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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:NEDD4L-MBD2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NEDD4L-MBD2
FusionPDB ID: 58422
FusionGDB2.0 ID: 58422
HgeneTgene
Gene symbol

NEDD4L

MBD2

Gene ID

23327

64174

Gene nameNEDD4 like E3 ubiquitin protein ligasedipeptidase 2
SynonymsNEDD4-2|NEDD4.2|PVNH7|RSP5|hNEDD4-2MBD2
Cytomap

18q21.31

16q22.1

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase NEDD4-likeHECT-type E3 ubiquitin transferase NED4Lneural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligaseubiquitin-protein ligase Rsp5dipeptidase 2
Modification date2020032920200313
UniProtAcc

Q96PU5

Main function of 5'-partner protein: FUNCTION: E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. Inhibits TGF-beta signaling by triggering SMAD2 and TGFBR1 ubiquitination and proteasome-dependent degradation. Promotes ubiquitination and internalization of various plasma membrane channels such as ENaC, SCN2A/Nav1.2, SCN3A/Nav1.3, SCN5A/Nav1.5, SCN9A/Nav1.7, SCN10A/Nav1.8, KCNA3/Kv1.3, KCNH2, EAAT1, KCNQ2/Kv7.2, KCNQ3/Kv7.3 or CLC5 (PubMed:26363003, PubMed:27445338). Promotes ubiquitination and degradation of SGK1 and TNK2. Ubiquitinates BRAT1 and this ubiquitination is enhanced in the presence of NDFIP1 (PubMed:25631046). Plays a role in dendrite formation by melanocytes (PubMed:23999003). Involved in the regulation of TOR signaling (PubMed:27694961). Ubiquitinates and regulates protein levels of NTRK1 once this one is activated by NGF (PubMed:27445338). {ECO:0000250|UniProtKB:Q8CFI0, ECO:0000269|PubMed:12911626, ECO:0000269|PubMed:15040001, ECO:0000269|PubMed:15217910, ECO:0000269|PubMed:15489223, ECO:0000269|PubMed:15496141, ECO:0000269|PubMed:15576372, ECO:0000269|PubMed:19144635, ECO:0000269|PubMed:23999003, ECO:0000269|PubMed:25631046, ECO:0000269|PubMed:26363003, ECO:0000269|PubMed:27445338, ECO:0000269|PubMed:27694961}.

Q9UBB5

Main function of 5'-partner protein: FUNCTION: Binds CpG islands in promoters where the DNA is methylated at position 5 of cytosine within CpG dinucleotides. Binds hemimethylated DNA as well. Recruits histone deacetylases and DNA methyltransferases. Acts as transcriptional repressor and plays a role in gene silencing. Functions as a scaffold protein, targeting GATAD2A and GATAD2B to chromatin to promote repression. May enhance the activation of some unmethylated cAMP-responsive promoters. {ECO:0000269|PubMed:10471499, ECO:0000269|PubMed:10947852, ECO:0000269|PubMed:12665568, ECO:0000269|PubMed:16415179, ECO:0000269|PubMed:24307175, ECO:0000269|PubMed:9774669}.
Ensembl transtripts involved in fusion geneENST idsENST00000256830, ENST00000356462, 
ENST00000382850, ENST00000400345, 
ENST00000589054, ENST00000256832, 
ENST00000357895, ENST00000431212, 
ENST00000435432, ENST00000456173, 
ENST00000456986, ENST00000586263, 
ENST00000588516, 
ENST00000398398, 
ENST00000579025, ENST00000583046, 
ENST00000256429, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score28 X 18 X 11=554413 X 7 X 7=637
# samples 3515
** MAII scorelog2(35/5544*10)=-3.98550043030488
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/637*10)=-2.08633087176042
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: NEDD4L [Title/Abstract] AND MBD2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: NEDD4L [Title/Abstract] AND MBD2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NEDD4L(55711940)-MBD2(51715381), # samples:1
Anticipated loss of major functional domain due to fusion event.NEDD4L-MBD2 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.
NEDD4L-MBD2 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.
NEDD4L-MBD2 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.
NEDD4L-MBD2 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.
* 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
HgeneNEDD4L

