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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:ZFP36_CSK

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: ZFP36_CSK
KinaseFusionDB ID: KFG7251
FusionGDB2.0 ID: KFG7251
HgeneTgene
Gene symbol

ZFP36

CSK

Gene ID

7538

1445

Gene nameZFP36 ring finger proteinC-terminal Src kinase
SynonymsG0S24|GOS24|NUP475|RNF162A|TIS11|TTP|zfp-36-
Cytomap

19q13.2

15q24.1

Type of geneprotein-codingprotein-coding
DescriptionmRNA decay activator protein ZFP36G0/G1 switch regulatory protein 24growth factor-inducible nuclear protein NUP475tristetraprolintristetraprolinezinc finger protein 36 homologzinc finger protein 36, C3H type, homologtyrosine-protein kinase CSKC-Src kinaseCSK, non-receptor tyrosine kinasec-src tyrosine kinaseprotein-tyrosine kinase CYL
Modification date2024030520240411
UniProtAcc

P26651

P41240

Ensembl transtripts involved in fusion geneENST idsENST00000597629, ENST00000248673, 
ENST00000594045, 
ENST00000220003, 
ENST00000439220, ENST00000567571, 
ENST00000309470, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: ZFP36 [Title/Abstract] AND CSK [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
HgeneZFP36

GO:0000288

nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay

23644599

HgeneZFP36

GO:0006402

mRNA catabolic process

10751406|11782475

HgeneZFP36

GO:0006402

mRNA catabolic process

10330172|20221403

HgeneZFP36

GO:0009611

response to wounding

27182009

HgeneZFP36

GO:0031086

nuclear-transcribed mRNA catabolic process, deadenylation-independent decay

11279239

HgeneZFP36

GO:0032680

regulation of tumor necrosis factor production

15014438

HgeneZFP36

GO:0042594

response to starvation

15014438

HgeneZFP36

GO:0043488

regulation of mRNA stability

9703499|11719186|15687258|20702587

HgeneZFP36

GO:0044344

cellular response to fibroblast growth factor stimulus

20166898

HgeneZFP36

GO:0045647

negative regulation of erythrocyte differentiation

20702587

HgeneZFP36

GO:0060213

positive regulation of nuclear-transcribed mRNA poly(A) tail shortening

10330172

HgeneZFP36

GO:0061158

3'-UTR-mediated mRNA destabilization

9703499|11719186|15687258|20221403|27193233

HgeneZFP36

GO:0070935

3'-UTR-mediated mRNA stabilization

15014438

HgeneZFP36

GO:0071222

cellular response to lipopolysaccharide

14766228

HgeneZFP36

GO:0071356

cellular response to tumor necrosis factor

20166898

HgeneZFP36

GO:0071364

cellular response to epidermal growth factor stimulus

20166898

HgeneZFP36

GO:0071385

cellular response to glucocorticoid stimulus

20166898

HgeneZFP36

GO:0097011

cellular response to granulocyte macrophage colony-stimulating factor stimulus

20166898

HgeneZFP36

GO:1900153

positive regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay

12748283

HgeneZFP36

GO:1901835

positive regulation of deadenylation-independent decapping of nuclear-transcribed mRNA

16364915

TgeneCSK

GO:0042997

negative regulation of Golgi to plasma membrane protein transport

20605918


check buttonKinase Fusion gene breakpoints across ZFP36 (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 CSK (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
CCLEU266B1ZFP36chr19

39898616

CSKchr15

75093038



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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)
ENST00000248673ENST00000220003ZFP36chr1939898616CSKchr15750930382976283

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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

