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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:SP3-PRCP (FusionGDB2 ID:HG6670TG5547)

Fusion Gene Summary for SP3-PRCP

check button Fusion gene summary
Fusion gene informationFusion gene name: SP3-PRCP
Fusion gene ID: hg6670tg5547
HgeneTgene
Gene symbol

SP3

PRCP

Gene ID

6670

5547

Gene nameSp3 transcription factorprolylcarboxypeptidase
SynonymsSPR2HUMPCP|PCP
Cytomap('SP3')('PRCP')

2q31.1

11q14.1

Type of geneprotein-codingprotein-coding
Descriptiontranscription factor Sp3GC-binding transcription factor Sp3specificity protein 3lysosomal Pro-X carboxypeptidaseangiotensinase Clysosomal carboxypeptidase Cproline carboxypeptidase
Modification date2020031320200313
UniProtAcc

Q02447

.
Ensembl transtripts involved in fusion geneENST00000310015, ENST00000418194, 
ENST00000455789, ENST00000483084, 
Fusion gene scores* DoF score12 X 8 X 9=8649 X 8 X 6=432
# samples 1811
** MAII scorelog2(18/864*10)=-2.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/432*10)=-1.97352778863881
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SP3 [Title/Abstract] AND PRCP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSP3(174819601)-PRCP(82564320), # samples:2
Anticipated loss of major functional domain due to fusion event.SP3-PRCP seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
SP3-PRCP seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
SP3-PRCP seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneSP3

GO:0006355

regulation of transcription, DNA-templated

12560508

HgeneSP3

GO:0045893

positive regulation of transcription, DNA-templated

12771217



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
ChimerDB4GBMTCGA-41-2572-01ASP3chr2

174819601

-PRCPchr11

82564320

-
ChimerDB4GBMTCGA-41-2572SP3chr2

174819600

-PRCPchr11

82564320

-


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Fusion Gene ORF analysis for SP3-PRCP

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-5UTRENST00000310015ENST00000535099SP3chr2

174819601

-PRCPchr11

82564320

-
5CDS-5UTRENST00000310015ENST00000535099SP3chr2

174819600

-PRCPchr11

82564320

-
5CDS-5UTRENST00000418194ENST00000535099SP3chr2

174819601

-PRCPchr11

82564320

-
5CDS-5UTRENST00000418194ENST00000535099SP3chr2

174819600

-PRCPchr11

82564320

-
5CDS-5UTRENST00000455789ENST00000535099SP3chr2

174819601

-PRCPchr11

82564320

-
5CDS-5UTRENST00000455789ENST00000535099SP3chr2

174819600

-PRCPchr11

82564320

-
5CDS-intronENST00000310015ENST00000525772SP3chr2

174819601

-PRCPchr11

82564320

-
5CDS-intronENST00000310015ENST00000525772SP3chr2

174819600

-PRCPchr11

82564320

-
5CDS-intronENST00000418194ENST00000525772SP3chr2

174819601

-PRCPchr11

82564320

-
5CDS-intronENST00000418194ENST00000525772SP3chr2

174819600

-PRCPchr11

82564320

-
5CDS-intronENST00000455789ENST00000525772SP3chr2

174819601

-PRCPchr11

82564320

-
5CDS-intronENST00000455789ENST00000525772SP3chr2

174819600

-PRCPchr11

82564320

-
Frame-shiftENST00000310015ENST00000313010SP3chr2

174819601

-PRCPchr11

82564320

-
Frame-shiftENST00000310015ENST00000313010SP3chr2

174819600

-PRCPchr11

82564320

-
Frame-shiftENST00000310015ENST00000393399SP3chr2

174819601

-PRCPchr11

82564320

-
Frame-shiftENST00000310015ENST00000393399SP3chr2

174819600

-PRCPchr11

82564320

-
Frame-shiftENST00000418194ENST00000313010SP3chr2

174819601

-PRCPchr11

82564320

-
Frame-shiftENST00000418194ENST00000313010SP3chr2

174819600

-PRCPchr11

82564320

-
Frame-shiftENST00000418194ENST00000393399SP3chr2

174819601

-PRCPchr11

82564320

-
Frame-shiftENST00000418194ENST00000393399SP3chr2

174819600

-PRCPchr11

82564320

-
Frame-shiftENST00000455789ENST00000313010SP3chr2

174819601

-PRCPchr11

82564320

-
Frame-shiftENST00000455789ENST00000313010SP3chr2

174819600

-PRCPchr11

82564320

-
Frame-shiftENST00000455789ENST00000393399SP3chr2

174819601

-PRCPchr11

82564320

-
Frame-shiftENST00000455789ENST00000393399SP3chr2

174819600

-PRCPchr11

82564320

-
intron-3CDSENST00000483084ENST00000313010SP3chr2

174819601

-PRCPchr11

82564320

-
intron-3CDSENST00000483084ENST00000313010SP3chr2

174819600

-PRCPchr11

82564320

-
intron-3CDSENST00000483084ENST00000393399SP3chr2

174819601

-PRCPchr11

82564320

-
intron-3CDSENST00000483084ENST00000393399SP3chr2

174819600

-PRCPchr11

82564320

-
intron-5UTRENST00000483084ENST00000535099SP3chr2

174819601

-PRCPchr11

82564320

-
intron-5UTRENST00000483084ENST00000535099SP3chr2

174819600

-PRCPchr11

82564320

-
intron-intronENST00000483084ENST00000525772SP3chr2

174819601

-PRCPchr11

82564320

-
intron-intronENST00000483084ENST00000525772SP3chr2

174819600

-PRCPchr11

82564320

-

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 SP3-PRCP


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 SP3-PRCP


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/:174819601/:82564320)
- 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
SP3

Q02447

.
FUNCTION: Transcriptional factor that can act as an activator or repressor depending on isoform and/or post-translational modifications. Binds to GT and GC boxes promoter elements. Competes with SP1 for the GC-box promoters. Weak activator of transcription but can activate a number of genes involved in different processes such as cell-cycle regulation, hormone-induction and house-keeping. {ECO:0000269|PubMed:10391891, ECO:0000269|PubMed:11812829, ECO:0000269|PubMed:12419227, ECO:0000269|PubMed:12837748, ECO:0000269|PubMed:15247228, ECO:0000269|PubMed:15494207, ECO:0000269|PubMed:15554904, ECO:0000269|PubMed:16781829, ECO:0000269|PubMed:17548428, ECO:0000269|PubMed:18187045, ECO:0000269|PubMed:18617891, ECO:0000269|PubMed:9278495}.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 SP3-PRCP


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 SP3-PRCP


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 SP3-PRCP


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 SP3-PRCP


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