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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:PDGFRB-NDE1 (FusionGDB2 ID:63861)

Fusion Gene Summary for PDGFRB-NDE1

check button Fusion gene summary
Fusion gene informationFusion gene name: PDGFRB-NDE1
Fusion gene ID: 63861
HgeneTgene
Gene symbol

PDGFRB

NDE1

Gene ID

5159

54820

Gene nameplatelet derived growth factor receptor betanudE neurodevelopment protein 1
SynonymsCD140B|IBGC4|IMF1|JTK12|KOGS|PDGFR|PDGFR-1|PDGFR1|PENTTHOM-TES-87|LIS4|MHAC|NDE|NUDE|NUDE1
Cytomap

5q32

16p13.11

Type of geneprotein-codingprotein-coding
Descriptionplatelet-derived growth factor receptor betaActivated tyrosine kinase PDGFRBCD140 antigen-like family member BNDEL1-PDGFRBPDGF-R-betaPDGFR-betabeta-type platelet-derived growth factor receptorplatelet-derived growth factor receptor 1platelet-derivnuclear distribution protein nudE homolog 1LIS1-interacting protein NUDE1, rat homologepididymis secretory sperm binding proteinnudE nuclear distribution E homolog 1nudE nuclear distribution gene E homolog 1
Modification date2020032920200313
UniProtAcc.

Q9NXR1

Ensembl transtripts involved in fusion geneENST00000261799, ENST00000523456, 
ENST00000342673, ENST00000396353, 
ENST00000396354, ENST00000396355, 
ENST00000571896, 
Fusion gene scores* DoF score4 X 4 X 4=649 X 10 X 6=540
# samples 411
** MAII scorelog2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/540*10)=-2.29545588352617
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PDGFRB [Title/Abstract] AND NDE1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPDGFRB(149508606)-NDE1(15784389), # samples:1
PDGFRB(149508606)-NDE1(15784639), # 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
HgenePDGFRB

GO:0007165

signal transduction

10821867

HgenePDGFRB

GO:0010863

positive regulation of phospholipase C activity

1653029

HgenePDGFRB

GO:0018108

peptidyl-tyrosine phosphorylation

1653029|2536956|2850496

HgenePDGFRB

GO:0030335

positive regulation of cell migration

17470632

HgenePDGFRB

GO:0032516

positive regulation of phosphoprotein phosphatase activity

7691811

HgenePDGFRB

GO:0038091

positive regulation of cell proliferation by VEGF-activated platelet derived growth factor receptor signaling pathway

17470632

HgenePDGFRB

GO:0043552

positive regulation of phosphatidylinositol 3-kinase activity

1314164

HgenePDGFRB

GO:0046777

protein autophosphorylation

1314164|2536956|2850496

HgenePDGFRB

GO:0048008

platelet-derived growth factor receptor signaling pathway

1314164|2536956

HgenePDGFRB

GO:0060326

cell chemotaxis

2554309|17991872


check buttonFusion gene breakpoints across PDGFRB (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 NDE1 (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
ChimerDB4chronic myeloid leukemiaDQ317513PDGFRBchr5

149508606

NDE1chr16

15784389

ChiTaRS5.0N/ADQ317513PDGFRBchr5

149508606

+NDE1chr16

15784639

-


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Fusion Gene ORF analysis for PDGFRB-NDE1

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
intron-intronENST00000261799ENST00000342673PDGFRBchr5

149508606

NDE1chr16

15784389

intron-intronENST00000261799ENST00000342673PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000261799ENST00000396353PDGFRBchr5

149508606

NDE1chr16

15784389

intron-intronENST00000261799ENST00000396353PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000261799ENST00000396354PDGFRBchr5

149508606

NDE1chr16

15784389

intron-intronENST00000261799ENST00000396354PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000261799ENST00000396355PDGFRBchr5

149508606

NDE1chr16

15784389

intron-intronENST00000261799ENST00000396355PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000261799ENST00000571896PDGFRBchr5

149508606

NDE1chr16

15784389

intron-intronENST00000261799ENST00000571896PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000523456ENST00000342673PDGFRBchr5

149508606

NDE1chr16

15784389

intron-intronENST00000523456ENST00000342673PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000523456ENST00000396353PDGFRBchr5

149508606

NDE1chr16

15784389

intron-intronENST00000523456ENST00000396353PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000523456ENST00000396354PDGFRBchr5

149508606

NDE1chr16

15784389

intron-intronENST00000523456ENST00000396354PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000523456ENST00000396355PDGFRBchr5

149508606

NDE1chr16

15784389

intron-intronENST00000523456ENST00000396355PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000523456ENST00000571896PDGFRBchr5

149508606

NDE1chr16

15784389

intron-intronENST00000523456ENST00000571896PDGFRBchr5

149508606

+NDE1chr16

15784639

-

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 PDGFRB-NDE1


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 PDGFRB-NDE1


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/:149508606/:15784389)
- 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
.NDE1

Q9NXR1

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: Required for centrosome duplication and formation and function of the mitotic spindle. Essential for the development of the cerebral cortex. May regulate the production of neurons by controlling the orientation of the mitotic spindle during division of cortical neuronal progenitors of the proliferative ventricular zone of the brain. Orientation of the division plane perpendicular to the layers of the cortex gives rise to two proliferative neuronal progenitors whereas parallel orientation of the division plane yields one proliferative neuronal progenitor and a post-mitotic neuron. A premature shift towards a neuronal fate within the progenitor population may result in an overall reduction in the final number of neurons and an increase in the number of neurons in the deeper layers of the cortex. {ECO:0000269|PubMed:17600710, ECO:0000269|PubMed:21529752}.

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 PDGFRB-NDE1


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 PDGFRB-NDE1


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 PDGFRB-NDE1


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 PDGFRB-NDE1


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