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Center for Computational Systems Medicine
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Kinase Fusion Gene Summary

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Kinase Fusion Gene Sample Information

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Kinase Fusion ORF Analysis

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Kinase Fusion Amino Acid Sequences

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Multiple Sequence Alignment of All Fusion Protein Isoforms

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Kinase Fusion Protein Functional Features

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Kinase Fusion Protein Structures

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Comparison of Fusion Protein Isoforms

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Comparison of Fusion Protein Sequences/Structures with Known Sequences/Structures from PDB

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pLDDT Scores and Difference Analysis of pLDDT Scores Between the Active Sites (Best) and Non-Active Sites.

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Ramachandran Plot of Kinase Fusion Protein Structure

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Potential Active Site Information

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Virtual Screening Results

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Kinase-Substrate Information

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Related Drugs with This Kinase Fusion Protein

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Related Disease with This Kinase Fusion Protein

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Clinical Trials of the Found Drugs/Small Molecules

Kinase Fusion Gene:CCDC88C_PDGFRB

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: CCDC88C_PDGFRB
KinaseFusionDB ID: KFG962
FusionGDB2.0 ID: KFG962
HgeneTgene
Gene symbol

CCDC88C

PDGFRB

Gene ID

440193

5159

Gene namecoiled-coil domain containing 88Cplatelet derived growth factor receptor beta
SynonymsDAPLE|HKRP2|HYC1|KIAA1509|SCA40CD140B|IBGC4|IMF1|JTK12|KOGS|PDGFR|PDGFR-1|PDGFR1|PENTT
Cytomap

14q32.11-q32.12

5q32

Type of geneprotein-codingprotein-coding
Descriptionprotein DapleDvl-associating protein with a high frequency of leucine residueshook-related protein 2spinocerebellar ataxia 40platelet-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-deriv
Modification date2024041120240413
UniProtAcc

Q9P219

P09619

Ensembl transtripts involved in fusion geneENST idsENST00000331194, ENST00000389856, 
ENST00000389857, ENST00000553403, 
ENST00000554165, 
ENST00000261799, 
ENST00000523456, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: CCDC88C [Title/Abstract] AND PDGFRB [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)
check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneCCDC88C

GO:0003383

apical constriction

30948426

HgeneCCDC88C

GO:0007264

small GTPase-mediated signal transduction

26126266

TgenePDGFRB

GO:0007165

signal transduction

10821867

TgenePDGFRB

GO:0010863

positive regulation of phospholipase C activity

1653029

TgenePDGFRB

GO:0018108

peptidyl-tyrosine phosphorylation

1653029|2536956|2850496

TgenePDGFRB

GO:0030335

positive regulation of cell migration

17470632

TgenePDGFRB

GO:0032516

positive regulation of phosphoprotein phosphatase activity

7691811

TgenePDGFRB

GO:0038091

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

17470632

TgenePDGFRB

GO:0046777

protein autophosphorylation

2536956|2850496

TgenePDGFRB

GO:0048008

platelet-derived growth factor receptor signaling pathway

1314164|2536956

TgenePDGFRB

GO:0051897

positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction

1314164

TgenePDGFRB

GO:0060326

cell chemotaxis

2554309|17991872


check buttonKinase Fusion gene breakpoints across CCDC88C (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonKinase Fusion gene breakpoints across PDGFRB (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.


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Kinase Fusion Gene Sample Information

check buttonKinase Fusion gene information.
check button Kinase Fusion gene information from four resources (ChiTars 5.0, ChimerDB 4.0, COSMIC, and CCLE)
* 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.
SourceSampleHgeneHchrHbpTgeneTchrTbp
ChimerKB4.CCDC88Cchr14

91791267

PDGFRBchr5

91791267



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Kinase Fusion ORF Analysis


check buttonKinase Fusion information from ORFfinder translation from full-length transcript sequence from KinaseFusionDB.
HenstTenstHgeneHchrHbpTgeneTchrTbpSeq length
(transcript)
Seq length
(amino acids)

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Kinase Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from KinaseFusionDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>Henst_Tenst_Hgene_Hchr_Hbp_Tgene_Tchr_Tbp_length(fusion AA)_AAseq

Multiple Sequence Alignment of All Fusion Protein Isoforms



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Kinase Fusion Protein Functional Features


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/:/:)
- 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
CCDC88C

Q9P219

PDGFRB

P09619

FUNCTION: Required for activation of guanine nucleotide-binding proteins (G-proteins) during non-canonical Wnt signaling (PubMed:26126266). Binds to ligand-activated Wnt receptor FZD7, displacing DVL1 from the FZD7 receptor and leading to inhibition of canonical Wnt signaling (PubMed:26126266). Acts as a non-receptor guanine nucleotide exchange factor by also binding to guanine nucleotide-binding protein G(i) alpha (Gi-alpha) subunits, leading to their activation (PubMed:26126266). Binding to Gi-alpha subunits displaces the beta and gamma subunits from the heterotrimeric G-protein complex, triggering non-canonical Wnt responses such as activation of RAC1 and PI3K-AKT signaling (PubMed:26126266). Promotes apical constriction of cells via ARHGEF18 (PubMed:30948426). {ECO:0000269|PubMed:26126266, ECO:0000269|PubMed:30948426}.FUNCTION: Tyrosine-protein kinase that acts as a cell-surface receptor for homodimeric PDGFB and PDGFD and for heterodimers formed by PDGFA and PDGFB, and plays an essential role in the regulation of embryonic development, cell proliferation, survival, differentiation, chemotaxis and migration. Plays an essential role in blood vessel development by promoting proliferation, migration and recruitment of pericytes and smooth muscle cells to endothelial cells. Plays a role in the migration of vascular smooth muscle cells and the formation of neointima at vascular injury sites. Required for normal development of the cardiovascular system. Required for normal recruitment of pericytes (mesangial cells) in the kidney glomerulus, and for normal formation of a branched network of capillaries in kidney glomeruli. Promotes rearrangement of the actin cytoskeleton and the formation of membrane ruffles. Binding of its cognate ligands - homodimeric PDGFB, heterodimers formed by PDGFA and PDGFB or homodimeric PDGFD -leads to the activation of several signaling cascades; the response depends on the nature of the bound ligand and is modulated by the formation of heterodimers between PDGFRA and PDGFRB. Phosphorylates PLCG1, PIK3R1, PTPN11, RASA1/GAP, CBL, SHC1 and NCK1. Activation of PLCG1 leads to the production of the cellular signaling molecules diacylglycerol and inositol 1,4,5-trisphosphate, mobilization of cytosolic Ca(2+) and the activation of protein kinase C. Phosphorylation of PIK3R1, the regulatory subunit of phosphatidylinositol 3-kinase, leads to the activation of the AKT1 signaling pathway. Phosphorylation of SHC1, or of the C-terminus of PTPN11, creates a binding site for GRB2, resulting in the activation of HRAS, RAF1 and down-stream MAP kinases, including MAPK1/ERK2 and/or MAPK3/ERK1. Promotes phosphorylation and activation of SRC family kinases. Promotes phosphorylation of PDCD6IP/ALIX and STAM. Receptor signaling is down-regulated by protein phosphatases that dephosphorylate the receptor and its down-stream effectors, and by rapid internalization of the activated 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}.

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.

check button - Retained domain in the 5'-partner of fusion protein (protein functional feature from UniProt).
PartnerHgeneeneHbpTgeneeneTbpENSTBPexonTotalExonProtein feature lociBPlociTotalLenFeatureNote


check button - Retained domain in the 3'-partner of fusion protein (protein functional feature from UniProt).
PartnerHgeneeneHbpTgeneeneTbpENSTBPexonTotalExonProtein feature lociBPlociTotalLenFeatureNote


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Kinase-Substrate Information of CCDC88C_PDGFRB


