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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:AGPS-PDE11A

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: AGPS-PDE11A
FusionPDB ID: 2984
FusionGDB2.0 ID: 2984
HgeneTgene
Gene symbol

AGPS

PDE11A

Gene ID

8540

50940

Gene namealkylglycerone phosphate synthasephosphodiesterase 11A
SynonymsADAP-S|ADAS|ADHAPS|ADPS|ALDHPSY|RCDP3PPNAD2
Cytomap

2q31.2

2q31.2

Type of geneprotein-codingprotein-coding
Descriptionalkyldihydroxyacetonephosphate synthase, peroxisomalaging-associated gene 5 proteinaging-associated protein 5alkyl-DHAP synthasedual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11AcAMP and cGMP cyclic nucleotide phosphodiesterase 11A
Modification date2020031320200313
UniProtAcc

O00116

Main function of 5'-partner protein: FUNCTION: Catalyzes the exchange of the acyl chain in acyl-dihydroxyacetonephosphate (acyl-DHAP) for a long chain fatty alcohol, yielding the first ether linked intermediate, i.e. alkyl-dihydroxyacetonephosphate (alkyl-DHAP), in the pathway of ether lipid biosynthesis. {ECO:0000269|PubMed:8399344, ECO:0000269|PubMed:9553082}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000264167, ENST00000409888, 
ENST00000497003, ENST00000389683, 
ENST00000409504, ENST00000449286, 
ENST00000450799, ENST00000286063, 
ENST00000358450, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 8 X 7=4488 X 5 X 6=240
# samples 1011
** MAII scorelog2(10/448*10)=-2.16349873228288
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/240*10)=-1.12553088208386
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: AGPS [Title/Abstract] AND PDE11A [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: AGPS [Title/Abstract] AND PDE11A [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)AGPS(178299145)-PDE11A(178576606), # samples:1
Anticipated loss of major functional domain due to fusion event.AGPS-PDE11A 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.
AGPS-PDE11A 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.
AGPS-PDE11A 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.
AGPS-PDE11A 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
HgeneAGPS

GO:0008610

lipid biosynthetic process

9553082



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/chr2:178299145/chr2:178576606)
- 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 AGPS (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 PDE11A (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)
ENST00000264167AGPSchr2178299145-ENST00000286063PDE11Achr2178576606-7501587681345425
ENST00000264167AGPSchr2178299145-ENST00000358450PDE11Achr2178576606-2684587681345425

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
ENST00000264167ENST00000286063AGPSchr2178299145-PDE11Achr2178576606-0.0003906160.9996094
ENST00000264167ENST00000358450AGPSchr2178299145-PDE11Achr2178576606-0.0012241960.9987758

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 AGPS-PDE11A

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
AGPSchr2178299145PDE11Achr2178576606587171QNTLGVNVEHKTTSKTAGFQDILTEV

