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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:URM1-TP53BP1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: URM1-TP53BP1
FusionPDB ID: 97100
FusionGDB2.0 ID: 97100
HgeneTgene
Gene symbol

URM1

TP53BP1

Gene ID

81605

7158

Gene nameubiquitin related modifier 1tumor protein p53 binding protein 1
SynonymsC9orf7453BP1|TDRD30|p202|p53BP1
Cytomap

9q34.11

15q15.3

Type of geneprotein-codingprotein-coding
Descriptionubiquitin-related modifier 1ubiquitin-related modifier 1 homologTP53-binding protein 1p53-binding protein 1tumor protein 53-binding protein, 1tumor suppressor p53-binding protein 1
Modification date2020031320200322
UniProtAcc.

Q12888

Main function of 5'-partner protein: FUNCTION: Double-strand break (DSB) repair protein involved in response to DNA damage, telomere dynamics and class-switch recombination (CSR) during antibody genesis (PubMed:12364621, PubMed:22553214, PubMed:23333306, PubMed:17190600, PubMed:21144835, PubMed:27153538, PubMed:28241136). Plays a key role in the repair of double-strand DNA breaks (DSBs) in response to DNA damage by promoting non-homologous end joining (NHEJ)-mediated repair of DSBs and specifically counteracting the function of the homologous recombination (HR) repair protein BRCA1 (PubMed:22553214, PubMed:23727112, PubMed:23333306, PubMed:27153538). In response to DSBs, phosphorylation by ATM promotes interaction with RIF1 and dissociation from NUDT16L1/TIRR, leading to recruitment to DSBs sites (PubMed:28241136). Recruited to DSBs sites by recognizing and binding histone H2A monoubiquitinated at 'Lys-15' (H2AK15Ub) and histone H4 dimethylated at 'Lys-20' (H4K20me2), two histone marks that are present at DSBs sites (PubMed:23760478, PubMed:27153538, PubMed:28241136, PubMed:17190600). Required for immunoglobulin class-switch recombination (CSR) during antibody genesis, a process that involves the generation of DNA DSBs (PubMed:23345425). Participates in the repair and the orientation of the broken DNA ends during CSR (By similarity). In contrast, it is not required for classic NHEJ and V(D)J recombination (By similarity). Promotes NHEJ of dysfunctional telomeres via interaction with PAXIP1 (PubMed:23727112). {ECO:0000250|UniProtKB:P70399, ECO:0000269|PubMed:12364621, ECO:0000269|PubMed:17190600, ECO:0000269|PubMed:21144835, ECO:0000269|PubMed:22553214, ECO:0000269|PubMed:23333306, ECO:0000269|PubMed:23345425, ECO:0000269|PubMed:23727112, ECO:0000269|PubMed:23760478, ECO:0000269|PubMed:27153538, ECO:0000269|PubMed:28241136}.
Ensembl transtripts involved in fusion geneENST idsENST00000483206, ENST00000372847, 
ENST00000372850, ENST00000372853, 
ENST00000452446, 
ENST00000263801, 
ENST00000382039, ENST00000382044, 
ENST00000450115, ENST00000605155, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score5 X 3 X 4=606 X 6 X 3=108
# samples 66
** MAII scorelog2(6/60*10)=0log2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: URM1 [Title/Abstract] AND TP53BP1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: URM1 [Title/Abstract] AND TP53BP1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)URM1(131140385)-TP53BP1(43762264), # samples:2
Anticipated loss of major functional domain due to fusion event.URM1-TP53BP1 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.
URM1-TP53BP1 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.
URM1-TP53BP1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
URM1-TP53BP1 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
URM1-TP53BP1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
URM1-TP53BP1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
TgeneTP53BP1

