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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 26467

FusionGeneSummary for PDGFRB_NDE1

check button Fusion gene summary
Fusion gene informationFusion gene name: PDGFRB_NDE1
Fusion gene ID: 26467
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 homolognudE nuclear distribution E homolog 1nudE nuclear distribution gene E homolog 1
Modification date2018052320180523
UniProtAcc

P09619

Q9NXR1

Ensembl transtripts involved in fusion geneENST00000261799, ENST00000523456, 
ENST00000396353, ENST00000396355, 
ENST00000396354, ENST00000342673, 
ENST00000571896, 
Fusion gene scores* DoF score3 X 3 X 2=1813 X 17 X 2=442
# samples 319
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(19/442*10)=-1.21804695106048
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]

Functional or gene categories assigned by FusionGDB annotation
* 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 button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1DQ317513PDGFRBchr5

149508606

+NDE1chr16

15784639

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-intronENST00000261799ENST00000396353PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000261799ENST00000396355PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000261799ENST00000396354PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000261799ENST00000342673PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000261799ENST00000571896PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000523456ENST00000396353PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000523456ENST00000396355PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000523456ENST00000396354PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000523456ENST00000342673PDGFRBchr5

149508606

+NDE1chr16

15784639

-
intron-intronENST00000523456ENST00000571896PDGFRBchr5

149508606

+NDE1chr16

15784639

-

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FusionProtFeatures for PDGFRB_NDE1


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

P09619

NDE1

Q9NXR1

Tyrosine-protein kinase that acts as cell-surfacereceptor for homodimeric PDGFB and PDGFD and for heterodimersformed by PDGFA and PDGFB, and plays an essential role in theregulation of embryonic development, cell proliferation, survival,differentiation, chemotaxis and migration. Plays an essential rolein blood vessel development by promoting proliferation, migrationand recruitment of pericytes and smooth muscle cells toendothelial cells. Plays a role in the migration of vascularsmooth muscle cells and the formation of neointima at vascularinjury sites. Required for normal development of thecardiovascular system. Required for normal recruitment ofpericytes (mesangial cells) in the kidney glomerulus, and fornormal formation of a branched network of capillaries in kidneyglomeruli. Promotes rearrangement of the actin cytoskeleton andthe formation of membrane ruffles. Binding of its cognate ligands- homodimeric PDGFB, heterodimers formed by PDGFA and PDGFB orhomodimeric PDGFD -leads to the activation of several signalingcascades; the response depends on the nature of the bound ligandand is modulated by the formation of heterodimers between PDGFRAand PDGFRB. Phosphorylates PLCG1, PIK3R1, PTPN11, RASA1/GAP, CBL,SHC1 and NCK1. Activation of PLCG1 leads to the production of thecellular signaling molecules diacylglycerol and inositol 1,4,5-trisphosphate, mobilization of cytosolic Ca(2+) and the activationof protein kinase C. Phosphorylation of PIK3R1, the regulatorysubunit of phosphatidylinositol 3-kinase, leads to the activationof the AKT1 signaling pathway. Phosphorylation of SHC1, or of theC-terminus of PTPN11, creates a binding site for GRB2, resultingin the activation of HRAS, RAF1 and down-stream MAP kinases,including MAPK1/ERK2 and/or MAPK3/ERK1. Promotes phosphorylationand activation of SRC family kinases. Promotes phosphorylation ofPDCD6IP/ALIX and STAM. Receptor signaling is down-regulated byprotein phosphatases that dephosphorylate the receptor and itsdown-stream effectors, and by rapid internalization of theactivated receptor. {ECO:0000269|PubMed:11297552,ECO:0000269|PubMed:11331881, ECO:0000269|PubMed:1314164,ECO:0000269|PubMed:1396585, ECO:0000269|PubMed:1653029,ECO:0000269|PubMed:1709159, ECO:0000269|PubMed:1846866,ECO:0000269|PubMed:20494825, ECO:0000269|PubMed:20529858,ECO:0000269|PubMed:21098708, ECO:0000269|PubMed:21679854,ECO:0000269|PubMed:21733313, ECO:0000269|PubMed:2554309,ECO:0000269|PubMed:26599395, ECO:0000269|PubMed:2835772,ECO:0000269|PubMed:2850496, ECO:0000269|PubMed:7685273,ECO:0000269|PubMed:7691811, ECO:0000269|PubMed:7692233,ECO:0000269|PubMed:8195171}. Required for centrosome duplication and formation andfunction of the mitotic spindle. Essential for the development ofthe cerebral cortex. May regulate the production of neurons bycontrolling the orientation of the mitotic spindle during divisionof cortical neuronal progenitors of the proliferative ventricularzone of the brain. Orientation of the division plane perpendicularto the layers of the cortex gives rise to two proliferativeneuronal progenitors whereas parallel orientation of the divisionplane yields one proliferative neuronal progenitor and a post-mitotic neuron. A premature shift towards a neuronal fate withinthe progenitor population may result in an overall reduction inthe final number of neurons and an increase in the number ofneurons 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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FusionGeneSequence for PDGFRB_NDE1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI 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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RelatedDrugs for PDGFRB_NDE1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgenePDGFRBP09619DB00619ImatinibPlatelet-derived growth factor receptor betasmall moleculeapproved
HgenePDGFRBP09619DB06589PazopanibPlatelet-derived growth factor receptor betasmall moleculeapproved
HgenePDGFRBP09619DB08896RegorafenibPlatelet-derived growth factor receptor betasmall moleculeapproved
HgenePDGFRBP09619DB00102BecaplerminPlatelet-derived growth factor receptor betabiotechapproved|investigational
HgenePDGFRBP09619DB00398SorafenibPlatelet-derived growth factor receptor betasmall moleculeapproved|investigational
HgenePDGFRBP09619DB01254DasatinibPlatelet-derived growth factor receptor betasmall moleculeapproved|investigational
HgenePDGFRBP09619DB01268SunitinibPlatelet-derived growth factor receptor betasmall moleculeapproved|investigational

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RelatedDiseases for PDGFRB_NDE1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePDGFRBC3554321BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 43UNIPROT
HgenePDGFRBC0023893Liver Cirrhosis, Experimental2CTD_human
HgenePDGFRBC0036341Schizophrenia2PSYGENET
HgenePDGFRBC0432284Infantile myofibromatosis2ORPHANET;UNIPROT
HgenePDGFRBC0004782Basal Ganglia Diseases1CTD_human
HgenePDGFRBC0006663Calcinosis1CTD_human
HgenePDGFRBC0036337Schizoaffective Disorder1PSYGENET
HgenePDGFRBC1866182Penttinen-Aula syndrome1ORPHANET;UNIPROT
HgenePDGFRBC4225270KOSAKI OVERGROWTH SYNDROME1UNIPROT
TgeneNDE1C0036341Schizophrenia4PSYGENET
TgeneNDE1C0033975Psychotic Disorders1PSYGENET
TgeneNDE1C0349204Nonorganic psychosis1PSYGENET