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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:TP53BP1-AP1G1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TP53BP1-AP1G1
FusionPDB ID: 93180
FusionGDB2.0 ID: 93180
HgeneTgene
Gene symbol

TP53BP1

AP1G1

Gene ID

7158

164

Gene nametumor protein p53 binding protein 1adaptor related protein complex 1 subunit gamma 1
Synonyms53BP1|TDRD30|p202|p53BP1ADTG|CLAPG1
Cytomap

15q15.3

16q22.2

Type of geneprotein-codingprotein-coding
DescriptionTP53-binding protein 1p53-binding protein 1tumor protein 53-binding protein, 1tumor suppressor p53-binding protein 1AP-1 complex subunit gamma-1adapter-related protein complex 1 subunit gamma-1adaptor protein complex AP-1 subunit gamma-1adaptor related protein complex 1 gamma 1 subunitclathrin assembly protein complex 1 gamma large chainclathrin assembly protein c
Modification date2020032220200313
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}.

O43747

Main function of 5'-partner protein: FUNCTION: Subunit of clathrin-associated adaptor protein complex 1 that plays a role in protein sorting in the late-Golgi/trans-Golgi network (TGN) and/or endosomes. The AP complexes mediate both the recruitment of clathrin to membranes and the recognition of sorting signals within the cytosolic tails of transmembrane cargo molecules. In association with AFTPH/aftiphilin in the aftiphilin/p200/gamma-synergin complex, involved in the trafficking of transferrin from early to recycling endosomes, and the membrane trafficking of furin and the lysosomal enzyme cathepsin D between the trans-Golgi network (TGN) and endosomes (PubMed:15758025). {ECO:0000269|PubMed:15758025}.
Ensembl transtripts involved in fusion geneENST idsENST00000263801, ENST00000382039, 
ENST00000382044, ENST00000450115, 
ENST00000605155, 
ENST00000564155, 
ENST00000570297, ENST00000299980, 
ENST00000393512, ENST00000423132, 
ENST00000433195, ENST00000569748, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 12 X 7=92412 X 12 X 5=720
# samples 1314
** MAII scorelog2(13/924*10)=-2.8293812283876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/720*10)=-2.36257007938471
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: TP53BP1 [Title/Abstract] AND AP1G1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: TP53BP1 [Title/Abstract] AND AP1G1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TP53BP1(43707791)-AP1G1(71773244), # samples:1
Anticipated loss of major functional domain due to fusion event.TP53BP1-AP1G1 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.
TP53BP1-AP1G1 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.
TP53BP1-AP1G1 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.
TP53BP1-AP1G1 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
HgeneTP53BP1

GO:0006303

double-strand break repair via nonhomologous end joining

23333306|23760478|28241136

HgeneTP53BP1

GO:0006974

cellular response to DNA damage stimulus

17500065|28241136

HgeneTP53BP1

GO:0045830

positive regulation of isotype switching

23345425

HgeneTP53BP1

GO:0051260

protein homooligomerization

23345425

HgeneTP53BP1

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/chr15:43707791/chr16:71773244)
- 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 TP53BP1 (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 AP1G1 (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)
ENST00000263801TP53BP1chr1543707791-ENST00000299980AP1G1chr1671773244-9845532725357961847
ENST00000263801TP53BP1chr1543707791-ENST00000423132AP1G1chr1671773244-7832532725357961847
ENST00000263801TP53BP1chr1543707791-ENST00000433195AP1G1chr1671773244-6972532725357961847
ENST00000263801TP53BP1chr1543707791-ENST00000569748AP1G1chr1671773244-6972532725357961847
ENST00000263801TP53BP1chr1543707791-ENST00000393512AP1G1chr1671773244-6470532725357961847
ENST00000382039TP53BP1chr1543707791-ENST00000299980AP1G1chr1671773244-951950016254701802
ENST00000382039TP53BP1chr1543707791-ENST00000423132AP1G1chr1671773244-750650016254701802
ENST00000382039TP53BP1chr1543707791-ENST00000433195AP1G1chr1671773244-664650016254701802
ENST00000382039TP53BP1chr1543707791-ENST00000569748AP1G1chr1671773244-664650016254701802
ENST00000382039TP53BP1chr1543707791-ENST00000393512AP1G1chr1671773244-614450016254701802
ENST00000382044TP53BP1chr1543707791-ENST00000299980AP1G1chr1671773244-9735521712856861852
ENST00000382044TP53BP1chr1543707791-ENST00000423132AP1G1chr1671773244-7722521712856861852
ENST00000382044TP53BP1chr1543707791-ENST00000433195AP1G1chr1671773244-6862521712856861852
ENST00000382044TP53BP1chr1543707791-ENST00000569748AP1G1chr1671773244-6862521712856861852
ENST00000382044TP53BP1chr1543707791-ENST00000393512AP1G1chr1671773244-6360521712856861852
ENST00000450115TP53BP1chr1543707791-ENST00000299980AP1G1chr1671773244-969151738456421852
ENST00000450115TP53BP1chr1543707791-ENST00000423132AP1G1chr1671773244-767851738456421852
ENST00000450115TP53BP1chr1543707791-ENST00000433195AP1G1chr1671773244-681851738456421852
ENST00000450115TP53BP1chr1543707791-ENST00000569748AP1G1chr1671773244-681851738456421852
ENST00000450115TP53BP1chr1543707791-ENST00000393512AP1G1chr1671773244-631651738456421852

