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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:TGFBR2_CLASP2

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: TGFBR2_CLASP2
KinaseFusionDB ID: KFG6515
FusionGDB2.0 ID: KFG6515
HgeneTgene
Gene symbol

TGFBR2

CLASP2

Gene ID

7048

23122

Gene nametransforming growth factor beta receptor 2cytoplasmic linker associated protein 2
SynonymsAAT3|FAA3|LDS1B|LDS2|LDS2B|MFS2|RIIC|TAAD2|TBR-ii|TBRII|TGFR-2|TGFbeta-RII|tbetaR-II-
Cytomap

3p24.1

3p22.3

Type of geneprotein-codingprotein-coding
DescriptionTGF-beta receptor type-2TGF-beta receptor type IIBTGF-beta type II receptortransforming growth factor beta receptor IItransforming growth factor beta receptor type IICtransforming growth factor, beta receptor II (70/80kDa)transforming growth factor,CLIP-associating protein 2CLIP-associating protein CLASP2multiple asters (Mast)-like homolog 2protein Orbit homolog 2
Modification date2024041620240407
UniProtAcc

P37173

O75122

Ensembl transtripts involved in fusion geneENST idsENST00000295754, ENST00000359013, 
ENST00000307312, ENST00000313350, 
ENST00000333778, ENST00000461133, 
ENST00000480013, ENST00000482896, 
ENST00000487200, ENST00000539981, 
ENST00000359576, ENST00000399362, 
ENST00000468888, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: TGFBR2 [Title/Abstract] AND CLASP2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TGFBR2(30715738)-CLASP2(33686395), # samples:1
check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneTGFBR2

GO:0006915

apoptotic process

17471240

HgeneTGFBR2

GO:0007179

transforming growth factor beta receptor signaling pathway

1333888|9311995|12015308|18453574

HgeneTGFBR2

GO:0009410

response to xenobiotic stimulus

17878231

HgeneTGFBR2

GO:0010718

positive regulation of epithelial to mesenchymal transition

26459119

HgeneTGFBR2

GO:0060391

positive regulation of SMAD protein signal transduction

18453574

HgeneTGFBR2

GO:0070723

response to cholesterol

17878231

HgeneTGFBR2

GO:2000563

positive regulation of CD4-positive, alpha-beta T cell proliferation

17164348


check buttonKinase Fusion gene breakpoints across TGFBR2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonKinase Fusion gene breakpoints across CLASP2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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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
ChimerDB4TCGA-L5-A4OJTGFBR2chr3

30715738

CLASP2chr3

33686395



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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/chr3:30715738/chr3:33686395)
- 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
TGFBR2

