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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:PPP6R3-SPTBN2 (FusionGDB2 ID:67895)

Fusion Gene Summary for PPP6R3-SPTBN2

check button Fusion gene summary
Fusion gene informationFusion gene name: PPP6R3-SPTBN2
Fusion gene ID: 67895
HgeneTgene
Gene symbol

PPP6R3

SPTBN2

Gene ID

55291

6712

Gene nameprotein phosphatase 6 regulatory subunit 3spectrin beta, non-erythrocytic 2
SynonymsC11orf23|PP6R3|SAP190|SAPL|SAPLa|SAPS3GTRAP41|SCA5|SCAR14
Cytomap

11q13.2

11q13.2

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein phosphatase 6 regulatory subunit 3SAPS domain family, member 3sporulation-induced transcript 4-associated protein SAPLspectrin beta chain, non-erythrocytic 2beta-III spectringlutamate transporter EAAT4-associated protein 41spectrin beta III sigma 2spectrin beta chain, brain 2spectrin, non-erythroid beta chain 2spinocerebellar ataxia 5 protein
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000393799, ENST00000530427, 
ENST00000393800, ENST00000534534, 
ENST00000524845, ENST00000265637, 
ENST00000524904, ENST00000393801, 
ENST00000265636, ENST00000529710, 
ENST00000527403, 
ENST00000533211, 
ENST00000309996, ENST00000529997, 
Fusion gene scores* DoF score34 X 21 X 15=107106 X 7 X 4=168
# samples 436
** MAII scorelog2(43/10710*10)=-4.63847801004816
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/168*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PPP6R3 [Title/Abstract] AND SPTBN2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPPP6R3(68228295)-SPTBN2(66483452), # samples:3
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
HgenePPP6R3

GO:0043666

regulation of phosphoprotein phosphatase activity

16716191

TgeneSPTBN2

GO:0016192

vesicle-mediated transport

9826670


check buttonFusion gene breakpoints across PPP6R3 (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 SPTBN2 (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
ChimerDB4BRCATCGA-GM-A3NW-01APPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
ChimerDB4BRCATCGA-GM-A3NW-01APPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
ChimerDB4BRCATCGA-GM-A3NW-01APPP6R3chr11

68228295

-SPTBN2chr11

66483452

-


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Fusion Gene ORF analysis for PPP6R3-SPTBN2

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-3CDSENST00000393799ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000393799ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000393799ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
3UTR-3CDSENST00000530427ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
3UTR-3CDSENST00000530427ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
3UTR-3CDSENST00000530427ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000393800ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000393800ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000393800ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000534534ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000534534ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000534534ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000524845ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000524845ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000524845ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000265637ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000265637ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000265637ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000524904ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000524904ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000524904ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000393801ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000393801ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000393801ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000265636ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000265636ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000265636ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000529710ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000529710ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
5UTR-3CDSENST00000529710ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
intron-3CDSENST00000527403ENST00000533211PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
intron-3CDSENST00000527403ENST00000309996PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-
intron-3CDSENST00000527403ENST00000529997PPP6R3chr11

68228295

+SPTBN2chr11

66483452

-

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 PPP6R3-SPTBN2


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 PPP6R3-SPTBN2


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 PPP6R3-SPTBN2


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 PPP6R3-SPTBN2


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 PPP6R3-SPTBN2


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 PPP6R3-SPTBN2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSPTBN2C0752123Spinocerebellar Ataxia Type 52CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneSPTBN2C1854369Spinocerebellar ataxia 142GENOMICS_ENGLAND
TgeneSPTBN2C3809327SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 142GENOMICS_ENGLAND;ORPHANET
TgeneSPTBN2C0036341Schizophrenia1PSYGENET
TgeneSPTBN2C0424605Developmental delay (disorder)1GENOMICS_ENGLAND
TgeneSPTBN2C0557874Global developmental delay1GENOMICS_ENGLAND
TgeneSPTBN2C0598589Inherited neuropathies1GENOMICS_ENGLAND