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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:PLEKHA6-DCAF5 (FusionGDB2 ID:65790)

Fusion Gene Summary for PLEKHA6-DCAF5

check button Fusion gene summary
Fusion gene informationFusion gene name: PLEKHA6-DCAF5
Fusion gene ID: 65790
HgeneTgene
Gene symbol

PLEKHA6

DCAF5

Gene ID

22874

8816

Gene namepleckstrin homology domain containing A6DDB1 and CUL4 associated factor 5
SynonymsPEPP-3|PEPP3BCRG2|BCRP2|D14S1461E|WDR22
Cytomap

1q32.1

14q24.1

Type of geneprotein-codingprotein-coding
Descriptionpleckstrin homology domain-containing family A member 6PH domain-containing family A member 6phosphoinositol 3-phosphate-binding protein 3DDB1- and CUL4-associated factor 5WD repeat-containing protein 22breakpoint cluster region protein, uterine leiomyoma, 2
Modification date2020031320200313
UniProtAcc.

Q96JK2

Ensembl transtripts involved in fusion geneENST00000272203, ENST00000414478, 
ENST00000485632, 
ENST00000341516, 
ENST00000554215, ENST00000556847, 
ENST00000557386, ENST00000389997, 
ENST00000553293, 
Fusion gene scores* DoF score15 X 17 X 8=204010 X 10 X 6=600
# samples 1911
** MAII scorelog2(19/2040*10)=-3.42449782852791
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/600*10)=-2.44745897697122
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PLEKHA6 [Title/Abstract] AND DCAF5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPLEKHA6(204234070)-DCAF5(69542128), # samples:1
Anticipated loss of major functional domain due to fusion event.PLEKHA6-DCAF5 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PLEKHA6-DCAF5 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* 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 PLEKHA6 (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 DCAF5 (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-DU-6403-01APLEKHA6chr1

204234070

-DCAF5chr14

69542128

-


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Fusion Gene ORF analysis for PLEKHA6-DCAF5

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
Frame-shiftENST00000272203ENST00000341516PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
Frame-shiftENST00000272203ENST00000554215PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
Frame-shiftENST00000272203ENST00000556847PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
Frame-shiftENST00000272203ENST00000557386PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
5CDS-intronENST00000272203ENST00000389997PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
5CDS-5UTRENST00000272203ENST00000553293PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
Frame-shiftENST00000414478ENST00000341516PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
Frame-shiftENST00000414478ENST00000554215PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
Frame-shiftENST00000414478ENST00000556847PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
Frame-shiftENST00000414478ENST00000557386PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
5CDS-intronENST00000414478ENST00000389997PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
5CDS-5UTRENST00000414478ENST00000553293PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
intron-3CDSENST00000485632ENST00000341516PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
intron-3CDSENST00000485632ENST00000554215PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
intron-3CDSENST00000485632ENST00000556847PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
intron-3CDSENST00000485632ENST00000557386PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
intron-intronENST00000485632ENST00000389997PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-
intron-5UTRENST00000485632ENST00000553293PLEKHA6chr1

204234070

-DCAF5chr14

69542128

-

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 PLEKHA6-DCAF5


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 PLEKHA6-DCAF5


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.DCAF5

Q96JK2

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: May function as a substrate receptor for CUL4-DDB1 E3 ubiquitin-protein ligase complex. {ECO:0000269|PubMed:16949367, ECO:0000269|PubMed:16964240}.

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 PLEKHA6-DCAF5


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 PLEKHA6-DCAF5


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 PLEKHA6-DCAF5


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 PLEKHA6-DCAF5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePLEKHA6C0036341Schizophrenia1PSYGENET