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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:OXSR1-MYD88 (FusionGDB2 ID:62056)

Fusion Gene Summary for OXSR1-MYD88

check button Fusion gene summary
Fusion gene informationFusion gene name: OXSR1-MYD88
Fusion gene ID: 62056
HgeneTgene
Gene symbol

OXSR1

MYD88

Gene ID

9943

4615

Gene nameoxidative stress responsive kinase 1MYD88 innate immune signal transduction adaptor
SynonymsOSR1MYD88D
Cytomap

3p22.2

3p22.2

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase OSR1oxidative stress responsive 1oxidative stress-responsive 1 proteinmyeloid differentiation primary response protein MyD88mutant myeloid differentiation primary response 88myeloid differentiation primary response 88myeloid differentiation primary response gene (88)
Modification date2020031320200327
UniProtAcc.

Q99836

Ensembl transtripts involved in fusion geneENST00000311806, ENST00000446845, 
ENST00000492714, 
ENST00000481122, 
ENST00000424893, ENST00000443433, 
ENST00000495303, ENST00000396334, 
ENST00000417037, 
Fusion gene scores* DoF score9 X 10 X 8=7206 X 4 X 2=48
# samples 126
** MAII scorelog2(12/720*10)=-2.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/48*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: OXSR1 [Title/Abstract] AND MYD88 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointOXSR1(38232330)-MYD88(38181355), # samples:2
Anticipated loss of major functional domain due to fusion event.OXSR1-MYD88 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
OXSR1-MYD88 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
OXSR1-MYD88 seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
OXSR1-MYD88 seems lost the major protein functional domain in Tgene partner, which is a CGC 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
HgeneOXSR1

GO:0006468

protein phosphorylation

14707132

HgeneOXSR1

GO:0018107

peptidyl-threonine phosphorylation

24393035

HgeneOXSR1

GO:0035556

intracellular signal transduction

14707132

HgeneOXSR1

GO:0046777

protein autophosphorylation

22052202

TgeneMYD88

GO:0070935

3'-UTR-mediated mRNA stabilization

15294994


check buttonFusion gene breakpoints across OXSR1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across MYD88 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4LUSCTCGA-52-7809-01AOXSR1chr3

38232330

+MYD88chr3

38181355

+
ChimerDB4LUSCTCGA-52-7809-01AOXSR1chr3

38232330

-MYD88chr3

38182248

+
ChimerDB4LUSCTCGA-52-7809OXSR1chr3

38232330

+MYD88chr3

38181355

+


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Fusion Gene ORF analysis for OXSR1-MYD88

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-3UTRENST00000311806ENST00000481122OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-3UTRENST00000311806ENST00000481122OXSR1chr3

38232330

-MYD88chr3

38182248

+
5CDS-3UTRENST00000446845ENST00000481122OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-3UTRENST00000446845ENST00000481122OXSR1chr3

38232330

-MYD88chr3

38182248

+
5CDS-intronENST00000311806ENST00000424893OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000311806ENST00000443433OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000311806ENST00000495303OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000446845ENST00000424893OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000446845ENST00000443433OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000446845ENST00000495303OXSR1chr3

38232330

+MYD88chr3

38181355

+
Frame-shiftENST00000311806ENST00000396334OXSR1chr3

38232330

-MYD88chr3

38182248

+
Frame-shiftENST00000311806ENST00000417037OXSR1chr3

38232330

-MYD88chr3

38182248

+
Frame-shiftENST00000311806ENST00000424893OXSR1chr3

38232330

-MYD88chr3

38182248

+
Frame-shiftENST00000446845ENST00000396334OXSR1chr3

38232330

-MYD88chr3

38182248

+
Frame-shiftENST00000446845ENST00000417037OXSR1chr3

38232330

-MYD88chr3

38182248

+
Frame-shiftENST00000446845ENST00000424893OXSR1chr3

38232330

-MYD88chr3

38182248

+
In-frameENST00000311806ENST00000396334OXSR1chr3

38232330

+MYD88chr3

38181355

+
In-frameENST00000311806ENST00000417037OXSR1chr3

38232330

+MYD88chr3

38181355

+
In-frameENST00000311806ENST00000443433OXSR1chr3

38232330

-MYD88chr3

38182248

+
In-frameENST00000311806ENST00000495303OXSR1chr3

38232330

-MYD88chr3

38182248

+
In-frameENST00000446845ENST00000396334OXSR1chr3

38232330

+MYD88chr3

38181355

+
In-frameENST00000446845ENST00000417037OXSR1chr3

38232330

+MYD88chr3

38181355

+
In-frameENST00000446845ENST00000443433OXSR1chr3

38232330

-MYD88chr3

38182248

+
In-frameENST00000446845ENST00000495303OXSR1chr3

38232330

-MYD88chr3

38182248

+
intron-3CDSENST00000492714ENST00000396334OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-3CDSENST00000492714ENST00000396334OXSR1chr3

