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Center for Computational Systems Medicine level2
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein Structure

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pLDDT scores

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Ramachandran Plot of Fusion Protein Structure

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:NEDD8-NRL

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NEDD8-NRL
FusionPDB ID: 58448
FusionGDB2.0 ID: 58448
HgeneTgene
Gene symbol

NEDD8

NRL

Gene ID

4738

4901

Gene nameNEDD8 ubiquitin like modifierneural retina leucine zipper
SynonymsNEDD-8D14S46E|NRL-MAF|RP27
Cytomap

14q12

14q11.2-q12

Type of geneprotein-codingprotein-coding
DescriptionNEDD8neddylinneural precursor cell expressed, developmentally down-regulated 8ubiquitin-like protein Nedd8neural retina-specific leucine zipper proteinneural retinal-specific leucine zipper
Modification date2020032720200313
UniProtAcc

UBE2F

P54845

Ensembl transtripts involved in fusion geneENST idsENST00000250495, ENST00000524927, 
ENST00000533242, 
ENST00000396995, 
ENST00000560550, ENST00000396997, 
ENST00000397002, ENST00000561028, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score1 X 2 X 1=24 X 5 X 4=80
# samples 26
** MAII scorelog2(2/2*10)=3.32192809488736log2(6/80*10)=-0.415037499278844
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: NEDD8 [Title/Abstract] AND NRL [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NEDD8(24701456)-NRL(24550777), # samples:2
Anticipated loss of major functional domain due to fusion event.NEDD8-NRL seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
NEDD8-NRL seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
NEDD8-NRL seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
NEDD8-NRL seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
NEDD8-NRL seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
NEDD8-NRL seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
NEDD8-NRL seems lost the major protein functional domain in Tgene partner, which is a transcription 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
HgeneNEDD8

GO:0045116

protein neddylation

10500095

TgeneNRL

GO:0045944

positive regulation of transcription by RNA polymerase II

8552602


check buttonFusion gene breakpoints across NEDD8 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across NRL (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4ESCATCGA-LN-A49L-01ANEDD8chr14

24701456

-NRLchr14

24550777

-
ChimerDB4ESCATCGA-LN-A49LNEDD8chr14

24700858

-NRLchr14

24550777

-
ChimerDB4ESCATCGA-LN-A49LNEDD8chr14

24701456

-NRLchr14

24550777

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000250495NEDD8chr1424701456-ENST00000397002NRLchr1424550777-1667205592194132
ENST00000524927NEDD8chr1424701456-ENST00000397002NRLchr1424550777-156710549294132

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
ENST00000250495ENST00000397002NEDD8chr1424701456-NRLchr1424550777-0.109487730.8905123
ENST00000524927ENST00000397002NEDD8chr1424701456-NRLchr1424550777-0.1104204650.88957953

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>58448_58448_1_NEDD8-NRL_NEDD8_chr14_24701456_ENST00000250495_NRL_chr14_24550777_ENST00000397002_length(amino acids)=132AA_BP=1
MGGATPPSPHYTTRCSERLRGRGGRGPRTRGRSRLAGHSEPCRDRAPGPGGPPRPAARPAGRPGGRARPPARAAAAAAWSDRPARSRGSS

--------------------------------------------------------------

>58448_58448_2_NEDD8-NRL_NEDD8_chr14_24701456_ENST00000524927_NRL_chr14_24550777_ENST00000397002_length(amino acids)=132AA_BP=1
MGGATPPSPHYTTRCSERLRGRGGRGPRTRGRSRLAGHSEPCRDRAPGPGGPPRPAARPAGRPGGRARPPARAAAAAAWSDRPARSRGSS

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr14:24701456/chr14:24550777)
- 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
NEDD8

UBE2F

NRL

P54845

185FUNCTION: Acts as a transcriptional activator which regulates the expression of several rod-specific genes, including RHO and PDE6B (PubMed:21981118). Functions also as a transcriptional coactivator, stimulating transcription mediated by the transcription factor CRX and NR2E3 (PubMed:17335001). Binds in a sequence-specific manner to the rhodopsin promoter (PubMed:17335001). {ECO:0000269|PubMed:17335001, ECO:0000269|PubMed:21981118}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneNRLchr14:24701456chr14:24550777ENST0000039699724159_222127.0238.0DomainbZIP
TgeneNRLchr14:24701456chr14:24550777ENST0000039700213159_222127.0238.0DomainbZIP
TgeneNRLchr14:24701456chr14:24550777ENST0000056102813159_222127.0238.0DomainbZIP
TgeneNRLchr14:24701456chr14:24550777ENST0000039699724159_185127.0238.0RegionBasic motif
TgeneNRLchr14:24701456chr14:24550777ENST0000039699724187_208127.0238.0RegionLeucine-zipper
TgeneNRLchr14:24701456chr14:24550777ENST0000039700213159_185127.0238.0RegionBasic motif
TgeneNRLchr14:24701456chr14:24550777ENST0000039700213187_208127.0238.0RegionLeucine-zipper
TgeneNRLchr14:24701456chr14:24550777ENST0000056102813159_185127.0238.0RegionBasic motif
TgeneNRLchr14:24701456chr14:24550777ENST0000056102813187_208127.0238.0RegionLeucine-zipper

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneNRLchr14:24701456chr14:24550777ENST000003969972430_93127.0238.0RegionMinimal transactivation domain (MTD)
TgeneNRLchr14:24701456chr14:24550777ENST000003970021330_93127.0238.0RegionMinimal transactivation domain (MTD)
TgeneNRLchr14:24701456chr14:24550777ENST000005610281330_93127.0238.0RegionMinimal transactivation domain (MTD)


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Fusion Protein Structures

check button PDB and CIF files of the predicted fusion proteins
* Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
Fusion protein PDB link (fusion AA seq ID in FusionPDB)HgeneHchrHbpHstrandTgeneTchrTbpTstrandAA seqLen(AA seq)
PDB file >>>74_NEDD8_24701456_NRL_24550777_ranked_0.pdbNEDD82470145624701456ENST00000397002NRLchr1424550777-
MGGATPPSPHYTTRCSERLRGRGGRGPRTRGRSRLAGHSEPCRDRAPGPGGPPRPAARPAGRPGGRARPPARAAAAAAWSDRPARSRGSS
132


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pLDDT score distribution

check button pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
NEDD8_pLDDT.png
all structure
all structure
NRL_pLDDT.png
all structure
all structure

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
all structure


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Ramachandran Plot of Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.
Fusion AA seq ID in FusionPDB and their Ramachandran plots

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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
NEDD8
NRL


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
HgeneNEDD8chr14:24701456chr14:24550777ENST00000250495-1470_726.082.0UBE1C


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Related Drugs to NEDD8-NRL


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to NEDD8-NRL


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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