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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:PHLDB1-NR4A1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PHLDB1-NR4A1
FusionPDB ID: 64962
FusionGDB2.0 ID: 64962
HgeneTgene
Gene symbol

PHLDB1

NR4A1

Gene ID

23187

3164

Gene namepleckstrin homology like domain family B member 1nuclear receptor subfamily 4 group A member 1
SynonymsLL5AGFRP1|HMR|N10|NAK-1|NGFIB|NP10|NUR77|TR3
Cytomap

11q23.3

12q13.13

Type of geneprotein-codingprotein-coding
Descriptionpleckstrin homology-like domain family B member 1LL5alphapleckstrin homology-like domain family B member 1 variant 3pleckstrin homology-like domain family B member 1 variant 4protein LL5-alphanuclear receptor subfamily 4 group A member 1ST-59TR3 orphan receptorearly response protein NAK1growth factor-inducible nuclear protein N10hormone receptornerve growth factor IB nuclear receptor variant 1nuclear hormone receptor NUR/77orphan nucle
Modification date2020032020200329
UniProtAcc.

P22736

Main function of 5'-partner protein: FUNCTION: Orphan nuclear receptor. May act concomitantly with NURR1 in regulating the expression of delayed-early genes during liver regeneration. Binds the NGFI-B response element (NBRE) 5'-AAAAGGTCA-3' (By similarity). May inhibit NF-kappa-B transactivation of IL2. Participates in energy homeostasis by sequestrating the kinase STK11 in the nucleus, thereby attenuating cytoplasmic AMPK activation. Plays a role in the vascular response to injury (By similarity). {ECO:0000250, ECO:0000250|UniProtKB:P12813, ECO:0000269|PubMed:15466594, ECO:0000269|PubMed:22983157}.
Ensembl transtripts involved in fusion geneENST idsENST00000356063, ENST00000361417, 
ENST00000524713, ENST00000527898, 
ENST00000534672, 
ENST00000547206, 
ENST00000243050, ENST00000394824, 
ENST00000394825, ENST00000548232, 
ENST00000360284, ENST00000545748, 
ENST00000550082, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score12 X 11 X 8=105615 X 14 X 4=840
# samples 1216
** MAII scorelog2(12/1056*10)=-3.13750352374993
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/840*10)=-2.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PHLDB1 [Title/Abstract] AND NR4A1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PHLDB1 [Title/Abstract] AND NR4A1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PHLDB1(118486926)-NR4A1(52448111), # samples:1
Anticipated loss of major functional domain due to fusion event.PHLDB1-NR4A1 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.
PHLDB1-NR4A1 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.
PHLDB1-NR4A1 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.
PHLDB1-NR4A1 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
TgeneNR4A1

GO:0002042

cell migration involved in sprouting angiogenesis

18059339

TgeneNR4A1

GO:0045944

positive regulation of transcription by RNA polymerase II

22427340



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/chr11:118486926/chr12:52448111)
- 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 PHLDB1 (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 NR4A1 (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)
ENST00000361417PHLDB1chr11118486926+ENST00000360284NR4A1chr1252448111+26707662522564770
ENST00000361417PHLDB1chr11118486926+ENST00000545748NR4A1chr1252448111+31227662522564770
ENST00000361417PHLDB1chr11118486926+ENST00000550082NR4A1chr1252448111+26707662522564770
ENST00000356063PHLDB1chr11118486926+ENST00000360284NR4A1chr1252448111+2337433782231717
ENST00000356063PHLDB1chr11118486926+ENST00000545748NR4A1chr1252448111+2789433782231717
ENST00000356063PHLDB1chr11118486926+ENST00000550082NR4A1chr1252448111+2337433782231717

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
ENST00000361417ENST00000360284PHLDB1chr11118486926+NR4A1chr1252448111+0.029682210.9703178
ENST00000361417ENST00000545748PHLDB1chr11118486926+NR4A1chr1252448111+0.0159781170.98402184
ENST00000361417ENST00000550082PHLDB1chr11118486926+NR4A1chr1252448111+0.029682210.9703178
ENST00000356063ENST00000360284PHLDB1chr11118486926+NR4A1chr1252448111+0.0366539550.963346
ENST00000356063ENST00000545748PHLDB1chr11118486926+NR4A1chr1252448111+0.0186015010.9813985
ENST00000356063ENST00000550082PHLDB1chr11118486926+NR4A1chr1252448111+0.0366539550.963346

