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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:WRAP53-CHD3 (FusionGDB2 ID:99383)

Fusion Gene Summary for WRAP53-CHD3

check button Fusion gene summary
Fusion gene informationFusion gene name: WRAP53-CHD3
Fusion gene ID: 99383
HgeneTgene
Gene symbol

WRAP53

CHD3

Gene ID

55135

1107

Gene nameWD repeat containing antisense to TP53chromodomain helicase DNA binding protein 3
SynonymsDKCB3|TCAB1|WDR79Mi-2a|Mi2-ALPHA|SNIBCPS|ZFH
Cytomap

17p13.1

17p13.1

Type of geneprotein-codingprotein-coding
Descriptiontelomerase Cajal body protein 1WD repeat-containing protein 79WD repeat-containing protein WRAP53WD40 protein Wrap53WD40 repeat-containing protein antisense to TP53WD40 repeat-containing protein encoding RNA antisense to p53WRAP53betachromodomain-helicase-DNA-binding protein 3ATP-dependent helicase CHD3CHD-3hZFHmi-2 autoantigen 240 kDa proteinzinc finger helicasezinc-finger helicase (Snf2-like)
Modification date2020031520200313
UniProtAcc.

Q12873

Ensembl transtripts involved in fusion geneENST00000316024, ENST00000396463, 
ENST00000431639, ENST00000457584, 
ENST00000534050, 
ENST00000330494, 
ENST00000358181, ENST00000380358, 
ENST00000570758, 
Fusion gene scores* DoF score5 X 4 X 5=10010 X 11 X 4=440
# samples 511
** MAII scorelog2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/440*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: WRAP53 [Title/Abstract] AND CHD3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointWRAP53(7589744)-CHD3(7811975), # 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
HgeneWRAP53

GO:0007004

telomere maintenance via telomerase

23685356|29695869|29804836

HgeneWRAP53

GO:0034337

RNA folding

29804836

HgeneWRAP53

GO:0045739

positive regulation of DNA repair

25512560

HgeneWRAP53

GO:0051973

positive regulation of telomerase activity

19179534|23685356|29804836

HgeneWRAP53

GO:0090666

scaRNA localization to Cajal body

19285445

HgeneWRAP53

GO:1904867

protein localization to Cajal body

22547674

HgeneWRAP53

GO:1905168

positive regulation of double-strand break repair via homologous recombination

25512560

HgeneWRAP53

GO:2000781

positive regulation of double-strand break repair

27715493

HgeneWRAP53

GO:2001034

positive regulation of double-strand break repair via nonhomologous end joining

25512560

TgeneCHD3

GO:0007051

spindle organization

17626165

TgeneCHD3

GO:0007098

centrosome cycle

17626165


check buttonFusion gene breakpoints across WRAP53 (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 CHD3 (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-YL-A9WL-01AWRAP53chr17

7589744

+CHD3chr17

7811975

-


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Fusion Gene ORF analysis for WRAP53-CHD3

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-intronENST00000316024ENST00000330494WRAP53chr17

7589744

+CHD3chr17

7811975

-
5UTR-intronENST00000316024ENST00000358181WRAP53chr17

7589744

+CHD3chr17

7811975

-
5UTR-intronENST00000316024ENST00000380358WRAP53chr17

7589744

+CHD3chr17

7811975

-
5UTR-intronENST00000316024ENST00000570758WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000396463ENST00000330494WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000396463ENST00000358181WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000396463ENST00000380358WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000396463ENST00000570758WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000431639ENST00000330494WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000431639ENST00000358181WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000431639ENST00000380358WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000431639ENST00000570758WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000457584ENST00000330494WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000457584ENST00000358181WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000457584ENST00000380358WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000457584ENST00000570758WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000534050ENST00000330494WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000534050ENST00000358181WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000534050ENST00000380358WRAP53chr17

7589744

+CHD3chr17

7811975

-
intron-intronENST00000534050ENST00000570758WRAP53chr17

7589744

+CHD3chr17

7811975

-

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 WRAP53-CHD3


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 WRAP53-CHD3


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/:7589744/:7811975)
- 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
.CHD3

Q12873

FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Component of the histone deacetylase NuRD complex which participates in the remodeling of chromatin by deacetylating histones (PubMed:9804427, PubMed:30397230). Involved in transcriptional repressiobn as part of the NuRD complex (PubMed:27068747). Required for anchoring centrosomal pericentrin in both interphase and mitosis, for spindle organization and centrosome integrity (PubMed:17626165). {ECO:0000269|PubMed:17626165, ECO:0000269|PubMed:27068747, ECO:0000269|PubMed:30397230, ECO:0000269|PubMed:9804427}.

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 WRAP53-CHD3


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 WRAP53-CHD3


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 WRAP53-CHD3


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 WRAP53-CHD3


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