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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:NBR1-RUNDC3A (FusionGDB2 ID:57142)

Fusion Gene Summary for NBR1-RUNDC3A

check button Fusion gene summary
Fusion gene informationFusion gene name: NBR1-RUNDC3A
Fusion gene ID: 57142
HgeneTgene
Gene symbol

NBR1

RUNDC3A

Gene ID

4077

10900

Gene nameNBR1 autophagy cargo receptorRUN domain containing 3A
Synonyms1A1-3B|IAI3B|M17S2|MIG19RAP2IP|RPIP-8|RPIP8
Cytomap

17q21.31

17q21.31

Type of geneprotein-codingprotein-coding
Descriptionnext to BRCA1 gene 1 proteinB-box proteincell migration-inducing gene 19 proteinmembrane component, chromosome 17, surface marker 2 (ovarian carcinoma antigen CA125)migration-inducing protein 19neighbor of BRCA1 gene 1RUN domain-containing protein 3ARaP2 interacting protein 8rap2-interacting protein 8
Modification date2020031320200320
UniProtAcc

Q14596

.
Ensembl transtripts involved in fusion geneENST00000341165, ENST00000422280, 
ENST00000542611, ENST00000590996, 
ENST00000389312, ENST00000589872, 
ENST00000426726, ENST00000590941, 
ENST00000225441, 
Fusion gene scores* DoF score5 X 5 X 5=1253 X 3 X 3=27
# samples 53
** MAII scorelog2(5/125*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: NBR1 [Title/Abstract] AND RUNDC3A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNBR1(41355803)-RUNDC3A(42395464), # samples:1
Anticipated loss of major functional domain due to fusion event.NBR1-RUNDC3A seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
NBR1-RUNDC3A seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneNBR1

GO:0016236

macroautophagy

19250911


check buttonFusion gene breakpoints across NBR1 (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 RUNDC3A (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
ChimerDB4BRCATCGA-EW-A2FS-01ANBR1chr17

41355803

-RUNDC3Achr17

42395464

+


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Fusion Gene ORF analysis for NBR1-RUNDC3A

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-shiftENST00000341165ENST00000426726NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
5CDS-intronENST00000341165ENST00000590941NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
5CDS-intronENST00000341165ENST00000225441NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
Frame-shiftENST00000422280ENST00000426726NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
5CDS-intronENST00000422280ENST00000590941NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
5CDS-intronENST00000422280ENST00000225441NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
intron-3CDSENST00000542611ENST00000426726NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
intron-intronENST00000542611ENST00000590941NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
intron-intronENST00000542611ENST00000225441NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
Frame-shiftENST00000590996ENST00000426726NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
5CDS-intronENST00000590996ENST00000590941NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
5CDS-intronENST00000590996ENST00000225441NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
Frame-shiftENST00000389312ENST00000426726NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
5CDS-intronENST00000389312ENST00000590941NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
5CDS-intronENST00000389312ENST00000225441NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
Frame-shiftENST00000589872ENST00000426726NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
5CDS-intronENST00000589872ENST00000590941NBR1chr17

41355803

-RUNDC3Achr17

42395464

+
5CDS-intronENST00000589872ENST00000225441NBR1chr17

41355803

-RUNDC3Achr17

42395464

+

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 NBR1-RUNDC3A


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 NBR1-RUNDC3A


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
NBR1

Q14596

.
FUNCTION: Acts probably as a receptor for selective autophagosomal degradation of ubiquitinated targets. {ECO:0000269|PubMed:19250911}.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.

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 NBR1-RUNDC3A


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 NBR1-RUNDC3A


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 NBR1-RUNDC3A


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 NBR1-RUNDC3A


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