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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:ATP9A-ZFP64

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ATP9A-ZFP64
FusionPDB ID: 8292
FusionGDB2.0 ID: 8292
HgeneTgene
Gene symbol

ATP9A

ZFP64

Gene ID

10079

55734

Gene nameATPase phospholipid transporting 9A (putative)ZFP64 zinc finger protein
SynonymsATPIIAZNF338
Cytomap

20q13.2

20q13.2

Type of geneprotein-codingprotein-coding
Descriptionprobable phospholipid-transporting ATPase IIAATPase type IV, phospholipid-transporting (P-type),(putative)ATPase, class II, type 9Aphospholipid-transporting ATPase IIAzinc finger protein 64zinc finger protein 338zinc finger protein 64 homolog
Modification date2020031320200327
UniProtAcc

O75110

Main function of 5'-partner protein: FUNCTION: Plays a role in regulating membrane trafficking of cargo proteins, namely endosome to plasma membrane recycling and endosome to trans-Golgi network retrograde transport (PubMed:27733620, PubMed:30213940). In complex with MON2 and DOP1B, regulates SNX3 retromer-mediated endosomal sorting of WLS, a transporter of Wnt morphogens in developing tissues. Participates in the formation of endosomal carriers that direct WLS trafficking back to Golgi, away from lysosomal degradation (PubMed:30213940). Appears to be implicated in intercellular communication by negatively regulating the release of exosomes (PubMed:30947313). The flippase activity towards membrane lipids and its role in membrane asymmetry remains to be proved (PubMed:30947313). {ECO:0000269|PubMed:27733620, ECO:0000269|PubMed:30213940, ECO:0000269|PubMed:30947313}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000311637, ENST00000338821, 
ENST00000402822, ENST00000477492, 
ENST00000371523, ENST00000477786, 
ENST00000216923, ENST00000346617, 
ENST00000371515, ENST00000361387, 
ENST00000371518, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score15 X 13 X 10=19505 X 5 X 3=75
# samples 166
** MAII scorelog2(16/1950*10)=-3.60733031374961
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/75*10)=-0.321928094887362
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ATP9A [Title/Abstract] AND ZFP64 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ATP9A [Title/Abstract] AND ZFP64 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ATP9A(50342358)-ZFP64(50715126), # samples:1
Anticipated loss of major functional domain due to fusion event.ATP9A-ZFP64 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.
ATP9A-ZFP64 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.
ATP9A-ZFP64 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.
ATP9A-ZFP64 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.
ATP9A-ZFP64 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ATP9A-ZFP64 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
ATP9A-ZFP64 seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID


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/chr20:50342358/chr20:50715126)
- 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 ATP9A (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 ZFP64 (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)
ENST00000477492ATP9Achr2050342358-ENST00000371518ZFP64chr2050715126-1405470214954246
ENST00000477492ATP9Achr2050342358-ENST00000361387ZFP64chr2050715126-21914702141644476

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
ENST00000477492ENST00000371518ATP9Achr2050342358-ZFP64chr2050715126-0.0796512140.92034876
ENST00000477492ENST00000361387ATP9Achr2050342358-ZFP64chr2050715126-0.065103660.93489635

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 ATP9A-ZFP64

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ATP9Achr2050342358ZFP64chr205071512647085NETWCTLYLLGSPASELDDDVPKANC

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Potential FusionNeoAntigen Information of ATP9A-ZFP64 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.
ATP9A-ZFP64_50342358_50715126.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)
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:22LLGSPASEL0.98830.5395817
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:13LLGSPASEL0.97140.7542817
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:27LLGSPASEL0.96260.6632817
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:17LLGSPASEL0.86590.5047817
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:38LLGSPASEL0.86170.7354817
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:19LLGSPASEL0.86010.5922817
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:22YLLGSPASEL0.99560.7157717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:60YLLGSPASEL0.99430.6775717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:67YLLGSPASEL0.99420.68717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:30YLLGSPASEL0.99420.68717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:24YLLGSPASEL0.99420.68717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:11YLLGSPASEL0.99390.7077717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:27YLLGSPASEL0.98940.7526717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:16YLLGSPASEL0.98880.5982717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:13YLLGSPASEL0.98850.8353717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:04YLLGSPASEL0.98770.7251717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:17YLLGSPASEL0.98420.6613717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:19YLLGSPASEL0.9640.5973717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:29YLLGSPASEL0.94430.6862717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:38YLLGSPASEL0.92640.8192717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:20YLLGSPASEL0.92240.6908717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:35YLLGSPASEL0.92060.7054717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:02YLLGSPASEL0.99590.5617717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:01YLLGSPASEL0.99420.68717
ATP9A-ZFP64chr2050342358chr2050715126470HLA-B15:73LLGSPASEL0.88580.9648817
ATP9A-ZFP64chr2050342358chr2050715126470HLA-B15:30LLGSPASEL0.76070.927817
ATP9A-ZFP64chr2050342358chr2050715126470HLA-A02:03YLLGSPASEL0.99560.8055717

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Potential FusionNeoAntigen Information of ATP9A-ZFP64 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 ATP9A-ZFP64

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
5835LYLLGSPASELDDDATP9AZFP64chr2050342358chr2050715126470

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ATP9A-ZFP64

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-B14:023BVN5835LYLLGSPASELDDD-6.47228-6.58568
HLA-B14:023BVN5835LYLLGSPASELDDD-5.17277-6.20807
HLA-B52:013W395835LYLLGSPASELDDD-5.78127-6.81657
HLA-B52:013W395835LYLLGSPASELDDD-5.54909-5.66249
HLA-A11:014UQ25835LYLLGSPASELDDD-6.10996-7.14526
HLA-A24:025HGA5835LYLLGSPASELDDD-6.56315-6.67655
HLA-A24:025HGA5835LYLLGSPASELDDD-4.43018-5.46548
HLA-B27:056PYJ5835LYLLGSPASELDDD-6.44184-7.47714
HLA-B27:056PYJ5835LYLLGSPASELDDD-5.32442-5.43782
HLA-B44:053DX85835LYLLGSPASELDDD-6.86074-6.97414
HLA-B44:053DX85835LYLLGSPASELDDD-6.38877-7.42407

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Vaccine Design for the FusionNeoAntigens of ATP9A-ZFP64

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
ATP9A-ZFP64chr2050342358chr2050715126717YLLGSPASELACCTACTGGGTTCCCCTGCTTCAGAACTTG
ATP9A-ZFP64chr2050342358chr2050715126817LLGSPASELTACTGGGTTCCCCTGCTTCAGAACTTG

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 ATP9A-ZFP64

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
UCSATP9A-ZFP64chr2050342358ENST00000477492chr2050715126ENST00000361387TCGA-NF-A5CP-01A

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Potential target of CAR-T therapy development for ATP9A-ZFP64

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
HgeneATP9Achr20:50342358chr20:50715126ENST00000338821-32870_911091048.0TransmembraneHelical
HgeneATP9Achr20:50342358chr20:50715126ENST00000402822-32370_91109927.0TransmembraneHelical

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 ATP9A-ZFP64

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 ATP9A-ZFP64

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