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Potential FusionNeoAntigen Information of AGPS-PDE11A 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.
AGPS-PDE11A_178299145_178576606.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)
AGPS-PDE11Achr2178299145chr2178576606587HLA-B15:17KTTSKTAGF0.98970.91691019
AGPS-PDE11Achr2178299145chr2178576606587HLA-B58:02KTTSKTAGF0.98930.90571019
AGPS-PDE11Achr2178299145chr2178576606587HLA-B15:16KTTSKTAGF0.98640.80371019
AGPS-PDE11Achr2178299145chr2178576606587HLA-B39:06EHKTTSKTA0.98150.7806817
AGPS-PDE11Achr2178299145chr2178576606587HLA-B57:03KTTSKTAGF0.9640.98071019
AGPS-PDE11Achr2178299145chr2178576606587HLA-B14:02EHKTTSKTA0.91540.6363817
AGPS-PDE11Achr2178299145chr2178576606587HLA-B14:01EHKTTSKTA0.91540.6363817
AGPS-PDE11Achr2178299145chr2178576606587HLA-A32:13KTTSKTAGF0.82240.79311019
AGPS-PDE11Achr2178299145chr2178576606587HLA-B50:02VEHKTTSKT0.70820.5225716
AGPS-PDE11Achr2178299145chr2178576606587HLA-B15:10EHKTTSKTA0.53450.5299817
AGPS-PDE11Achr2178299145chr2178576606587HLA-B41:01VEHKTTSKT0.22470.7781716
AGPS-PDE11Achr2178299145chr2178576606587HLA-B15:37EHKTTSKTA0.19810.5182817
AGPS-PDE11Achr2178299145chr2178576606587HLA-B50:01VEHKTTSKT0.11040.5466716
AGPS-PDE11Achr2178299145chr2178576606587HLA-B45:01VEHKTTSKTA0.95910.81717
AGPS-PDE11Achr2178299145chr2178576606587HLA-B50:02VEHKTTSKTA0.93360.574717
AGPS-PDE11Achr2178299145chr2178576606587HLA-B41:01VEHKTTSKTA0.80660.7988717
AGPS-PDE11Achr2178299145chr2178576606587HLA-B50:01VEHKTTSKTA0.64570.5974717
AGPS-PDE11Achr2178299145chr2178576606587HLA-C15:04KTTSKTAGF0.87970.8581019
AGPS-PDE11Achr2178299145chr2178576606587HLA-B40:06VEHKTTSKTA0.96810.6293717
AGPS-PDE11Achr2178299145chr2178576606587HLA-B57:04KTTSKTAGF0.99360.67811019
AGPS-PDE11Achr2178299145chr2178576606587HLA-B58:06KTTSKTAGF0.99040.6691019
AGPS-PDE11Achr2178299145chr2178576606587HLA-A32:01KTTSKTAGF0.98410.80091019
AGPS-PDE11Achr2178299145chr2178576606587HLA-B57:02KTTSKTAGF0.95810.86081019
AGPS-PDE11Achr2178299145chr2178576606587HLA-C15:09KTTSKTAGF0.87970.8581019
AGPS-PDE11Achr2178299145chr2178576606587HLA-B15:09EHKTTSKTA0.64230.5538817
AGPS-PDE11Achr2178299145chr2178576606587HLA-B50:05VEHKTTSKT0.11040.5466716
AGPS-PDE11Achr2178299145chr2178576606587HLA-B50:04VEHKTTSKT0.11040.5466716
AGPS-PDE11Achr2178299145chr2178576606587HLA-B50:04VEHKTTSKTA0.64570.5974717
AGPS-PDE11Achr2178299145chr2178576606587HLA-B50:05VEHKTTSKTA0.64570.5974717

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Potential FusionNeoAntigen Information of AGPS-PDE11A 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.
AGPS-PDE11A_178299145_178576606.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)
AGPS-PDE11Achr2178299145chr2178576606587DRB1-1421TLGVNVEHKTTSKTA217
AGPS-PDE11Achr2178299145chr2178576606587DRB1-1480TLGVNVEHKTTSKTA217

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Fusion breakpoint peptide structures of AGPS-PDE11A

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
6432NVEHKTTSKTAGFQAGPSPDE11Achr2178299145chr2178576606587

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of AGPS-PDE11A

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-B14:023BVN6432NVEHKTTSKTAGFQ-7.9962-8.1096
HLA-B14:023BVN6432NVEHKTTSKTAGFQ-5.70842-6.74372
HLA-B52:013W396432NVEHKTTSKTAGFQ-6.83737-6.95077
HLA-B52:013W396432NVEHKTTSKTAGFQ-4.4836-5.5189
HLA-A11:014UQ26432NVEHKTTSKTAGFQ-10.0067-10.1201
HLA-A11:014UQ26432NVEHKTTSKTAGFQ-9.03915-10.0745
HLA-A24:025HGA6432NVEHKTTSKTAGFQ-6.56204-6.67544
HLA-A24:025HGA6432NVEHKTTSKTAGFQ-5.42271-6.45801
HLA-B44:053DX86432NVEHKTTSKTAGFQ-7.85648-8.89178
HLA-B44:053DX86432NVEHKTTSKTAGFQ-5.3978-5.5112
HLA-A02:016TDR6432NVEHKTTSKTAGFQ-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of AGPS-PDE11A

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
AGPS-PDE11Achr2178299145chr21785766061019KTTSKTAGFACCTCTAAAACTGCTGGGTTTCAAGAC
AGPS-PDE11Achr2178299145chr2178576606716VEHKTTSKTCATAAAACTACCTCTAAAACTGCTGGG
AGPS-PDE11Achr2178299145chr2178576606717VEHKTTSKTACATAAAACTACCTCTAAAACTGCTGGGTTT
AGPS-PDE11Achr2178299145chr2178576606817EHKTTSKTAAAAACTACCTCTAAAACTGCTGGGTTT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
AGPS-PDE11Achr2178299145chr2178576606217TLGVNVEHKTTSKTAGGAGTAAATGTGGAGCATAAAACTACCTCTAAAACTGCTGGGTTT

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Information of the samples that have these potential fusion neoantigens of AGPS-PDE11A

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
LIHCAGPS-PDE11Achr2178299145ENST00000264167chr2178576606ENST00000286063TCGA-FV-A496-01A

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Potential target of CAR-T therapy development for AGPS-PDE11A

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 AGPS-PDE11A

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 AGPS-PDE11A

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