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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:MDM2-PPM1H

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MDM2-PPM1H
FusionPDB ID: 52415
FusionGDB2.0 ID: 52415
HgeneTgene
Gene symbol

MDM2

PPM1H

Gene ID

4193

57460

Gene nameMDM2 proto-oncogeneprotein phosphatase, Mg2+/Mn2+ dependent 1H
SynonymsACTFS|HDMX|LSKB|hdm2ARHCL1|NERPP-2C|URCC2
Cytomap

12q15

12q14.1-q14.2

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, humprotein phosphatase 1Hneurite extension-related protein phosphatase related to PP2Cprotein phosphatase 1H (PP2C domain containing)ras homolog gene family, member C like 1
Modification date2020032920200327
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, 
ENST00000551214, ENST00000228705, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score39 X 20 X 11=858012 X 10 X 6=720
# samples 4711
** MAII scorelog2(47/8580*10)=-4.19024498582191
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/720*10)=-2.71049338280502
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: MDM2 [Title/Abstract] AND PPM1H [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: MDM2 [Title/Abstract] AND PPM1H [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MDM2(69230529)-PPM1H(63195940), # samples:1
Anticipated loss of major functional domain due to fusion event.MDM2-PPM1H 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-PPM1H 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-PPM1H 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-PPM1H 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/chr12:63195940)
- 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 PPM1H (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)
ENST00000462284MDM2chr1269230529+ENST00000228705PPM1Hchr1263195940-686112202662353695
ENST00000356290MDM2chr1269230529+ENST00000228705PPM1Hchr1263195940-63366952511828525
ENST00000540827MDM2chr1269230529+ENST00000228705PPM1Hchr1263195940-62616202511753500
ENST00000258149MDM2chr1269230529+ENST00000228705PPM1Hchr1263195940-668110402512173640
ENST00000258148MDM2chr1269230529+ENST00000228705PPM1Hchr1263195940-6408767141900628
ENST00000350057MDM2chr1269230529+ENST00000228705PPM1Hchr1263195940-646682501958652
ENST00000360430MDM2chr1269230529+ENST00000228705PPM1Hchr1263195940-595631501448482
ENST00000299252MDM2chr1269230529+ENST00000228705PPM1Hchr1263195940-603139001523507

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
ENST00000462284ENST00000228705MDM2chr1269230529+PPM1Hchr1263195940-0.0009166120.9990834
ENST00000356290ENST00000228705MDM2chr1269230529+PPM1Hchr1263195940-0.0012191210.9987809
ENST00000540827ENST00000228705MDM2chr1269230529+PPM1Hchr1263195940-0.0007008410.99929917
ENST00000258149ENST00000228705MDM2chr1269230529+PPM1Hchr1263195940-0.0004108030.99958926
ENST00000258148ENST00000228705MDM2chr1269230529+PPM1Hchr1263195940-0.0003948730.9996051
ENST00000350057ENST00000228705MDM2chr1269230529+PPM1Hchr1263195940-0.0005179220.9994821
ENST00000360430ENST00000228705MDM2chr1269230529+PPM1Hchr1263195940-0.0004422940.9995577
ENST00000299252ENST00000228705MDM2chr1269230529+PPM1Hchr1263195940-0.0004263960.99957365

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 MDM2-PPM1H

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
MDM2chr1269230529PPM1Hchr12631959401040263TDSFEEDPEISLAESEGVSCHYWSLF
MDM2chr1269230529PPM1Hchr12631959401220318TDSFEEDPEISLAESEGVSCHYWSLF
MDM2chr1269230529PPM1Hchr1263195940315105TDSFEEDPEISLAESEGVSCHYWSLF
MDM2chr1269230529PPM1Hchr1263195940390130TDSFEEDPEISLAESEGVSCHYWSLF
MDM2chr1269230529PPM1Hchr1263195940620123TDSFEEDPEISLAESEGVSCHYWSLF
MDM2chr1269230529PPM1Hchr1263195940695148TDSFEEDPEISLAESEGVSCHYWSLF
MDM2chr1269230529PPM1Hchr1263195940767251TDSFEEDPEISLAESEGVSCHYWSLF
MDM2chr1269230529PPM1Hchr1263195940825275TDSFEEDPEISLAESEGVSCHYWSLF

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Potential FusionNeoAntigen Information of MDM2-PPM1H 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-PPM1H_69230529_63195940.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-PPM1Hchr1269230529chr1263195940767HLA-B44:03AESEGVSCHY0.99890.94031222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B18:01AESEGVSCHY0.90970.89021222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:02AESEGVSCHYW0.99990.50821223
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:03AESEGVSCHYW0.99990.9641223
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:05AESEGVSCHYW0.99980.56261223
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:08AESEGVSCHYW0.99990.6561223
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:09AESEGVSCHYW0.99980.65271223
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:10AESEGVSCHYW0.98710.70671223
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B18:11AESEGVSCH0.44190.8661221
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:26AESEGVSCHY0.99890.94031222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:13AESEGVSCHY0.99890.94031222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:07AESEGVSCHY0.99890.94031222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B15:12AESEGVSCHY0.9350.82961222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B15:53AESEGVSCHY0.93350.85021222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B18:05AESEGVSCHY0.90970.89021222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B18:11AESEGVSCHY0.89250.87251222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B15:54AESEGVSCHY0.84460.81831222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B35:28AESEGVSCHY0.82820.8621222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B48:02AESEGVSCHY0.68120.8431222
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:26AESEGVSCHYW0.99990.9641223
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:13AESEGVSCHYW0.99990.9641223
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:22AESEGVSCHYW0.99990.50821223
MDM2-PPM1Hchr1269230529chr1263195940767HLA-B44:07AESEGVSCHYW0.99990.9641223