GO:0003254

regulation of membrane depolarization

15217910

HgeneNEDD4L

GO:0006511

ubiquitin-dependent protein catabolic process

21463633

HgeneNEDD4L

GO:0010038

response to metal ion

11244092

HgeneNEDD4L

GO:0016567

protein ubiquitination

15217910|25631046

HgeneNEDD4L

GO:0034765

regulation of ion transmembrane transport

17289006

HgeneNEDD4L

GO:0042391

regulation of membrane potential

17289006

HgeneNEDD4L

GO:0043161

proteasome-mediated ubiquitin-dependent protein catabolic process

21463633

HgeneNEDD4L

GO:0060306

regulation of membrane repolarization

21463633

HgeneNEDD4L

GO:0070936

protein K48-linked ubiquitination

21463633

HgeneNEDD4L

GO:1901016

regulation of potassium ion transmembrane transporter activity

17289006

HgeneNEDD4L

GO:1901017

negative regulation of potassium ion transmembrane transporter activity

21463633

HgeneNEDD4L

GO:1901380

negative regulation of potassium ion transmembrane transport

21463633

HgeneNEDD4L

GO:1902306

negative regulation of sodium ion transmembrane transport

15217910

HgeneNEDD4L

GO:1903861

positive regulation of dendrite extension

23999003

HgeneNEDD4L

GO:2000009

negative regulation of protein localization to cell surface

21463633

HgeneNEDD4L

GO:2000650

negative regulation of sodium ion transmembrane transporter activity

15217910



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/chr18:55711940/chr18:51715381)
- 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 buttonRetention analysis results 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, are available here.

check buttonFusion gene breakpoints across NEDD4L (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 MBD2 (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 Amino Acid Sequences


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)
ENST00000356462NEDD4Lchr1855711940+ENST00000256429MBD2chr1851715381-3491342210875221
ENST00000400345NEDD4Lchr1855711940+ENST00000256429MBD2chr1851715381-3480331199864221
ENST00000589054NEDD4Lchr1855711940+ENST00000256429MBD2chr1851715381-3474325193858221
ENST00000382850NEDD4Lchr1855711940+ENST00000256429MBD2chr1851715381-331016129694221
ENST00000256830NEDD4Lchr1855711940+ENST00000256429MBD2chr1851715381-3197480581193

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
ENST00000356462ENST00000256429NEDD4Lchr1855711940+MBD2chr1851715381-0.0012736540.9987263
ENST00000400345ENST00000256429NEDD4Lchr1855711940+MBD2chr1851715381-0.0012762490.9987237
ENST00000589054ENST00000256429NEDD4Lchr1855711940+MBD2chr1851715381-0.0012553780.9987446
ENST00000382850ENST00000256429NEDD4Lchr1855711940+MBD2chr1851715381-0.0011161080.9988839
ENST00000256830ENST00000256429NEDD4Lchr1855711940+MBD2chr1851715381-0.0010120640.998988

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for NEDD4L-MBD2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
NEDD4Lchr1855711940MBD2chr185171538116144GLGEPVYGLSEDEGKPDLNTTLPIRQ
NEDD4Lchr1855711940MBD2chr185171538132544GLGEPVYGLSEDEGKPDLNTTLPIRQ
NEDD4Lchr1855711940MBD2chr185171538133144GLGEPVYGLSEDEGKPDLNTTLPIRQ
NEDD4Lchr1855711940MBD2chr185171538134244GLGEPVYGLSEDEGKPDLNTTLPIRQ
NEDD4Lchr1855711940MBD2chr18517153814816GLGEPVYGLSEDEGKPDLNTTLPIRQ

