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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:C12orf49-MDM2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: C12orf49-MDM2
FusionPDB ID: 10837
FusionGDB2.0 ID: 10837
HgeneTgene
Gene symbol

C12orf49

MDM2

Gene ID

79794

4193

Gene namechromosome 12 open reading frame 49MDM2 proto-oncogene
Synonyms-ACTFS|HDMX|LSKB|hdm2
Cytomap

12q24.22

12q15

Type of geneprotein-codingprotein-coding
DescriptionUPF0454 protein C12orf49E3 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, hum
Modification date2020031320200329
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 idsENST00000261318, ENST00000536380, 
ENST00000548356, 
ENST00000258148, 
ENST00000299252, ENST00000348801, 
ENST00000350057, ENST00000360430, 
ENST00000393410, ENST00000393412, 
ENST00000393413, ENST00000478070, 
ENST00000517852, ENST00000544125, 
ENST00000544561, ENST00000545204, 
ENST00000258149, ENST00000356290, 
ENST00000428863, ENST00000462284, 
ENST00000540827, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 4 X 2=6412 X 10 X 6=720
# samples 612
** MAII scorelog2(6/64*10)=-0.0931094043914815
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/720*10)=-2.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: C12orf49 [Title/Abstract] AND MDM2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: C12orf49 [Title/Abstract] AND MDM2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)C12orf49(117175595)-MDM2(69229609), # samples:2
Anticipated loss of major functional domain due to fusion event.C12orf49-MDM2 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.
C12orf49-MDM2 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.
C12orf49-MDM2 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.
C12orf49-MDM2 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.
C12orf49-MDM2 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
C12orf49-MDM2 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
TgeneMDM2

GO:0000122

negative regulation of transcription by RNA polymerase II

9271120|17310983

TgeneMDM2

GO:0006511

ubiquitin-dependent protein catabolic process

11278372|15314173|16173922|17310983

TgeneMDM2

GO:0016567

protein ubiquitination

9450543|15878855|19656744|20153724

TgeneMDM2

GO:0031648

protein destabilization

9529249|10360174|15314173

TgeneMDM2

GO:0032436

positive regulation of proteasomal ubiquitin-dependent protein catabolic process

11278372

TgeneMDM2

GO:0034504

protein localization to nucleus

10360174

TgeneMDM2

GO:0042176

regulation of protein catabolic process

9153395

TgeneMDM2

GO:0043518

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

9529249|10360174

TgeneMDM2

GO:0045184

establishment of protein localization

10360174

TgeneMDM2

GO:0045892

negative regulation of transcription, DNA-templated

9271120

TgeneMDM2

GO:0065003

protein-containing complex assembly

10608892|12915590

TgeneMDM2

GO:0071157

negative regulation of cell cycle arrest

9529249

TgeneMDM2

GO:0071480

cellular response to gamma radiation

16213212

TgeneMDM2

GO:0072717

cellular response to actinomycin D

15314173

TgeneMDM2

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/chr12:117175595/chr12:69229609)
- 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 C12orf49 (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 MDM2 (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)
ENST00000261318C12orf49chr12117175594-ENST00000462284MDM2chr1269229608+66672721611081306
ENST00000261318C12orf49chr12117175594-ENST00000356290MDM2chr1269229608+66642721611081306
ENST00000261318C12orf49chr12117175594-ENST00000540827MDM2chr1269229608+66642721611081306
ENST00000261318C12orf49chr12117175594-ENST00000258149MDM2chr1269229608+66642721611081306
ENST00000261318C12orf49chr12117175594-ENST00000428863MDM2chr1269229608+65862721611003280
ENST00000536380C12orf49chr12117175594-ENST00000462284MDM2chr1269229608+66752801691089306
ENST00000536380C12orf49chr12117175594-ENST00000356290MDM2chr1269229608+66722801691089306
ENST00000536380C12orf49chr12117175594-ENST00000540827MDM2chr1269229608+66722801691089306
ENST00000536380C12orf49chr12117175594-ENST00000258149MDM2chr1269229608+66722801691089306
ENST00000536380C12orf49chr12117175594-ENST00000428863MDM2chr1269229608+65942801691011280
ENST00000261318C12orf49chr12117175595-ENST00000462284MDM2chr1269229609+66672721611081306
ENST00000261318C12orf49chr12117175595-ENST00000356290MDM2chr1269229609+66642721611081306
ENST00000261318C12orf49chr12117175595-ENST00000540827MDM2chr1269229609+66642721611081306
ENST00000261318C12orf49chr12117175595-ENST00000258149MDM2chr1269229609+66642721611081306
ENST00000261318C12orf49chr12117175595-ENST00000428863MDM2chr1269229609+65862721611003280
ENST00000536380C12orf49chr12117175595-ENST00000462284MDM2chr1269229609+66752801691089306
ENST00000536380C12orf49chr12117175595-ENST00000356290MDM2chr1269229609+66722801691089306
ENST00000536380C12orf49chr12117175595-ENST00000540827MDM2chr1269229609+66722801691089306
ENST00000536380C12orf49chr12117175595-ENST00000258149MDM2chr1269229609+66722801691089306
ENST00000536380C12orf49chr12117175595-ENST00000428863MDM2chr1269229609+65942801691011280
ENST00000261318C12orf49chr12117175595-ENST00000393412MDM2chr1269233054+1088272161847228
ENST00000261318C12orf49chr12117175595-ENST00000258148MDM2chr1269233054+866272161847228
ENST00000536380C12orf49chr12117175595-ENST00000393412MDM2chr1269233054+1096280169855228
ENST00000536380C12orf49chr12117175595-ENST00000258148MDM2chr1269233054+874280169855228