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
PDGFRBP09619humanPDGFRBP09619Y1021PNEGDNDyIIPLPDP
PDGFRBP09619humanPDGFRAP16234Y754ERKEVsKysDIQRsLPK_Tyr_Ser-Thr
PDGFRBP09619humanPDGFRBP09619Y1009LDTSSVLyTAVQPNE
PDGFRBP09619humanPTK2Q05397Y5___MAAAyLDPNLNH
PDGFRBP09619humanABL2P42684Y272KCNKPTVyGVsPIHD
PDGFRBP09619humanPDGFRBP09619Y579VSSDGHEyIyVDPMQ
PDGFRBP09619humanPDGFRBP09619Y562LWQKKPRyEIRWKVI
PDGFRBP09619humanTHOC5Q13769Y225EIEVKKEyLSSLQPRFmiP_Thoc5
PDGFRBP09619humanABL2P42684Y139EKLRVLGyNQNGEWSSH3_1
PDGFRBP09619humanPLCG1P19174Y783EGRNPGFyVEANPMP
PDGFRBP09619humanPDGFRBP09619Y740TGESDGGyMDMSKDEPK_Tyr_Ser-Thr
PDGFRBP09619humanABL2P42684Y439RLMtGDtytAHAGAkPK_Tyr_Ser-Thr
PDGFRBP09619humanFYNP06241Y28sLNQssGyRyGTDPT
PDGFRBP09619humanETV6P41212Y17IkQERIsytPPEsPV
PDGFRBP09619humanPTK2Q05397Y194ALEKKSNyEVLEkDVFERM_M
PDGFRBP09619humanPDGFRBP09619Y763DMKGDVKyADIESSNPK_Tyr_Ser-Thr
PDGFRBP09619humanTNK2Q07912Y635PLPPPPAyDDVAQDE
PDGFRBP09619humanPDGFRBP09619Y581SDGHEyIyVDPMQLP
PDGFRBP09619humanABL2P42684Y116PNLFVALyDFVAsGDSH3_1
PDGFRBP09619humanABL2P42684Y303GGQyGEVyVGVWKKyPK_Tyr_Ser-Thr
PDGFRBP09619humanMUC1P15941Y1218tyHtHGRyVPPsstD
PDGFRBP09619humanABL2P42684Y310yVGVWKKysLtVAVKPK_Tyr_Ser-Thr
PDGFRBP09619humanPDGFRBP09619Y857DIMRDSNyISKGSTFPK_Tyr_Ser-Thr
PDGFRBP09619humanPDGFRBP09619Y775SSNyMAPyDNyVPSAPK_Tyr_Ser-Thr
PDGFRBP09619humanMUC1P15941Y1203IFPARDtyHPMsEyP
PDGFRBP09619humanPDGFRBP09619Y771ADIESSNyMAPyDNyPK_Tyr_Ser-Thr
PDGFRBP09619humanABL2P42684Y161QGWVPsNyItPVNSL
PDGFRBP09619humanETV6P41212Y27PEsPVPsyAsstPLH
PDGFRBP09619humanSRCP12931Y419RLIEDNEytARQGAkPK_Tyr_Ser-Thr
PDGFRBP09619humanPDGFRBP09619Y751SKDESVDyVPMLDMKPK_Tyr_Ser-Thr
PDGFRBP09619humanABL2P42684Y299HKLGGGQyGEVyVGVPK_Tyr_Ser-Thr
PDGFRBP09619humanPDGFRBP09619Y778yMAPyDNyVPSAPERPK_Tyr_Ser-Thr


check button Biological Network Integration of This Kinase and Substrates
(GeneMANIA website)

