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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:F2RL1-CYSTM1 (FusionGDB2 ID:HG2150TG84418)

Fusion Gene Summary for F2RL1-CYSTM1

check button Fusion gene summary
Fusion gene informationFusion gene name: F2RL1-CYSTM1
Fusion gene ID: hg2150tg84418
HgeneTgene
Gene symbol

F2RL1

CYSTM1

Gene ID

2150

84418

Gene nameF2R like trypsin receptor 1cysteine rich transmembrane module containing 1
SynonymsGPR11|PAR2C5orf32|ORF1-FL49
Cytomap('F2RL1')('CYSTM1')

5q13.3

5q31.3

Type of geneprotein-codingprotein-coding
Descriptionproteinase-activated receptor 2G-protein coupled receptor 11coagulation factor II (thrombin) receptor-like 1protease-activated receptor 2thrombin receptor-like 1cysteine-rich and transmembrane domain-containing protein 1UPF0467 protein C5orf32putative nuclear protein ORF1-FL49
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000296677, 
Fusion gene scores* DoF score2 X 2 X 2=826 X 7 X 13=2366
# samples 234
** MAII scorelog2(2/8*10)=1.32192809488736log2(34/2366*10)=-2.79884342220209
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: F2RL1 [Title/Abstract] AND CYSTM1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointF2RL1(76115089)-CYSTM1(139622890), # samples:1
Anticipated loss of major functional domain due to fusion event.F2RL1-CYSTM1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
F2RL1-CYSTM1 seems lost the major protein functional domain in Hgene 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
HgeneF2RL1

GO:0002690

positive regulation of leukocyte chemotaxis

17991872

HgeneF2RL1

GO:0002741

positive regulation of cytokine secretion involved in immune response

11441110

HgeneF2RL1

GO:0007204

positive regulation of cytosolic calcium ion concentration

10725339

HgeneF2RL1

GO:0010804

negative regulation of tumor necrosis factor-mediated signaling pathway

19781631

HgeneF2RL1

GO:0030193

regulation of blood coagulation

17848177

HgeneF2RL1

GO:0030836

positive regulation of actin filament depolymerization

17500066

HgeneF2RL1

GO:0032930

positive regulation of superoxide anion generation

11714832

HgeneF2RL1

GO:0034145

positive regulation of toll-like receptor 4 signaling pathway

18622013

HgeneF2RL1

GO:0035926

chemokine (C-C motif) ligand 2 secretion

21501162

HgeneF2RL1

GO:0042119

neutrophil activation

15155775

HgeneF2RL1

GO:0043122

regulation of I-kappaB kinase/NF-kappaB signaling

18453611

HgeneF2RL1

GO:0043123

positive regulation of I-kappaB kinase/NF-kappaB signaling

11413129

HgeneF2RL1

GO:0043311

positive regulation of eosinophil degranulation

11714832

HgeneF2RL1

GO:0045944

positive regulation of transcription by RNA polymerase II

16410250

HgeneF2RL1

GO:0046328

regulation of JNK cascade

16410250

HgeneF2RL1

GO:0046329

negative regulation of JNK cascade

19781631

HgeneF2RL1

GO:0046330

positive regulation of JNK cascade

11413129

HgeneF2RL1

GO:0050702

interleukin-1 beta secretion

15155775

HgeneF2RL1

GO:0050900

leukocyte migration

15155775

HgeneF2RL1

GO:0050927

positive regulation of positive chemotaxis

17991872

HgeneF2RL1

GO:0051607

defense response to virus

18453611|19494303

HgeneF2RL1

GO:0060100

positive regulation of phagocytosis, engulfment

21501162

HgeneF2RL1

GO:0061028

establishment of endothelial barrier

20826780

HgeneF2RL1

GO:0070374

positive regulation of ERK1 and ERK2 cascade

10725339

HgeneF2RL1

GO:0070963

positive regulation of neutrophil mediated killing of gram-negative bacterium

21501162

HgeneF2RL1

GO:0072608

interleukin-10 secretion

18453611

HgeneF2RL1

GO:0090195

chemokine secretion

19494303|21501162

HgeneF2RL1

GO:0090198

negative regulation of chemokine secretion

19865078

HgeneF2RL1

GO:0097029

mature conventional dendritic cell differentiation

16478888

HgeneF2RL1

GO:2000484

positive regulation of interleukin-8 secretion

15155775|17404307|18622013|19865078

HgeneF2RL1

GO:2000778

positive regulation of interleukin-6 secretion

11447194|15155775



check button Fusion gene information
* 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
ChimerDB4STADTCGA-D7-A4Z0-01AF2RL1chr5

76115089

+CYSTM1chr5

139622890

+


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Fusion Gene ORF analysis for F2RL1-CYSTM1

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-3UTRENST00000296677ENST00000509789F2RL1chr5

76115089

+CYSTM1chr5

139622890

+
Frame-shiftENST00000296677ENST00000261811F2RL1chr5

76115089

+CYSTM1chr5

139622890

+

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 F2RL1-CYSTM1


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)
F2RL1chr576115089+CYSTM1chr5139622889+0.0010692980.99893063
F2RL1chr576115089+CYSTM1chr5139622889+0.0010692980.99893063


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%

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Fusion Protein Features for F2RL1-CYSTM1


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/:76115089/:139622890)
- 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 F2RL1-CYSTM1


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 F2RL1-CYSTM1


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 F2RL1-CYSTM1


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 F2RL1-CYSTM1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneF2RL1C0021368Inflammation2CTD_human
HgeneF2RL1C0017160Gastroenteritis1CTD_human
HgeneF2RL1C0025202melanoma1CTD_human
HgeneF2RL1C0033774Pruritus1CTD_human
HgeneF2RL1C0151744Myocardial Ischemia1CTD_human
TgeneC0023893Liver Cirrhosis, Experimental1CTD_human