GO:0006303

double-strand break repair via nonhomologous end joining

23333306|23760478|28241136

TgeneTP53BP1

GO:0006974

cellular response to DNA damage stimulus

17500065|28241136

TgeneTP53BP1

GO:0045830

positive regulation of isotype switching

23345425

TgeneTP53BP1

GO:0051260

protein homooligomerization

23345425

TgeneTP53BP1

GO:2000042

negative regulation of double-strand break repair via homologous recombination

23333306|23345425



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/chr9:131140385/chr15:43762264)
- 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 URM1 (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 TP53BP1 (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)
ENST00000372853URM1chr9131140385+ENST00000263801TP53BP1chr1543762264-5096168849211637
ENST00000372853URM1chr9131140385+ENST00000382039TP53BP1chr1543762264-4941168847711587
ENST00000372853URM1chr9131140385+ENST00000382044TP53BP1chr1543762264-5091168849211637
ENST00000372853URM1chr9131140385+ENST00000450115TP53BP1chr1543762264-5083168849151635
ENST00000452446URM1chr9131140385+ENST00000263801TP53BP1chr1543762264-5096168849211637
ENST00000452446URM1chr9131140385+ENST00000382039TP53BP1chr1543762264-4941168847711587
ENST00000452446URM1chr9131140385+ENST00000382044TP53BP1chr1543762264-5091168849211637
ENST00000452446URM1chr9131140385+ENST00000450115TP53BP1chr1543762264-5083168849151635
ENST00000372850URM1chr9131140385+ENST00000263801TP53BP1chr1543762264-50541262048791619
ENST00000372850URM1chr9131140385+ENST00000382039TP53BP1chr1543762264-48991262047291569
ENST00000372850URM1chr9131140385+ENST00000382044TP53BP1chr1543762264-50491262048791619
ENST00000372850URM1chr9131140385+ENST00000450115TP53BP1chr1543762264-50411262048731617

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
ENST00000372853ENST00000263801URM1chr9131140385+TP53BP1chr1543762264-0.000693980.99930596
ENST00000372853ENST00000382039URM1chr9131140385+TP53BP1chr1543762264-0.0005173110.99948263
ENST00000372853ENST00000382044URM1chr9131140385+TP53BP1chr1543762264-0.0006975260.9993025
ENST00000372853ENST00000450115URM1chr9131140385+TP53BP1chr1543762264-0.0005467970.99945325
ENST00000452446ENST00000263801URM1chr9131140385+TP53BP1chr1543762264-0.000693980.99930596
ENST00000452446ENST00000382039URM1chr9131140385+TP53BP1chr1543762264-0.0005173110.99948263
ENST00000452446ENST00000382044URM1chr9131140385+TP53BP1chr1543762264-0.0006975260.9993025
ENST00000452446ENST00000450115URM1chr9131140385+TP53BP1chr1543762264-0.0005467970.99945325
ENST00000372850ENST00000263801URM1chr9131140385+TP53BP1chr1543762264-0.0006532110.9993468
ENST00000372850ENST00000382039URM1chr9131140385+TP53BP1chr1543762264-0.0004880480.99951196
ENST00000372850ENST00000382044URM1chr9131140385+TP53BP1chr1543762264-0.0006565670.99934345
ENST00000372850ENST00000450115URM1chr9131140385+TP53BP1chr1543762264-0.0005146440.9994854

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 URM1-TP53BP1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
URM1chr9131140385TP53BP1chr154376226412634IKKHRVTLPGQEEPYKPMDTSVLSEE
URM1chr9131140385TP53BP1chr154376226416852IKKHRVTLPGQEEPYKPMDTSVLSEE

