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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:PHF1-IVNS1ABP

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PHF1-IVNS1ABP
FusionPDB ID: 64807
FusionGDB2.0 ID: 64807
HgeneTgene
Gene symbol

PHF1

IVNS1ABP

Gene ID

5252

10625

Gene namePHD finger protein 1influenza virus NS1A binding protein
SynonymsMTF2L2|PCL1|PHF2|TDRD19C|hPHF1ARA3|FLARA3|HSPC068|KLHL39|ND1|NS-1|NS1-BP|NS1BP
Cytomap

6p21.32

1q25.3

Type of geneprotein-codingprotein-coding
DescriptionPHD finger protein 1hPCl1polycomb-like 1polycomb-like protein 1testicular tissue protein Li 140tudor domain containing 19Cinfluenza virus NS1A-binding proteinNCX downstream gene 1NS1-binding proteinaryl hydrocarbon receptor-associated 3aryl hydrocarbon receptor-associated protein 3kelch-like family member 39kelch-like protein 39
Modification date2020031320200320
UniProtAcc.

Q9Y6Y0

Main function of 5'-partner protein: FUNCTION: Involved in many cell functions, including pre-mRNA splicing, the aryl hydrocarbon receptor (AHR) pathway, F-actin organization and protein ubiquitination. Plays a role in the dynamic organization of the actin skeleton as a stabilizer of actin filaments by association with F-actin through Kelch repeats (By similarity). Protects cells from cell death induced by actin destabilization (By similarity). Functions as modifier of the AHR/Aryl hydrocarbon receptor pathway increasing the concentration of AHR available to activate transcription (PubMed:16582008). In addition, functions as a negative regulator of BCR(KLHL20) E3 ubiquitin ligase complex to prevent ubiquitin-mediated proteolysis of PML and DAPK1, two tumor suppressors (PubMed:25619834). Inhibits pre-mRNA splicing (in vitro) (PubMed:9696811). {ECO:0000250|UniProtKB:Q920Q8, ECO:0000269|PubMed:16582008, ECO:0000269|PubMed:25619834, ECO:0000269|PubMed:9696811}.; FUNCTION: (Microbial infection) Involved in the alternative splicing of influenza A virus M1 mRNA through interaction with HNRNPK, thereby facilitating the generation of viral M2 protein. {ECO:0000269|PubMed:23825951, ECO:0000269|PubMed:9696811}.
Ensembl transtripts involved in fusion geneENST idsENST00000459809, ENST00000374512, 
ENST00000374516, ENST00000427869, 
ENST00000442136, ENST00000454914, 
ENST00000475137, ENST00000487460, 
ENST00000367498, ENST00000392007, 
ENST00000459929, ENST00000367497, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 3 X 3=2717 X 9 X 9=1377
# samples 318
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(18/1377*10)=-2.93545974780529
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PHF1 [Title/Abstract] AND IVNS1ABP [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PHF1 [Title/Abstract] AND IVNS1ABP [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PHF1(33380199)-IVNS1ABP(185274775), # samples:1
Anticipated loss of major functional domain due to fusion event.PHF1-IVNS1ABP 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.
PHF1-IVNS1ABP 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
HgenePHF1

GO:0006974

cellular response to DNA damage stimulus

23142980



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/chr6:33380199/chr1:185274775)
- 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 PHF1 (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 IVNS1ABP (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)
ENST00000374512PHF1chr633380199+ENST00000367498IVNS1ABPchr1185274775-33494302711701476
ENST00000374516PHF1chr633380199+ENST00000367498IVNS1ABPchr1185274775-33494302711701476

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
ENST00000374512ENST00000367498PHF1chr633380199+IVNS1ABPchr1185274775-0.000304560.9996954
ENST00000374516ENST00000367498PHF1chr633380199+IVNS1ABPchr1185274775-0.000304560.9996954

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 PHF1-IVNS1ABP

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PHF1chr633380199IVNS1ABPchr118527477543053WTDGLLYLGTIKKVQTLYYSADHKLL