P37173

CLASP2

O75122

FUNCTION: Transmembrane serine/threonine kinase forming with the TGF-beta type I serine/threonine kinase receptor, TGFBR1, the non-promiscuous receptor for the TGF-beta cytokines TGFB1, TGFB2 and TGFB3. Transduces the TGFB1, TGFB2 and TGFB3 signal from the cell surface to the cytoplasm and thus regulates a plethora of physiological and pathological processes including cell cycle arrest in epithelial and hematopoietic cells, control of mesenchymal cell proliferation and differentiation, wound healing, extracellular matrix production, immunosuppression and carcinogenesis. The formation of the receptor complex composed of 2 TGFBR1 and 2 TGFBR2 molecules symmetrically bound to the cytokine dimer results in the phosphorylation and activation of TGFBR1 by the constitutively active TGFBR2. Activated TGFBR1 phosphorylates SMAD2 which dissociates from the receptor and interacts with SMAD4. The SMAD2-SMAD4 complex is subsequently translocated to the nucleus where it modulates the transcription of the TGF-beta-regulated genes. This constitutes the canonical SMAD-dependent TGF-beta signaling cascade. Also involved in non-canonical, SMAD-independent TGF-beta signaling pathways. {ECO:0000269|PubMed:7774578}.; FUNCTION: [Isoform 1]: Has transforming growth factor beta-activated receptor activity. {ECO:0000269|PubMed:8635485}.; FUNCTION: [Isoform 2]: Has transforming growth factor beta-activated receptor activity. {ECO:0000269|PubMed:8635485}.; FUNCTION: [Isoform 3]: Binds TGFB1, TGFB2 and TGFB3 in the picomolar affinity range without the participation of additional receptors. Blocks activation of SMAD2 and SMAD3 by TGFB1. {ECO:0000269|PubMed:34568316}.FUNCTION: Microtubule plus-end tracking protein that promotes the stabilization of dynamic microtubules (PubMed:26003921). Involved in the nucleation of noncentrosomal microtubules originating from the trans-Golgi network (TGN). Required for the polarization of the cytoplasmic microtubule arrays in migrating cells towards the leading edge of the cell. May act at the cell cortex to enhance the frequency of rescue of depolymerizing microtubules by attaching their plus-ends to cortical platforms composed of ERC1 and PHLDB2 (PubMed:16824950). This cortical microtubule stabilizing activity is regulated at least in part by phosphatidylinositol 3-kinase signaling. Also performs a similar stabilizing function at the kinetochore which is essential for the bipolar alignment of chromosomes on the mitotic spindle (PubMed:16866869, PubMed:16914514). Acts as a mediator of ERBB2-dependent stabilization of microtubules at the cell cortex. {ECO:0000269|PubMed:11290329, ECO:0000269|PubMed:15631994, ECO:0000269|PubMed:16824950, ECO:0000269|PubMed:16866869, ECO:0000269|PubMed:16914514, ECO:0000269|PubMed:17543864, ECO:0000269|PubMed:20937854, ECO:0000269|PubMed:26003921}.

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 TGFBR2_CLASP2


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
TGFBR2P37173humanTGFBR1P36897T185kDLIyDMttsGsGsGTGF_beta_GS
TGFBR2P37173humanUSP2O75604S207ENYGRKGsASQVPSQ
TGFBR2P37173humanTGFBR2P37173S213TRkLMEFsEHCAIIL
TGFBR2P37173humanUSP2O75604S225SRVPEIIsPTYRPIG
TGFBR2P37173humanTGFBR1P36897S187LIyDMttsGsGsGLPTGF_beta_GS
TGFBR2P37173humanENGP17813S634VAVAAPAssESSStN
TGFBR2P37173humanTGFBR2P37173Y259KGRFAEVykAKLkQNPK_Tyr_Ser-Thr
TGFBR2P37173humanTGFBR1P36897S191MttsGsGsGLPLLVQTGF_beta_GS
TGFBR2P37173humanTGFBR2P37173S416sVDDLANsGQVGTARPK_Tyr_Ser-Thr
TGFBR2P37173humanTGFBR2P37173Y424GQVGTARyMAPEVLEPK_Tyr_Ser-Thr
TGFBR2P37173humanTGFBR2P37173S409LRLDPTLsVDDLANsPK_Tyr_Ser-Thr
TGFBR2P37173humanTGFBR1P36897S189yDMttsGsGsGLPLLTGF_beta_GS
TGFBR2P37173humanENGP17813S635AVAAPAssESSStNH
TGFBR2P37173humanTGFBR2P37173Y336AKGNLQEyLTRHVISPK_Tyr_Ser-Thr
TGFBR2P37173humanTGFBR1P36897T200LPLLVQRtIARtIVLTGF_beta_GS
TGFBR2P37173humanTGFBR1P36897T186DLIyDMttsGsGsGLTGF_beta_GS


