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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:DYRK1B-CNOT3 (FusionGDB2 ID:24720)

Fusion Gene Summary for DYRK1B-CNOT3

check button Fusion gene summary
Fusion gene informationFusion gene name: DYRK1B-CNOT3
Fusion gene ID: 24720
HgeneTgene
Gene symbol

DYRK1B

CNOT3

Gene ID

9149

4849

Gene namedual specificity tyrosine phosphorylation regulated kinase 1BCCR4-NOT transcription complex subunit 3
SynonymsAOMS3|MIRKIDDSADF|LENG2|NOT3|NOT3H
Cytomap

19q13.2

19q13.42

Type of geneprotein-codingprotein-coding
Descriptiondual specificity tyrosine-phosphorylation-regulated kinase 1Bdual specificity tyrosine-(Y)-phosphorylation regulated kinase 1Bminibrain-related kinasemirk protein kinaseCCR4-NOT transcription complex subunit 3CCR4-associated factor 3NOT3 (negative regulator of transcription 3, yeast) homologleukocyte receptor cluster member 2
Modification date2020031320200313
UniProtAcc

Q9Y463

O75175

Ensembl transtripts involved in fusion geneENST00000323039, ENST00000348817, 
ENST00000430012, ENST00000601972, 
ENST00000593685, ENST00000597639, 
ENST00000221232, ENST00000358389, 
ENST00000406403, ENST00000496327, 
Fusion gene scores* DoF score3 X 3 X 3=275 X 5 X 4=100
# samples 35
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DYRK1B [Title/Abstract] AND CNOT3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDYRK1B(40324662)-CNOT3(54655962), # 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
HgeneDYRK1B

GO:0006468

protein phosphorylation

11980910

HgeneDYRK1B

GO:0045893

positive regulation of transcription, DNA-templated

11980910


check buttonFusion gene breakpoints across DYRK1B (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 CNOT3 (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
ChimerDB4Non-Cancer235NDYRK1Bchr19

40324662

-CNOT3chr19

54655962

+


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Fusion Gene ORF analysis for DYRK1B-CNOT3

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
5UTR-3CDSENST00000323039ENST00000221232DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000323039ENST00000358389DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000323039ENST00000406403DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000348817ENST00000221232DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000348817ENST00000358389DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000348817ENST00000406403DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000430012ENST00000221232DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000430012ENST00000358389DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000430012ENST00000406403DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000601972ENST00000221232DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000601972ENST00000358389DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3CDSENST00000601972ENST00000406403DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3UTRENST00000323039ENST00000496327DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3UTRENST00000348817ENST00000496327DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3UTRENST00000430012ENST00000496327DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
5UTR-3UTRENST00000601972ENST00000496327DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
intron-3CDSENST00000593685ENST00000221232DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
intron-3CDSENST00000593685ENST00000358389DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
intron-3CDSENST00000593685ENST00000406403DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
intron-3CDSENST00000597639ENST00000221232DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
intron-3CDSENST00000597639ENST00000358389DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
intron-3CDSENST00000597639ENST00000406403DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
intron-3UTRENST00000593685ENST00000496327DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+
intron-3UTRENST00000597639ENST00000496327DYRK1Bchr19

40324662

-CNOT3chr19

54655962

+

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 DYRK1B-CNOT3


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)
DYRK1Bchr1940324662-CNOT3chr1954655962+0.1014053750.8985946
DYRK1Bchr1940324662-CNOT3chr1954655962+0.1014053750.8985946

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 DYRK1B-CNOT3


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/:40324662/:54655962)
- 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
DYRK1B

Q9Y463

CNOT3

O75175

FUNCTION: Dual-specificity kinase which possesses both serine/threonine and tyrosine kinase activities. Enhances the transcriptional activity of TCF1/HNF1A and FOXO1. Inhibits epithelial cell migration. Mediates colon carcinoma cell survival in mitogen-poor environments. Inhibits the SHH and WNT1 pathways, thereby enhancing adipogenesis. In addition, promotes expression of the gluconeogenic enzyme glucose-6-phosphatase catalytic subunit 1 (G6PC1). {ECO:0000269|PubMed:10910078, ECO:0000269|PubMed:11980910, ECO:0000269|PubMed:14500717, ECO:0000269|PubMed:24827035}.FUNCTION: Component of the CCR4-NOT complex which is one of the major cellular mRNA deadenylases and is linked to various cellular processes including bulk mRNA degradation, miRNA-mediated repression, translational repression during translational initiation and general transcription regulation. Additional complex functions may be a consequence of its influence on mRNA expression. May be involved in metabolic regulation; may be involved in recruitment of the CCR4-NOT complex to deadenylation target mRNAs involved in energy metabolism. Involved in mitotic progression and regulation of the spindle assembly checkpoint by regulating the stability of MAD1L1 mRNA. Can repress transcription and may link the CCR4-NOT complex to transcriptional regulation; the repressive function may involve histone deacetylases. Involved in the maintenance of embryonic stem (ES) cell identity. {ECO:0000269|PubMed:14707134, ECO:0000269|PubMed:22342980, ECO:0000269|PubMed:22367759}.

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 DYRK1B-CNOT3


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 DYRK1B-CNOT3


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 DYRK1B-CNOT3


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 DYRK1B-CNOT3


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