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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 27485

FusionGeneSummary for PLCB1_SMOX

check button Fusion gene summary
Fusion gene informationFusion gene name: PLCB1_SMOX
Fusion gene ID: 27485
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

20p12.3

20p13

Type of geneprotein-codingprotein-coding
Description1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-11-phosphatidyl-D-myo-inositol-4,5-bisphosphateinositoltrisphosphohydrolasemonophosphatidylinositol phosphodiesterasephosphoinositidase Cphospholipase C, beta 1 (phosphoinositide-specificspermine oxidaseflavin containing amine oxidaseflavin-containing spermine oxidasepolyamine oxidase 1putative cyclin G1 interacting protein
Modification date2018051920180523
UniProtAcc

Q9NQ66

Q9NWM0

Ensembl transtripts involved in fusion geneENST00000378641, ENST00000338037, 
ENST00000378637, ENST00000494924, 
ENST00000278795, ENST00000305958, 
ENST00000339123, ENST00000484515, 
ENST00000346595, ENST00000379460, 
Fusion gene scores* DoF score13 X 9 X 9=10534 X 3 X 4=48
# samples 114
** MAII scorelog2(11/1053*10)=-3.25893000750106
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
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]

Functional or gene categories assigned by FusionGDB annotation
* 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 three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGALDCOADTCGA-D5-5541-01APLCB1chr20

8714039

+SMOXchr20

4101627

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
5CDS-intronENST00000378641ENST00000278795PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000305958PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000339123PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000484515PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000346595PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378641ENST00000379460PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000278795PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000305958PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000339123PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000484515PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000346595PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000338037ENST00000379460PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000278795PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000305958PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000339123PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000484515PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000346595PLCB1chr20

8714039

+SMOXchr20

4101627

+
5CDS-intronENST00000378637ENST00000379460PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000278795PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000305958PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000339123PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000484515PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000346595PLCB1chr20

8714039

+SMOXchr20

4101627

+
3UTR-intronENST00000494924ENST00000379460PLCB1chr20

8714039

+SMOXchr20

4101627

+

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FusionProtFeatures for PLCB1_SMOX


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PLCB1

Q9NQ66

SMOX

Q9NWM0


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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FusionGeneSequence for PLCB1_SMOX


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI 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
PLCB1TRPM7, SLC9A3R1, SPTBN1, KRIT1, PCF11, GNA11, GNAQ, PLCB1, CTBP1, CTBP2, TFCP2, CEP76, BTN2A1, PTGER3, GAN, DEF8SMOXALDH1A3, CCT6B, HERC1, CCT3, CCT2, FLNC, TRIM25, MCPH1


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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RelatedDrugs for PLCB1_SMOX


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for PLCB1_SMOX


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePLCB1C0005586Bipolar Disorder1PSYGENET
HgenePLCB1C0009375Colonic Neoplasms1CTD_human
HgenePLCB1C0030193Pain1CTD_human
HgenePLCB1C0036341Schizophrenia1CTD_human
HgenePLCB1C0041696Unipolar Depression1PSYGENET
HgenePLCB1C1269683Major Depressive Disorder1PSYGENET
HgenePLCB1C3463824MYELODYSPLASTIC SYNDROME1CTD_human
TgeneSMOXC0038454Cerebrovascular accident1CTD_human
TgeneSMOXC0525045Mood Disorders1PSYGENET