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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:KDM6B-DDX42 (FusionGDB2 ID:41918)

Fusion Gene Summary for KDM6B-DDX42

check button Fusion gene summary
Fusion gene informationFusion gene name: KDM6B-DDX42
Fusion gene ID: 41918
HgeneTgene
Gene symbol

KDM6B

DDX42

Gene ID

23135

11325

Gene namelysine demethylase 6BDEAD-box helicase 42
SynonymsJMJD3|NEDCFSADDX42P|RHELP|RNAHP|SF3B8|SF3b125
Cytomap

17p13.1

17q23.3

Type of geneprotein-codingprotein-coding
Descriptionlysine-specific demethylase 6BjmjC domain-containing protein 3jumonji domain containing 3, histone lysine demethylasejumonji domain-containing protein 3lysine (K)-specific demethylase 6BATP-dependent RNA helicase DDX42DEAD (Asp-Glu-Ala-Asp) box helicase 42DEAD (Asp-Glu-Ala-Asp) box polypeptide 42SF3b DEAD box proteinsplicing factor 3B-associated 125 kDa proteinsplicing factor 3b, subunit 8
Modification date2020031320200313
UniProtAcc

O15054

Q86XP3

Ensembl transtripts involved in fusion geneENST00000572030, ENST00000254846, 
ENST00000448097, 
ENST00000389924, 
ENST00000578681, ENST00000583590, 
ENST00000359353, ENST00000457800, 
ENST00000582985, 
Fusion gene scores* DoF score8 X 5 X 7=28015 X 18 X 10=2700
# samples 818
** MAII scorelog2(8/280*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(18/2700*10)=-3.90689059560852
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KDM6B [Title/Abstract] AND DDX42 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointKDM6B(7743342)-DDX42(61864393), # samples:2
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
TgeneDDX42

GO:0008104

protein localization

19377511


check buttonFusion gene breakpoints across KDM6B (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 DDX42 (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
ChimerDB4PRADTCGA-HC-7818KDM6Bchr17

7743342

+DDX42chr17

61864393

+


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Fusion Gene ORF analysis for KDM6B-DDX42

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-5UTRENST00000572030ENST00000389924KDM6Bchr17

7743342

+DDX42chr17

61864393

+
3UTR-5UTRENST00000572030ENST00000578681KDM6Bchr17

7743342

+DDX42chr17

61864393

+
3UTR-5UTRENST00000572030ENST00000583590KDM6Bchr17

7743342

+DDX42chr17

61864393

+
3UTR-intronENST00000572030ENST00000359353KDM6Bchr17

7743342

+DDX42chr17

61864393

+
3UTR-intronENST00000572030ENST00000457800KDM6Bchr17

7743342

+DDX42chr17

61864393

+
3UTR-intronENST00000572030ENST00000582985KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-5UTRENST00000254846ENST00000389924KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-5UTRENST00000254846ENST00000578681KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-5UTRENST00000254846ENST00000583590KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-5UTRENST00000448097ENST00000389924KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-5UTRENST00000448097ENST00000578681KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-5UTRENST00000448097ENST00000583590KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-intronENST00000254846ENST00000359353KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-intronENST00000254846ENST00000457800KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-intronENST00000254846ENST00000582985KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-intronENST00000448097ENST00000359353KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-intronENST00000448097ENST00000457800KDM6Bchr17

7743342

+DDX42chr17

61864393

+
5UTR-intronENST00000448097ENST00000582985KDM6Bchr17

7743342

+DDX42chr17

61864393

+

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 KDM6B-DDX42


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)
KDM6Bchr177743342+DDX42chr1761864393+0.985028860.014971143
KDM6Bchr177743342+DDX42chr1761864393+0.985028860.014971143

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 KDM6B-DDX42


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/:7743342/:61864393)
- 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
KDM6B

O15054

DDX42

Q86XP3

FUNCTION: Histone demethylase that specifically demethylates 'Lys-27' of histone H3, thereby playing a central role in histone code (PubMed:17825402, PubMed:17851529, PubMed:17713478, PubMed:18003914). Demethylates trimethylated and dimethylated H3 'Lys-27' (PubMed:17825402, PubMed:17851529, PubMed:17713478, PubMed:18003914). Plays a central role in regulation of posterior development, by regulating HOX gene expression (PubMed:17851529). Involved in inflammatory response by participating in macrophage differentiation in case of inflammation by regulating gene expression and macrophage differentiation (PubMed:17825402). Plays a demethylase-independent role in chromatin remodeling to regulate T-box family member-dependent gene expression by acting as a link between T-box factors and the SMARCA4-containing SWI/SNF remodeling complex (By similarity). {ECO:0000250|UniProtKB:Q5NCY0, ECO:0000269|PubMed:17713478, ECO:0000269|PubMed:17825402, ECO:0000269|PubMed:17851529, ECO:0000269|PubMed:18003914, ECO:0000269|PubMed:28262558}.FUNCTION: ATP-dependent RNA helicase. Binds to partially double-stranded RNAs (dsRNAs) in order to unwind RNA secondary structures. Unwinding is promoted in the presence of single-strand binding proteins. Mediates also RNA duplex formation thereby displacing the single-strand RNA binding protein. ATP and ADP modulate its activity: ATP binding and hydrolysis by DDX42 triggers RNA strand separation, whereas the ADP-bound form of the protein triggers annealing of complementary RNA strands. Involved in the survival of cells by interacting with TP53BP2 and thereby counteracting the apoptosis-stimulating activity of TP53BP2. Relocalizes TP53BP2 to the cytoplasm. {ECO:0000269|PubMed:16397294, ECO:0000269|PubMed:19377511}.

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 KDM6B-DDX42


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 KDM6B-DDX42


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 KDM6B-DDX42


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 KDM6B-DDX42


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