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Potential FusionNeoAntigen Information of URM1-TP53BP1 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.
URM1-TP53BP1_131140385_43762264.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)
URM1-TP53BP1chr9131140385chr1543762264126HLA-B35:08LPGQEEPY0.8560.9467715
URM1-TP53BP1chr9131140385chr1543762264126HLA-B48:01GQEEPYKPM0.99290.6852918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B39:13GQEEPYKPM0.86290.9337918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B15:03GQEEPYKPM0.63330.8776918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B15:17VTLPGQEEPY0.98340.9613515
URM1-TP53BP1chr9131140385chr1543762264126HLA-B58:01VTLPGQEEPY0.91690.9828515
URM1-TP53BP1chr9131140385chr1543762264126HLA-B15:16VTLPGQEEPY0.89970.9321515
URM1-TP53BP1chr9131140385chr1543762264126HLA-A30:08VTLPGQEEPYK0.99130.7961516
URM1-TP53BP1chr9131140385chr1543762264126HLA-B35:03EPYKPMDTSVL0.98440.77581223
URM1-TP53BP1chr9131140385chr1543762264126HLA-B35:02EPYKPMDTSVL0.96940.83371223
URM1-TP53BP1chr9131140385chr1543762264126HLA-B35:04EPYKPMDTSVL0.96940.83371223
URM1-TP53BP1chr9131140385chr1543762264126HLA-B48:03GQEEPYKPM0.97260.5536918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B39:08GQEEPYKPM0.79680.967918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B15:31TLPGQEEPY0.69240.9394615
URM1-TP53BP1chr9131140385chr1543762264126HLA-B42:02EPYKPMDTSV0.9560.59971222
URM1-TP53BP1chr9131140385chr1543762264126HLA-B15:05VTLPGQEEPY0.93610.948515
URM1-TP53BP1chr9131140385chr1543762264126HLA-B39:10EPYKPMDTSV0.37220.88871222
URM1-TP53BP1chr9131140385chr1543762264126HLA-B42:02EPYKPMDTSVL0.99660.54831223
URM1-TP53BP1chr9131140385chr1543762264126HLA-B73:01HRVTLPGQEEP0.99660.9133314
URM1-TP53BP1chr9131140385chr1543762264126HLA-B42:01EPYKPMDTSVL0.99490.53871223
URM1-TP53BP1chr9131140385chr1543762264126HLA-B39:10EPYKPMDTSVL0.97080.82051223
URM1-TP53BP1chr9131140385chr1543762264126HLA-B35:12EPYKPMDTSVL0.96940.83371223
URM1-TP53BP1chr9131140385chr1543762264126HLA-B40:12GQEEPYKPM0.97260.5536918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B40:49GQEEPYKPM0.95970.527918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B40:21GQEEPYKPM0.92110.6083918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B39:02GQEEPYKPM0.91590.9373918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B15:73GQEEPYKPM0.79040.9524918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B15:30GQEEPYKPM0.6760.9012918
URM1-TP53BP1chr9131140385chr1543762264126HLA-B57:04VTLPGQEEPY0.99380.872515
URM1-TP53BP1chr9131140385chr1543762264126HLA-B15:20VTLPGQEEPY0.93910.9698515
URM1-TP53BP1chr9131140385chr1543762264126HLA-B67:01EPYKPMDTSV0.52650.73281222
URM1-TP53BP1chr9131140385chr1543762264126HLA-B67:01EPYKPMDTSVL0.97390.57381223
URM1-TP53BP1chr9131140385chr1543762264126HLA-B35:09EPYKPMDTSVL0.96940.83371223

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Potential FusionNeoAntigen Information of URM1-TP53BP1 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.
URM1-TP53BP1_131140385_43762264.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)
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0101EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0101QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0105EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0105QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0107EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0107QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0109EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0111EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0111QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0113EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0113QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0115EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0117EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0117QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0119EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0119QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0121EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0121QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0125EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0125QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0127EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0127QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0129EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0131EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0131QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0401EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0401QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0405EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0407EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0407QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0409EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0417EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0419EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0419QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0424EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0424QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0429EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0430EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0431EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0431QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0433EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0433QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0434EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0434QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0435EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0435QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0438EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0438QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0443EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0443QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0445EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0447EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0447QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0448EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0454EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0457EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0461EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0461QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0462EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0462QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0463EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0463QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0464EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0464QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0469EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0469QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0469GQEEPYKPMDTSVLS924
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0472EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0474EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0474QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0475EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0475QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0476EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0476QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0477EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0480EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0482EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0482QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0482GQEEPYKPMDTSVLS924
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0483EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0484EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0486EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0487EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0489EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0807EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0819EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0825EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0825QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0832EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-0834EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1001EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1001QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1003EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1003QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1216EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1446EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1446QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1511EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1515EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1527EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1527QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1531EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1534EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1534QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1601EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1601QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1602EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1602QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1602GQEEPYKPMDTSVLS924
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1603EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1603QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1604EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1604QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1605EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1605QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1607EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1607QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1608EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1608QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1609EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1609QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1610EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1610QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1611EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1611QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1611GQEEPYKPMDTSVLS924
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1612EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1612QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1612GQEEPYKPMDTSVLS924
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1614EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1614QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1614GQEEPYKPMDTSVLS924
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1616EEPYKPMDTSVLSEE1126
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1616QEEPYKPMDTSVLSE1025
URM1-TP53BP1chr9131140385chr1543762264126DRB1-1616GQEEPYKPMDTSVLS924

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Fusion breakpoint peptide structures of URM1-TP53BP1

