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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:PLCB1-SMOX (FusionGDB2 ID:HG23236TG54498)

Fusion Gene Summary for PLCB1-SMOX

check button Fusion gene summary
Fusion gene informationFusion gene name: PLCB1-SMOX
Fusion gene ID: hg23236tg54498
HgeneTgene
Gene symbol

PLCB1

SMOX

Gene ID

23236

54498

Gene namephospholipase C beta 1spermine oxidase
SynonymsEIEE12|PI-PLC|PLC-154|PLC-I|PLC-beta-1|PLC154|PLCB1A|PLCB1BC20orf16|PAO|PAO-1|PAO1|PAOH|PAOH1|SMO
Cytomap('PLCB1')('SMOX')

20p12.3

20p13

Type of geneprotein-codingprotein-coding
Description1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-11-phosphatidyl-D-myo-inositol-4,5-bisphosphateinositoltrisphosphohydrolasemonophosphatidylinositol phosphodiesterasephosphoinositidase Cphosphoinositide phospholipase Cphospholipase C, spermine oxidaseflavin containing amine oxidaseflavin-containing spermine oxidasepolyamine oxidase 1putative cyclin G1 interacting protein
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000494924, ENST00000338037, 
ENST00000378637, ENST00000378641, 
Fusion gene scores* DoF score24 X 20 X 10=48006 X 5 X 4=120
# samples 226
** MAII scorelog2(22/4800*10)=-4.44745897697122
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PLCB1 [Title/Abstract] AND SMOX [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPLCB1(8714039)-SMOX(4101627), # 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
HgenePLCB1

GO:0035722

interleukin-12-mediated signaling pathway

11743656

HgenePLCB1

GO:0035723

interleukin-15-mediated signaling pathway

11743656

HgenePLCB1

GO:0046330

positive regulation of JNK cascade

9500449

HgenePLCB1

GO:0070498

interleukin-1-mediated signaling pathway

8872139

TgeneSMOX

GO:0006598

polyamine catabolic process

12477380



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
ChimerDB4COADTCGA-D5-5541-01APLCB1chr20

8714039

+SMOXchr20

4101627

+


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Fusion Gene ORF analysis for PLCB1-SMOX

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-intronENST00000494924ENST00000278795PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000305958PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000339123PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000346595PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000379460PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000484515PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000278795PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000305958PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000339123PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000346595PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000379460PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000484515PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000278795PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000305958PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000339123PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000346595PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000379460PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000484515PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000278795PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000305958PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000339123PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000346595PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000379460PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000484515PLCB1chr20

8714039

+SMOXchr20

4101627

+

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 PLCB1-SMOX


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)


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Fusion Protein Features for PLCB1-SMOX


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/:8714039/:4101627)
- 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 PLCB1-SMOX


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 PLCB1-SMOX


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 PLCB1-SMOX


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 PLCB1-SMOX


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePLCB1C0037769West Syndrome2ORPHANET
HgenePLCB1C0005586Bipolar Disorder1PSYGENET
HgenePLCB1C0007102Malignant tumor of colon1CTD_human
HgenePLCB1C0009375Colonic Neoplasms1CTD_human
HgenePLCB1C0030193Pain1CTD_human
HgenePLCB1C0036341Schizophrenia1CTD_human
HgenePLCB1C0041696Unipolar Depression1PSYGENET
HgenePLCB1C0234230Pain, Burning1CTD_human
HgenePLCB1C0234238Ache1CTD_human
HgenePLCB1C0234254Radiating pain1CTD_human
HgenePLCB1C0458257Pain, Splitting1CTD_human
HgenePLCB1C0458259Pain, Crushing1CTD_human
HgenePLCB1C0751407Pain, Migratory1CTD_human
HgenePLCB1C0751408Suffering, Physical1CTD_human
HgenePLCB1C1269683Major Depressive Disorder1PSYGENET
HgenePLCB1C2713368Hematopoetic Myelodysplasia1CTD_human
HgenePLCB1C3150988EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 121CTD_human;GENOMICS_ENGLAND
HgenePLCB1C3463824MYELODYSPLASTIC SYNDROME1CTD_human
TgeneC0038454Cerebrovascular accident1CTD_human
TgeneC0238281Middle Cerebral Artery Syndrome1CTD_human
TgeneC0525045Mood Disorders1PSYGENET
TgeneC0740376Middle Cerebral Artery Thrombosis1CTD_human
TgeneC0740391Middle Cerebral Artery Occlusion1CTD_human
TgeneC0740392Infarction, Middle Cerebral Artery1CTD_human
TgeneC0751845Middle Cerebral Artery Embolus1CTD_human
TgeneC0751846Left Middle Cerebral Artery Infarction1CTD_human
TgeneC0751847Embolic Infarction, Middle Cerebral Artery1CTD_human
TgeneC0751848Thrombotic Infarction, Middle Cerebral Artery1CTD_human
TgeneC0751849Right Middle Cerebral Artery Infarction1CTD_human
TgeneC0751956Acute Cerebrovascular Accidents1CTD_human