FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

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

leaf

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

leaf

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

leaf

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

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

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

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:MDM2-POLR3B

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MDM2-POLR3B
FusionPDB ID: 52414
FusionGDB2.0 ID: 52414
HgeneTgene
Gene symbol

MDM2

POLR3B

Gene ID

4193

55703

Gene nameMDM2 proto-oncogeneRNA polymerase III subunit B
SynonymsACTFS|HDMX|LSKB|hdm2C128|HLD8|INMAP|RPC2
Cytomap

12q15

12q23.3

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase Mdm2MDM2 oncogene, E3 ubiquitin protein ligaseMDM2 proto-oncogene, E3 ubiquitin protein ligaseMdm2, p53 E3 ubiquitin protein ligase homologMdm2, transformed 3T3 cell double minute 2, p53 binding proteindouble minute 2, humDNA-directed RNA polymerase III subunit RPC2DNA-directed RNA polymerase III 127.6 kDa polypeptideDNA-directed RNA polymerase III subunit BRNA polymerase III subunit C2interphase nucleus and mitotic apparatus associated proteinpolymerase (RNA) III (DN
Modification date2020032920200313
UniProtAcc

Q00987

Main function of 5'-partner protein: FUNCTION: E3 ubiquitin-protein ligase that mediates ubiquitination of p53/TP53, leading to its degradation by the proteasome. Inhibits p53/TP53- and p73/TP73-mediated cell cycle arrest and apoptosis by binding its transcriptional activation domain. Also acts as a ubiquitin ligase E3 toward itself and ARRB1. Permits the nuclear export of p53/TP53. Promotes proteasome-dependent ubiquitin-independent degradation of retinoblastoma RB1 protein. Inhibits DAXX-mediated apoptosis by inducing its ubiquitination and degradation. Component of the TRIM28/KAP1-MDM2-p53/TP53 complex involved in stabilizing p53/TP53. Also component of the TRIM28/KAP1-ERBB4-MDM2 complex which links growth factor and DNA damage response pathways. Mediates ubiquitination and subsequent proteasome degradation of DYRK2 in nucleus. Ubiquitinates IGF1R and SNAI1 and promotes them to proteasomal degradation (PubMed:12821780, PubMed:15053880, PubMed:15195100, PubMed:15632057, PubMed:16337594, PubMed:17290220, PubMed:19098711, PubMed:19219073, PubMed:19837670, PubMed:19965871, PubMed:20173098, PubMed:20385133, PubMed:20858735, PubMed:22128911). Ubiquitinates DCX, leading to DCX degradation and reduction of the dendritic spine density of olfactory bulb granule cells (By similarity). Ubiquitinates DLG4, leading to proteasomal degradation of DLG4 which is required for AMPA receptor endocytosis (By similarity). Negatively regulates NDUFS1, leading to decreased mitochondrial respiration, marked oxidative stress, and commitment to the mitochondrial pathway of apoptosis (PubMed:30879903). Binds NDUFS1 leading to its cytosolic retention rather than mitochondrial localization resulting in decreased supercomplex assembly (interactions between complex I and complex III), decreased complex I activity, ROS production, and apoptosis (PubMed:30879903). {ECO:0000250|UniProtKB:P23804, ECO:0000269|PubMed:12821780, ECO:0000269|PubMed:15053880, ECO:0000269|PubMed:15195100, ECO:0000269|PubMed:15632057, ECO:0000269|PubMed:16337594, ECO:0000269|PubMed:17290220, ECO:0000269|PubMed:19098711, ECO:0000269|PubMed:19219073, ECO:0000269|PubMed:19837670, ECO:0000269|PubMed:19965871, ECO:0000269|PubMed:20173098, ECO:0000269|PubMed:20385133, ECO:0000269|PubMed:20858735, ECO:0000269|PubMed:22128911, ECO:0000269|PubMed:30879903}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000258148, ENST00000258149, 
ENST00000299252, ENST00000350057, 
ENST00000356290, ENST00000360430, 
ENST00000462284, ENST00000540827, 
ENST00000348801, ENST00000393410, 
ENST00000393412, ENST00000393413, 
ENST00000428863, ENST00000478070, 
ENST00000517852, ENST00000544125, 
ENST00000544561, ENST00000545204, 
ENST00000549195, ENST00000228347, 
ENST00000539066, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score39 X 20 X 11=85802 X 2 X 2=8
# samples 472
** MAII scorelog2(47/8580*10)=-4.19024498582191
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Fusion gene context

PubMed: MDM2 [Title/Abstract] AND POLR3B [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: MDM2 [Title/Abstract] AND POLR3B [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MDM2(69230529)-POLR3B(106820975), # samples:1
Anticipated loss of major functional domain due to fusion event.MDM2-POLR3B 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.
MDM2-POLR3B 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.
MDM2-POLR3B 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.
MDM2-POLR3B 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
HgeneMDM2

GO:0000122

negative regulation of transcription by RNA polymerase II

9271120|17310983

HgeneMDM2

GO:0006511

ubiquitin-dependent protein catabolic process

11278372|15314173|16173922|17310983

HgeneMDM2

GO:0016567

protein ubiquitination

9450543|15878855|19656744|20153724

HgeneMDM2

GO:0031648

protein destabilization

9529249|10360174|15314173

HgeneMDM2

GO:0032436

positive regulation of proteasomal ubiquitin-dependent protein catabolic process

11278372

HgeneMDM2

GO:0034504

protein localization to nucleus

10360174

HgeneMDM2

GO:0042176

regulation of protein catabolic process

9153395

HgeneMDM2

GO:0043518

negative regulation of DNA damage response, signal transduction by p53 class mediator

9529249|10360174

HgeneMDM2

GO:0045184

establishment of protein localization

10360174

HgeneMDM2

GO:0045892

negative regulation of transcription, DNA-templated

9271120

HgeneMDM2

GO:0065003

protein-containing complex assembly

10608892|12915590

HgeneMDM2

GO:0071157

negative regulation of cell cycle arrest

9529249

HgeneMDM2

GO:0071480

cellular response to gamma radiation

16213212

HgeneMDM2

GO:0072717

cellular response to actinomycin D

15314173

HgeneMDM2

GO:1901797

negative regulation of signal transduction by p53 class mediator

16173922



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/chr12:69230529/chr12:106820975)
- 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 MDM2 (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 POLR3B (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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)
ENST00000462284MDM2chr1269230529+ENST00000228347POLR3Bchr12106820975+4170122026635201084
ENST00000462284MDM2chr1269230529+ENST00000539066POLR3Bchr12106820975+4168122026635201084
ENST00000356290MDM2chr1269230529+ENST00000228347POLR3Bchr12106820975+36456952512995914
ENST00000356290MDM2chr1269230529+ENST00000539066POLR3Bchr12106820975+36436952512995914
ENST00000540827MDM2chr1269230529+ENST00000228347POLR3Bchr12106820975+35706202512920889
ENST00000540827MDM2chr1269230529+ENST00000539066POLR3Bchr12106820975+35686202512920889
ENST00000258149MDM2chr1269230529+ENST00000228347POLR3Bchr12106820975+3990104025133401029
ENST00000258149MDM2chr1269230529+ENST00000539066POLR3Bchr12106820975+3988104025133401029
ENST00000258148MDM2chr1269230529+ENST00000228347POLR3Bchr12106820975+37177671430671017
ENST00000258148MDM2chr1269230529+ENST00000539066POLR3Bchr12106820975+37157671430671017
ENST00000350057MDM2chr1269230529+ENST00000228347POLR3Bchr12106820975+3775825031251041
ENST00000350057MDM2chr1269230529+ENST00000539066POLR3Bchr12106820975+3773825031251041
ENST00000360430MDM2chr1269230529+ENST00000228347POLR3Bchr12106820975+326531502615871
ENST00000360430MDM2chr1269230529+ENST00000539066POLR3Bchr12106820975+326331502615871
ENST00000299252MDM2chr1269230529+ENST00000228347POLR3Bchr12106820975+334039002690896
ENST00000299252MDM2chr1269230529+ENST00000539066POLR3Bchr12106820975+333839002690896

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
ENST00000462284ENST00000228347MDM2chr1269230529+POLR3Bchr12106820975+0.0002129270.99978703
ENST00000462284ENST00000539066MDM2chr1269230529+POLR3Bchr12106820975+0.0002143830.9997856
ENST00000356290ENST00000228347MDM2chr1269230529+POLR3Bchr12106820975+0.0003818640.99961805
ENST00000356290ENST00000539066MDM2chr1269230529+POLR3Bchr12106820975+0.0003853010.9996147
ENST00000540827ENST00000228347MDM2chr1269230529+POLR3Bchr12106820975+0.0003130910.99968696
ENST00000540827ENST00000539066MDM2chr1269230529+POLR3Bchr12106820975+0.000315690.99968433
ENST00000258149ENST00000228347MDM2chr1269230529+POLR3Bchr12106820975+0.0002229260.99977714
ENST00000258149ENST00000539066MDM2chr1269230529+POLR3Bchr12106820975+0.0002237080.9997763
ENST00000258148ENST00000228347MDM2chr1269230529+POLR3Bchr12106820975+0.0001796590.9998204
ENST00000258148ENST00000539066MDM2chr1269230529+POLR3Bchr12106820975+0.0001809110.9998191
ENST00000350057ENST00000228347MDM2chr1269230529+POLR3Bchr12106820975+0.0001675160.9998325
ENST00000350057ENST00000539066MDM2chr1269230529+POLR3Bchr12106820975+0.0001691310.99983084
ENST00000360430ENST00000228347MDM2chr1269230529+POLR3Bchr12106820975+0.0004173550.9995827
ENST00000360430ENST00000539066MDM2chr1269230529+POLR3Bchr12106820975+0.0004211220.9995789
ENST00000299252ENST00000228347MDM2chr1269230529+POLR3Bchr12106820975+0.0003440140.99965596
ENST00000299252ENST00000539066MDM2chr1269230529+POLR3Bchr12106820975+0.0003461510.9996538

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

Top

Fusion Protein Breakpoint Sequences for MDM2-POLR3B

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
MDM2chr1269230529POLR3Bchr121068209751040263TDSFEEDPEISLALLSLLFEDLFKKF
MDM2chr1269230529POLR3Bchr121068209751220318TDSFEEDPEISLALLSLLFEDLFKKF
MDM2chr1269230529POLR3Bchr12106820975315105TDSFEEDPEISLALLSLLFEDLFKKF
MDM2chr1269230529POLR3Bchr12106820975390130TDSFEEDPEISLALLSLLFEDLFKKF
MDM2chr1269230529POLR3Bchr12106820975620123TDSFEEDPEISLALLSLLFEDLFKKF
MDM2chr1269230529POLR3Bchr12106820975695148TDSFEEDPEISLALLSLLFEDLFKKF
MDM2chr1269230529POLR3Bchr12106820975767251TDSFEEDPEISLALLSLLFEDLFKKF
MDM2chr1269230529POLR3Bchr12106820975825275TDSFEEDPEISLALLSLLFEDLFKKF

Top

Potential FusionNeoAntigen Information of MDM2-POLR3B 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.
MDM2-POLR3B_69230529_106820975.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)
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B35:03DPEISLAL0.94540.8064614
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B35:02DPEISLAL0.85380.8124614
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B35:04DPEISLAL0.85380.8124614
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B15:17ISLALLSLL0.98640.8923918
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B15:16ISLALLSLL0.98030.6333918
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B57:03ISLALLSLL0.94410.9714918
MDM2-POLR3Bchr1269230529chr12106820975767HLA-A32:13SLALLSLLF0.86950.98441019
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B35:03DPEISLALL0.86810.7902615
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B15:25SLALLSLLF0.78660.97561019
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B35:04DPEISLALL0.62750.8184615
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B35:02DPEISLALL0.62750.8184615
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B13:01SLALLSLLF0.07260.98861019
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B57:03ISLALLSLLF0.9940.9688919
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B44:03EEDPEISLAL0.96470.9103414
MDM2-POLR3Bchr1269230529chr12106820975767HLA-A02:04ALLSLLFEDL0.9570.80321222
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B45:01EEDPEISLAL0.86710.6828414
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B39:13FEEDPEISLAL0.99640.7895314
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B35:12DPEISLAL0.85380.8124614
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B39:10DPEISLAL0.8230.7228614
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B35:12DPEISLALL0.62750.8184615
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B15:05SLALLSLLF0.5630.93681019
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B39:10DPEISLALL0.48250.7721615
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B39:08EEDPEISLAL0.95590.6088414
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B39:08FEEDPEISLAL0.9960.6877314
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B35:09DPEISLAL0.85380.8124614
MDM2-POLR3Bchr1269230529chr12106820975767HLA-A25:01EISLALLSL0.99350.9267817
MDM2-POLR3Bchr1269230529chr12106820975767HLA-A68:02EISLALLSL0.98890.5087817
MDM2-POLR3Bchr1269230529chr12106820975767HLA-A32:01SLALLSLLF0.91040.98711019
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B15:27SLALLSLLF0.85180.96841019
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B15:24SLALLSLLF0.83630.97881019
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B15:13SLALLSLLF0.6890.80911019
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B35:09DPEISLALL0.62750.8184615
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B15:20SLALLSLLF0.60880.95461019
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B40:04EEDPEISLAL0.98340.5893414
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B44:07EEDPEISLAL0.96470.9103414
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B44:13EEDPEISLAL0.96470.9103414
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B44:26EEDPEISLAL0.96470.9103414
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B39:11EEDPEISLAL0.95770.6191414
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B39:31EEDPEISLAL0.93280.8719414
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B18:08EEDPEISLAL0.63310.7762414
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B40:04FEEDPEISLAL0.99990.6389314
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B39:02FEEDPEISLAL0.99650.7987314
MDM2-POLR3Bchr1269230529chr12106820975767HLA-B41:03FEEDPEISLAL0.96530.5787314