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
9485TLPGQEEPYKPMDTURM1TP53BP1chr9131140385chr1543762264126

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of URM1-TP53BP1

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-B14:023BVN9485TLPGQEEPYKPMDT-7.63753-7.75093
HLA-B14:023BVN9485TLPGQEEPYKPMDT-4.36349-5.39879
HLA-B52:013W399485TLPGQEEPYKPMDT-6.74822-6.86162
HLA-B52:013W399485TLPGQEEPYKPMDT-4.96916-6.00446
HLA-A24:025HGA9485TLPGQEEPYKPMDT-8.26666-9.30196
HLA-A24:025HGA9485TLPGQEEPYKPMDT-7.6208-7.7342
HLA-B27:036PZ59485TLPGQEEPYKPMDT0.0420189-0.993281
HLA-B44:053DX89485TLPGQEEPYKPMDT-5.06122-5.17462
HLA-B44:053DX89485TLPGQEEPYKPMDT-4.87073-5.90603

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Vaccine Design for the FusionNeoAntigens of URM1-TP53BP1

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
URM1-TP53BP1chr9131140385chr15437622641222EPYKPMDTSVCCTATAAGCCAATGGACACGTCAGTGTTAT
URM1-TP53BP1chr9131140385chr15437622641223EPYKPMDTSVLCCTATAAGCCAATGGACACGTCAGTGTTATCTG
URM1-TP53BP1chr9131140385chr1543762264314HRVTLPGQEEPGAGTCACTTTGCCTGGACAGGAGGAACCCTATA
URM1-TP53BP1chr9131140385chr1543762264515VTLPGQEEPYCTTTGCCTGGACAGGAGGAACCCTATAAGC
URM1-TP53BP1chr9131140385chr1543762264516VTLPGQEEPYKCTTTGCCTGGACAGGAGGAACCCTATAAGCCAA
URM1-TP53BP1chr9131140385chr1543762264615TLPGQEEPYTGCCTGGACAGGAGGAACCCTATAAGC
URM1-TP53BP1chr9131140385chr1543762264715LPGQEEPYCTGGACAGGAGGAACCCTATAAGC
URM1-TP53BP1chr9131140385chr1543762264918GQEEPYKPMAGGAGGAACCCTATAAGCCAATGGACA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
URM1-TP53BP1chr9131140385chr15437622641025QEEPYKPMDTSVLSEAGGAACCCTATAAGCCAATGGACACGTCAGTGTTATCTGAAGAAG
URM1-TP53BP1chr9131140385chr15437622641126EEPYKPMDTSVLSEEAACCCTATAAGCCAATGGACACGTCAGTGTTATCTGAAGAAGGAG
URM1-TP53BP1chr9131140385chr1543762264924GQEEPYKPMDTSVLSAGGAGGAACCCTATAAGCCAATGGACACGTCAGTGTTATCTGAAG

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Information of the samples that have these potential fusion neoantigens of URM1-TP53BP1

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
STADURM1-TP53BP1chr9131140385ENST00000372850chr1543762264ENST00000263801TCGA-BR-8060-01A

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Potential target of CAR-T therapy development for URM1-TP53BP1

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 URM1-TP53BP1

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 URM1-TP53BP1

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
TgeneTP53BP1C0006142Malignant neoplasm of breast1CTD_human
TgeneTP53BP1C0007102Malignant tumor of colon1CTD_human
TgeneTP53BP1C0007131Non-Small Cell Lung Carcinoma1CTD_human
TgeneTP53BP1C0009375Colonic Neoplasms1CTD_human
TgeneTP53BP1C0017636Glioblastoma1CTD_human
TgeneTP53BP1C0024232Lymphatic Metastasis1CTD_human
TgeneTP53BP1C0334588Giant Cell Glioblastoma1CTD_human
TgeneTP53BP1C0678222Breast Carcinoma1CTD_human
TgeneTP53BP1C0919267ovarian neoplasm1CTD_human
TgeneTP53BP1C1140680Malignant neoplasm of ovary1CTD_human
TgeneTP53BP1C1257931Mammary Neoplasms, Human1CTD_human
TgeneTP53BP1C1458155Mammary Neoplasms1CTD_human
TgeneTP53BP1C1621958Glioblastoma Multiforme1CTD_human
TgeneTP53BP1C4704874Mammary Carcinoma, Human1CTD_human