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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:NLK_UTP20

Kinase Fusion Protein Summary

check button Kinase Fusion gene summary
Kinase Fusion partner gene informationKinase Fusion gene name: NLK_UTP20
KinaseFusionDB ID: KFG4213
FusionGDB2.0 ID: KFG4213
HgeneTgene
Gene symbol

NLK

UTP20

Gene ID

51701

27340

Gene namenemo like kinaseUTP20 small subunit processome component
Synonyms-1A6/DRIM|DRIM
Cytomap

17q11.2

12q23.2

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase NLKsmall subunit processome component 20 homologNNP73UTP20 small subunit (SSU) processome componentUTP20, small subunit (SSU) processome component, homologdown regulated in metastasisdown-regulated in metastasis proteinnovel nucleolar protein 73
Modification date2024040320240305
UniProtAcc

Q9UBE8

O75691

Ensembl transtripts involved in fusion geneENST idsENST00000407008, ENST00000582037, 
ENST00000583517, 
ENST00000261637, 
Context (manual curation of fusion genes in KinaseFusionDB)

PubMed: NLK [Title/Abstract] AND UTP20 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NLK(26463909)-UTP20(101702359), # 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
HgeneNLK

GO:0050821

protein stabilization

25512613

HgeneNLK

GO:0071470

cellular response to osmotic stress

26588989

HgeneNLK

GO:1904262

negative regulation of TORC1 signaling

26588989

TgeneUTP20

GO:0042274

ribosomal small subunit biogenesis

34516797


check buttonKinase Fusion gene breakpoints across NLK (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 UTP20 (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
ChiTaRS5.0FN176744NLKchr17

26463909

UTP20chr12

101702359



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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/:26463909/:101702359)
- 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
NLK

Q9UBE8

UTP20

O75691

FUNCTION: Serine/threonine-protein kinase that regulates a number of transcription factors with key roles in cell fate determination (PubMed:14960582, PubMed:12482967, PubMed:15004007, PubMed:15764709, PubMed:20061393, PubMed:20874444, PubMed:21454679). Positive effector of the non-canonical Wnt signaling pathway, acting downstream of WNT5A, MAP3K7/TAK1 and HIPK2 (PubMed:15004007, PubMed:15764709). Negative regulator of the canonical Wnt/beta-catenin signaling pathway (PubMed:12482967). Binds to and phosphorylates TCF7L2/TCF4 and LEF1, promoting the dissociation of the TCF7L2/LEF1/beta-catenin complex from DNA, as well as the ubiquitination and subsequent proteolysis of LEF1 (PubMed:21454679). Together these effects inhibit the transcriptional activation of canonical Wnt/beta-catenin target genes (PubMed:12482967, PubMed:21454679). Negative regulator of the Notch signaling pathway (PubMed:20118921). Binds to and phosphorylates NOTCH1, thereby preventing the formation of a transcriptionally active ternary complex of NOTCH1, RBPJ/RBPSUH and MAML1 (PubMed:20118921). Negative regulator of the MYB family of transcription factors (PubMed:15082531). Phosphorylation of MYB leads to its subsequent proteolysis while phosphorylation of MYBL1 and MYBL2 inhibits their interaction with the coactivator CREBBP (PubMed:15082531). Other transcription factors may also be inhibited by direct phosphorylation of CREBBP itself (PubMed:15082531). Acts downstream of IL6 and MAP3K7/TAK1 to phosphorylate STAT3, which is in turn required for activation of NLK by MAP3K7/TAK1 (PubMed:15004007, PubMed:15764709). Upon IL1B stimulus, cooperates with ATF5 to activate the transactivation activity of C/EBP subfamily members (PubMed:25512613). Phosphorylates ATF5 but also stabilizes ATF5 protein levels in a kinase-independent manner (PubMed:25512613). Acts as an inhibitor of the mTORC1 complex in response to osmotic stress by mediating phosphorylation of RPTOR, thereby preventing recruitment of the mTORC1 complex to lysosomes (PubMed:26588989). {ECO:0000269|PubMed:12482967, ECO:0000269|PubMed:14960582, ECO:0000269|PubMed:15004007, ECO:0000269|PubMed:15082531, ECO:0000269|PubMed:15764709, ECO:0000269|PubMed:20061393, ECO:0000269|PubMed:20118921, ECO:0000269|PubMed:20874444, ECO:0000269|PubMed:21454679, ECO:0000269|PubMed:25512613, ECO:0000269|PubMed:26588989}.FUNCTION: Part of the small subunit (SSU) processome, first precursor of the small eukaryotic ribosomal subunit. During the assembly of the SSU processome in the nucleolus, many ribosome biogenesis factors, an RNA chaperone and ribosomal proteins associate with the nascent pre-rRNA and work in concert to generate RNA folding, modifications, rearrangements and cleavage as well as targeted degradation of pre-ribosomal RNA by the RNA exosome. Involved in 18S pre-rRNA processing. Associates with U3 snoRNA. {ECO:0000269|PubMed:17498821, ECO:0000269|PubMed:34516797}.

