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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:MST1R-FNDC3B (FusionGDB2 ID:55432)

Fusion Gene Summary for MST1R-FNDC3B

check button Fusion gene summary
Fusion gene informationFusion gene name: MST1R-FNDC3B
Fusion gene ID: 55432
HgeneTgene
Gene symbol

MST1R

FNDC3B

Gene ID

4486

64778

Gene namemacrophage stimulating 1 receptorfibronectin type III domain containing 3B
SynonymsCD136|CDw136|NPCA3|PTK8|RON|SEAFAD104|PRO4979|YVTM2421
Cytomap

3p21.31

3q26.31

Type of geneprotein-codingprotein-coding
Descriptionmacrophage-stimulating protein receptorMSP receptorPTK8 protein tyrosine kinase 8S13 avian erythroblastosis oncogene homologS13 erythroblastosis oncogene homologc-met-related tyrosine kinasep185-Ronfibronectin type III domain-containing protein 3BHCV NS5A-binding protein 37factor for adipocyte differentiation 104
Modification date2020031320200313
UniProtAcc

Q04912

Q53EP0

Ensembl transtripts involved in fusion geneENST00000296474, ENST00000344206, 
ENST00000476794, ENST00000336824, 
ENST00000392699, ENST00000415807, 
ENST00000416957, ENST00000421757, 
ENST00000423424, 
Fusion gene scores* DoF score2 X 2 X 2=821 X 23 X 11=5313
# samples 228
** MAII scorelog2(2/8*10)=1.32192809488736log2(28/5313*10)=-4.2460279805281
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MST1R [Title/Abstract] AND FNDC3B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMST1R(49932600)-FNDC3B(171904502), # samples:2
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
HgeneMST1R

GO:0009615

response to virus

12676986

HgeneMST1R

GO:0043406

positive regulation of MAP kinase activity

12676986

HgeneMST1R

GO:0051897

positive regulation of protein kinase B signaling

12676986


check buttonFusion gene breakpoints across MST1R (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 FNDC3B (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
ChimerDB4LUADTCGA-95-7039-01AMST1Rchr3

49932600

-FNDC3Bchr3

171904502

+


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Fusion Gene ORF analysis for MST1R-FNDC3B

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-3UTRENST00000296474ENST00000476794MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-3UTRENST00000344206ENST00000476794MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000296474ENST00000336824MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000296474ENST00000392699MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000296474ENST00000415807MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000296474ENST00000416957MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000296474ENST00000421757MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000296474ENST00000423424MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000344206ENST00000336824MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000344206ENST00000392699MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000344206ENST00000415807MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000344206ENST00000416957MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000344206ENST00000421757MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+
5CDS-intronENST00000344206ENST00000423424MST1Rchr3

49932600

-FNDC3Bchr3

171904502

+

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 MST1R-FNDC3B


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.
genomic feature of top 1%

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Fusion Protein Features for MST1R-FNDC3B


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/:49932600/:171904502)
- 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
MST1R

Q04912

FNDC3B

Q53EP0

FUNCTION: Receptor tyrosine kinase that transduces signals from the extracellular matrix into the cytoplasm by binding to MST1 ligand. Regulates many physiological processes including cell survival, migration and differentiation. Ligand binding at the cell surface induces autophosphorylation of RON on its intracellular domain that provides docking sites for downstream signaling molecules. Following activation by ligand, interacts with the PI3-kinase subunit PIK3R1, PLCG1 or the adapter GAB1. Recruitment of these downstream effectors by RON leads to the activation of several signaling cascades including the RAS-ERK, PI3 kinase-AKT, or PLCgamma-PKC. RON signaling activates the wound healing response by promoting epithelial cell migration, proliferation as well as survival at the wound site. Plays also a role in the innate immune response by regulating the migration and phagocytic activity of macrophages. Alternatively, RON can also promote signals such as cell migration and proliferation in response to growth factors other than MST1 ligand. {ECO:0000269|PubMed:18836480, ECO:0000269|PubMed:7939629, ECO:0000269|PubMed:9764835}.FUNCTION: May be a positive regulator of adipogenesis. {ECO:0000269|PubMed:15564382}.

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 MST1R-FNDC3B


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 MST1R-FNDC3B


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 MST1R-FNDC3B


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 MST1R-FNDC3B


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