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Potential FusionNeoAntigen Information of PHF1-IVNS1ABP 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.
PHF1-IVNS1ABP_33380199_185274775.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)
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:01TIKKVQTLY0.99940.7465918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:25TIKKVQTLY0.99890.7909918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:02TIKKVQTLY0.99550.8446918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:17GTIKKVQTL0.99380.8791817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:16GTIKKVQTL0.98660.7981817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B57:03GTIKKVQTL0.9790.9711817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A30:08GTIKKVQTL0.91110.7344817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B48:01GTIKKVQTL0.82580.6844817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A02:21GTIKKVQTL0.80360.6101817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A32:13GTIKKVQTL0.77660.942817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B13:01GTIKKVQTL0.35480.9709817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A32:13TIKKVQTLY0.30030.7487918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:01GTIKKVQTLY0.9970.7023818
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:17GTIKKVQTLY0.99480.7384818
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B08:01YLGTIKKVQTL0.99780.6441617
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:17GTIKKVQTLYY0.9970.6867819
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A02:22YLGTIKKVQTL0.99110.6833617
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A02:04YLGTIKKVQTL0.96410.719617
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A02:17YLGTIKKVQTL0.95660.5547617
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C15:04GTIKKVQTL0.99980.8995817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C15:06GTIKKVQTL0.99970.933817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C03:07GTIKKVQTL0.99940.971817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C03:19GTIKKVQTL0.99920.9715817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C03:08GTIKKVQTL0.9990.8704817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:21TIKKVQTLY0.99470.7481918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C12:12GTIKKVQTL0.99420.9021817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C12:04GTIKKVQTL0.9930.9924817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C06:03GTIKKVQTL0.99290.9895817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:05TIKKVQTLY0.95780.7758918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C03:14GTIKKVQTL0.94850.9666817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C02:06GTIKKVQTL0.92610.9359817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:04TIKKVQTLY0.89850.7537918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:31TIKKVQTLY0.89750.7811918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C15:04TIKKVQTLY0.81820.734918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C01:30GTIKKVQTL0.72870.9589817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C12:16IKKVQTLYY0.12270.82071019
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:07GTIKKVQTLY0.99760.5046818
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C15:09GTIKKVQTL0.99980.8995817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C15:05GTIKKVQTL0.99950.928817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C15:02GTIKKVQTL0.99950.8659817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:34TIKKVQTLY0.99940.7465918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:33TIKKVQTLY0.99940.7465918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:125TIKKVQTLY0.99940.7465918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:27TIKKVQTLY0.99930.757918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:135TIKKVQTLY0.99930.7927918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:50TIKKVQTLY0.99920.6995918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C03:05GTIKKVQTL0.99890.9033817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:39TIKKVQTLY0.99880.6426918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C03:17GTIKKVQTL0.99870.9664817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:11TIKKVQTLY0.99860.7153918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:08TIKKVQTLY0.99830.7057918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C03:67GTIKKVQTL0.99760.9713817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B35:43TIKKVQTLY0.99740.705918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C03:03GTIKKVQTL0.99710.9812817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:24TIKKVQTLY0.99710.7807918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C03:04GTIKKVQTL0.99710.9812817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:35TIKKVQTLY0.9970.6947918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C06:06GTIKKVQTL0.99690.9891817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C16:02GTIKKVQTL0.99490.9908817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C16:04GTIKKVQTL0.99460.9656817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:53TIKKVQTLY0.99450.7187918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B35:11TIKKVQTLY0.99410.7505918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C12:03GTIKKVQTL0.99370.974817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C16:01GTIKKVQTL0.99260.9709817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B58:06GTIKKVQTL0.99130.8856817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C07:04GTIKKVQTL0.99070.9563817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C07:22GTIKKVQTL0.99040.7266817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C06:02GTIKKVQTL0.99040.9911817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C06:17GTIKKVQTL0.99040.9911817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:12TIKKVQTLY0.98850.6574918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A32:01GTIKKVQTL0.98190.8821817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C03:06GTIKKVQTL0.97130.9805817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:20TIKKVQTLY0.95860.8634918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C12:02GTIKKVQTL0.9470.9736817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B57:02GTIKKVQTL0.9380.9128817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C06:08GTIKKVQTL0.93550.9798817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B35:28TIKKVQTLY0.93080.9039918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C02:02GTIKKVQTL0.9030.9681817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C02:10GTIKKVQTL0.9030.9681817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B35:20TIKKVQTLY0.89070.9221918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C15:09TIKKVQTLY0.81820.734918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A02:14GTIKKVQTL0.81030.5165817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A02:06GTIKKVQTL0.80360.6101817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A25:01TIKKVQTLY0.8010.597918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C17:01GTIKKVQTL0.79930.8975817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C12:02TIKKVQTLY0.72140.8583918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C07:17IKKVQTLYY0.7070.79751019
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:73GTIKKVQTL0.6970.9128817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:30GTIKKVQTL0.68660.8959817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A25:01GTIKKVQTL0.6410.8374817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B07:13GTIKKVQTL0.3110.8629817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:53IKKVQTLYY0.24480.53541019
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B40:21GTIKKVQTL0.22190.5824817
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C02:10TIKKVQTLY0.16930.8828918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C02:02TIKKVQTLY0.16930.8828918
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B48:02IKKVQTLYY0.12190.63611019
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C06:17LYLGTIKKV0.11640.9929514
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C06:02LYLGTIKKV0.11640.9929514
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C06:08LYLGTIKKV0.01130.9822514
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-C06:06LYLGTIKKV0.0040.9817514
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:135TIKKVQTLYY0.99960.7168919
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:35TIKKVQTLYY0.99920.5572919
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B57:04GTIKKVQTLY0.99860.6417818
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-A02:03LLYLGTIKKV0.99780.6347414
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:34GTIKKVQTLY0.9970.7023818
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:33GTIKKVQTLY0.9970.7023818
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:125GTIKKVQTLY0.9970.7023818
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:35GTIKKVQTLY0.99650.683818
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:135GTIKKVQTLY0.99640.771818
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B15:50GTIKKVQTLY0.99590.7321818
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B08:18YLGTIKKVQTL0.99780.6441617
PHF1-IVNS1ABPchr633380199chr1185274775430HLA-B08:12YLGTIKKVQTL0.85720.7814617

