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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:NUP205-DVL2 (FusionGDB2 ID:60640)

Fusion Gene Summary for NUP205-DVL2

check button Fusion gene summary
Fusion gene informationFusion gene name: NUP205-DVL2
Fusion gene ID: 60640
HgeneTgene
Gene symbol

NUP205

DVL2

Gene ID

23165

1856

Gene namenucleoporin 205dishevelled segment polarity protein 2
SynonymsC7orf14|NPHS13-
Cytomap

7q33

17p13.1

Type of geneprotein-codingprotein-coding
Descriptionnuclear pore complex protein Nup205205 kDa nucleoporinnucleoporin Nup205segment polarity protein dishevelled homolog DVL-2dishevelled 2 (homologous to Drosophila dsh)dishevelled, dsh homolog 2
Modification date2020031320200327
UniProtAcc.

O14641

Ensembl transtripts involved in fusion geneENST00000285968, ENST00000440390, 
ENST00000489493, 
ENST00000005340, 
ENST00000575458, ENST00000574642, 
Fusion gene scores* DoF score8 X 9 X 7=5042 X 2 X 2=8
# samples 93
** MAII scorelog2(9/504*10)=-2.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/8*10)=1.90689059560852
Context

PubMed: NUP205 [Title/Abstract] AND DVL2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNUP205(135330979)-DVL2(7133474), # samples:3
Anticipated loss of major functional domain due to fusion event.NUP205-DVL2 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
NUP205-DVL2 seems lost the major protein functional domain in Hgene 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
TgeneDVL2

GO:0006366

transcription by RNA polymerase II

11742073

TgeneDVL2

GO:0043507

positive regulation of JUN kinase activity

17593335

TgeneDVL2

GO:0044340

canonical Wnt signaling pathway involved in regulation of cell proliferation

18787224

TgeneDVL2

GO:0045893

positive regulation of transcription, DNA-templated

12805222|17593335

TgeneDVL2

GO:0051091

positive regulation of DNA-binding transcription factor activity

17593335

TgeneDVL2

GO:0060070

canonical Wnt signaling pathway

17593335

TgeneDVL2

GO:0060071

Wnt signaling pathway, planar cell polarity pathway

12805222


check buttonFusion gene breakpoints across NUP205 (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 DVL2 (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-V1-A9ZR-01ANUP205chr7

135330979

+DVL2chr17

7133474

-
ChimerDB4PRADTCGA-V1-A9ZRNUP205chr7

135330979

+DVL2chr17

7133474

-
ChimerDB4PRADTCGA-V1-A9ZR-01ANUP205chr7

135330979

-DVL2chr17

7133474

-


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Fusion Gene ORF analysis for NUP205-DVL2

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-shiftENST00000285968ENST00000005340NUP205chr7

135330979

+DVL2chr17

7133474

-
5CDS-intronENST00000285968ENST00000575458NUP205chr7

135330979

+DVL2chr17

7133474

-
5CDS-5UTRENST00000285968ENST00000574642NUP205chr7

135330979

+DVL2chr17

7133474

-
intron-3CDSENST00000440390ENST00000005340NUP205chr7

135330979

+DVL2chr17

7133474

-
intron-intronENST00000440390ENST00000575458NUP205chr7

135330979

+DVL2chr17

7133474

-
intron-5UTRENST00000440390ENST00000574642NUP205chr7

135330979

+DVL2chr17

7133474

-
intron-3CDSENST00000489493ENST00000005340NUP205chr7

135330979

+DVL2chr17

7133474

-
intron-intronENST00000489493ENST00000575458NUP205chr7

135330979

+DVL2chr17

7133474

-
intron-5UTRENST00000489493ENST00000574642NUP205chr7

135330979

+DVL2chr17

7133474

-

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 NUP205-DVL2


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 NUP205-DVL2


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
.DVL2

O14641

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: Plays a role in the signal transduction pathways mediated by multiple Wnt genes. Participates both in canonical and non-canonical Wnt signaling by binding to the cytoplasmic C-terminus of frizzled family members and transducing the Wnt signal to down-stream effectors. Promotes internalization and degradation of frizzled proteins upon Wnt signaling. {ECO:0000250|UniProtKB:Q60838, ECO:0000269|PubMed:19252499}.

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 NUP205-DVL2


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 NUP205-DVL2


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 NUP205-DVL2


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 NUP205-DVL2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNUP205C0029401Osteitis Deformans1CTD_human
HgeneNUP205C1868672NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE1CTD_human;ORPHANET
HgeneNUP205C4225165NEPHROTIC SYNDROME, TYPE 131CTD_human;GENOMICS_ENGLAND;UNIPROT