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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:NCS1-YWHAE (FusionGDB2 ID:57555)

Fusion Gene Summary for NCS1-YWHAE

check button Fusion gene summary
Fusion gene informationFusion gene name: NCS1-YWHAE
Fusion gene ID: 57555
HgeneTgene
Gene symbol

NCS1

YWHAE

Gene ID

23413

7531

Gene nameneuronal calcium sensor 1tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon
SynonymsFLUP|FREQ14-3-3E|HEL2|KCIP-1|MDCR|MDS
Cytomap

9q34.11

17p13.3

Type of geneprotein-codingprotein-coding
Descriptionneuronal calcium sensor 1frequenin homologfrequenin-like proteinfrequenin-like ubiquitous protein14-3-3 protein epsilon14-3-3 epsilonepididymis luminal protein 2mitochondrial import stimulation factor L subunitprotein kinase C inhibitor protein-1tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptidetyrosine
Modification date2020031320200327
UniProtAcc

P62166

P62258

Ensembl transtripts involved in fusion geneENST00000372398, ENST00000493042, 
ENST00000458469, 
ENST00000264335, 
ENST00000571732, ENST00000573026, 
ENST00000575977, ENST00000498643, 
Fusion gene scores* DoF score6 X 5 X 6=18025 X 13 X 12=3900
# samples 632
** MAII scorelog2(6/180*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(32/3900*10)=-3.60733031374961
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NCS1 [Title/Abstract] AND YWHAE [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNCS1(132935006)-YWHAE(1265302), # samples:1
Anticipated loss of major functional domain due to fusion event.NCS1-YWHAE seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
NCS1-YWHAE seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
NCS1-YWHAE seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
* 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
TgeneYWHAE

GO:0000165

MAPK cascade

12917326

TgeneYWHAE

GO:0034605

cellular response to heat

12917326

TgeneYWHAE

GO:0046827

positive regulation of protein export from nucleus

12917326

TgeneYWHAE

GO:0051480

regulation of cytosolic calcium ion concentration

18029012

TgeneYWHAE

GO:0060306

regulation of membrane repolarization

11953308

TgeneYWHAE

GO:1901016

regulation of potassium ion transmembrane transporter activity

11953308

TgeneYWHAE

GO:1901020

negative regulation of calcium ion transmembrane transporter activity

18029012

TgeneYWHAE

GO:1902309

negative regulation of peptidyl-serine dephosphorylation

11953308

TgeneYWHAE

GO:1905913

negative regulation of calcium ion export across plasma membrane

18029012


check buttonFusion gene breakpoints across NCS1 (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 YWHAE (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
ChimerDB4GBMTCGA-06-5415-01ANCS1chr9

132935006

+YWHAEchr17

1265302

-


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Fusion Gene ORF analysis for NCS1-YWHAE

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
Frame-shiftENST00000372398ENST00000264335NCS1chr9

132935006

+YWHAEchr17

1265302

-
Frame-shiftENST00000372398ENST00000571732NCS1chr9

132935006

+YWHAEchr17

1265302

-
5CDS-intronENST00000372398ENST00000573026NCS1chr9

132935006

+YWHAEchr17

1265302

-
5CDS-intronENST00000372398ENST00000575977NCS1chr9

132935006

+YWHAEchr17

1265302

-
5CDS-intronENST00000372398ENST00000498643NCS1chr9

132935006

+YWHAEchr17

1265302

-
intron-3CDSENST00000493042ENST00000264335NCS1chr9

132935006

+YWHAEchr17

1265302

-
intron-3CDSENST00000493042ENST00000571732NCS1chr9

132935006

+YWHAEchr17

1265302

-
intron-intronENST00000493042ENST00000573026NCS1chr9

132935006

+YWHAEchr17

1265302

-
intron-intronENST00000493042ENST00000575977NCS1chr9

132935006

+YWHAEchr17

1265302

-
intron-intronENST00000493042ENST00000498643NCS1chr9

132935006

+YWHAEchr17

1265302

-
intron-3CDSENST00000458469ENST00000264335NCS1chr9

132935006

+YWHAEchr17

1265302

-
intron-3CDSENST00000458469ENST00000571732NCS1chr9

132935006

+YWHAEchr17

1265302

-
intron-intronENST00000458469ENST00000573026NCS1chr9

132935006

+YWHAEchr17

1265302

-
intron-intronENST00000458469ENST00000575977NCS1chr9

132935006

+YWHAEchr17

1265302

-
intron-intronENST00000458469ENST00000498643NCS1chr9

132935006

+YWHAEchr17

1265302

-

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 NCS1-YWHAE


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)

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.

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Fusion Protein Features for NCS1-YWHAE


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NCS1

P62166

YWHAE

P62258

FUNCTION: Neuronal calcium sensor, regulator of G protein-coupled receptor phosphorylation in a calcium dependent manner. Directly regulates GRK1 (RHOK), but not GRK2 to GRK5. Can substitute for calmodulin (By similarity). Stimulates PI4KB kinase activity (By similarity). Involved in long-term synaptic plasticity through its interaction with PICK1 (By similarity). May also play a role in neuron differentiation through inhibition of the activity of N-type voltage-gated calcium channel (By similarity). {ECO:0000250}.FUNCTION: Adapter protein implicated in the regulation of a large spectrum of both general and specialized signaling pathways. Binds to a large number of partners, usually by recognition of a phosphoserine or phosphothreonine motif. Binding generally results in the modulation of the activity of the binding partner (By similarity). Positively regulates phosphorylated protein HSF1 nuclear export to the cytoplasm (PubMed:12917326). {ECO:0000250|UniProtKB:P62261, ECO:0000269|PubMed:12917326}.

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 NCS1-YWHAE


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 NCS1-YWHAE


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 NCS1-YWHAE


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneNCS1P62166DB11348Calcium PhosphateLigandSmall moleculeApproved
HgeneNCS1P62166DB11348Calcium PhosphateLigandSmall moleculeApproved
HgeneNCS1P62166DB11348Calcium PhosphateLigandSmall moleculeApproved
HgeneNCS1P62166DB14481Calcium phosphate dihydrateSmall moleculeApproved
HgeneNCS1P62166DB14481Calcium phosphate dihydrateSmall moleculeApproved
HgeneNCS1P62166DB14481Calcium phosphate dihydrateSmall moleculeApproved
HgeneNCS1P62166DB11093Calcium citrateLigandSmall moleculeApproved|Investigational
HgeneNCS1P62166DB11093Calcium citrateLigandSmall moleculeApproved|Investigational
HgeneNCS1P62166DB11093Calcium citrateLigandSmall moleculeApproved|Investigational

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Related Diseases for NCS1-YWHAE


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNCS1C0005586Bipolar Disorder2PSYGENET
HgeneNCS1C0036341Schizophrenia2PSYGENET
HgeneNCS1C0600427Cocaine Dependence1PSYGENET
TgeneYWHAEC0036341Schizophrenia4PSYGENET
TgeneYWHAEC0005586Bipolar Disorder2PSYGENET
TgeneYWHAEC0206630Endometrial Stromal Sarcoma2ORPHANET
TgeneYWHAEC0027627Neoplasm Metastasis1CTD_human
TgeneYWHAEC0265219Miller Dieker syndrome1ORPHANET
TgeneYWHAEC0334488Clear cell sarcoma of kidney1ORPHANET
TgeneYWHAEC2750748Chromosome 17p13.3 Duplication Syndrome1ORPHANET
TgeneYWHAEC4707092Distal 17p13.3 microdeletion syndrome1ORPHANET