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
ENST00000261318ENST00000462284C12orf49chr12117175594-MDM2chr1269229608+8.46E-050.9999155
ENST00000261318ENST00000356290C12orf49chr12117175594-MDM2chr1269229608+8.38E-050.9999162
ENST00000261318ENST00000540827C12orf49chr12117175594-MDM2chr1269229608+8.38E-050.9999162
ENST00000261318ENST00000258149C12orf49chr12117175594-MDM2chr1269229608+8.38E-050.9999162
ENST00000261318ENST00000428863C12orf49chr12117175594-MDM2chr1269229608+0.0001818720.99981815
ENST00000536380ENST00000462284C12orf49chr12117175594-MDM2chr1269229608+8.39E-050.9999161
ENST00000536380ENST00000356290C12orf49chr12117175594-MDM2chr1269229608+8.32E-050.9999168
ENST00000536380ENST00000540827C12orf49chr12117175594-MDM2chr1269229608+8.32E-050.9999168
ENST00000536380ENST00000258149C12orf49chr12117175594-MDM2chr1269229608+8.32E-050.9999168
ENST00000536380ENST00000428863C12orf49chr12117175594-MDM2chr1269229608+0.0001808250.9998192
ENST00000261318ENST00000462284C12orf49chr12117175595-MDM2chr1269229609+8.46E-050.9999155
ENST00000261318ENST00000356290C12orf49chr12117175595-MDM2chr1269229609+8.38E-050.9999162
ENST00000261318ENST00000540827C12orf49chr12117175595-MDM2chr1269229609+8.38E-050.9999162
ENST00000261318ENST00000258149C12orf49chr12117175595-MDM2chr1269229609+8.38E-050.9999162
ENST00000261318ENST00000428863C12orf49chr12117175595-MDM2chr1269229609+0.0001818720.99981815
ENST00000536380ENST00000462284C12orf49chr12117175595-MDM2chr1269229609+8.39E-050.9999161
ENST00000536380ENST00000356290C12orf49chr12117175595-MDM2chr1269229609+8.32E-050.9999168
ENST00000536380ENST00000540827C12orf49chr12117175595-MDM2chr1269229609+8.32E-050.9999168
ENST00000536380ENST00000258149C12orf49chr12117175595-MDM2chr1269229609+8.32E-050.9999168
ENST00000536380ENST00000428863C12orf49chr12117175595-MDM2chr1269229609+0.0001808250.9998192
ENST00000261318ENST00000393412C12orf49chr12117175595-MDM2chr1269233054+0.0013268380.9986732
ENST00000261318ENST00000258148C12orf49chr12117175595-MDM2chr1269233054+0.0019663370.9980337
ENST00000536380ENST00000393412C12orf49chr12117175595-MDM2chr1269233054+0.0013713460.99862874
ENST00000536380ENST00000258148C12orf49chr12117175595-MDM2chr1269233054+0.0018843550.99811566

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 C12orf49-MDM2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
C12orf49chr12117175594MDM2chr126922960827237LSLVYFLSSTFKQDLDAGVSEHSGDW
C12orf49chr12117175594MDM2chr126922960828037LSLVYFLSSTFKQDLDAGVSEHSGDW
C12orf49chr12117175595MDM2chr126922960927237LSLVYFLSSTFKQDLDAGVSEHSGDW
C12orf49chr12117175595MDM2chr126922960928037LSLVYFLSSTFKQDLDAGVSEHSGDW
C12orf49chr12117175595MDM2chr126923305427237LSLVYFLSSTFKQDYWKCTSCNEMNP
C12orf49chr12117175595MDM2chr126923305428037LSLVYFLSSTFKQDYWKCTSCNEMNP

