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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:NEK1-RPS6KC1 (FusionGDB2 ID:58509)

Fusion Gene Summary for NEK1-RPS6KC1

check button Fusion gene summary
Fusion gene informationFusion gene name: NEK1-RPS6KC1
Fusion gene ID: 58509
HgeneTgene
Gene symbol

NEK1

RPS6KC1

Gene ID

4750

26750

Gene nameNIMA related kinase 1ribosomal protein S6 kinase C1
SynonymsALS24|NY-REN-55|SRPS2|SRPS2A|SRTD6RPK118|RSKL1|S6K-delta-1|S6PKh1|humS6PKh1
Cytomap

4q33

1q32.3

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase Nek1NIMA (never in mitosis gene a)-related kinase 1never in mitosis A-related kinase 1nimA-related protein kinase 1protein-serine/threonine kinaserenal carcinoma antigen NY-REN-55ribosomal protein S6 kinase delta-152 kDa ribosomal protein S6 kinaseSPHK1-binding proteinribosomal S6 kinase-like protein with two PSK domains 118 kDa proteinribosomal protein S6 kinase, 52kDa, polypeptide 1
Modification date2020032920200320
UniProtAcc

Q96PY6

.
Ensembl transtripts involved in fusion geneENST00000439128, ENST00000507142, 
ENST00000510533, ENST00000511633, 
ENST00000512193, 
ENST00000366959, 
ENST00000366960, ENST00000543470, 
ENST00000490299, ENST00000543354, 
Fusion gene scores* DoF score7 X 7 X 3=1479 X 8 X 2=144
# samples 79
** MAII scorelog2(7/147*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/144*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NEK1 [Title/Abstract] AND RPS6KC1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNEK1(170533170)-RPS6KC1(213415910), # samples:2
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneNEK1

GO:0006468

protein phosphorylation

19158487


check buttonFusion gene breakpoints across NEK1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across RPS6KC1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ABI596518NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
ChiTaRS5.0N/ABI596864NEK1chr4

170533170

-RPS6KC1chr1

213415910

+


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Fusion Gene ORF analysis for NEK1-RPS6KC1

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
5UTR-3CDSENST00000439128ENST00000366959NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000439128ENST00000366960NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000439128ENST00000543470NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000507142ENST00000366959NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000507142ENST00000366960NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000507142ENST00000543470NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000510533ENST00000366959NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000510533ENST00000366960NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000510533ENST00000543470NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000511633ENST00000366959NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000511633ENST00000366960NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000511633ENST00000543470NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000512193ENST00000366959NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000512193ENST00000366960NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3CDSENST00000512193ENST00000543470NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3UTRENST00000439128ENST00000490299NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3UTRENST00000439128ENST00000543354NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3UTRENST00000507142ENST00000490299NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3UTRENST00000507142ENST00000543354NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3UTRENST00000510533ENST00000490299NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3UTRENST00000510533ENST00000543354NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3UTRENST00000511633ENST00000490299NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3UTRENST00000511633ENST00000543354NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3UTRENST00000512193ENST00000490299NEK1chr4

170533170

-RPS6KC1chr1

213415910

+
5UTR-3UTRENST00000512193ENST00000543354NEK1chr4

170533170

-RPS6KC1chr1

213415910

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for NEK1-RPS6KC1


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
NEK1chr4170533170-RPS6KC1chr1213415911+0.180082050.819918
NEK1chr4170533170-RPS6KC1chr1213415911+0.180082050.819918

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.
genomic feature of top 1%

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Fusion Protein Features for NEK1-RPS6KC1


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/:170533170/:213415910)
- 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
NEK1

Q96PY6

.
FUNCTION: Phosphorylates serines and threonines, but also appears to possess tyrosine kinase activity (PubMed:20230784). Involved in DNA damage checkpoint control and for proper DNA damage repair (PubMed:20230784). In response to injury that includes DNA damage, NEK1 phosphorylates VDAC1 to limit mitochondrial cell death (PubMed:20230784). May be implicated in the control of meiosis (By similarity). Involved in cilium assembly (PubMed:21211617). {ECO:0000250|UniProtKB:P51954, ECO:0000269|PubMed:20230784, ECO:0000269|PubMed:21211617}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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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Fusion Gene Sequence for NEK1-RPS6KC1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for NEK1-RPS6KC1


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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Related Drugs for NEK1-RPS6KC1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for NEK1-RPS6KC1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource