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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:PPP2CB-MYOC (FusionGDB2 ID:67548)

Fusion Gene Summary for PPP2CB-MYOC

check button Fusion gene summary
Fusion gene informationFusion gene name: PPP2CB-MYOC
Fusion gene ID: 67548
HgeneTgene
Gene symbol

PPP2CB

MYOC

Gene ID

5516

4653

Gene nameprotein phosphatase 2 catalytic subunit betamyocilin
SynonymsPP2Abeta|PP2CBGLC1A|GPOA|JOAG|JOAG1|TIGR
Cytomap

8p12

1q24.3

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein phosphatase 2A catalytic subunit beta isoformPP2A-betaprotein phosphatase 2 (formerly 2A), catalytic subunit, beta isoformprotein phosphatase 2, catalytic subunit, beta isoformprotein phosphatase 2, catalytic subunit, beta isomyocilinjuvenile-onset open-angle glaucoma 1mutated trabecular meshwork-induced glucocorticoid response proteinmyocilin 55 kDa subunitmyocilin trabecular meshwork inducible glucocorticoid response proteintrabecular meshwork inducible glucocorticoid r
Modification date2020031320200322
UniProtAcc.

Q8IZQ8

Ensembl transtripts involved in fusion geneENST00000520500, ENST00000221138, 
ENST00000518564, 
ENST00000037502, 
Fusion gene scores* DoF score6 X 5 X 5=1501 X 1 X 1=1
# samples 71
** MAII scorelog2(7/150*10)=-1.09953567355091
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: PPP2CB [Title/Abstract] AND MYOC [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPPP2CB(30669836)-MYOC(171607862), # samples:1
Anticipated loss of major functional domain due to fusion event.PPP2CB-MYOC seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
PPP2CB-MYOC seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene 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
TgeneMYOC

GO:0001649

osteoblast differentiation

23629661

TgeneMYOC

GO:0001953

negative regulation of cell-matrix adhesion

17984096

TgeneMYOC

GO:0014068

positive regulation of phosphatidylinositol 3-kinase signaling

21656515

TgeneMYOC

GO:0030335

positive regulation of cell migration

21656515

TgeneMYOC

GO:0035024

negative regulation of Rho protein signal transduction

17984096

TgeneMYOC

GO:0043408

regulation of MAPK cascade

23629661

TgeneMYOC

GO:0051496

positive regulation of stress fiber assembly

19188438

TgeneMYOC

GO:0051497

negative regulation of stress fiber assembly

17984096

TgeneMYOC

GO:0051894

positive regulation of focal adhesion assembly

18855004

TgeneMYOC

GO:0051897

positive regulation of protein kinase B signaling

21656515

TgeneMYOC

GO:0051901

positive regulation of mitochondrial depolarization

17516541

TgeneMYOC

GO:1900026

positive regulation of substrate adhesion-dependent cell spreading

18855004


check buttonFusion gene breakpoints across PPP2CB (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 MYOC (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
ChimerDB4BLCATCGA-BT-A3PK-01APPP2CBchr8

30669836

-MYOCchr1

171607862

-


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Fusion Gene ORF analysis for PPP2CB-MYOC

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
intron-3CDSENST00000520500ENST00000037502PPP2CBchr8

30669836

-MYOCchr1

171607862

-
Frame-shiftENST00000221138ENST00000037502PPP2CBchr8

30669836

-MYOCchr1

171607862

-
Frame-shiftENST00000518564ENST00000037502PPP2CBchr8

30669836

-MYOCchr1

171607862

-

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 PPP2CB-MYOC


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 PPP2CB-MYOC


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
.MYOC

Q8IZQ8

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: Smooth muscle cells (SM) and cardiac muscle cells-specific transcriptional factor which uses the canonical single or multiple CArG boxes DNA sequence. Acts as a cofactor of serum response factor (SRF) with the potential to modulate SRF-target genes. Plays a crucial role in cardiogenesis, urinary bladder development, and differentiation of the smooth muscle cell lineage (myogenesis) (By similarity). {ECO:0000250, ECO:0000269|PubMed:12640126, ECO:0000269|PubMed:31513549}.

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 PPP2CB-MYOC


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 PPP2CB-MYOC


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 PPP2CB-MYOC


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 PPP2CB-MYOC


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMYOCC1842028GLAUCOMA 1, OPEN ANGLE, A36CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneMYOCC0020302Hydrophthalmos3ORPHANET
TgeneMYOCC0017601Glaucoma1CTD_human
TgeneMYOCC0017612Glaucoma, Open-Angle1CTD_human
TgeneMYOCC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneMYOCC0271148Secondary Open Angle Glaucoma1CTD_human
TgeneMYOCC0339573Glaucoma, Primary Open Angle1CTD_human
TgeneMYOCC1856439GLAUCOMA 3, PRIMARY CONGENITAL, A1GENOMICS_ENGLAND;UNIPROT
TgeneMYOCC2981140Glaucoma of childhood1ORPHANET