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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:NBEA-BRCA2 (FusionGDB2 ID:57402)

Fusion Gene Summary for NBEA-BRCA2

check button Fusion gene summary
Fusion gene informationFusion gene name: NBEA-BRCA2
Fusion gene ID: 57402
HgeneTgene
Gene symbol

NBEA

BRCA2

Gene ID

26960

675

Gene nameneurobeachinBRCA2 DNA repair associated
SynonymsBCL8B|LYST2BRCC2|BROVCA2|FACD|FAD|FAD1|FANCD|FANCD1|GLM3|PNCA2|XRCC11
Cytomap

13q13.3

13q13.1

Type of geneprotein-codingprotein-coding
Descriptionneurobeachinlysosomal-trafficking regulator 2breast cancer type 2 susceptibility proteinBRCA1/BRCA2-containing complex, subunit 2Fanconi anemia group D1 proteinbreast and ovarian cancer susceptibility gene, early onsetbreast and ovarian cancer susceptibility protein 2breast cancer 2 tumor suppr
Modification date2020032820200329
UniProtAcc

Q8NFP9

P51587

Ensembl transtripts involved in fusion geneENST00000310336, ENST00000379939, 
ENST00000400445, ENST00000540320, 
ENST00000379922, ENST00000461581, 
ENST00000537702, 
ENST00000380152, 
ENST00000544455, 
Fusion gene scores* DoF score15 X 15 X 7=15751 X 1 X 1=1
# samples 151
** MAII scorelog2(15/1575*10)=-3.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: NBEA [Title/Abstract] AND BRCA2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNBEA(35770439)-BRCA2(32899213), # samples:2
Anticipated loss of major functional domain due to fusion event.NBEA-BRCA2 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
NBEA-BRCA2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
NBEA-BRCA2 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
NBEA-BRCA2 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
NBEA-BRCA2 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
TgeneBRCA2

GO:0000724

double-strand break repair via homologous recombination

20729832

TgeneBRCA2

GO:0033600

negative regulation of mammary gland epithelial cell proliferation

15930293

TgeneBRCA2

GO:0043966

histone H3 acetylation

9619837

TgeneBRCA2

GO:0043967

histone H4 acetylation

9619837

TgeneBRCA2

GO:0045893

positive regulation of transcription, DNA-templated

9126734

TgeneBRCA2

GO:0070200

establishment of protein localization to telomere

21076401


check buttonFusion gene breakpoints across NBEA (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 BRCA2 (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
ChimerDB4SARCTCGA-DX-A48J-01ANBEAchr13

35770439

-BRCA2chr13

32899213

+
ChimerDB4SARCTCGA-DX-A48J-01ANBEAchr13

35770439

+BRCA2chr13

32899213

+


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Fusion Gene ORF analysis for NBEA-BRCA2

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-shiftENST00000310336ENST00000380152NBEAchr13

35770439

+BRCA2chr13

32899213

+
Frame-shiftENST00000310336ENST00000544455NBEAchr13

35770439

+BRCA2chr13

32899213

+
Frame-shiftENST00000379939ENST00000380152NBEAchr13

35770439

+BRCA2chr13

32899213

+
Frame-shiftENST00000379939ENST00000544455NBEAchr13

35770439

+BRCA2chr13

32899213

+
Frame-shiftENST00000400445ENST00000380152NBEAchr13

35770439

+BRCA2chr13

32899213

+
Frame-shiftENST00000400445ENST00000544455NBEAchr13

35770439

+BRCA2chr13

32899213

+
Frame-shiftENST00000540320ENST00000380152NBEAchr13

35770439

+BRCA2chr13

32899213

+
Frame-shiftENST00000540320ENST00000544455NBEAchr13

35770439

+BRCA2chr13

32899213

+
intron-3CDSENST00000379922ENST00000380152NBEAchr13

35770439

+BRCA2chr13

32899213

+
intron-3CDSENST00000379922ENST00000544455NBEAchr13

35770439

+BRCA2chr13

32899213

+
intron-3CDSENST00000461581ENST00000380152NBEAchr13

35770439

+BRCA2chr13

32899213

+
intron-3CDSENST00000461581ENST00000544455NBEAchr13

35770439

+BRCA2chr13

32899213

+
intron-3CDSENST00000537702ENST00000380152NBEAchr13

35770439

+BRCA2chr13

32899213

+
intron-3CDSENST00000537702ENST00000544455NBEAchr13

35770439

+BRCA2chr13

32899213

+

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 NBEA-BRCA2


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)
NBEAchr1335770439+BRCA2chr1332899212+0.0001239320.999876
NBEAchr1335770439+BRCA2chr1332899212+0.0001239320.999876

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 NBEA-BRCA2


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/:35770439/:32899213)
- 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
NBEA

Q8NFP9

BRCA2

P51587

FUNCTION: Binds to type II regulatory subunits of protein kinase A and anchors/targets them to the membrane. May anchor the kinase to cytoskeletal and/or organelle-associated proteins (By similarity). {ECO:0000250}.FUNCTION: Involved in double-strand break repair and/or homologous recombination. Binds RAD51 and potentiates recombinational DNA repair by promoting assembly of RAD51 onto single-stranded DNA (ssDNA). Acts by targeting RAD51 to ssDNA over double-stranded DNA, enabling RAD51 to displace replication protein-A (RPA) from ssDNA and stabilizing RAD51-ssDNA filaments by blocking ATP hydrolysis. Part of a PALB2-scaffolded HR complex containing RAD51C and which is thought to play a role in DNA repair by HR. May participate in S phase checkpoint activation. Binds selectively to ssDNA, and to ssDNA in tailed duplexes and replication fork structures. May play a role in the extension step after strand invasion at replication-dependent DNA double-strand breaks; together with PALB2 is involved in both POLH localization at collapsed replication forks and DNA polymerization activity. In concert with NPM1, regulates centrosome duplication. Interacts with the TREX-2 complex (transcription and export complex 2) subunits PCID2 and SEM1, and is required to prevent R-loop-associated DNA damage and thus transcription-associated genomic instability. Silencing of BRCA2 promotes R-loop accumulation at actively transcribed genes in replicating and non-replicating cells, suggesting that BRCA2 mediates the control of R-loop associated genomic instability, independently of its known role in homologous recombination (PubMed:24896180). {ECO:0000269|PubMed:15115758, ECO:0000269|PubMed:15199141, ECO:0000269|PubMed:15671039, ECO:0000269|PubMed:18317453, ECO:0000269|PubMed:20729832, ECO:0000269|PubMed:20729858, ECO:0000269|PubMed:20729859, ECO:0000269|PubMed:21084279, ECO:0000269|PubMed:21719596, ECO:0000269|PubMed:24485656, ECO:0000269|PubMed:24896180}.

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 NBEA-BRCA2


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 NBEA-BRCA2


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 NBEA-BRCA2


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 NBEA-BRCA2


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