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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:NOTCH2NL-CTSS (FusionGDB2 ID:59390)

Fusion Gene Summary for NOTCH2NL-CTSS

check button Fusion gene summary
Fusion gene informationFusion gene name: NOTCH2NL-CTSS
Fusion gene ID: 59390
HgeneTgene
Gene symbol

NOTCH2NL

CTSS

Gene ID

100996763

1520

Gene namenotch 2 N-terminal like Bcathepsin S
SynonymsN2N|NOTCH2NL|NOTCH2NLA-
Cytomap

1q21.2

1q21.3

Type of geneprotein-codingprotein-coding
Descriptionnotch homolog 2 N-terminal-like protein BNotch homolog 2 N-terminal-like protein Anotch homolog 2 N-terminal-like proteincathepsin S
Modification date2020031320200329
UniProtAcc.

P25774

Ensembl transtripts involved in fusion geneENST00000362074, ENST00000344859, 
ENST00000369340, ENST00000479995, 
ENST00000368985, ENST00000448301, 
ENST00000480760, 
Fusion gene scores* DoF score23 X 4 X 14=128814 X 15 X 9=1890
# samples 2219
** MAII scorelog2(22/1288*10)=-2.54955716458996
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(19/1890*10)=-3.31431491077749
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NOTCH2NL [Title/Abstract] AND CTSS [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNOTCH2NL(145209436)-CTSS(150724484), # samples:1
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
HgeneNOTCH2NL

GO:0021987

cerebral cortex development

29561261|29856954|29856955

HgeneNOTCH2NL

GO:0045747

positive regulation of Notch signaling pathway

29856954|29856955

TgeneCTSS

GO:0006508

proteolysis

12788072|22864553

TgeneCTSS

GO:0010447

response to acidic pH

22864553

TgeneCTSS

GO:0016485

protein processing

22864553

TgeneCTSS

GO:0030574

collagen catabolic process

22952693

TgeneCTSS

GO:0034769

basement membrane disassembly

22952693

TgeneCTSS

GO:0048002

antigen processing and presentation of peptide antigen

8612130

TgeneCTSS

GO:0051603

proteolysis involved in cellular protein catabolic process

22952693

TgeneCTSS

GO:2001259

positive regulation of cation channel activity

22864553


check buttonFusion gene breakpoints across NOTCH2NL (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 CTSS (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
ChimerDB4BLCATCGA-FD-A3B7-01ANOTCH2NLchr1

145209436

+CTSSchr1

150724484

-


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Fusion Gene ORF analysis for NOTCH2NL-CTSS

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-3CDSENST00000362074ENST00000368985NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
5UTR-3CDSENST00000362074ENST00000448301NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
5UTR-5UTRENST00000362074ENST00000480760NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
5UTR-3CDSENST00000344859ENST00000368985NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
5UTR-3CDSENST00000344859ENST00000448301NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
5UTR-5UTRENST00000344859ENST00000480760NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
intron-3CDSENST00000369340ENST00000368985NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
intron-3CDSENST00000369340ENST00000448301NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
intron-5UTRENST00000369340ENST00000480760NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
intron-3CDSENST00000479995ENST00000368985NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
intron-3CDSENST00000479995ENST00000448301NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-
intron-5UTRENST00000479995ENST00000480760NOTCH2NLchr1

145209436

+CTSSchr1

150724484

-

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 NOTCH2NL-CTSS


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 NOTCH2NL-CTSS


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
.CTSS

P25774

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Thiol protease. Key protease responsible for the removal of the invariant chain from MHC class II molecules and MHC class II antigen presentation (PubMed:30612035). The bond-specificity of this proteinase is in part similar to the specificities of cathepsin L. {ECO:0000269|PubMed:30612035}.

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 NOTCH2NL-CTSS


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 NOTCH2NL-CTSS


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 NOTCH2NL-CTSS


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneCTSSP25774DB12010FostamatinibInhibitorSmall moleculeApproved|Investigational

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Related Diseases for NOTCH2NL-CTSS


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneCTSSC0011616Contact Dermatitis1CTD_human
TgeneCTSSC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneCTSSC0027626Neoplasm Invasiveness1CTD_human
TgeneCTSSC0028754Obesity1CTD_human
TgeneCTSSC0162351Contact hypersensitivity1CTD_human