>ENST00000248673_ENST00000220003_ZFP36_chr19_39898616_CSK_chr15_75093038_length(amino acids)=283
MPSTSCHPHPLRPLQPPPPPRATRLSYVGPSQRVGAAATGPSASLPMAWASCARPIATPNTRRNSVTSSTSRAAAPTALAATSSTTLAKT
WRPRATLLCFARASASPACPLAAGPHHHHQAWPALPCPPAPSRPPAPHHHLGTFHCHPLPSLLPLAPPWLEETPPQSVAPPAEGPLLSAS
GGPWVAWFGPPLYSPWDPTLMNMPAAAAAWGALTLPSSRREFLHHPSPWQPPGDSPSSIASLFLSDKVTARSDQLDLSGEPRLLHCGLCM

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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/chr19:/chr15:)
- 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
ZFP36

P26651

CSK

P41240

FUNCTION: Zinc-finger RNA-binding protein that destabilizes several cytoplasmic AU-rich element (ARE)-containing mRNA transcripts by promoting their poly(A) tail removal or deadenylation, and hence provide a mechanism for attenuating protein synthesis (PubMed:9703499, PubMed:10330172, PubMed:10751406, PubMed:11279239, PubMed:12115244, PubMed:12748283, PubMed:15187101, PubMed:15634918, PubMed:17030620, PubMed:16702957, PubMed:20702587, PubMed:20221403, PubMed:21775632, PubMed:27193233, PubMed:23644599, PubMed:25815583, PubMed:31439631). Acts as an 3'-untranslated region (UTR) ARE mRNA-binding adapter protein to communicate signaling events to the mRNA decay machinery (PubMed:15687258, PubMed:23644599). Recruits deadenylase CNOT7 (and probably the CCR4-NOT complex) via association with CNOT1, and hence promotes ARE-mediated mRNA deadenylation (PubMed:23644599). Functions also by recruiting components of the cytoplasmic RNA decay machinery to the bound ARE-containing mRNAs (PubMed:11719186, PubMed:12748283, PubMed:15687258, PubMed:16364915). Self regulates by destabilizing its own mRNA (PubMed:15187101). Binds to 3'-UTR ARE of numerous mRNAs and of its own mRNA (PubMed:10330172, PubMed:10751406, PubMed:12115244, PubMed:15187101, PubMed:15634918, PubMed:17030620, PubMed:16702957, PubMed:19188452, PubMed:20702587, PubMed:20221403, PubMed:21775632, PubMed:25815583). Plays a role in anti-inflammatory responses; suppresses tumor necrosis factor (TNF)-alpha production by stimulating ARE-mediated TNF-alpha mRNA decay and several other inflammatory ARE-containing mRNAs in interferon (IFN)- and/or lipopolysaccharide (LPS)-induced macrophages (By similarity). Also plays a role in the regulation of dendritic cell maturation at the post-transcriptional level, and hence operates as part of a negative feedback loop to limit the inflammatory response (PubMed:18367721). Promotes ARE-mediated mRNA decay of hypoxia-inducible factor HIF1A mRNA during the response of endothelial cells to hypoxia (PubMed:21775632). Positively regulates early adipogenesis of preadipocytes by promoting ARE-mediated mRNA decay of immediate early genes (IEGs) (By similarity). Negatively regulates hematopoietic/erythroid cell differentiation by promoting ARE-mediated mRNA decay of the transcription factor STAT5B mRNA (PubMed:20702587). Plays a role in maintaining skeletal muscle satellite cell quiescence by promoting ARE-mediated mRNA decay of the myogenic determination factor