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 PHLDB1-NR4A1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PHLDB1chr11118486926NR4A1chr1252448111433118DGLPVRQPTRLTQEMPCIQAQYGTPA
PHLDB1chr11118486926NR4A1chr1252448111766171DGLPVRQPTRLTQEMPCIQAQYGTPA

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Potential FusionNeoAntigen Information of PHLDB1-NR4A1 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.
PHLDB1-NR4A1_118486926_52448111.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)
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B50:02QEMPCIQA0.99970.83021220
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B45:01QEMPCIQA0.99950.98941220
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B41:01QEMPCIQA0.97720.98621220
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B50:01QEMPCIQA0.9040.96771220
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:02QPTRLTQEM0.9990.6129615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:05QPTRLTQEM0.99890.5968615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:01QPTRLTQEM0.94920.8651615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:05QPTRLTQEM0.92650.7915615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:08QPTRLTQEM0.91390.8775615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:03QPTRLTQEM0.90630.8489615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B53:01QPTRLTQEM0.76630.7857615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:02QPTRLTQEM0.60440.9745615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:04QPTRLTQEM0.60440.9745615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B82:01QPTRLTQEM0.36950.7019615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B81:01QPTRLTQEM0.18750.8315615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:03QEMPCIQAQY0.99920.9651222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B47:01QEMPCIQAQY0.99690.68831222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:05QEMPCIQAQY0.99350.56391222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B18:01QEMPCIQAQY0.97330.84621222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:05RQPTRLTQEM0.95040.6229515
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:02RQPTRLTQEM0.93320.7088515
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:03QEMPCIQAQYG0.96770.94441223
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:03TQEMPCIQAQY0.92020.96541122
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B40:06QEMPCIQA0.99970.90551220
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B42:02QPTRLTQEM0.98070.8697615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B42:01QPTRLTQEM0.97460.8629615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B73:01TRLTQEMPC0.95550.776817
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:12QPTRLTQEM0.91530.6569615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:04QPTRLTQEM0.84730.6243615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B56:04QPTRLTQEM0.76680.8289615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B39:10QPTRLTQEM0.62290.983615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:12QPTRLTQEM0.60440.9745615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:09QEMPCIQAQY0.9990.55251222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:04RQPTRLTQEM0.96080.7173515
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:12RQPTRLTQEM0.9430.7776515
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:10QEMPCIQAQY0.90870.68851222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B42:01RQPTRLTQEM0.89670.8178515
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B15:31QEMPCIQAQY0.85650.92141222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-C07:46VRQPTRLTQEM0.99520.9179415
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:09QEMPCIQAQYG0.97160.75421223
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B50:05QEMPCIQA0.9040.96771220
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B50:04QEMPCIQA0.9040.96771220
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:09QPTRLTQEM0.99910.6013615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:22QPTRLTQEM0.9990.6129615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:23QPTRLTQEM0.95060.8969615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:77QPTRLTQEM0.94920.8651615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:30QPTRLTQEM0.93190.8153615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:17QPTRLTQEM0.93190.8153615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:11QPTRLTQEM0.90450.9204615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:13QPTRLTQEM0.89910.8519615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:24QPTRLTQEM0.8550.8378615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B59:01QPTRLTQEM0.79760.8716615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B56:02QPTRLTQEM0.76680.8289615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B08:12QPTRLTQEM0.74660.9364615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B55:04QPTRLTQEM0.72240.7854615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B67:01QPTRLTQEM0.65490.9825615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:22QPTRLTQEM0.64560.7642615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:09QPTRLTQEM0.60440.9745615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:26QPTRLTQEM0.5540.6082615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B53:02QPTRLTQEM0.54590.7075615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B51:05QPTRLTQEM0.42890.5673615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B51:06QPTRLTQEM0.38190.636615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B82:02QPTRLTQEM0.36950.7019615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:43QPTRLTQEM0.19780.9173615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B15:08QPTRLTQEM0.17330.9175615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B15:11QPTRLTQEM0.16690.9226615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B18:07QPTRLTQEM0.10050.8152615
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:13QEMPCIQAQY0.99920.9651222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:07QEMPCIQAQY0.99920.9651222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:26QEMPCIQAQY0.99920.9651222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B18:04QEMPCIQAQY0.97990.85421222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B18:08QEMPCIQAQY0.97930.85621222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B18:07QEMPCIQAQY0.97910.81251222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B18:05QEMPCIQAQY0.97330.84621222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:26RQPTRLTQEM0.97280.5082515
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B15:53QEMPCIQAQY0.96850.8051222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B18:11QEMPCIQAQY0.96830.86681222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B15:12QEMPCIQAQY0.96760.83651222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B18:06QEMPCIQAQY0.96740.85251222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:09RQPTRLTQEM0.93490.6901515
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B07:22RQPTRLTQEM0.93320.7088515
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B18:03QEMPCIQAQY0.91660.83511222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:28QEMPCIQAQY0.87570.94461222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B48:02QEMPCIQAQY0.83920.94041222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B35:20QEMPCIQAQY0.83550.94881222
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B27:06VRQPTRLTQEM0.99980.6208415
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:26QEMPCIQAQYG0.96770.94441223
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:13QEMPCIQAQYG0.96770.94441223
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:07QEMPCIQAQYG0.96770.94441223
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:07TQEMPCIQAQY0.92020.96541122
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:26TQEMPCIQAQY0.92020.96541122
PHLDB1-NR4A1chr11118486926chr1252448111433HLA-B44:13TQEMPCIQAQY0.92020.96541122