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Potential FusionNeoAntigen Information of MDM2-PPM1H 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-PPM1H_69230529_63195940.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-PPM1Hchr1269230529chr1263195940767DRB1-0901EEDPEISLAESEGVS419
MDM2-PPM1Hchr1269230529chr1263195940767DRB1-0904EEDPEISLAESEGVS419
MDM2-PPM1Hchr1269230529chr1263195940767DRB1-0906EEDPEISLAESEGVS419
MDM2-PPM1Hchr1269230529chr1263195940767DRB1-0906DPEISLAESEGVSCH621
MDM2-PPM1Hchr1269230529chr1263195940767DRB1-0906EDPEISLAESEGVSC520
MDM2-PPM1Hchr1269230529chr1263195940767DRB1-0909EEDPEISLAESEGVS419
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0101TDSFEEDPEISLAES015
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0101DSFEEDPEISLAESE116
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0104TDSFEEDPEISLAES015
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0104DSFEEDPEISLAESE116
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0105TDSFEEDPEISLAES015
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0108TDSFEEDPEISLAES015
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0108DSFEEDPEISLAESE116
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0109TDSFEEDPEISLAES015
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0111TDSFEEDPEISLAES015
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0111DSFEEDPEISLAESE116
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0112TDSFEEDPEISLAES015
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0112DSFEEDPEISLAESE116
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0113TDSFEEDPEISLAES015
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0113DSFEEDPEISLAESE116
MDM2-PPM1Hchr1269230529chr1263195940767DRB3-0114TDSFEEDPEISLAES015

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Fusion breakpoint peptide structures of MDM2-PPM1H

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
1302DPEISLAESEGVSCMDM2PPM1Hchr1269230529chr1263195940767

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of MDM2-PPM1H

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-B14:023BVN1302DPEISLAESEGVSC-6.46878-6.66328
HLA-B14:023BVN1302DPEISLAESEGVSC-4.33704-5.09154
HLA-B52:013W391302DPEISLAESEGVSC-6.45088-7.20538
HLA-B52:013W391302DPEISLAESEGVSC-6.08714-6.28164
HLA-A11:014UQ21302DPEISLAESEGVSC-7.67344-8.42794
HLA-A24:025HGA1302DPEISLAESEGVSC-7.49907-7.69357
HLA-A24:025HGA1302DPEISLAESEGVSC-4.36357-5.11807
HLA-B27:056PYJ1302DPEISLAESEGVSC-8.53231-9.28681
HLA-B44:053DX81302DPEISLAESEGVSC-5.69992-5.89442
HLA-B44:053DX81302DPEISLAESEGVSC-3.58931-4.34381
HLA-A02:016TDR1302DPEISLAESEGVSC-7.78181-7.97631

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Vaccine Design for the FusionNeoAntigens of MDM2-PPM1H

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-PPM1Hchr1269230529chr12631959401221AESEGVSCHGCTGAATCCGAGGGTGTTTCCTGCCAC
MDM2-PPM1Hchr1269230529chr12631959401222AESEGVSCHYGCTGAATCCGAGGGTGTTTCCTGCCACTAT
MDM2-PPM1Hchr1269230529chr12631959401223AESEGVSCHYWGCTGAATCCGAGGGTGTTTCCTGCCACTATTGG

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-PPM1Hchr1269230529chr1263195940015TDSFEEDPEISLAESACAGATTCATTTGAAGAAGATCCTGAAATTTCCTTAGCTGAATCC
MDM2-PPM1Hchr1269230529chr1263195940116DSFEEDPEISLAESEGATTCATTTGAAGAAGATCCTGAAATTTCCTTAGCTGAATCCGAG
MDM2-PPM1Hchr1269230529chr1263195940419EEDPEISLAESEGVSGAAGAAGATCCTGAAATTTCCTTAGCTGAATCCGAGGGTGTTTCC
MDM2-PPM1Hchr1269230529chr1263195940520EDPEISLAESEGVSCGAAGATCCTGAAATTTCCTTAGCTGAATCCGAGGGTGTTTCCTGC
MDM2-PPM1Hchr1269230529chr1263195940621DPEISLAESEGVSCHGATCCTGAAATTTCCTTAGCTGAATCCGAGGGTGTTTCCTGCCAC

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Information of the samples that have these potential fusion neoantigens of MDM2-PPM1H

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
GBMMDM2-PPM1Hchr1269230529ENST00000258148chr1263195940ENST00000228705TCGA-19-2624

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Potential target of CAR-T therapy development for MDM2-PPM1H

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 MDM2-PPM1H

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 MDM2-PPM1H

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