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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: 25661

FusionGeneSummary for OXSR1_MYD88

check button Fusion gene summary
Fusion gene informationFusion gene name: OXSR1_MYD88
Fusion gene ID: 25661
HgeneTgene
Gene symbol

OXSR1

MYD88

Gene ID

9943

4615

Gene nameoxidative stress responsive 1myeloid differentiation primary response 88
SynonymsOSR1MYD88D
Cytomap

3p22.2

3p22.2

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase OSR1oxidative stress-responsive 1 proteinmyeloid differentiation primary response protein MyD88mutant myeloid differentiation primary response 88myeloid differentiation primary response gene (88)
Modification date2018052320180527
UniProtAcc

O95747

Q99836

Ensembl transtripts involved in fusion geneENST00000446845, ENST00000311806, 
ENST00000492714, 
ENST00000417037, 
ENST00000396334, ENST00000424893, 
ENST00000495303, ENST00000443433, 
ENST00000481122, 
Fusion gene scores* DoF score10 X 9 X 6=5402 X 3 X 2=12
# samples 102
** MAII scorelog2(10/540*10)=-2.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/12*10)=0.736965594166206
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]

Functional or gene categories assigned by FusionGDB annotationOncogene involved fusion gene, in-frame and retained their domain.
* 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

TgeneMYD88

GO:0070935

3'-UTR-mediated mRNA stabilization

15294994


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
TCGARVLUSCTCGA-52-7809-01AOXSR1chr3

38232330

+MYD88chr3

38182248

+
TCGALDLUSCTCGA-52-7809-01AOXSR1chr3

38232330

+MYD88chr3

38181355

+
* 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
Frame-shiftENST00000446845ENST00000417037OXSR1chr3

38232330

+MYD88chr3

38182248

+
Frame-shiftENST00000446845ENST00000396334OXSR1chr3

38232330

+MYD88chr3

38182248

+
Frame-shiftENST00000446845ENST00000424893OXSR1chr3

38232330

+MYD88chr3

38182248

+
In-frameENST00000446845ENST00000495303OXSR1chr3

38232330

+MYD88chr3

38182248

+
In-frameENST00000446845ENST00000443433OXSR1chr3

38232330

+MYD88chr3

38182248

+
5CDS-3UTRENST00000446845ENST00000481122OXSR1chr3

38232330

+MYD88chr3

38182248

+
Frame-shiftENST00000311806ENST00000417037OXSR1chr3

38232330

+MYD88chr3

38182248

+
Frame-shiftENST00000311806ENST00000396334OXSR1chr3

38232330

+MYD88chr3

38182248

+
Frame-shiftENST00000311806ENST00000424893OXSR1chr3

38232330

+MYD88chr3

38182248

+
In-frameENST00000311806ENST00000495303OXSR1chr3

38232330

+MYD88chr3

38182248

+
In-frameENST00000311806ENST00000443433OXSR1chr3

38232330

+MYD88chr3

38182248

+
5CDS-3UTRENST00000311806ENST00000481122OXSR1chr3

38232330

+MYD88chr3

38182248

+
intron-3CDSENST00000492714ENST00000417037OXSR1chr3

38232330

+MYD88chr3

38182248

+
intron-3CDSENST00000492714ENST00000396334OXSR1chr3

38232330

+MYD88chr3

38182248

+
intron-3CDSENST00000492714ENST00000424893OXSR1chr3

38232330

+MYD88chr3

38182248

+
intron-3CDSENST00000492714ENST00000495303OXSR1chr3

38232330

+MYD88chr3

38182248

+
intron-3CDSENST00000492714ENST00000443433OXSR1chr3

38232330

+MYD88chr3

38182248

+
intron-3UTRENST00000492714ENST00000481122OXSR1chr3

38232330

+MYD88chr3

38182248

+
In-frameENST00000446845ENST00000417037OXSR1chr3

38232330

+MYD88chr3

38181355

+
In-frameENST00000446845ENST00000396334OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000446845ENST00000424893OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000446845ENST00000495303OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000446845ENST00000443433OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-3UTRENST00000446845ENST00000481122OXSR1chr3

