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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:DCTN2-DENND3 (FusionGDB2 ID:21680)

Fusion Gene Summary for DCTN2-DENND3

check button Fusion gene summary
Fusion gene informationFusion gene name: DCTN2-DENND3
Fusion gene ID: 21680
HgeneTgene
Gene symbol

DCTN2

DENND3

Gene ID

10540

22898

Gene namedynactin subunit 2DENN domain containing 3
SynonymsDCTN50|DYNAMITIN|HEL-S-77|RBP50-
Cytomap

12q13.3

8q24.3

Type of geneprotein-codingprotein-coding
Descriptiondynactin subunit 250 kDa dynein-associated polypeptidedynactin 2 (p50)dynactin complex 50 kDa subunitepididymis secretory protein Li 77epididymis secretory sperm binding proteinp50 dynamitinDENN domain-containing protein 3DENN/MADD domain containing 3
Modification date2020031320200313
UniProtAcc

Q13561

A2RUS2

Ensembl transtripts involved in fusion geneENST00000434715, ENST00000537439, 
ENST00000543672, ENST00000548249, 
ENST00000551400, 
ENST00000262585, 
ENST00000424248, ENST00000518347, 
ENST00000518806, ENST00000519811, 
ENST00000523308, 
Fusion gene scores* DoF score15 X 9 X 6=8105 X 6 X 4=120
# samples 166
** MAII scorelog2(16/810*10)=-2.33985000288462
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DCTN2 [Title/Abstract] AND DENND3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDCTN2(57925798)-DENND3(142160933), # samples:3
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 DCTN2 (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 DENND3 (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
ChimerDB4LGGTCGA-P5-A72U-01ADCTN2chr12

57925798

-DENND3chr8

142160933

+
ChimerDB4LGGTCGA-P5-A72UDCTN2chr12

57925798

-DENND3chr8

142160933

+


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Fusion Gene ORF analysis for DCTN2-DENND3

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-intronENST00000434715ENST00000262585DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000434715ENST00000424248DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000434715ENST00000518347DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000434715ENST00000518806DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000434715ENST00000519811DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000434715ENST00000523308DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000537439ENST00000262585DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000537439ENST00000424248DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000537439ENST00000518347DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000537439ENST00000518806DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000537439ENST00000519811DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000537439ENST00000523308DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000543672ENST00000262585DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000543672ENST00000424248DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000543672ENST00000518347DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000543672ENST00000518806DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000543672ENST00000519811DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000543672ENST00000523308DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000548249ENST00000262585DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000548249ENST00000424248DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000548249ENST00000518347DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000548249ENST00000518806DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000548249ENST00000519811DCTN2chr12

57925798

-DENND3chr8

142160933

+
5CDS-intronENST00000548249ENST00000523308DCTN2chr12

57925798

-DENND3chr8

142160933

+
intron-intronENST00000551400ENST00000262585DCTN2chr12

57925798

-DENND3chr8

142160933

+
intron-intronENST00000551400ENST00000424248DCTN2chr12

57925798

-DENND3chr8

142160933

+
intron-intronENST00000551400ENST00000518347DCTN2chr12

57925798

-DENND3chr8

142160933

+
intron-intronENST00000551400ENST00000518806DCTN2chr12

57925798

-DENND3chr8

142160933

+
intron-intronENST00000551400ENST00000519811DCTN2chr12

57925798

-DENND3chr8

142160933

+
intron-intronENST00000551400ENST00000523308DCTN2chr12

57925798

-DENND3chr8

142160933

+

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 DCTN2-DENND3


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)
DCTN2chr1257925797-DENND3chr8142160932+0.000351060.9996489
DCTN2chr1257925797-DENND3chr8142160932+0.000351060.9996489
DCTN2chr1257925797-DENND3chr8142160932+0.000351060.9996489
DCTN2chr1257925797-DENND3chr8142160932+0.000351060.9996489

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 DCTN2-DENND3


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/:57925798/:142160933)
- 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
DCTN2

Q13561

DENND3

A2RUS2

FUNCTION: Modulates cytoplasmic dynein binding to an organelle, and plays a role in prometaphase chromosome alignment and spindle organization during mitosis. Involved in anchoring microtubules to centrosomes. May play a role in synapse formation during brain development.FUNCTION: Guanine nucleotide exchange factor (GEF) activating RAB12. Promotes the exchange of GDP to GTP, converting inactive GDP-bound RAB12 into its active GTP-bound form (PubMed:20937701). Regulates autophagy in response to starvation through RAB12 activation. Starvation leads to ULK1/2-dependent phosphorylation of Ser-472 and Ser-490, which in turn allows recruitment of 14-3-3 adapter proteins and leads to up-regulation of GEF activity towards RAB12 (By similarity). Also plays a role in protein transport from recycling endosomes to lysosomes, regulating, for instance, the degradation of the transferrin receptor and of the amino acid transporter PAT4 (PubMed:20937701). Starvation also induces phosphorylation at Tyr-858, which leads to up-regulated GEF activity and initiates autophagy (By similarity). {ECO:0000250|UniProtKB:A2RT67, ECO:0000269|PubMed:20937701}.

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 DCTN2-DENND3


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 DCTN2-DENND3


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 DCTN2-DENND3


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 DCTN2-DENND3


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