MYOD1 mRNA (By similarity). Associates also with and regulates the expression of non-ARE-containing target mRNAs at the post-transcriptional level, such as MHC class I mRNAs (PubMed:18367721). Participates in association with argonaute RISC catalytic components in the ARE-mediated mRNA decay mechanism; assists microRNA (miRNA) targeting ARE-containing mRNAs (PubMed:15766526). May also play a role in the regulation of cytoplasmic mRNA decapping; enhances decapping of ARE-containing RNAs, in vitro (PubMed:16364915). Involved in the delivery of target ARE-mRNAs to processing bodies (PBs) (PubMed:17369404). In addition to its cytosolic mRNA-decay function, affects nuclear pre-mRNA processing (By similarity). Negatively regulates nuclear poly(A)-binding protein PABPN1-stimulated polyadenylation activity on ARE-containing pre-mRNA during LPS-stimulated macrophages (By similarity). Also involved in the regulation of stress granule (SG) and P-body (PB) formation and fusion (By similarity). Plays a role in the regulation of keratinocyte proliferation, differentiation and apoptosis (PubMed:27182009). Plays a role as a tumor suppressor by inhibiting cell proliferation in breast cancer cells (PubMed:26926077). {ECO:0000250|UniProtKB:P22893, ECO:0000269|PubMed:10330172, ECO:0000269|PubMed:10751406, ECO:0000269|PubMed:11279239, ECO:0000269|PubMed:11719186, ECO:0000269|PubMed:12115244, ECO:0000269|PubMed:12748283, ECO:0000269|PubMed:15187101, ECO:0000269|PubMed:15634918, ECO:0000269|PubMed:15687258, ECO:0000269|PubMed:15766526, ECO:0000269|PubMed:16364915, ECO:0000269|PubMed:16702957, ECO:0000269|PubMed:17030620, ECO:0000269|PubMed:17369404, ECO:0000269|PubMed:18367721, ECO:0000269|PubMed:19188452, ECO:0000269|PubMed:20221403, ECO:0000269|PubMed:20702587, ECO:0000269|PubMed:21775632, ECO:0000269|PubMed:23644599, ECO:0000269|PubMed:25815583, ECO:0000269|PubMed:26926077, ECO:0000269|PubMed:27182009, ECO:0000269|PubMed:27193233, ECO:0000269|PubMed:31439631, ECO:0000269|PubMed:9703499}.; FUNCTION: (Microbial infection) Negatively regulates HTLV-1 TAX-dependent transactivation of viral long terminal repeat (LTR) promoter. {ECO:0000269|PubMed:14679154}.FUNCTION: Non-receptor tyrosine-protein kinase that plays an important role in the regulation of cell growth, differentiation, migration and immune response. Phosphorylates tyrosine residues located in the C-terminal tails of Src-family kinases (SFKs) including LCK, SRC, HCK, FYN, LYN, CSK or YES1. Upon tail phosphorylation, Src-family members engage in intramolecular interactions between the phosphotyrosine tail and the SH2 domain that result in an inactive conformation. To inhibit SFKs, CSK is recruited to the plasma membrane via binding to transmembrane proteins or adapter proteins located near the plasma membrane. Suppresses signaling by various surface receptors, including T-cell receptor (TCR) and B-cell receptor (BCR) by phosphorylating and maintaining inactive several positive effectors such as FYN or LCK. {ECO:0000269|PubMed:1639064, ECO:0000269|PubMed:9281320}.