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Potential FusionNeoAntigen Information of PHF1-IVNS1ABP 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.
PHF1-IVNS1ABP_33380199_185274775.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)
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1201LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1201YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1201GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1201LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1203LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1203YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1203GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1203LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1204LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1204YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1204GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1205LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1205YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1205GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1205LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1206LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1206YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1206GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1206LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1207LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1207YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1207GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1207LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1208LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1208GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1208YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1208LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1209LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1209YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1209GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1210LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1210YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1210GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1210LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1211LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1211GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1211YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1211LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1212LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1212GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1212YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1212LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1213LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1213GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1213YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1213LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1214LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1214YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1214GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1214LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1215LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1215GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1215YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1215LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1216LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1217LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1217YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1217GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1217LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1218LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1218GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1218YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1218LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1219LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1219GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1219YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1220LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1220GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1221LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1221GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1221YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1222LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1222YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1223LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1223GTIKKVQTLYYSADH823
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1223YLGTIKKVQTLYYSA621
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1223LYLGTIKKVQTLYYS520
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1377LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1431LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB1-1452LGTIKKVQTLYYSAD722
PHF1-IVNS1ABPchr633380199chr1185274775430DRB5-0101TDGLLYLGTIKKVQT116
PHF1-IVNS1ABPchr633380199chr1185274775430DRB5-0102TDGLLYLGTIKKVQT116
PHF1-IVNS1ABPchr633380199chr1185274775430DRB5-0102WTDGLLYLGTIKKVQ015
PHF1-IVNS1ABPchr633380199chr1185274775430DRB5-0105TDGLLYLGTIKKVQT116
PHF1-IVNS1ABPchr633380199chr1185274775430DRB5-0108NTDGLLYLGTIKKVQT116
PHF1-IVNS1ABPchr633380199chr1185274775430DRB5-0108NWTDGLLYLGTIKKVQ015
PHF1-IVNS1ABPchr633380199chr1185274775430DRB5-0113TDGLLYLGTIKKVQT116
PHF1-IVNS1ABPchr633380199chr1185274775430DRB5-0114TDGLLYLGTIKKVQT116
PHF1-IVNS1ABPchr633380199chr1185274775430DRB5-0205TDGLLYLGTIKKVQT116
PHF1-IVNS1ABPchr633380199chr1185274775430DRB5-0205WTDGLLYLGTIKKVQ015