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 NLK_UTP20


check button Phosphorylation target of the kinase
(phosphosite, 03-17-2024)
KinaseKinase UniProt AccKinase speciesSubstrateSubstrate UniProt AccSubstrate phosphorylated residuesSubstrate phosphorylated sites (+/-7AA)Domain
NLKQ9UBE8humanNCOA3Q9Y6Q9S857PPYNRAVsLDsPVsV
NLKQ9UBE8humanLEF1Q9UJU2S166tysDEHFsPGSHPSHCTNNB1_binding
NLKQ9UBE8humanSMAD4Q13485S138YHYERVVsPGIDLSG
NLKQ9UBE8humanTCF7L2Q9NQB0T212TYSNEHFtPGNPPPHCTNNB1_binding
NLKQ9UBE8humanESR1P03372S104FPPLNsVsPsPLMLLOest_recep
NLKQ9UBE8humanLEF1Q9UJU2S132YMSNGSLsPPIPRTSCTNNB1_binding
NLKQ9UBE8humanLEF1Q9UJU2S200IPtFyPLsPGGVGQICTNNB1_binding
NLKQ9UBE8humanNCOA3Q9Y6Q9S860NRAVsLDsPVsVGss
NLKQ9UBE8humanSMAD2Q15796S250TGsPAELsPTTLsPV
NLKQ9UBE8humanNCOA3Q9Y6Q9S543SLLSTLSsPGPKLDNNCOA_u2
NLKQ9UBE8humanSMAD4Q13485T9DNMSITNtPTSNDAC
NLKQ9UBE8humanYAP1P46937S128QHVRAHssPAsLQLG
NLKQ9UBE8humanFOXO1Q12778S329stIsGRLsPIMtEQD
NLKQ9UBE8humanNCOA3Q9Y6Q9T24KRKLPCDtPGQGLtC
NLKQ9UBE8humanTCF7L2Q9NQB0T201PHHVHPLtPLITYSNCTNNB1_binding
NLKQ9UBE8humanESR1P03372S118LHPPPQLsPFLQPHGOest_recep
NLKQ9UBE8humanSMAD3P84022S208DAGsPNLsPNPMsPA
NLKQ9UBE8humanESR1P03372S106PLNsVsPsPLMLLHPOest_recep
NLKQ9UBE8humanNCOA3Q9Y6Q9S867sPVsVGssPPVKNIS
NLKQ9UBE8humanESR1P03372S167GGRERLAsTNDkGSMOest_recep
NLKQ9UBE8humanRPTORQ8N122S863LtQsAPAsPtNkGVH
NLKQ9UBE8humanLEF1Q9UJU2T265IPHPAIVtPQVKQEH
NLKQ9UBE8humanLEF1Q9UJU2T155SHAVHPLtPLItysDCTNNB1_binding
NLKQ9UBE8humanNCOA3Q9Y6Q9S505SPVAGVHsPMAsSGNNCOA_u2


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
NLKIDDescription0.00e+00
NLKGO:0010718positive regulation of epithelial to mesenchymal transition6.04e-08
NLKGO:0048339paraxial mesoderm development6.04e-08
NLKGO:0010717regulation of epithelial to mesenchymal transition5.26e-07
NLKGO:0007498mesoderm development1.02e-06
NLKGO:0060485mesenchyme development1.02e-06
NLKGO:0048340paraxial mesoderm morphogenesis2.13e-06
NLKGO:0072132mesenchyme morphogenesis2.13e-06
NLKGO:0001837epithelial to mesenchymal transition2.13e-06
NLKGO:0048762mesenchymal cell differentiation1.31e-05
NLKGO:0062009secondary palate development2.72e-05
NLKGO:0060070canonical Wnt signaling pathway2.72e-05
NLKGO:0030325adrenal gland development2.80e-05
NLKGO:0060562epithelial tube morphogenesis2.80e-05
NLKGO:0030111regulation of Wnt signaling pathway2.80e-05
NLKGO:0003299muscle hypertrophy in response to stress2.80e-05
NLKGO:0014887cardiac muscle adaptation2.80e-05
NLKGO:0014898cardiac muscle hypertrophy in response to stress2.80e-05
NLKGO:1904019epithelial cell apoptotic process3.64e-05
NLKGO:0010614negative regulation of cardiac muscle hypertrophy3.64e-05
NLKGO:0072073kidney epithelium development3.87e-05
NLKGO:0014741negative regulation of muscle hypertrophy3.91e-05
NLKGO:0001701in utero embryonic development3.93e-05
NLKGO:0048754branching morphogenesis of an epithelial tube3.93e-05
NLKGO:0048732gland development6.62e-05
NLKGO:0061138morphogenesis of a branching epithelium6.93e-05
NLKGO:0016055Wnt signaling pathway6.93e-05
NLKGO:0198738cell-cell signaling by wnt6.93e-05
NLKGO:0032924activin receptor signaling pathway6.93e-05
NLKGO:0007369gastrulation7.85e-05
NLKGO:0050673epithelial cell proliferation7.85e-05
NLKGO:0001763morphogenesis of a branching structure8.34e-05
NLKGO:0014888striated muscle adaptation8.63e-05
NLKGO:0009952anterior/posterior pattern specification1.06e-04
NLKGO:0045599negative regulation of fat cell differentiation1.11e-04
NLKGO:0001756somitogenesis1.37e-04
NLKGO:0010611regulation of cardiac muscle hypertrophy1.40e-04
NLKGO:0045444fat cell differentiation1.47e-04
NLKGO:0014743regulation of muscle hypertrophy1.47e-04
NLKGO:1902893regulation of miRNA transcription1.47e-04
NLKGO:0061614miRNA transcription1.50e-04
NLKGO:0001649osteoblast differentiation1.59e-04
NLKGO:0009880embryonic pattern specification1.59e-04
NLKGO:0001707mesoderm formation1.59e-04
NLKGO:0060828regulation of canonical Wnt signaling pathway1.59e-04
NLKGO:0003007heart morphogenesis1.59e-04
NLKGO:0014706striated muscle tissue development1.59e-04
NLKGO:0048332mesoderm morphogenesis1.63e-04
NLKGO:0007492endoderm development2.00e-04
NLKGO:0060395SMAD protein signal transduction2.03e-04

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Related Drugs to NLK_UTP20


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 NLK-UTP20 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 NLK_UTP20


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