human
HgenePPARGC1708349Hereditary Diffuse Gastric Cancer2CTD_human
HgenePPARGC0001418Adenocarcinoma1CTD_human
HgenePPARGC0004153Atherosclerosis1CTD_human
HgenePPARGC0004763Barrett Esophagus1CTD_human
HgenePPARGC0007102Malignant tumor of colon1CTD_human;UNIPROT
HgenePPARGC0009375Colonic Neoplasms1CTD_human
HgenePPARGC0009402Colorectal Carcinoma1CTD_human
HgenePPARGC0009404Colorectal Neoplasms1CTD_human
HgenePPARGC0010346Crohn Disease1CTD_human
HgenePPARGC0011849Diabetes Mellitus1CTD_human
HgenePPARGC0011859Lipoatrophic Diabetes Mellitus1ORPHANET
HgenePPARGC0011881Diabetic Nephropathy1CTD_human
HgenePPARGC0017658Glomerulonephritis1CTD_human
HgenePPARGC0017667Nodular glomerulosclerosis1CTD_human
HgenePPARGC0018801Heart failure1CTD_human
HgenePPARGC0018802Congestive heart failure1CTD_human
HgenePPARGC0023212Left-Sided Heart Failure1CTD_human
HgenePPARGC0023645Lichen planus follicularis1GENOMICS_ENGLAND
HgenePPARGC0023794Lipoidosis1CTD_human
HgenePPARGC0023903Liver neoplasms1CTD_human
HgenePPARGC0025517Metabolic Diseases1CTD_human
HgenePPARGC0027746Nerve Degeneration1CTD_human
HgenePPARGC0029408Degenerative polyarthritis1CTD_human
HgenePPARGC0030246Pustulosis of Palms and Soles1CTD_human
HgenePPARGC0030625Passive Cutaneous Anaphylaxis1GENOMICS_ENGLAND
HgenePPARGC0033860Psoriasis1CTD_human
HgenePPARGC0035078Kidney Failure1CTD_human
HgenePPARGC0038525Subarachnoid Hemorrhage1CTD_human
HgenePPARGC0040136Thyroid Neoplasm1CTD_human
HgenePPARGC0079772T-Cell Lymphoma1CTD_human
HgenePPARGC0085278Antiphospholipid Syndrome1CTD_human
HgenePPARGC0085413Polycystic Kidney, Autosomal Dominant1CTD_human
HgenePPARGC0086743Osteoarthrosis Deformans1CTD_human
HgenePPARGC0086873Pseudopelade1GENOMICS_ENGLAND
HgenePPARGC0151468Thyroid Gland Follicular Adenoma1CTD_human
HgenePPARGC0156147Crohn's disease of large bowel1CTD_human
HgenePPARGC0205641Adenocarcinoma, Basal Cell1CTD_human
HgenePPARGC0205642Adenocarcinoma, Oxyphilic1CTD_human
HgenePPARGC0205643Carcinoma, Cribriform1CTD_human
HgenePPARGC0205644Carcinoma, Granular Cell1CTD_human
HgenePPARGC0205645Adenocarcinoma, Tubular1CTD_human
HgenePPARGC0206726gliosarcoma1ORPHANET
HgenePPARGC0221032Familial generalized lipodystrophy1ORPHANET
HgenePPARGC0221406Pituitary-dependent Cushing's disease1CTD_human
HgenePPARGC0235527Heart Failure, Right-Sided1CTD_human
HgenePPARGC0236811Chronobiology Disorders1CTD_human
HgenePPARGC0242339Dyslipidemias1CTD_human
HgenePPARGC0242488Acute Lung Injury1CTD_human
HgenePPARGC0267380Crohn's disease of the ileum1CTD_human
HgenePPARGC0270192Perinatal Subarachnoid Hemorrhage1CTD_human
HgenePPARGC0271694Familial partial lipodystrophy1CTD_human
HgenePPARGC0282548Leukostasis1CTD_human
HgenePPARGC0334588Giant Cell Glioblastoma1ORPHANET
HgenePPARGC0345904Malignant neoplasm of liver1CTD_human
HgenePPARGC0472383Subarachnoid Hemorrhage, Spontaneous1CTD_human
HgenePPARGC0525045Mood Disorders1PSYGENET
HgenePPARGC0549473Thyroid carcinoma1CTD_human
HgenePPARGC0598784Dyslipoproteinemias1CTD_human
HgenePPARGC0678202Regional enteritis1CTD_human
HgenePPARGC0751220Inappropriate ACTH Secretion Syndrome1CTD_human
HgenePPARGC0751530Subarachnoid Hemorrhage, Aneurysmal1CTD_human
HgenePPARGC0795688Subarachnoid Hemorrhage, Intracranial1CTD_human
HgenePPARGC0813142Circadian Rhythm Disorders1CTD_human
HgenePPARGC0887800Psychogenic Inversion of Circadian Rhythm1CTD_human
HgenePPARGC0887850Polycystic Kidney, Type 1 Autosomal Dominant Disease1CTD_human
HgenePPARGC0949272IIeocolitis1CTD_human
HgenePPARGC1258085Barrett Epithelium1CTD_human
HgenePPARGC1563937Atherogenesis1CTD_human
HgenePPARGC1565489Renal Insufficiency1CTD_human
HgenePPARGC1704377Bright Disease1CTD_human
HgenePPARGC1720859Familial Partial Lipodystrophy, Type 11CTD_human
HgenePPARGC1720860Familial Partial Lipodystrophy, Type 21CTD_human
HgenePPARGC1959583Myocardial Failure1CTD_human
HgenePPARGC1961112Heart Decompensation1CTD_human
HgenePPARGC2239176Liver carcinoma1CTD_human
HgenePPARGC2751306Polycystic kidney disease, type 21CTD_human
HgenePPARGC2931367Thyroid cancer, follicular1CTD_human
HgenePPARGC2936846Scarring alopecia1GENOMICS_ENGLAND
TgenePAX8C0151516Thyroid Hypoplasia4GENOMICS_ENGLAND;ORPHANET
TgenePAX8C0238463Papillary thyroid carcinoma4ORPHANET
TgenePAX8C1869118HYPOTHYROIDISM, CONGENITAL, DUE TO THYROID DYSGENESIS3CTD_human;GENOMICS_ENGLAND;UNIPROT
TgenePAX8C0009402Colorectal Carcinoma1CTD_human
TgenePAX8C0009404Colorectal Neoplasms1CTD_human
TgenePAX8C0010308Congenital Hypothyroidism1GENOMICS_ENGLAND
TgenePAX8C0266283Ectopic thyroid tissue (disorder)1ORPHANET
TgenePAX8C1563716Thyroid Dysgenesis1GENOMICS_ENGLAND
TgenePAX8C2931367Thyroid cancer, follicular1CTD_human