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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: 22964

FusionGeneSummary for MYD88_ARHGEF10L

check button Fusion gene summary
Fusion gene informationFusion gene name: MYD88_ARHGEF10L
Fusion gene ID: 22964
HgeneTgene
Gene symbol

MYD88

ARHGEF10L

Gene ID

4615

55160

Gene namemyeloid differentiation primary response 88Rho guanine nucleotide exchange factor 10 like
SynonymsMYD88DGrinchGEF
Cytomap

3p22.2

1p36.13

Type of geneprotein-codingprotein-coding
Descriptionmyeloid differentiation primary response protein MyD88mutant myeloid differentiation primary response 88myeloid differentiation primary response gene (88)rho guanine nucleotide exchange factor 10-like proteinRho guanine nucleotide exchange factor (GEF) 10-like
Modification date2018052720180523
UniProtAcc

Q99836

Q9HCE6

Ensembl transtripts involved in fusion geneENST00000417037, ENST00000396334, 
ENST00000424893, ENST00000495303, 
ENST00000443433, ENST00000481122, 
ENST00000434513, ENST00000361221, 
ENST00000452522, ENST00000375415, 
ENST00000375420, ENST00000469726, 
ENST00000375408, ENST00000167825, 
Fusion gene scores* DoF score3 X 3 X 1=98 X 8 X 3=192
# samples 510
** MAII scorelog2(5/9*10)=2.47393118833241
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(10/192*10)=-0.941106310946431
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MYD88 [Title/Abstract] AND ARHGEF10L [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgeneMYD88

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
ChiTaRS3.1BE161378MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
ChiTaRS3.1BE161373MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
* 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
3UTR-intronENST00000417037ENST00000434513MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000417037ENST00000361221MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000417037ENST00000452522MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000417037ENST00000375415MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000417037ENST00000375420MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000417037ENST00000469726MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000417037ENST00000375408MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000417037ENST00000167825MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000396334ENST00000434513MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000396334ENST00000361221MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000396334ENST00000452522MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000396334ENST00000375415MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000396334ENST00000375420MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000396334ENST00000469726MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000396334ENST00000375408MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000396334ENST00000167825MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000424893ENST00000434513MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000424893ENST00000361221MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000424893ENST00000452522MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000424893ENST00000375415MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000424893ENST00000375420MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000424893ENST00000469726MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000424893ENST00000375408MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000424893ENST00000167825MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000495303ENST00000434513MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000495303ENST00000361221MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000495303ENST00000452522MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000495303ENST00000375415MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000495303ENST00000375420MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000495303ENST00000469726MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000495303ENST00000375408MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000495303ENST00000167825MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000443433ENST00000434513MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000443433ENST00000361221MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000443433ENST00000452522MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000443433ENST00000375415MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-intronENST00000443433ENST00000375420MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000443433ENST00000469726MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000443433ENST00000375408MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
3UTR-3UTRENST00000443433ENST00000167825MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
intron-intronENST00000481122ENST00000434513MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
intron-intronENST00000481122ENST00000361221MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
intron-intronENST00000481122ENST00000452522MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
intron-intronENST00000481122ENST00000375415MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
intron-intronENST00000481122ENST00000375420MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
intron-3UTRENST00000481122ENST00000469726MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
intron-3UTRENST00000481122ENST00000375408MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-
intron-3UTRENST00000481122ENST00000167825MYD88chr3

38182836

-ARHGEF10Lchr1

18021736

-

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FusionProtFeatures for MYD88_ARHGEF10L


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MYD88

Q99836

ARHGEF10L

Q9HCE6


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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FusionGeneSequence for MYD88_ARHGEF10L


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 MYD88_ARHGEF10L


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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RelatedDrugs for MYD88_ARHGEF10L


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 MYD88_ARHGEF10L


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMYD88C0007621Neoplastic Cell Transformation1CTD_human
HgeneMYD88C0014457Eosinophilia1CTD_human
HgeneMYD88C0020538Hypertensive disease1CTD_human
HgeneMYD88C0021368Inflammation1CTD_human
HgeneMYD88C0024301Lymphoma, Follicular1CTD_human
HgeneMYD88C0027626Neoplasm Invasiveness1CTD_human
HgeneMYD88C0032285Pneumonia1CTD_human
HgeneMYD88C0035126Reperfusion Injury1CTD_human
HgeneMYD88C0079744Diffuse Large B-Cell Lymphoma1CTD_human
HgeneMYD88C0344315Depressed mood1PSYGENET
HgeneMYD88C2677092MYD88 Deficiency1CTD_human;ORPHANET;UNIPROT