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
ENST00000263801ENST00000299980TP53BP1chr1543707791-AP1G1chr1671773244-0.0003327280.9996673
ENST00000263801ENST00000423132TP53BP1chr1543707791-AP1G1chr1671773244-0.00057380.99942625
ENST00000263801ENST00000433195TP53BP1chr1543707791-AP1G1chr1671773244-0.0008452040.9991548
ENST00000263801ENST00000569748TP53BP1chr1543707791-AP1G1chr1671773244-0.0008452040.9991548
ENST00000263801ENST00000393512TP53BP1chr1543707791-AP1G1chr1671773244-0.0011522810.9988477
ENST00000382039ENST00000299980TP53BP1chr1543707791-AP1G1chr1671773244-0.0003011290.9996989
ENST00000382039ENST00000423132TP53BP1chr1543707791-AP1G1chr1671773244-0.0005699670.99943
ENST00000382039ENST00000433195TP53BP1chr1543707791-AP1G1chr1671773244-0.0008828250.9991172
ENST00000382039ENST00000569748TP53BP1chr1543707791-AP1G1chr1671773244-0.0008828250.9991172
ENST00000382039ENST00000393512TP53BP1chr1543707791-AP1G1chr1671773244-0.0012248530.9987752
ENST00000382044ENST00000299980TP53BP1chr1543707791-AP1G1chr1671773244-0.0003115080.9996885
ENST00000382044ENST00000423132TP53BP1chr1543707791-AP1G1chr1671773244-0.0005713910.9994286
ENST00000382044ENST00000433195TP53BP1chr1543707791-AP1G1chr1671773244-0.000855460.99914455
ENST00000382044ENST00000569748TP53BP1chr1543707791-AP1G1chr1671773244-0.000855460.99914455
ENST00000382044ENST00000393512TP53BP1chr1543707791-AP1G1chr1671773244-0.0011923020.99880767
ENST00000450115ENST00000299980TP53BP1chr1543707791-AP1G1chr1671773244-0.000300760.99969923
ENST00000450115ENST00000423132TP53BP1chr1543707791-AP1G1chr1671773244-0.0005567390.99944323
ENST00000450115ENST00000433195TP53BP1chr1543707791-AP1G1chr1671773244-0.0008482620.9991517
ENST00000450115ENST00000569748TP53BP1chr1543707791-AP1G1chr1671773244-0.0008482620.9991517
ENST00000450115ENST00000393512TP53BP1chr1543707791-AP1G1chr1671773244-0.0011898680.9988102

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 TP53BP1-AP1G1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
TP53BP1chr1543707791AP1G1chr167177324450011646PAKRGRKSATVKPGAPAAAPAPASVP
TP53BP1chr1543707791AP1G1chr167177324451731696PAKRGRKSATVKPGAPAAAPAPASVP
TP53BP1chr1543707791AP1G1chr167177324452171696PAKRGRKSATVKPGAPAAAPAPASVP
TP53BP1chr1543707791AP1G1chr167177324453271691PAKRGRKSATVKPGAPAAAPAPASVP