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
TgeneZFP3639898616CSK75093038ENST00000248673013195_4490451DomainNote=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159
TgeneZFP3639898616CSK75093038ENST00000248673014195_4490451DomainNote=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159
TgeneZFP3639898616CSK75093038ENST00000248673015195_4490451DomainNote=Protein kinase;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00159
TgeneZFP3639898616CSK75093038ENST0000024867301382_1710451DomainNote=SH2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00191
TgeneZFP3639898616CSK75093038ENST0000024867301482_1710451DomainNote=SH2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00191
TgeneZFP3639898616CSK75093038ENST0000024867301582_1710451DomainNote=SH2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00191


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Kinase Fusion Protein Structures

check button CIF files of the predicted kinase fusion proteins
* Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
Kinase Fusion protein CIF link (fusion AA seq ID in KinaseFusionDB)HenstTenstHgeneHchrHbpTgeneTchrTbpAA seqLen(AA seq)
PDB file >>>570_ZFP36_CSKENST00000248673ENST00000220003ZFP36chr1939898616CSKchr1575093038
MPSTSCHPHPLRPLQPPPPPRATRLSYVGPSQRVGAAATGPSASLPMAWASCARPIATPNTRRNSVTSSTSRAAAPTALAATSSTTLAKT
WRPRATLLCFARASASPACPLAAGPHHHHQAWPALPCPPAPSRPPAPHHHLGTFHCHPLPSLLPLAPPWLEETPPQSVAPPAEGPLLSAS
GGPWVAWFGPPLYSPWDPTLMNMPAAAAAWGALTLPSSRREFLHHPSPWQPPGDSPSSIASLFLSDKVTARSDQLDLSGEPRLLHCGLCM
283
3D view using mol* of 570_ZFP36_CSK
PDB file >>>TKFP_967_ZFP36_CSKENST00000248673ENST00000220003ZFP36chr1939898616CSKchr1575093038
MPSTSCHPHPLRPLQPPPPPRATRLSYVGPSQRVGAAATGPSASLPMAWASCARPIATPNTRRNSVTSSTSRAAAPTALAATSSTTLAKT
WRPRATLLCFARASASPACPLAAGPHHHHQAWPALPCPPAPSRPPAPHHHLGTFHCHPLPSLLPLAPPWLEETPPQSVAPPAEGPLLSAS
GGPWVAWFGPPLYSPWDPTLMNMPAAAAAWGALTLPSSRREFLHHPSPWQPPGDSPSSIASLFLSDKVTARSDQLDLSGEPRLLHCGLCM
283_ZFP36_CSK


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Comparison of Fusion Protein Isoforms

check button Superimpose the 3D Structures Among All Fusion Protein Isoforms
* Download the pdb file and open it from the molstar online viewer.

check button Comparison of the Secondary Structures of Fusion Protein Isoforms

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

ZFP36_CSK does not have any known PDB structures.

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pLDDT score distribution

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
* The blue color at the bottom marks the best active site residues.


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Potential Active Site Information


check button The potential binding sites of these fusion proteins were identified using SiteMap, a module of the Schrodinger suite.
Kinase Fusion AA seq ID in KinaseFusionDBSite scoreSizeDscoreVolumeExposureEnclosureContactPhobicPhilicBalanceDon/AccResidues

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Ramachandran Plot of Kinase Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.

570_ZFP36_CSK_ramachandran.png
all structure ZFP36-CSK

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Virtual Screening Results


check button Distribution of the average docking score across all approved kinase inhibitors.
Distribution of the number of occurrence across all approved kinase inhibitors.
5'-kinase fusion protein case
3'-kinase fusion protein case

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check button Drug information from DrugBank of the top 20 interacting small molecules.
* The detailed information of individual kinase inhibitors are available in the download page.
Fusion gene name infoDrugDocking scoreGlide g scoreGlide energy

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Kinase-Substrate Information of ZFP36_CSK


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
CSKP41240humanEEF2P13639Y265kkLWGDryFDPANGkGTP_EFTU
CSKP41240humanYES1P07947Y537FtAtEPQyQPGENL_
CSKP41240humanPTPRCP08575Y1218MVSTFEQyQFLyDVIY_phosphatase
CSKP41240humanLCKP06239Y505FTAtEGQyQPQP___
CSKP41240humanSRCP12931Y530FTstEPQyQPGENL_
CSKP41240humanHCKP08631Y411RVIEDNEytAREGAkPK_Tyr_Ser-Thr
CSKP41240humanMAPTP10636-8Y29DRKDQGGytMHQDQE
CSKP41240humanMAPTP10636-8Y197KsGDRsGyssPGsPG
CSKP41240humanEEF2P13639Y373kYRCELLyEGPPDDE
CSKP41240humanSRCP12931Y419RLIEDNEytARQGAkPK_Tyr_Ser-Thr
CSKP41240humanFYNP06241Y531FtAtEPQyQPGENL_