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Fusion breakpoint peptide structures of PHF1-IVNS1ABP

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
10711YLGTIKKVQTLYYSPHF1IVNS1ABPchr633380199chr1185274775430

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PHF1-IVNS1ABP

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-B14:023BVN10711YLGTIKKVQTLYYS-4.62424-5.65954
HLA-B14:023BVN10711YLGTIKKVQTLYYS-4.1114-4.2248
HLA-B52:013W3910711YLGTIKKVQTLYYS-6.8001-6.9135
HLA-B52:013W3910711YLGTIKKVQTLYYS-6.46104-7.49634
HLA-A24:025HGA10711YLGTIKKVQTLYYS-9.1447-9.2581
HLA-A24:025HGA10711YLGTIKKVQTLYYS-6.01279-7.04809
HLA-B44:053DX810711YLGTIKKVQTLYYS-5.02862-5.14202
HLA-B44:053DX810711YLGTIKKVQTLYYS-4.60714-5.64244

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Vaccine Design for the FusionNeoAntigens of PHF1-IVNS1ABP

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
PHF1-IVNS1ABPchr633380199chr11852747751019IKKVQTLYYATCAAAAAGGTTCAAACCTTGTACTAC
PHF1-IVNS1ABPchr633380199chr1185274775414LLYLGTIKKVCTGCTATACTTGGGTACCATCAAAAAGGTT
PHF1-IVNS1ABPchr633380199chr1185274775514LYLGTIKKVCTATACTTGGGTACCATCAAAAAGGTT
PHF1-IVNS1ABPchr633380199chr1185274775617YLGTIKKVQTLTACTTGGGTACCATCAAAAAGGTTCAAACCTTG
PHF1-IVNS1ABPchr633380199chr1185274775817GTIKKVQTLGGTACCATCAAAAAGGTTCAAACCTTG
PHF1-IVNS1ABPchr633380199chr1185274775818GTIKKVQTLYGGTACCATCAAAAAGGTTCAAACCTTGTAC
PHF1-IVNS1ABPchr633380199chr1185274775819GTIKKVQTLYYGGTACCATCAAAAAGGTTCAAACCTTGTACTAC
PHF1-IVNS1ABPchr633380199chr1185274775918TIKKVQTLYACCATCAAAAAGGTTCAAACCTTGTAC
PHF1-IVNS1ABPchr633380199chr1185274775919TIKKVQTLYYACCATCAAAAAGGTTCAAACCTTGTACTAC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PHF1-IVNS1ABPchr633380199chr1185274775015WTDGLLYLGTIKKVQTGGACTGATGGGCTGCTATACTTGGGTACCATCAAAAAGGTTCAA
PHF1-IVNS1ABPchr633380199chr1185274775116TDGLLYLGTIKKVQTACTGATGGGCTGCTATACTTGGGTACCATCAAAAAGGTTCAAACC
PHF1-IVNS1ABPchr633380199chr1185274775520LYLGTIKKVQTLYYSCTATACTTGGGTACCATCAAAAAGGTTCAAACCTTGTACTACTCA
PHF1-IVNS1ABPchr633380199chr1185274775621YLGTIKKVQTLYYSATACTTGGGTACCATCAAAAAGGTTCAAACCTTGTACTACTCAGCT
PHF1-IVNS1ABPchr633380199chr1185274775722LGTIKKVQTLYYSADTTGGGTACCATCAAAAAGGTTCAAACCTTGTACTACTCAGCTGAT
PHF1-IVNS1ABPchr633380199chr1185274775823GTIKKVQTLYYSADHGGTACCATCAAAAAGGTTCAAACCTTGTACTACTCAGCTGATCAC

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Information of the samples that have these potential fusion neoantigens of PHF1-IVNS1ABP

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
LGGPHF1-IVNS1ABPchr633380199ENST00000374512chr1185274775ENST00000367498TCGA-DU-5853

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Potential target of CAR-T therapy development for PHF1-IVNS1ABP

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 PHF1-IVNS1ABP

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 PHF1-IVNS1ABP

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