38232330

+MYD88chr3

38181355

+
In-frameENST00000311806ENST00000417037OXSR1chr3

38232330

+MYD88chr3

38181355

+
In-frameENST00000311806ENST00000396334OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000311806ENST00000424893OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000311806ENST00000495303OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-intronENST00000311806ENST00000443433OXSR1chr3

38232330

+MYD88chr3

38181355

+
5CDS-3UTRENST00000311806ENST00000481122OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-3CDSENST00000492714ENST00000417037OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-3CDSENST00000492714ENST00000396334OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-intronENST00000492714ENST00000424893OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-intronENST00000492714ENST00000495303OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-intronENST00000492714ENST00000443433OXSR1chr3

38232330

+MYD88chr3

38181355

+
intron-3UTRENST00000492714ENST00000481122OXSR1chr3

38232330

+MYD88chr3

38181355

+

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FusionProtFeatures for OXSR1_MYD88


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
OXSR1

O95747

MYD88

Q99836

Regulates downstream kinases in response toenvironmental stress. May also have a function in regulating theactin cytoskeleton. {ECO:0000269|PubMed:14707132,ECO:0000303|PubMed:14707132}.

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_3197528Nucleotide bindingATP
TgeneMYD88chr3:38232330chr3:38181355ENST00000443433+04159_296122205DomainTIR
TgeneMYD88chr3:38232330chr3:38181355ENST00000495303+03159_296-2160DomainTIR
TgeneMYD88chr3:38232330chr3:38181355ENST00000495303+0354_109-2160DomainDeath
TgeneMYD88chr3:38232330chr3:38181355ENST00000495303+03110_155-2160RegionIntermediate domain

- In-frame and not-retained protein feature among the 13 regional features.
>
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneOXSR1chr3:38232330chr3:38181355ENST00000311806+31817_29197528DomainProtein kinase
TgeneMYD88chr3:38232330chr3:38181355ENST00000443433+0454_109122205DomainDeath
TgeneMYD88chr3:38232330chr3:38181355ENST00000443433+04110_155122205RegionIntermediate domain


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FusionGeneSequence for OXSR1_MYD88


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 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
OXSR1ELAVL1, TGFBR1, TGFBR2, APP, RNASEH2C, CDK9, SLFN5, ANP32A, ADSL, API5, BTF3L4, UBA6, RPL17, USP5, AIFM1, MAD2L1, EGFR, RELL2, RELT, ACAD10, MARS, OARD1, PFKP, THUMPD1, NTRK1, BAG6, SNW1, CDC5L, RELL1, FGB, SNRNP27, ICMTMYD88SPOP, TLR2, TLR4, TLR5, TLR9, TLR3, IRAK1, RAC1, IRAK2, IRAK3, IL1R1, IRAK4, TIRAP, MYD88, TRAF6, MAP3K7, IL1RAP, IRF7, LRRFIP1, LRRFIP2, FLII, CISH, SARM1, SQSTM1, HDAC6, CBLB, TNIP1, TRAF3, STAP2, BTK, PELI1, IRF5, SMAD6, SMURF1, BST2, IL1RL1, TNFRSF13B, IKBKE, SASH1, SYK, SMAD3, SIAH1, USP7, TXN, FADD, MBIP, TLR7, POLR1C, MAL, MDM2, PRDX1, PFKL, SIAH2, CD93, IKBKG, IRF4, CYLD


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 OXSR1_MYD88


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 OXSR1_MYD88


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneOXSR1C0020538Hypertensive disease1CTD_human
HgeneOXSR1C0036341Schizophrenia1PSYGENET
TgeneMYD88C0007621Neoplastic Cell Transformation1CTD_human
TgeneMYD88C0014457Eosinophilia1CTD_human
TgeneMYD88C0020538Hypertensive disease1CTD_human
TgeneMYD88C0021368Inflammation1CTD_human
TgeneMYD88C0024301Lymphoma, Follicular1CTD_human
TgeneMYD88C0027626Neoplasm Invasiveness1CTD_human
TgeneMYD88C0032285Pneumonia1CTD_human
TgeneMYD88C0035126Reperfusion Injury1CTD_human
TgeneMYD88C0079744Diffuse Large B-Cell Lymphoma1CTD_human
TgeneMYD88C0344315Depressed mood1PSYGENET
TgeneMYD88C2677092MYD88 Deficiency1CTD_human;ORPHANET;UNIPROT