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Potential FusionNeoAntigen Information of TP53BP1-AP1G1 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.
TP53BP1-AP1G1_43707791_71773244.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)
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B55:01KPGAPAAA0.95390.751119
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B55:01TVKPGAPAA0.96090.6197918
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-A30:08KSATVKPGA0.96020.587615
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-A30:08TVKPGAPAA0.94790.8239918
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B08:09TVKPGAPAA0.9170.7107918
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-A30:08ATVKPGAPA0.80650.7097817
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B56:01TVKPGAPAA0.80140.8101918
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B55:01KPGAPAAAPA0.90270.76921121
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-A30:08ATVKPGAPAA0.87460.8225818
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B56:01KPGAPAAAPA0.84250.8741121
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B54:01TVKPGAPAA0.98570.8647918
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B78:01TVKPGAPAA0.31720.9255918
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-A30:01TVKPGAPAA0.9480.9149918
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B56:05TVKPGAPAA0.75910.8429918
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B78:02TVKPGAPAA0.21550.9272918
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-B55:02KPGAPAAAPA0.88510.89891121
TP53BP1-AP1G1chr1543707791chr16717732445327HLA-A30:01ATVKPGAPAA0.86020.919818

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Potential FusionNeoAntigen Information of TP53BP1-AP1G1 in HLA II

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

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

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Fusion breakpoint peptide structures of TP53BP1-AP1G1

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
4590KSATVKPGAPAAAPTP53BP1AP1G1chr1543707791chr16717732445327

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of TP53BP1-AP1G1

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-B14:023BVN4590KSATVKPGAPAAAP-7.29174-7.40514
HLA-B14:023BVN4590KSATVKPGAPAAAP-4.74919-5.78449
HLA-B52:013W394590KSATVKPGAPAAAP-5.07451-5.18791
HLA-B52:013W394590KSATVKPGAPAAAP-2.86294-3.89824
HLA-A11:014UQ24590KSATVKPGAPAAAP-4.62205-5.65735
HLA-A24:025HGA4590KSATVKPGAPAAAP-11.701-11.8144
HLA-A24:025HGA4590KSATVKPGAPAAAP-4.6967-5.732
HLA-B44:053DX84590KSATVKPGAPAAAP-5.76162-5.87502
HLA-B44:053DX84590KSATVKPGAPAAAP-3.98447-5.01977
HLA-A02:016TDR4590KSATVKPGAPAAAP-2.29826-3.33356

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Vaccine Design for the FusionNeoAntigens of TP53BP1-AP1G1

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
TP53BP1-AP1G1chr1543707791chr16717732441119KPGAPAAAAACCTGGTGCTCCAGCTGCTGCTC
TP53BP1-AP1G1chr1543707791chr16717732441121KPGAPAAAPAAACCTGGTGCTCCAGCTGCTGCTCCTGCCC
TP53BP1-AP1G1chr1543707791chr1671773244615KSATVKPGAAGTCTGCCACAGTAAAACCTGGTGCTC
TP53BP1-AP1G1chr1543707791chr1671773244817ATVKPGAPACCACAGTAAAACCTGGTGCTCCAGCTG
TP53BP1-AP1G1chr1543707791chr1671773244818ATVKPGAPAACCACAGTAAAACCTGGTGCTCCAGCTGCTG
TP53BP1-AP1G1chr1543707791chr1671773244918TVKPGAPAACAGTAAAACCTGGTGCTCCAGCTGCTG

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

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Information of the samples that have these potential fusion neoantigens of TP53BP1-AP1G1

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
THCATP53BP1-AP1G1chr1543707791ENST00000263801chr1671773244ENST00000299980TCGA-DJ-A3V2

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Potential target of CAR-T therapy development for TP53BP1-AP1G1

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 TP53BP1-AP1G1

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 TP53BP1-AP1G1

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
HgeneTP53BP1C0006142Malignant neoplasm of breast1CTD_human
HgeneTP53BP1C0007102Malignant tumor of colon1CTD_human
HgeneTP53BP1C0007131Non-Small Cell Lung Carcinoma1CTD_human
HgeneTP53BP1C0009375Colonic Neoplasms1CTD_human
HgeneTP53BP1C0017636Glioblastoma1CTD_human
HgeneTP53BP1C0024232Lymphatic Metastasis1CTD_human
HgeneTP53BP1C0334588Giant Cell Glioblastoma1CTD_human
HgeneTP53BP1C0678222Breast Carcinoma1CTD_human
HgeneTP53BP1C0919267ovarian neoplasm1CTD_human
HgeneTP53BP1C1140680Malignant neoplasm of ovary1CTD_human
HgeneTP53BP1C1257931Mammary Neoplasms, Human1CTD_human
HgeneTP53BP1C1458155Mammary Neoplasms1CTD_human
HgeneTP53BP1C1621958Glioblastoma Multiforme1CTD_human
HgeneTP53BP1C4704874Mammary Carcinoma, Human1CTD_human