FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:PPP1R37-BCL3 (FusionGDB2 ID:67901)

Fusion Gene Summary for PPP1R37-BCL3

check button Fusion gene summary
Fusion gene informationFusion gene name: PPP1R37-BCL3
Fusion gene ID: 67901
HgeneTgene
Gene symbol

PPP1R37

BCL3

Gene ID

284352

602

Gene nameprotein phosphatase 1 regulatory subunit 37BCL3 transcription coactivator
SynonymsLRRC68BCL4|D19S37
Cytomap

19q13.32

19q13.32

Type of geneprotein-codingprotein-coding
Descriptionprotein phosphatase 1 regulatory subunit 37leucine rich repeat containing 68leucine-rich repeat-containing protein 68B-cell lymphoma 3 proteinB cell CLL/lymphoma 3B-cell leukemia/lymphoma 3B-cell lymphoma 3-encoded proteinBCL-3chronic lymphatic leukemia proteinproto-oncogene BCL3
Modification date2020031320200313
UniProtAcc

O75864

P20749

Ensembl transtripts involved in fusion geneENST00000496125, ENST00000221462, 
ENST00000421905, 
ENST00000164227, 
ENST00000487394, 
Fusion gene scores* DoF score20 X 7 X 13=18207 X 7 X 5=245
# samples 277
** MAII scorelog2(27/1820*10)=-2.75290713803523
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/245*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PPP1R37 [Title/Abstract] AND BCL3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPPP1R37(45596785)-BCL3(45254484), # samples:2
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
HgenePPP1R37

GO:0010923

negative regulation of phosphatase activity

19389623

TgeneBCL3

GO:0006351

transcription, DNA-templated

16306601

TgeneBCL3

GO:0006974

cellular response to DNA damage stimulus

16384933

TgeneBCL3

GO:0007249

I-kappaB kinase/NF-kappaB signaling

8196632

TgeneBCL3

GO:0009615

response to virus

16306601

TgeneBCL3

GO:0010225

response to UV-C

16384933

TgeneBCL3

GO:0042981

regulation of apoptotic process

16732314

TgeneBCL3

GO:0043066

negative regulation of apoptotic process

16384933

TgeneBCL3

GO:0045892

negative regulation of transcription, DNA-templated

16306601

TgeneBCL3

GO:0045893

positive regulation of transcription, DNA-templated

16384933


check buttonFusion gene breakpoints across PPP1R37 (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 BCL3 (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-XJ-A9DX-01APPP1R37chr19

45596785

+BCL3chr19

45254484

+
ChimerDB4UCECTCGA-B5-A3S1-01APPP1R37chr19

45596785

+BCL3chr19

45254484

+


Top

Fusion Gene ORF analysis for PPP1R37-BCL3

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-intronENST00000496125ENST00000164227PPP1R37chr19

45596785

+BCL3chr19

45254484

+
3UTR-intronENST00000496125ENST00000487394PPP1R37chr19

45596785

+BCL3chr19

45254484

+
5CDS-intronENST00000221462ENST00000164227PPP1R37chr19

45596785

+BCL3chr19

45254484

+
5CDS-intronENST00000221462ENST00000487394PPP1R37chr19

45596785

+BCL3chr19

45254484

+
5CDS-intronENST00000421905ENST00000164227PPP1R37chr19

45596785

+BCL3chr19

45254484

+
5CDS-intronENST00000421905ENST00000487394PPP1R37chr19

45596785

+BCL3chr19

45254484

+

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

Top

Fusion Genomic Features for PPP1R37-BCL3


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)
PPP1R37chr1945596785+BCL3chr1945254483+6.39E-111
PPP1R37chr1945596785+BCL3chr1945254483+6.39E-111

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.
genomic feature of top 1%

Top

Fusion Protein Features for PPP1R37-BCL3


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/:45596785/:45254484)
- 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
PPP1R37

O75864

BCL3

P20749

FUNCTION: Inhibits phosphatase activity of protein phosphatase 1 (PP1) complexes. {ECO:0000269|PubMed:19389623}.FUNCTION: Contributes to the regulation of transcriptional activation of NF-kappa-B target genes. In the cytoplasm, inhibits the nuclear translocation of the NF-kappa-B p50 subunit. In the nucleus, acts as transcriptional activator that promotes transcription of NF-kappa-B target genes. Contributes to the regulation of cell proliferation (By similarity). {ECO:0000250, ECO:0000269|PubMed:8453667}.

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


Top

Fusion Gene Sequence for PPP1R37-BCL3


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.

Top

Fusion Gene PPI Analysis for PPP1R37-BCL3


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


Top

Related Drugs for PPP1R37-BCL3


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

Related Diseases for PPP1R37-BCL3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource