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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:ZNF91-ASF1B

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ZNF91-ASF1B
FusionPDB ID: 103099
FusionGDB2.0 ID: 103099
HgeneTgene
Gene symbol

ZNF91

ASF1B

Gene ID

7644

55723

Gene namezinc finger protein 91anti-silencing function 1B histone chaperone
SynonymsHPF7|HTF10CIA-II
Cytomap

19p12

19p13.12

Type of geneprotein-codingprotein-coding
Descriptionzinc finger protein 91zinc finger protein 91 (HPF7, HTF10)zinc finger protein HPF7zinc finger protein HTF10histone chaperone ASF1BASF1 anti-silencing function 1 homolog BCCG1-interacting factor A-IIanti-silencing function protein 1 homolog BhAsf1hAsf1bhCIA-II
Modification date2020031320200313
UniProtAcc.

Q9NVP2

Main function of 5'-partner protein: FUNCTION: Histone chaperone that facilitates histone deposition and histone exchange and removal during nucleosome assembly and disassembly. Cooperates with chromatin assembly factor 1 (CAF-1) to promote replication-dependent chromatin assembly. Does not participate in replication-independent nucleosome deposition which is mediated by ASF1A and HIRA. Required for spermatogenesis. {ECO:0000269|PubMed:11897662, ECO:0000269|PubMed:12842904, ECO:0000269|PubMed:14718166, ECO:0000269|PubMed:15664198, ECO:0000269|PubMed:16151251}.
Ensembl transtripts involved in fusion geneENST idsENST00000300619, ENST00000397082, 
ENST00000599743, ENST00000596528, 
ENST00000474890, ENST00000592798, 
ENST00000263382, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 8 X 7=6167 X 5 X 6=210
# samples 118
** MAII scorelog2(11/616*10)=-2.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/210*10)=-1.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ZNF91 [Title/Abstract] AND ASF1B [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ZNF91 [Title/Abstract] AND ASF1B [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ZNF91(23578127)-ASF1B(14232520), # samples:3
Anticipated loss of major functional domain due to fusion event.ZNF91-ASF1B 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.
ZNF91-ASF1B 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
HgeneZNF91

GO:0045892

negative regulation of transcription, DNA-templated

25274305

HgeneZNF91

GO:0070895

negative regulation of transposon integration

25274305

TgeneASF1B

GO:0006335

DNA replication-dependent nucleosome assembly

14718166

TgeneASF1B

GO:0006336

DNA replication-independent nucleosome assembly

14718166



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/chr19:23578127/chr19:14232520)
- 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 ZNF91 (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 ASF1B (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)
ENST00000599743ZNF91chr1923578127-ENST00000263382ASF1Bchr1914232520-146713325516163
ENST00000300619ZNF91chr1923578127-ENST00000263382ASF1Bchr1914232520-157023620619199
ENST00000397082ZNF91chr1923578127-ENST00000263382ASF1Bchr1914232520-145612214505163

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
ENST00000599743ENST00000263382ZNF91chr1923578127-ASF1Bchr1914232520-0.0176305340.9823695
ENST00000300619ENST00000263382ZNF91chr1923578127-ASF1Bchr1914232520-0.0133168010.9866832
ENST00000397082ENST00000263382ZNF91chr1923578127-ASF1Bchr1914232520-0.01884890.98115104

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 ZNF91-ASF1B

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ZNF91chr1923578127ASF1Bchr191423252012236TAKMPGTPGSLEMADAPNPSLIPETD
ZNF91chr1923578127ASF1Bchr191423252013336TAKMPGTPGSLEMADAPNPSLIPETD
ZNF91chr1923578127ASF1Bchr191423252023672TAKMPGTPGSLEMADAPNPSLIPETD

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Potential FusionNeoAntigen Information of ZNF91-ASF1B 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.
ZNF91-ASF1B_23578127_14232520.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)
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:03MADAPNPSL0.99460.92821221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B15:10MADAPNPSL0.99110.52461221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:04MADAPNPSL0.98350.96841221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:02MADAPNPSL0.98350.96841221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:08MADAPNPSL0.98270.92411221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B15:37MADAPNPSL0.97750.53411221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:01MADAPNPSL0.97010.93721221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:01MADAPNPSL0.96130.93611221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B45:01LEMADAPNP0.93430.91211019
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-A02:21MADAPNPSL0.92880.66011221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:13MADAPNPSL0.92740.93391221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:05MADAPNPSL0.90170.6761221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-A02:35MADAPNPSL0.87750.5461221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B50:02LEMADAPNP0.76250.74971019
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B50:01LEMADAPNP0.40150.7771019
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B41:01LEMADAPNP0.28110.92591019
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:04EMADAPNPSL0.77430.91281121
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:02EMADAPNPSL0.77430.91281121
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:13LEMADAPNPSL0.99750.94641021
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:15MADAPNPSL10.95361221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C04:07MADAPNPSL10.76131221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C05:09MADAPNPSL10.93761221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C04:10MADAPNPSL10.7391221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C01:17MADAPNPSL0.99990.95391221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:07MADAPNPSL0.99980.97621221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:19MADAPNPSL0.99980.98361221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:08MADAPNPSL0.99970.87821221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C15:06MADAPNPSL0.99970.92141221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C15:04MADAPNPSL0.99960.8991221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C04:06MADAPNPSL0.99950.83611221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C01:30MADAPNPSL0.99930.94111221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:04MADAPNPSL0.99910.94581221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:13MADAPNPSL0.99910.94581221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:03MADAPNPSL0.99740.97121221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C04:14MADAPNPSL0.99350.80541221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:14MADAPNPSL0.99180.97571221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:08MADAPNPSL0.98980.83391221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:09MADAPNPSL0.98540.61221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:12MADAPNPSL0.98350.96841221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C07:13MADAPNPSL0.97940.88861221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C02:06MADAPNPSL0.97240.95221221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:10MADAPNPSL0.96720.931221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C06:03MADAPNPSL0.96410.9881221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B14:03MADAPNPSL0.96090.76241221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C07:29MADAPNPSL0.95630.92871221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B15:21MADAPNPSL0.94890.92751221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-A02:07MADAPNPSL0.93450.54521221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C12:12MADAPNPSL0.91620.94891221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:05MADAPNPSL0.9030.93111221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B78:01MADAPNPSL0.88380.50791221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B51:07MADAPNPSL0.87840.74161221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B07:12MADAPNPSL0.79910.53481221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B42:02MADAPNPSL0.38650.57631221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B42:01MADAPNPSL0.36340.56871221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C05:09MADAPNPSLI10.90441222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:15MADAPNPSLI0.99990.94351222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C05:09EMADAPNPSL0.99970.91531121
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:15EMADAPNPSL0.99940.95481121
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C04:06MADAPNPSLI0.99790.81751222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:13MADAPNPSLI0.98460.93271222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:04MADAPNPSLI0.98460.93271222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:03MADAPNPSLI0.85720.96851222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:12EMADAPNPSL0.77430.91281121
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:15LEMADAPNPSL10.97181021
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C05:09LEMADAPNPSL10.94241021
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:03LEMADAPNPSL0.99980.97531021
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:08LEMADAPNPSL0.99910.90661021
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C04:03MADAPNPSL10.81991221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C18:01MADAPNPSL10.7791221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:02MADAPNPSL10.95361221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C05:01MADAPNPSL10.93761221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C04:01MADAPNPSL10.76131221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C01:03MADAPNPSL0.99990.91841221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C01:02MADAPNPSL0.99990.95211221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:03MADAPNPSL0.99980.9871221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:04MADAPNPSL0.99980.9871221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C06:06MADAPNPSL0.99980.98461221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:67MADAPNPSL0.99970.97841221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C15:05MADAPNPSL0.99960.87891221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C15:09MADAPNPSL0.99960.8991221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:05MADAPNPSL0.99950.91051221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C15:02MADAPNPSL0.99950.86041221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:17MADAPNPSL0.99940.97391221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C04:04MADAPNPSL0.99930.82391221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:06MADAPNPSL0.99910.98991221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:02MADAPNPSL0.99880.97071221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:01MADAPNPSL0.99740.97121221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:13MADAPNPSL0.9950.93051221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C16:01MADAPNPSL0.99290.97731221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C16:02MADAPNPSL0.98990.98941221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C16:04MADAPNPSL0.98860.97981221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:11MADAPNPSL0.98540.83321221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:09MADAPNPSL0.98350.96841221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:02MADAPNPSL0.97080.93271221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B67:01MADAPNPSL0.97080.821221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:77MADAPNPSL0.97010.93721221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B39:31MADAPNPSL0.96790.93741221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:23MADAPNPSL0.96790.93431221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C07:04MADAPNPSL0.96230.90891221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:11MADAPNPSL0.95740.9281221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C17:01MADAPNPSL0.95470.93561221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B15:09MADAPNPSL0.94250.77171221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-A02:14MADAPNPSL0.9340.56421221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C12:03MADAPNPSL0.93320.97121221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C02:10MADAPNPSL0.9290.96561221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C02:02MADAPNPSL0.9290.96561221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-A02:06MADAPNPSL0.92880.66011221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:17MADAPNPSL0.90020.85241221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:30MADAPNPSL0.90020.85241221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B78:02MADAPNPSL0.8960.62291221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B07:13MADAPNPSL0.86090.81741221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B57:02MADAPNPSL0.85430.88611221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C12:02MADAPNPSL0.85320.95781221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-A69:01MADAPNPSL0.80220.68121221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:24MADAPNPSL0.78670.91971221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B08:12MADAPNPSL0.59010.77841221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B50:04LEMADAPNP0.40150.7771019
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B50:05LEMADAPNP0.40150.7771019
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B15:30MADAPNPSL0.39210.89231221
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C04:03MADAPNPSLI10.78241222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C05:01MADAPNPSLI10.90441222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:02MADAPNPSLI0.99990.94351222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C05:01EMADAPNPSL0.99970.91531121
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:02EMADAPNPSL0.99940.95481121
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C03:06MADAPNPSLI0.98820.98961222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:01MADAPNPSLI0.85720.96851222
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-A69:01EMADAPNPSL0.83230.53951121
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B35:09EMADAPNPSL0.77430.91281121
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C05:01LEMADAPNPSL10.94241021
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:02LEMADAPNPSL10.97181021
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B40:04LEMADAPNPSL0.99990.77791021
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-C08:01LEMADAPNPSL0.99980.97531021
ZNF91-ASF1Bchr1923578127chr1914232520236HLA-B41:03LEMADAPNPSL0.99750.75781021

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Potential FusionNeoAntigen Information of ZNF91-ASF1B 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 ZNF91-ASF1B

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
9539TPGSLEMADAPNPSZNF91ASF1Bchr1923578127chr1914232520236

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ZNF91-ASF1B

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-B14:023BVN9539TPGSLEMADAPNPS-7.15543-7.26883
HLA-B14:023BVN9539TPGSLEMADAPNPS-4.77435-5.80965
HLA-B52:013W399539TPGSLEMADAPNPS-6.80875-6.92215
HLA-B52:013W399539TPGSLEMADAPNPS-4.20386-5.23916
HLA-A11:014UQ29539TPGSLEMADAPNPS-7.5194-8.5547
HLA-A11:014UQ29539TPGSLEMADAPNPS-6.9601-7.0735
HLA-A24:025HGA9539TPGSLEMADAPNPS-7.52403-7.63743
HLA-A24:025HGA9539TPGSLEMADAPNPS-5.82433-6.85963
HLA-B27:056PYJ9539TPGSLEMADAPNPS-3.28285-4.31815
HLA-B44:053DX89539TPGSLEMADAPNPS-5.91172-6.94702
HLA-B44:053DX89539TPGSLEMADAPNPS-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of ZNF91-ASF1B

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
ZNF91-ASF1Bchr1923578127chr19142325201019LEMADAPNPCTAGAAATGGCCGACGCCCCCAACCCA
ZNF91-ASF1Bchr1923578127chr19142325201021LEMADAPNPSLCTAGAAATGGCCGACGCCCCCAACCCATCCCTC
ZNF91-ASF1Bchr1923578127chr19142325201121EMADAPNPSLGAAATGGCCGACGCCCCCAACCCATCCCTC
ZNF91-ASF1Bchr1923578127chr19142325201221MADAPNPSLATGGCCGACGCCCCCAACCCATCCCTC
ZNF91-ASF1Bchr1923578127chr19142325201222MADAPNPSLIATGGCCGACGCCCCCAACCCATCCCTCATC

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 ZNF91-ASF1B

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
PCPGZNF91-ASF1Bchr1923578127ENST00000300619chr1914232520ENST00000263382TCGA-S7-A7WP-01A

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Potential target of CAR-T therapy development for ZNF91-ASF1B

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 ZNF91-ASF1B

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 ZNF91-ASF1B

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