check button Enriched GO biological processes of the phosphorylation target genes of the kinase
KinaseGOIDGO termP.adjust
PDGFRBIDDescription0.00e+00
PDGFRBGO:0018108peptidyl-tyrosine phosphorylation1.87e-08
PDGFRBGO:0018212peptidyl-tyrosine modification1.87e-08
PDGFRBGO:0038093Fc receptor signaling pathway6.42e-06
PDGFRBGO:0036120cellular response to platelet-derived growth factor stimulus4.63e-05
PDGFRBGO:0036119response to platelet-derived growth factor4.63e-05
PDGFRBGO:0002433immune response-regulating cell surface receptor signaling pathway involved in phagocytosis4.63e-05
PDGFRBGO:0038096Fc-gamma receptor signaling pathway involved in phagocytosis4.63e-05
PDGFRBGO:0002431Fc receptor mediated stimulatory signaling pathway6.79e-05
PDGFRBGO:0002862negative regulation of inflammatory response to antigenic stimulus6.79e-05
PDGFRBGO:0038094Fc-gamma receptor signaling pathway6.79e-05
PDGFRBGO:0010863positive regulation of phospholipase C activity8.77e-05
PDGFRBGO:1900274regulation of phospholipase C activity9.45e-05
PDGFRBGO:0051897positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction1.34e-04
PDGFRBGO:0002861regulation of inflammatory response to antigenic stimulus1.52e-04
PDGFRBGO:0010518positive regulation of phospholipase activity1.52e-04
PDGFRBGO:0048013ephrin receptor signaling pathway1.61e-04
PDGFRBGO:0046777protein autophosphorylation1.87e-04
PDGFRBGO:0048008platelet-derived growth factor receptor signaling pathway2.11e-04
PDGFRBGO:0010517regulation of phospholipase activity2.11e-04
PDGFRBGO:0060193positive regulation of lipase activity2.11e-04
PDGFRBGO:0048010vascular endothelial growth factor receptor signaling pathway2.11e-04
PDGFRBGO:0051896regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction3.46e-04
PDGFRBGO:0060191regulation of lipase activity4.05e-04
PDGFRBGO:0002437inflammatory response to antigenic stimulus4.19e-04
PDGFRBGO:0043491phosphatidylinositol 3-kinase/protein kinase B signal transduction5.64e-04
PDGFRBGO:0002429immune response-activating cell surface receptor signaling pathway7.80e-04
PDGFRBGO:0035791platelet-derived growth factor receptor-beta signaling pathway8.61e-04
PDGFRBGO:0007173epidermal growth factor receptor signaling pathway8.61e-04
PDGFRBGO:0033674positive regulation of kinase activity8.77e-04
PDGFRBGO:0002768immune response-regulating cell surface receptor signaling pathway9.40e-04
PDGFRBGO:2001243negative regulation of intrinsic apoptotic signaling pathway9.40e-04
PDGFRBGO:0072224metanephric glomerulus development1.11e-03
PDGFRBGO:0038127ERBB signaling pathway1.14e-03
PDGFRBGO:2000811negative regulation of anoikis1.18e-03
PDGFRBGO:0055003cardiac myofibril assembly1.24e-03
PDGFRBGO:0061298retina vasculature development in camera-type eye1.24e-03
PDGFRBGO:0050900leukocyte migration1.29e-03
PDGFRBGO:0043552positive regulation of phosphatidylinositol 3-kinase activity1.45e-03
PDGFRBGO:0051347positive regulation of transferase activity1.46e-03
PDGFRBGO:0050921positive regulation of chemotaxis1.49e-03
PDGFRBGO:0002223stimulatory C-type lectin receptor signaling pathway1.54e-03
PDGFRBGO:1990840response to lectin1.54e-03
PDGFRBGO:1990858cellular response to lectin1.54e-03
PDGFRBGO:0034614cellular response to reactive oxygen species1.60e-03
PDGFRBGO:2000209regulation of anoikis1.60e-03
PDGFRBGO:0090218positive regulation of lipid kinase activity1.85e-03
PDGFRBGO:0050731positive regulation of peptidyl-tyrosine phosphorylation1.97e-03
PDGFRBGO:0002757immune response-activating signaling pathway1.99e-03
PDGFRBGO:0032102negative regulation of response to external stimulus2.07e-03

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Related Drugs to CCDC88C_PDGFRB


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

check button Distribution of the number of studies mentioning CCDC88C-PDGFRB and kinase inhibitors the PubMed Abstract (04-01-2024)

Fusion gene - drug pair 1Fusion gene - drug pair 2PMIDPublication dateDOIStudy title

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Related Diseases to CCDC88C_PDGFRB


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Related diseases from the literature mentioned this fusion gene and drug.
(PubMed, 04-01-2024)
MeSH IDMeSH term

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePDGFRBC3554321BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 46CTD_human;GENOMICS_ENGLAND;UNIPROT
TgenePDGFRBC0393590Fahr's syndrome (disorder)3GENOMICS_ENGLAND;ORPHANET
TgenePDGFRBC4225270Kosaki overgrowth syndrome3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgenePDGFRBC4551572MYOFIBROMATOSIS, INFANTILE, 13GENOMICS_ENGLAND;UNIPROT
TgenePDGFRBC0013421Dystonia2GENOMICS_ENGLAND
TgenePDGFRBC0023480Leukemia, Myelomonocytic, Chronic2ORPHANET
TgenePDGFRBC0023893Liver Cirrhosis, Experimental2CTD_human
TgenePDGFRBC0036341Schizophrenia2PSYGENET
TgenePDGFRBC0432284Infantile myofibromatosis2CTD_human;GENOMICS_ENGLAND;ORPHANET


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Clinical Trials of the Found Drugs/Small Molecules


check button Statistics of the Clinical Trials of the Found Kinase Inibitors from clinicaltrials.gov (06-17-2024)

check button Clinical Trials from clinicaltrials.gov (06-17-2024)

Fusion GeneKinase InhibitorNCT IDStudy StatusPhasesDisease# EnrolmentDate