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Potential FusionNeoAntigen Information of C12orf49-MDM2 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.
C12orf49-MDM2_117175594_69229608.msa
C12orf49-MDM2_117175595_69233054.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)
C12orf49-MDM2chr12117175594chr1269229608272HLA-C16:01LSSTFKQDL0.66790.9813615
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:01STFKQDYW0.99950.9405816
C12orf49-MDM2chr12117175595chr1269233054272HLA-B58:02STFKQDYW0.99840.8784816
C12orf49-MDM2chr12117175595chr1269233054272HLA-B58:01STFKQDYW0.99830.8308816
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:03STFKQDYW0.99650.9771816
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:01SSTFKQDYW0.99780.945716
C12orf49-MDM2chr12117175595chr1269233054272HLA-B58:01SSTFKQDYW0.99690.8067716
C12orf49-MDM2chr12117175595chr1269233054272HLA-B58:02SSTFKQDYW0.99540.8635716
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:03SSTFKQDYW0.97640.9722716
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:01LSSTFKQDYW0.99970.9392616
C12orf49-MDM2chr12117175595chr1269233054272HLA-B58:02LSSTFKQDYW0.99890.8567616
C12orf49-MDM2chr12117175595chr1269233054272HLA-B58:01LSSTFKQDYW0.99870.8191616
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:03LSSTFKQDYW0.99470.9818616
C12orf49-MDM2chr12117175595chr1269233054272HLA-C15:04LSSTFKQDY0.61590.7391615
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:10STFKQDYW0.99950.9405816
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:04STFKQDYW0.99880.6185816
C12orf49-MDM2chr12117175595chr1269233054272HLA-B58:06STFKQDYW0.99830.7633816
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:02STFKQDYW0.99780.8392816
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:10SSTFKQDYW0.99780.945716
C12orf49-MDM2chr12117175595chr1269233054272HLA-B58:06SSTFKQDYW0.99270.7467716
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:04SSTFKQDYW0.98890.6264716
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:02SSTFKQDYW0.97490.821716
C12orf49-MDM2chr12117175595chr1269233054272HLA-C15:09LSSTFKQDY0.61590.7391615
C12orf49-MDM2chr12117175595chr1269233054272HLA-C16:01LSSTFKQDY0.12940.9394615
C12orf49-MDM2chr12117175595chr1269233054272HLA-C16:02LSSTFKQDY0.06240.9514615
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:10LSSTFKQDYW0.99970.9392616
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:04LSSTFKQDYW0.99950.6677616
C12orf49-MDM2chr12117175595chr1269233054272HLA-B58:06LSSTFKQDYW0.99730.7619616
C12orf49-MDM2chr12117175595chr1269233054272HLA-B57:02LSSTFKQDYW0.99690.8709616

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Potential FusionNeoAntigen Information of C12orf49-MDM2 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.
C12orf49-MDM2_117175594_69229608.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)
C12orf49-MDM2chr12117175594chr1269229608272DRB1-0407SLVYFLSSTFKQDLD116
C12orf49-MDM2chr12117175594chr1269229608272DRB1-0462SSTFKQDLDAGVSEH722
C12orf49-MDM2chr12117175594chr1269229608272DRB1-0472SSTFKQDLDAGVSEH722
C12orf49-MDM2chr12117175594chr1269229608272DRB1-0472LSSTFKQDLDAGVSE621
C12orf49-MDM2chr12117175594chr1269229608272DRB1-0474SLVYFLSSTFKQDLD116
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0101SSTFKQDLDAGVSEH722
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0101LSSTFKQDLDAGVSE621
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0104SSTFKQDLDAGVSEH722
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0104LSSTFKQDLDAGVSE621
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0105SSTFKQDLDAGVSEH722
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0105LSSTFKQDLDAGVSE621
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0108SSTFKQDLDAGVSEH722
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0108LSSTFKQDLDAGVSE621
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0109SSTFKQDLDAGVSEH722
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0109LSSTFKQDLDAGVSE621
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0111SSTFKQDLDAGVSEH722
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0111LSSTFKQDLDAGVSE621
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0112SSTFKQDLDAGVSEH722
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0112LSSTFKQDLDAGVSE621
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0113SSTFKQDLDAGVSEH722
C12orf49-MDM2chr12117175594chr1269229608272DRB3-0113LSSTFKQDLDAGVSE621

