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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:DMWD-DYNLRB1 (FusionGDB2 ID:23270)

Fusion Gene Summary for DMWD-DYNLRB1

check button Fusion gene summary
Fusion gene informationFusion gene name: DMWD-DYNLRB1
Fusion gene ID: 23270
HgeneTgene
Gene symbol

DMWD

DYNLRB1

Gene ID

1762

83658

Gene nameDM1 locus, WD repeat containingdynein light chain roadblock-type 1
SynonymsD19S593E|DMR-N9|DMRN9|gene59BITH|BLP|DNCL2A|DNLC2A|ROBLD1
Cytomap

19q13.32

20q11.22

Type of geneprotein-codingprotein-coding
Descriptiondystrophia myotonica WD repeat-containing proteindystrophia myotonica, WD repeat containingdystrophia myotonica-containing WD repeat motif proteinprotein 59dynein light chain roadblock-type 1ROBL/LC7-like 1bithoraxoid-like proteindynein, cytoplasmic, light polypeptide 2Adynein-associated protein Km23roadblock domain-containing protein 1
Modification date2020031320200320
UniProtAcc

Q09019

Q9NP97

Ensembl transtripts involved in fusion geneENST00000270223, ENST00000377735, 
ENST00000601370, 
ENST00000357156, 
ENST00000374846, ENST00000480759, 
ENST00000300469, ENST00000417166, 
Fusion gene scores* DoF score6 X 3 X 6=10817 X 12 X 12=2448
# samples 823
** MAII scorelog2(8/108*10)=-0.432959407276106
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(23/2448*10)=-3.41189779174828
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DMWD [Title/Abstract] AND DYNLRB1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDMWD(46289254)-DYNLRB1(33128686), # samples:1
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

check buttonFusion gene breakpoints across DMWD (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 DYNLRB1 (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
ChimerDB4COADTCGA-AA-3488-01ADMWDchr19

46289254

-DYNLRB1chr20

33128686

+


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Fusion Gene ORF analysis for DMWD-DYNLRB1

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
intron-3UTRENST00000270223ENST00000357156DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-3UTRENST00000270223ENST00000374846DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-3UTRENST00000270223ENST00000480759DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-3UTRENST00000377735ENST00000357156DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-3UTRENST00000377735ENST00000374846DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-3UTRENST00000377735ENST00000480759DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-3UTRENST00000601370ENST00000357156DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-3UTRENST00000601370ENST00000374846DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-3UTRENST00000601370ENST00000480759DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-intronENST00000270223ENST00000300469DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-intronENST00000270223ENST00000417166DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-intronENST00000377735ENST00000300469DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-intronENST00000377735ENST00000417166DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-intronENST00000601370ENST00000300469DMWDchr19

46289254

-DYNLRB1chr20

33128686

+
intron-intronENST00000601370ENST00000417166DMWDchr19

46289254

-DYNLRB1chr20

33128686

+

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 DMWD-DYNLRB1


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.

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Fusion Protein Features for DMWD-DYNLRB1


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/:46289254/:33128686)
- 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
DMWD

Q09019

DYNLRB1

Q9NP97

FUNCTION: Acts as one of several non-catalytic accessory components of the cytoplasmic dynein 1 complex that are thought to be involved in linking dynein to cargos and to adapter proteins that regulate dynein function. Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules.

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 DMWD-DYNLRB1


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 DMWD-DYNLRB1


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 DMWD-DYNLRB1


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 DMWD-DYNLRB1


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