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Potential FusionNeoAntigen Information of PHLDB1-NR4A1 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 PHLDB1-NR4A1

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
7485QPTRLTQEMPCIQAPHLDB1NR4A1chr11118486926chr1252448111433

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PHLDB1-NR4A1

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-B14:023BVN7485QPTRLTQEMPCIQA-6.85534-6.96874
HLA-B14:023BVN7485QPTRLTQEMPCIQA-4.27547-5.31077
HLA-B52:013W397485QPTRLTQEMPCIQA-5.43417-5.54757
HLA-B52:013W397485QPTRLTQEMPCIQA-5.12682-6.16212
HLA-A11:014UQ27485QPTRLTQEMPCIQA-8.67447-8.78787
HLA-A11:014UQ27485QPTRLTQEMPCIQA-5.23618-6.27148
HLA-A24:025HGA7485QPTRLTQEMPCIQA-7.29782-7.41122
HLA-A24:025HGA7485QPTRLTQEMPCIQA-4.4495-5.4848
HLA-B27:056PYJ7485QPTRLTQEMPCIQA-0.698164-1.73346
HLA-B44:053DX87485QPTRLTQEMPCIQA-5.39484-6.43014
HLA-B44:053DX87485QPTRLTQEMPCIQA-5.26994-5.38334

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Vaccine Design for the FusionNeoAntigens of PHLDB1-NR4A1

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
PHLDB1-NR4A1chr11118486926chr12524481111122TQEMPCIQAQYCTCAGGAGATGCCCTGTATCCAAGCCCAATATG
PHLDB1-NR4A1chr11118486926chr12524481111220QEMPCIQAAGGAGATGCCCTGTATCCAAGCCC
PHLDB1-NR4A1chr11118486926chr12524481111222QEMPCIQAQYAGGAGATGCCCTGTATCCAAGCCCAATATG
PHLDB1-NR4A1chr11118486926chr12524481111223QEMPCIQAQYGAGGAGATGCCCTGTATCCAAGCCCAATATGGGA
PHLDB1-NR4A1chr11118486926chr1252448111415VRQPTRLTQEMTCCGGCAGCCTACCCGGCTCACTCAGGAGATGC
PHLDB1-NR4A1chr11118486926chr1252448111515RQPTRLTQEMGGCAGCCTACCCGGCTCACTCAGGAGATGC
PHLDB1-NR4A1chr11118486926chr1252448111615QPTRLTQEMAGCCTACCCGGCTCACTCAGGAGATGC
PHLDB1-NR4A1chr11118486926chr1252448111817TRLTQEMPCCCCGGCTCACTCAGGAGATGCCCTGTA

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 PHLDB1-NR4A1

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
STADPHLDB1-NR4A1chr11118486926ENST00000356063chr1252448111ENST00000360284TCGA-D7-A4Z0-01A

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Potential target of CAR-T therapy development for PHLDB1-NR4A1

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 PHLDB1-NR4A1

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 PHLDB1-NR4A1

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