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
CSKIDDescription0.00e+00
CSKGO:0038094Fc-gamma receptor signaling pathway4.27e-13
CSKGO:0038093Fc receptor signaling pathway6.25e-12
CSKGO:0002433immune response-regulating cell surface receptor signaling pathway involved in phagocytosis3.99e-11
CSKGO:0038096Fc-gamma receptor signaling pathway involved in phagocytosis3.99e-11
CSKGO:0002431Fc receptor mediated stimulatory signaling pathway9.76e-11
CSKGO:0018108peptidyl-tyrosine phosphorylation3.27e-08
CSKGO:0018212peptidyl-tyrosine modification3.27e-08
CSKGO:0002862negative regulation of inflammatory response to antigenic stimulus5.72e-08
CSKGO:0002429immune response-activating cell surface receptor signaling pathway5.72e-08
CSKGO:0002768immune response-regulating cell surface receptor signaling pathway8.55e-08
CSKGO:0002861regulation of inflammatory response to antigenic stimulus1.85e-07
CSKGO:0031295T cell costimulation1.85e-07
CSKGO:0031294lymphocyte costimulation2.02e-07
CSKGO:0002757immune response-activating signaling pathway3.99e-07
CSKGO:0050728negative regulation of inflammatory response4.21e-07
CSKGO:0050777negative regulation of immune response4.25e-07
CSKGO:0002764immune response-regulating signaling pathway4.58e-07
CSKGO:0006909phagocytosis7.82e-07
CSKGO:0002437inflammatory response to antigenic stimulus9.38e-07
CSKGO:0050870positive regulation of T cell activation9.38e-07
CSKGO:1903039positive regulation of leukocyte cell-cell adhesion1.41e-06
CSKGO:0031348negative regulation of defense response2.83e-06
CSKGO:0022409positive regulation of cell-cell adhesion2.83e-06
CSKGO:0051251positive regulation of lymphocyte activation3.05e-06
CSKGO:0036120cellular response to platelet-derived growth factor stimulus3.05e-06
CSKGO:0036119response to platelet-derived growth factor3.81e-06
CSKGO:0002696positive regulation of leukocyte activation5.26e-06
CSKGO:0050863regulation of T cell activation5.26e-06
CSKGO:1903037regulation of leukocyte cell-cell adhesion5.26e-06
CSKGO:0050867positive regulation of cell activation5.89e-06
CSKGO:0050900leukocyte migration5.89e-06
CSKGO:0007159leukocyte cell-cell adhesion7.55e-06
CSKGO:0050727regulation of inflammatory response7.86e-06
CSKGO:0050731positive regulation of peptidyl-tyrosine phosphorylation1.05e-05
CSKGO:0032102negative regulation of response to external stimulus1.35e-05
CSKGO:0045785positive regulation of cell adhesion1.35e-05
CSKGO:0022407regulation of cell-cell adhesion1.46e-05
CSKGO:2000116regulation of cysteine-type endopeptidase activity1.71e-05
CSKGO:0046777protein autophosphorylation1.80e-05
CSKGO:0048013ephrin receptor signaling pathway2.23e-05
CSKGO:0050730regulation of peptidyl-tyrosine phosphorylation3.11e-05
CSKGO:0052548regulation of endopeptidase activity7.30e-05
CSKGO:0052547regulation of peptidase activity9.80e-05
CSKGO:0045862positive regulation of proteolysis1.51e-04
CSKGO:0071801regulation of podosome assembly2.35e-04
CSKGO:2001233regulation of apoptotic signaling pathway2.40e-04
CSKGO:2001056positive regulation of cysteine-type endopeptidase activity3.14e-04
CSKGO:0050852T cell receptor signaling pathway4.27e-04
CSKGO:0071800podosome assembly4.73e-04

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Related Drugs to ZFP36_CSK


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 ZFP36-CSK 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 ZFP36_CSK


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