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Potential FusionNeoAntigen Information of NEDD4L-MBD2 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
NEDD4L-MBD2_55711940_51715381.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
NEDD4L-MBD2chr1855711940chr185171538148HLA-B45:01SEDEGKPDL0.86770.5055918
NEDD4L-MBD2chr1855711940chr185171538148HLA-B39:13SEDEGKPDL0.45430.7631918
NEDD4L-MBD2chr1855711940chr185171538148HLA-B41:01SEDEGKPDL0.3670.6836918
NEDD4L-MBD2chr1855711940chr185171538148HLA-B40:06SEDEGKPDL0.99810.5365918
NEDD4L-MBD2chr1855711940chr185171538148HLA-B39:08SEDEGKPDL0.56590.6358918
NEDD4L-MBD2chr1855711940chr185171538148HLA-B39:09SEDEGKPDL0.50470.5132918
NEDD4L-MBD2chr1855711940chr185171538148HLA-B39:05SEDEGKPDL0.37750.7408918
NEDD4L-MBD2chr1855711940chr185171538148HLA-B39:08LSEDEGKPDL0.93290.6618818
NEDD4L-MBD2chr1855711940chr185171538148HLA-B39:08GLSEDEGKPDL0.97920.7523718
NEDD4L-MBD2chr1855711940chr185171538148HLA-B40:04SEDEGKPDL0.99750.5693918
NEDD4L-MBD2chr1855711940chr185171538148HLA-B39:11SEDEGKPDL0.56360.5877918
NEDD4L-MBD2chr1855711940chr185171538148HLA-B39:31SEDEGKPDL0.45140.7571918
NEDD4L-MBD2chr1855711940chr185171538148HLA-B39:02SEDEGKPDL0.41390.7614918

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Potential FusionNeoAntigen Information of NEDD4L-MBD2 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)

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Fusion breakpoint peptide structures of NEDD4L-MBD2

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
10650YGLSEDEGKPDLNTNEDD4LMBD2chr1855711940chr185171538148

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of NEDD4L-MBD2

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN10650YGLSEDEGKPDLNT-7.9962-8.1096
HLA-B14:023BVN10650YGLSEDEGKPDLNT-5.70842-6.74372
HLA-B52:013W3910650YGLSEDEGKPDLNT-6.83737-6.95077
HLA-B52:013W3910650YGLSEDEGKPDLNT-4.4836-5.5189
HLA-A11:014UQ210650YGLSEDEGKPDLNT-10.0067-10.1201
HLA-A11:014UQ210650YGLSEDEGKPDLNT-9.03915-10.0745
HLA-A24:025HGA10650YGLSEDEGKPDLNT-6.56204-6.67544
HLA-A24:025HGA10650YGLSEDEGKPDLNT-5.42271-6.45801
HLA-B44:053DX810650YGLSEDEGKPDLNT-7.85648-8.89178
HLA-B44:053DX810650YGLSEDEGKPDLNT-5.3978-5.5112
HLA-A02:016TDR10650YGLSEDEGKPDLNT-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of NEDD4L-MBD2

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
NEDD4L-MBD2chr1855711940chr1851715381718GLSEDEGKPDLGGACTTTCCGAAGACGAGGGTAAACCAGACTTG
NEDD4L-MBD2chr1855711940chr1851715381818LSEDEGKPDLCTTTCCGAAGACGAGGGTAAACCAGACTTG
NEDD4L-MBD2chr1855711940chr1851715381918SEDEGKPDLTCCGAAGACGAGGGTAAACCAGACTTG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence

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Information of the samples that have these potential fusion neoantigens of NEDD4L-MBD2

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
THCANEDD4L-MBD2chr1855711940ENST00000256830chr1851715381ENST00000256429TCGA-ET-A40P

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Potential target of CAR-T therapy development for NEDD4L-MBD2

check button Predicted 3D structure. We used RoseTTAFold.

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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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Related Drugs to NEDD4L-MBD2

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 NEDD4L-MBD2

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