38232330

-MYD88chr3

38182248

+
intron-3CDSENST00000492714ENST00000417037OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-3CDSENST00000492714ENST00000417037OXSR1chr3

38232330

-MYD88chr3

38182248

+
intron-3CDSENST00000492714ENST00000424893OXSR1chr3

38232330

-MYD88chr3

38182248

+
intron-3CDSENST00000492714ENST00000443433OXSR1chr3

38232330

-MYD88chr3

38182248

+
intron-3CDSENST00000492714ENST00000495303OXSR1chr3

38232330

-MYD88chr3

38182248

+
intron-3UTRENST00000492714ENST00000481122OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-3UTRENST00000492714ENST00000481122OXSR1chr3

38232330

-MYD88chr3

38182248

+
intron-intronENST00000492714ENST00000424893OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-intronENST00000492714ENST00000443433OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-intronENST00000492714ENST00000495303OXSR1chr3

38232330

+MYD88chr3

38181355

+

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 OXSR1-MYD88


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)
OXSR1chr338232330+MYD88chr338181354+0.0003247220.9996753
OXSR1chr338232330+MYD88chr338181354+0.0003247220.9996753
OXSR1chr338232330+MYD88chr338181354+0.0003247220.9996753
OXSR1chr338232330+MYD88chr338181354+0.0003247220.9996753

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.
genomic feature

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 OXSR1-MYD88


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/chr3:38232330/chr3:38181355)
- 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
.MYD88

Q99836

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: Adapter protein involved in the Toll-like receptor and IL-1 receptor signaling pathway in the innate immune response (PubMed:15361868, PubMed:18292575). Acts via IRAK1, IRAK2, IRF7 and TRAF6, leading to NF-kappa-B activation, cytokine secretion and the inflammatory response (PubMed:15361868, PubMed:24316379, PubMed:19506249). Increases IL-8 transcription (PubMed:9013863). Involved in IL-18-mediated signaling pathway. Activates IRF1 resulting in its rapid migration into the nucleus to mediate an efficient induction of IFN-beta, NOS2/INOS, and IL12A genes. MyD88-mediated signaling in intestinal epithelial cells is crucial for maintenance of gut homeostasis and controls the expression of the antimicrobial lectin REG3G in the small intestine (By similarity). {ECO:0000250|UniProtKB:P22366, ECO:0000269|PubMed:15361868, ECO:0000269|PubMed:18292575, ECO:0000269|PubMed:19506249, ECO:0000269|PubMed:20855887, ECO:0000269|PubMed:24316379, ECO:0000269|PubMed:9013863}.

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
HgeneOXSR1chr3:38232330chr3:38181355ENST00000311806+31823_3197528.0Nucleotide bindingATP
HgeneOXSR1chr3:38232330chr3:38182248ENST00000311806-31823_3197528.0Nucleotide bindingATP
TgeneMYD88chr3:38232330chr3:38181355ENST0000044343304159_293122205.0DomainTIR
TgeneMYD88chr3:38232330chr3:38181355ENST0000049530303159_2930160.0DomainTIR
TgeneMYD88chr3:38232330chr3:38181355ENST000004953030354_1090160.0DomainDeath
TgeneMYD88chr3:38232330chr3:38182248ENST0000049530303159_293122160.0DomainTIR
TgeneMYD88chr3:38232330chr3:38181355ENST0000049530303110_1550160.0RegionIntermediate domain

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneOXSR1chr3:38232330chr3:38181355ENST00000311806+31817_29197528.0DomainProtein kinase
HgeneOXSR1chr3:38232330chr3:38182248ENST00000311806-31817_29197528.0DomainProtein kinase
TgeneMYD88chr3:38232330chr3:38181355ENST000004434330454_109122205.0DomainDeath
TgeneMYD88chr3:38232330chr3:38182248ENST0000044343314159_293167205.0DomainTIR
TgeneMYD88chr3:38232330chr3:38182248ENST000004434331454_109167205.0DomainDeath
TgeneMYD88chr3:38232330chr3:38182248ENST000004953030354_109122160.0DomainDeath
TgeneMYD88chr3:38232330chr3:38181355ENST0000044343304110_155122205.0RegionIntermediate domain
TgeneMYD88chr3:38232330chr3:38182248ENST0000044343314110_155167205.0RegionIntermediate domain
TgeneMYD88chr3:38232330chr3:38182248ENST0000049530303110_155122160.0RegionIntermediate domain


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Fusion Gene Sequence for OXSR1-MYD88


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 OXSR1-MYD88


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 OXSR1-MYD88


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 OXSR1-MYD88


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