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
TGFBR2IDDescription0.00e+00
TGFBR2GO:0062042regulation of cardiac epithelial to mesenchymal transition1.70e-07
TGFBR2GO:0003198epithelial to mesenchymal transition involved in endocardial cushion formation3.22e-07
TGFBR2GO:0003272endocardial cushion formation1.54e-06
TGFBR2GO:0060317cardiac epithelial to mesenchymal transition2.11e-06
TGFBR2GO:0003203endocardial cushion morphogenesis3.01e-06
TGFBR2GO:0003197endocardial cushion development5.20e-06
TGFBR2GO:0072132mesenchyme morphogenesis5.74e-06
TGFBR2GO:0010718positive regulation of epithelial to mesenchymal transition5.74e-06
TGFBR2GO:0003208cardiac ventricle morphogenesis8.41e-06
TGFBR2GO:0060411cardiac septum morphogenesis8.41e-06
TGFBR2GO:0048844artery morphogenesis1.05e-05
TGFBR2GO:0090100positive regulation of transmembrane receptor protein serine/threonine kinase signaling pathway2.08e-05
TGFBR2GO:0003279cardiac septum development2.08e-05
TGFBR2GO:0010717regulation of epithelial to mesenchymal transition2.08e-05
TGFBR2GO:0060840artery development2.08e-05
TGFBR2GO:0003206cardiac chamber morphogenesis2.76e-05
TGFBR2GO:0003231cardiac ventricle development2.76e-05
TGFBR2GO:0003205cardiac chamber development6.06e-05
TGFBR2GO:0003222ventricular trabecula myocardium morphogenesis6.39e-05
TGFBR2GO:0001837epithelial to mesenchymal transition6.49e-05
TGFBR2GO:0007179transforming growth factor beta receptor signaling pathway1.32e-04
TGFBR2GO:0003148outflow tract septum morphogenesis1.67e-04
TGFBR2GO:0048762mesenchymal cell differentiation1.73e-04
TGFBR2GO:0003007heart morphogenesis1.73e-04
TGFBR2GO:0060391positive regulation of SMAD protein signal transduction1.73e-04
TGFBR2GO:0071560cellular response to transforming growth factor beta stimulus2.01e-04
TGFBR2GO:0070723response to cholesterol2.01e-04
TGFBR2GO:0071559response to transforming growth factor beta2.01e-04
TGFBR2GO:0048562embryonic organ morphogenesis2.01e-04
TGFBR2GO:0090092regulation of transmembrane receptor protein serine/threonine kinase signaling pathway2.01e-04
TGFBR2GO:0061384heart trabecula morphogenesis2.13e-04
TGFBR2GO:0036314response to sterol2.44e-04
TGFBR2GO:0060485mesenchyme development2.44e-04
TGFBR2GO:0001569branching involved in blood vessel morphogenesis2.47e-04
TGFBR2GO:0035909aorta morphogenesis2.67e-04
TGFBR2GO:0007517muscle organ development2.84e-04
TGFBR2GO:0060412ventricular septum morphogenesis3.25e-04
TGFBR2GO:0048701embryonic cranial skeleton morphogenesis3.47e-04
TGFBR2GO:0055010ventricular cardiac muscle tissue morphogenesis3.60e-04
TGFBR2GO:0061383trabecula morphogenesis3.60e-04
TGFBR2GO:0032924activin receptor signaling pathway3.78e-04
TGFBR2GO:0007178transmembrane receptor protein serine/threonine kinase signaling pathway3.78e-04
TGFBR2GO:0003002regionalization4.16e-04
TGFBR2GO:0060390regulation of SMAD protein signal transduction4.16e-04
TGFBR2GO:0048568embryonic organ development4.75e-04
TGFBR2GO:0003229ventricular cardiac muscle tissue development4.78e-04
TGFBR2GO:0055008cardiac muscle tissue morphogenesis5.13e-04
TGFBR2GO:0007389pattern specification process5.13e-04
TGFBR2GO:0001947heart looping5.53e-04

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Related Drugs to TGFBR2_CLASP2


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 TGFBR2-CLASP2 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 TGFBR2_CLASP2


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


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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