Top

Potential FusionNeoAntigen Information of MDM2-POLR3B 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.
MDM2-POLR3B_69230529_106820975.msa

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)
MDM2-POLR3Bchr1269230529chr12106820975767DRB3-0101TDSFEEDPEISLALL015
MDM2-POLR3Bchr1269230529chr12106820975767DRB3-0104TDSFEEDPEISLALL015
MDM2-POLR3Bchr1269230529chr12106820975767DRB3-0105TDSFEEDPEISLALL015
MDM2-POLR3Bchr1269230529chr12106820975767DRB3-0108TDSFEEDPEISLALL015
MDM2-POLR3Bchr1269230529chr12106820975767DRB3-0111TDSFEEDPEISLALL015
MDM2-POLR3Bchr1269230529chr12106820975767DRB3-0112TDSFEEDPEISLALL015
MDM2-POLR3Bchr1269230529chr12106820975767DRB3-0113TDSFEEDPEISLALL015

Top

Fusion breakpoint peptide structures of MDM2-POLR3B

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
1303DPEISLALLSLLFEMDM2POLR3Bchr1269230529chr12106820975767

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of MDM2-POLR3B

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-B14:023BVN1303DPEISLALLSLLFE-7.15543-7.26883
HLA-B14:023BVN1303DPEISLALLSLLFE-4.77435-5.80965
HLA-B52:013W391303DPEISLALLSLLFE-6.80875-6.92215
HLA-B52:013W391303DPEISLALLSLLFE-4.20386-5.23916
HLA-A11:014UQ21303DPEISLALLSLLFE-7.5194-8.5547
HLA-A11:014UQ21303DPEISLALLSLLFE-6.9601-7.0735
HLA-A24:025HGA1303DPEISLALLSLLFE-7.52403-7.63743
HLA-A24:025HGA1303DPEISLALLSLLFE-5.82433-6.85963
HLA-B27:056PYJ1303DPEISLALLSLLFE-3.28285-4.31815
HLA-B44:053DX81303DPEISLALLSLLFE-5.91172-6.94702
HLA-B44:053DX81303DPEISLALLSLLFE-4.24346-4.35686

Top

Vaccine Design for the FusionNeoAntigens of MDM2-POLR3B

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
MDM2-POLR3Bchr1269230529chr121068209751019SLALLSLLFTCCTTAGCTCTTTTATCTCTTCTTTTT
MDM2-POLR3Bchr1269230529chr121068209751222ALLSLLFEDLGCTCTTTTATCTCTTCTTTTTGAAGACTTG
MDM2-POLR3Bchr1269230529chr12106820975314FEEDPEISLALTTTGAAGAAGATCCTGAAATTTCCTTAGCTCTT
MDM2-POLR3Bchr1269230529chr12106820975414EEDPEISLALGAAGAAGATCCTGAAATTTCCTTAGCTCTT
MDM2-POLR3Bchr1269230529chr12106820975614DPEISLALGATCCTGAAATTTCCTTAGCTCTT
MDM2-POLR3Bchr1269230529chr12106820975615DPEISLALLGATCCTGAAATTTCCTTAGCTCTTTTA
MDM2-POLR3Bchr1269230529chr12106820975817EISLALLSLGAAATTTCCTTAGCTCTTTTATCTCTT
MDM2-POLR3Bchr1269230529chr12106820975918ISLALLSLLATTTCCTTAGCTCTTTTATCTCTTCTT
MDM2-POLR3Bchr1269230529chr12106820975919ISLALLSLLFATTTCCTTAGCTCTTTTATCTCTTCTTTTT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
MDM2-POLR3Bchr1269230529chr12106820975015TDSFEEDPEISLALLACAGATTCATTTGAAGAAGATCCTGAAATTTCCTTAGCTCTTTTA

Top

Information of the samples that have these potential fusion neoantigens of MDM2-POLR3B

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
SARCMDM2-POLR3Bchr1269230529ENST00000258148chr12106820975ENST00000228347TCGA-DX-A48N-01A

Top

Potential target of CAR-T therapy development for MDM2-POLR3B

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

Top

Related Drugs to MDM2-POLR3B

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

Top

Related Diseases to MDM2-POLR3B

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