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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:PTMA-PPIE (FusionGDB2 ID:HG5757TG10450)

Fusion Gene Summary for PTMA-PPIE

check button Fusion gene summary
Fusion gene informationFusion gene name: PTMA-PPIE
Fusion gene ID: hg5757tg10450
HgeneTgene
Gene symbol

PTMA

PPIE

Gene ID

5757

10450

Gene nameprothymosin alphapeptidylprolyl isomerase E
SynonymsTMSACYP-33|CYP33
Cytomap('PTMA')('PPIE')

2q37.1

1p34.2

Type of geneprotein-codingprotein-coding
Descriptionprothymosin alphagene sequence 28prothymosin alpha proteinprothymosin-I+/-peptidyl-prolyl cis-trans isomerase EPPIase Ecyclophilin-33peptidylprolyl isomerase E (cyclophilin E)rotamase E
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000409115, ENST00000341369, 
ENST00000409321, ENST00000409683, 
ENST00000410064, ENST00000466801, 
Fusion gene scores* DoF score19 X 19 X 8=28888 X 9 X 3=216
# samples 2010
** MAII scorelog2(20/2888*10)=-3.85199883711245
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/216*10)=-1.11103131238874
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PTMA [Title/Abstract] AND PPIE [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPTMA(232578241)-PPIE(40204568), # 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
TgenePPIE

GO:0000398

mRNA splicing, via spliceosome

28076346

TgenePPIE

GO:0000413

protein peptidyl-prolyl isomerization

20676357



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
ChiTaRS5.0N/ABQ923234PTMAchr2

232578241

+PPIEchr1

40204568

+


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Fusion Gene ORF analysis for PTMA-PPIE

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
3UTR-5UTRENST00000409115ENST00000324379PTMAchr2

232578241

+PPIEchr1

40204568

+
3UTR-5UTRENST00000409115ENST00000356511PTMAchr2

232578241

+PPIEchr1

40204568

+
3UTR-5UTRENST00000409115ENST00000372830PTMAchr2

232578241

+PPIEchr1

40204568

+
3UTR-5UTRENST00000409115ENST00000470213PTMAchr2

232578241

+PPIEchr1

40204568

+
3UTR-intronENST00000409115ENST00000480169PTMAchr2

232578241

+PPIEchr1

40204568

+
5CDS-5UTRENST00000341369ENST00000324379PTMAchr2

232578241

+PPIEchr1

40204568

+
5CDS-5UTRENST00000341369ENST00000356511PTMAchr2

232578241

+PPIEchr1

40204568

+
5CDS-5UTRENST00000341369ENST00000372830PTMAchr2

232578241

+PPIEchr1

40204568

+
5CDS-5UTRENST00000341369ENST00000470213PTMAchr2

232578241

+PPIEchr1

40204568

+
5CDS-intronENST00000341369ENST00000480169PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000409321ENST00000324379PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000409321ENST00000356511PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000409321ENST00000372830PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000409321ENST00000470213PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000409683ENST00000324379PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000409683ENST00000356511PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000409683ENST00000372830PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000409683ENST00000470213PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000410064ENST00000324379PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000410064ENST00000356511PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000410064ENST00000372830PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000410064ENST00000470213PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000466801ENST00000324379PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000466801ENST00000356511PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000466801ENST00000372830PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-5UTRENST00000466801ENST00000470213PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-intronENST00000409321ENST00000480169PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-intronENST00000409683ENST00000480169PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-intronENST00000410064ENST00000480169PTMAchr2

232578241

+PPIEchr1

40204568

+
intron-intronENST00000466801ENST00000480169PTMAchr2

232578241

+PPIEchr1

40204568

+

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 PTMA-PPIE


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)
PTMAchr2232578246+PPIEchr140204572+0.50579090.49420908
PTMAchr2232578246+PPIEchr140204572+0.50579090.49420908


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.
genomic feature of top 1%

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Fusion Protein Features for PTMA-PPIE


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/:232578241/:40204568)
- 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
..
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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 PTMA-PPIE


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 PTMA-PPIE


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 PTMA-PPIE


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 PTMA-PPIE


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePTMAC0001430Adenoma1CTD_human
HgenePTMAC0015695Fatty Liver1CTD_human
HgenePTMAC0024121Lung Neoplasms1CTD_human
HgenePTMAC0035412Rhabdomyosarcoma1CTD_human
HgenePTMAC0205646Adenoma, Basal Cell1CTD_human
HgenePTMAC0205647Follicular adenoma1CTD_human
HgenePTMAC0205648Adenoma, Microcystic1CTD_human
HgenePTMAC0205649Adenoma, Monomorphic1CTD_human
HgenePTMAC0205650Papillary adenoma1CTD_human
HgenePTMAC0205651Adenoma, Trabecular1CTD_human
HgenePTMAC0242379Malignant neoplasm of lung1CTD_human
HgenePTMAC2711227Steatohepatitis1CTD_human