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Fusion breakpoint peptide structures of C12orf49-MDM2

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
5669LSSTFKQDLDAGVSC12orf49MDM2chr12117175594chr1269229608272
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
5670LSSTFKQDYWKCTSC12orf49MDM2chr12117175595chr1269233054272

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of C12orf49-MDM2

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-B14:023BVN5669LSSTFKQDLDAGVS-7.9962-8.1096
HLA-B14:023BVN5669LSSTFKQDLDAGVS-5.70842-6.74372
HLA-B52:013W395669LSSTFKQDLDAGVS-6.83737-6.95077
HLA-B52:013W395669LSSTFKQDLDAGVS-4.4836-5.5189
HLA-A11:014UQ25669LSSTFKQDLDAGVS-10.0067-10.1201
HLA-A11:014UQ25669LSSTFKQDLDAGVS-9.03915-10.0745
HLA-A24:025HGA5669LSSTFKQDLDAGVS-6.56204-6.67544
HLA-A24:025HGA5669LSSTFKQDLDAGVS-5.42271-6.45801
HLA-B44:053DX85669LSSTFKQDLDAGVS-7.85648-8.89178
HLA-B44:053DX85669LSSTFKQDLDAGVS-5.3978-5.5112
HLA-A02:016TDR5669LSSTFKQDLDAGVS-3.37154-4.40684
HLA-B14:023BVN5670LSSTFKQDYWKCTS-7.62002-7.73342
HLA-B14:023BVN5670LSSTFKQDYWKCTS-3.26509-4.30039
HLA-B52:013W395670LSSTFKQDYWKCTS-7.21379-7.32719
HLA-B52:013W395670LSSTFKQDYWKCTS-4.63393-5.66923
HLA-A11:014UQ25670LSSTFKQDYWKCTS-10.622-10.7354
HLA-A24:025HGA5670LSSTFKQDYWKCTS-7.29499-8.33029
HLA-A24:025HGA5670LSSTFKQDYWKCTS-6.47841-6.59181
HLA-B44:053DX85670LSSTFKQDYWKCTS-5.65986-5.77326
HLA-B44:053DX85670LSSTFKQDYWKCTS-4.37611-5.41141
HLA-A02:016TDR5670LSSTFKQDYWKCTS2.618021.58272

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Vaccine Design for the FusionNeoAntigens of C12orf49-MDM2

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
C12orf49-MDM2chr12117175594chr1269229608615LSSTFKQDLCTCAGCAGCACCTTCAAGCAGGATCTT
C12orf49-MDM2chr12117175595chr1269233054615LSSTFKQDYCTCAGCAGCACCTTCAAGCAGGACTAT
C12orf49-MDM2chr12117175595chr1269233054616LSSTFKQDYWCTCAGCAGCACCTTCAAGCAGGACTATTGG
C12orf49-MDM2chr12117175595chr1269233054716SSTFKQDYWAGCAGCACCTTCAAGCAGGACTATTGG
C12orf49-MDM2chr12117175595chr1269233054816STFKQDYWAGCACCTTCAAGCAGGACTATTGG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
C12orf49-MDM2chr12117175594chr1269229608116SLVYFLSSTFKQDLDTCGCTCGTCTACTTCCTCAGCAGCACCTTCAAGCAGGATCTTGAT
C12orf49-MDM2chr12117175594chr1269229608621LSSTFKQDLDAGVSECTCAGCAGCACCTTCAAGCAGGATCTTGATGCTGGTGTAAGTGAA
C12orf49-MDM2chr12117175594chr1269229608722SSTFKQDLDAGVSEHAGCAGCACCTTCAAGCAGGATCTTGATGCTGGTGTAAGTGAACAT

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Information of the samples that have these potential fusion neoantigens of C12orf49-MDM2

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
GBMC12orf49-MDM2chr12117175595ENST00000261318chr1269233054ENST00000258148TCGA-06-5856-01A
GBMC12orf49-MDM2chr12117175594ENST00000261318chr1269229608ENST00000258149TCGA-06-5856

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Potential target of CAR-T therapy development for C12orf49-MDM2

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
HgeneC12orf49chr12:117175594chr12:69229608ENST00000261318-1517_3537206.0TransmembraneHelical
HgeneC12orf49chr12:117175595chr12:69229609ENST00000261318-1517_3537206.0TransmembraneHelical
HgeneC12orf49chr12:117175595chr12:69233054ENST00000261318-1517_3537206.0TransmembraneHelical

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 C12orf49-MDM2

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 C12orf49-MDM2

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