FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:NIPBL-FYN (FusionGDB2 ID:59198)

Fusion Gene Summary for NIPBL-FYN

check button Fusion gene summary
Fusion gene informationFusion gene name: NIPBL-FYN
Fusion gene ID: 59198
HgeneTgene
Gene symbol

NIPBL

FYN

Gene ID

25836

2534

Gene nameNIPBL cohesin loading factorFYN proto-oncogene, Src family tyrosine kinase
SynonymsCDLS|CDLS1|IDN3|IDN3-B|Scc2SLK|SYN|p59-FYN
Cytomap

5p13.2

6q21

Type of geneprotein-codingprotein-coding
Descriptionnipped-B-like proteinNipped-B homologSCC2 homologdelanginsister chromatid cohesion 2 homologtyrosine-protein kinase FynFYN oncogene related to SRC, FGR, YESOKT3-induced calcium influx regulatorc-syn protooncogeneproto-oncogene Synproto-oncogene c-Fynsrc-like kinasesrc/yes-related noveltyrosine kinase p59fyn(T)
Modification date2020031320200327
UniProtAcc

Q6KC79

C1orf168

Ensembl transtripts involved in fusion geneENST00000282516, ENST00000448238, 
ENST00000504430, 
ENST00000229470, 
ENST00000229471, ENST00000354650, 
ENST00000356013, ENST00000368667, 
ENST00000368678, ENST00000368682, 
ENST00000538466, ENST00000476769, 
Fusion gene scores* DoF score26 X 13 X 16=540819 X 14 X 12=3192
# samples 4327
** MAII scorelog2(43/5408*10)=-3.65268658669272
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(27/3192*10)=-3.56342933917152
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NIPBL [Title/Abstract] AND FYN [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNIPBL(36877280)-FYN(111995833), # 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
HgeneNIPBL

GO:0000122

negative regulation of transcription by RNA polymerase II

18854353

HgeneNIPBL

GO:0031065

positive regulation of histone deacetylation

18854353

HgeneNIPBL

GO:0045892

negative regulation of transcription, DNA-templated

18854353

HgeneNIPBL

GO:0071921

cohesin loading

22628566

TgeneFYN

GO:0050852

T cell receptor signaling pathway

7722293


check buttonFusion gene breakpoints across NIPBL (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 FYN (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
ChimerDB4STADTCGA-CD-8531-01ANIPBLchr5

36877280

+FYNchr6

111995833

-


Top

Fusion Gene ORF analysis for NIPBL-FYN

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-3CDSENST00000282516ENST00000229470NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000282516ENST00000229471NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000282516ENST00000354650NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000282516ENST00000356013NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000282516ENST00000368667NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000282516ENST00000368678NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000282516ENST00000368682NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000282516ENST00000538466NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000448238ENST00000229470NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000448238ENST00000229471NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000448238ENST00000354650NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000448238ENST00000356013NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000448238ENST00000368667NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000448238ENST00000368678NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000448238ENST00000368682NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-3CDSENST00000448238ENST00000538466NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-intronENST00000282516ENST00000476769NIPBLchr5

36877280

+FYNchr6

111995833

-
5UTR-intronENST00000448238ENST00000476769NIPBLchr5

36877280

+FYNchr6

111995833

-
intron-3CDSENST00000504430ENST00000229470NIPBLchr5

36877280

+FYNchr6

111995833

-
intron-3CDSENST00000504430ENST00000229471NIPBLchr5

36877280

+FYNchr6

111995833

-
intron-3CDSENST00000504430ENST00000354650NIPBLchr5

36877280

+FYNchr6

111995833

-
intron-3CDSENST00000504430ENST00000356013NIPBLchr5

36877280

+FYNchr6

111995833

-
intron-3CDSENST00000504430ENST00000368667NIPBLchr5

36877280

+FYNchr6

111995833

-
intron-3CDSENST00000504430ENST00000368678NIPBLchr5

36877280

+FYNchr6

111995833

-
intron-3CDSENST00000504430ENST00000368682NIPBLchr5

36877280

+FYNchr6

111995833

-
intron-3CDSENST00000504430ENST00000538466NIPBLchr5

36877280

+FYNchr6

111995833

-
intron-intronENST00000504430ENST00000476769NIPBLchr5

36877280

+FYNchr6

111995833

-

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

Top

Fusion Genomic Features for NIPBL-FYN


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.

Top

Fusion Protein Features for NIPBL-FYN


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/:36877280/:111995833)
- 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
NIPBL

Q6KC79

FYN

C1orf168

FUNCTION: Plays an important role in the loading of the cohesin complex on to DNA. Forms a heterodimeric complex (also known as cohesin loading complex) with MAU2/SCC4 which mediates the loading of the cohesin complex onto chromatin (PubMed:22628566, PubMed:28914604). Plays a role in cohesin loading at sites of DNA damage. Its recruitment to double-strand breaks (DSBs) sites occurs in a CBX3-, RNF8- and RNF168-dependent manner whereas its recruitment to UV irradiation-induced DNA damage sites occurs in a ATM-, ATR-, RNF8- and RNF168-dependent manner (PubMed:28167679). Along with ZNF609, promotes cortical neuron migration during brain development by regulating the transcription of crucial genes in this process. Preferentially binds promoters containing paused RNA polymerase II. Up-regulates the expression of SEMA3A, NRP1, PLXND1 and GABBR2 genes, among others (By similarity). {ECO:0000250|UniProtKB:Q6KCD5, ECO:0000269|PubMed:22628566, ECO:0000269|PubMed:28167679, ECO:0000269|PubMed:28914604}.728

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


Top

Fusion Gene Sequence for NIPBL-FYN


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.

Top

Fusion Gene PPI Analysis for NIPBL-FYN


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


Top

Related Drugs for NIPBL-FYN


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

Top

Related Diseases for NIPBL-FYN


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