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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:WAC-APBB1IP

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: WAC-APBB1IP
FusionPDB ID: 98660
FusionGDB2.0 ID: 98660
HgeneTgene
Gene symbol

WAC

APBB1IP

Gene ID

51322

54518

Gene nameWW domain containing adaptor with coiled-coilamyloid beta precursor protein binding family B member 1 interacting protein
SynonymsBM-016|DESSH|PRO1741|Wwp4INAG1|PREL1|RARP1|RIAM
Cytomap

10p12.1|10p12.1-p11.2

10p12.1

Type of geneprotein-codingprotein-coding
DescriptionWW domain-containing adapter protein with coiled-coilamyloid beta A4 precursor protein-binding family B member 1-interacting proteinAPBB1-interacting protein 1PREL-1RARP-1Rap1-GTP-interacting adaptor moleculeRap1-interacting adaptor moleculeproline rich EVH1 ligand 1proline-rich protein 73rap1-GTP-i
Modification date2020031320200313
UniProtAcc.

Q7Z5R6

Main function of 5'-partner protein: FUNCTION: Appears to function in the signal transduction from Ras activation to actin cytoskeletal remodeling. Suppresses insulin-induced promoter activities through AP1 and SRE. Mediates Rap1-induced adhesion. {ECO:0000269|PubMed:14530287, ECO:0000269|PubMed:15469846}.
Ensembl transtripts involved in fusion geneENST idsENST00000532233, ENST00000347934, 
ENST00000354911, ENST00000375646, 
ENST00000375664, ENST00000428935, 
ENST00000376236, ENST00000356785, 
ENST00000493857, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score17 X 16 X 8=21766 X 9 X 5=270
# samples 227
** MAII scorelog2(22/2176*10)=-3.30610312772568
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/270*10)=-1.94753258010586
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: WAC [Title/Abstract] AND APBB1IP [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: WAC [Title/Abstract] AND APBB1IP [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)WAC(28824686)-APBB1IP(26849034), # samples:2
WAC(28872434)-APBB1IP(26855890), # samples:2
APBB1IP(26727782)-WAC(28897115), # samples:1
Anticipated loss of major functional domain due to fusion event.WAC-APBB1IP 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.
WAC-APBB1IP 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.
WAC-APBB1IP 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.
WAC-APBB1IP 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.
WAC-APBB1IP seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
WAC-APBB1IP seems lost the major protein functional domain in Hgene partner, which is a essential gene 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/chr10:28824686/chr10:26849034)
- 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 WAC (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 APBB1IP (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)
ENST00000375664WACchr1028872434+ENST00000376236APBB1IPchr1026855890+16988554571347296
ENST00000375646WACchr1028872434+ENST00000376236APBB1IPchr1026855890+14075641661056296
ENST00000347934WACchr1028872434+ENST00000376236APBB1IPchr1026855890+14916481711175334
ENST00000354911WACchr1028872434+ENST00000376236APBB1IPchr1026855890+1385542651069334
ENST00000428935WACchr1028872434+ENST00000376236APBB1IPchr1026855890+130946616993325
ENST00000375664WACchr1028872436+ENST00000376236APBB1IPchr1026855885+16988554571347296
ENST00000375646WACchr1028872436+ENST00000376236APBB1IPchr1026855885+14075641661056296
ENST00000347934WACchr1028872436+ENST00000376236APBB1IPchr1026855885+14916481711175334
ENST00000354911WACchr1028872436+ENST00000376236APBB1IPchr1026855885+1385542651069334
ENST00000428935WACchr1028872436+ENST00000376236APBB1IPchr1026855885+130946616993325

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
ENST00000375664ENST00000376236WACchr1028872434+APBB1IPchr1026855890+0.0356805850.9643194
ENST00000375646ENST00000376236WACchr1028872434+APBB1IPchr1026855890+0.0350999240.9649001
ENST00000347934ENST00000376236WACchr1028872434+APBB1IPchr1026855890+0.027655220.97234476
ENST00000354911ENST00000376236WACchr1028872434+APBB1IPchr1026855890+0.0262147240.9737853
ENST00000428935ENST00000376236WACchr1028872434+APBB1IPchr1026855890+0.024362460.97563756
ENST00000375664ENST00000376236WACchr1028872436+APBB1IPchr1026855885+0.0356805850.9643194
ENST00000375646ENST00000376236WACchr1028872436+APBB1IPchr1026855885+0.0350999240.9649001
ENST00000347934ENST00000376236WACchr1028872436+APBB1IPchr1026855885+0.027655220.97234476
ENST00000354911ENST00000376236WACchr1028872436+APBB1IPchr1026855885+0.0262147240.9737853
ENST00000428935ENST00000376236WACchr1028872436+APBB1IPchr1026855885+0.024362460.97563756

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 WAC-APBB1IP

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
WACchr1028872434APBB1IPchr1026855890466150SNPSNNPSKTSDADKKPALGNHHDPA
WACchr1028872434APBB1IPchr1026855890542159SNPSNNPSKTSDADKKPALGNHHDPA
WACchr1028872434APBB1IPchr1026855890564133LIQAITQAKLQMQIRSQPSGTTTTRQ
WACchr1028872434APBB1IPchr1026855890648159SNPSNNPSKTSDADKKPALGNHHDPA
WACchr1028872434APBB1IPchr1026855890855133LIQAITQAKLQMQIRSQPSGTTTTRQ
WACchr1028872436APBB1IPchr1026855885466150SNPSNNPSKTSDADKKPALGNHHDPA
WACchr1028872436APBB1IPchr1026855885542159SNPSNNPSKTSDADKKPALGNHHDPA
WACchr1028872436APBB1IPchr1026855885564133LIQAITQAKLQMQIRSQPSGTTTTRQ
WACchr1028872436APBB1IPchr1026855885648159SNPSNNPSKTSDADKKPALGNHHDPA
WACchr1028872436APBB1IPchr1026855885855133LIQAITQAKLQMQIRSQPSGTTTTRQ

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Potential FusionNeoAntigen Information of WAC-APBB1IP 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.
WAC-APBB1IP_28872434_26855890.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)
WAC-APBB1IPchr1028872434chr1026855890648HLA-B08:09DADKKPAL0.99580.63811119
WAC-APBB1IPchr1028872434chr1026855890564HLA-B48:01TQAKLQMQI0.9440.7096514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B13:02TQAKLQMQI0.80480.8296514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B38:01TQAKLQMQI0.65260.951514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B38:02TQAKLQMQI0.62830.948514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B13:01TQAKLQMQI0.620.9331514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B39:13TQAKLQMQI0.57870.9252514
WAC-APBB1IPchr1028872434chr1026855890564HLA-A32:13TQAKLQMQI0.52460.9298514
WAC-APBB1IPchr1028872434chr1026855890648HLA-B39:13SDADKKPAL0.47240.7771019
WAC-APBB1IPchr1028872434chr1026855890564HLA-B52:01TQAKLQMQI0.24850.9387514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B13:02ITQAKLQMQI0.50380.5084414
WAC-APBB1IPchr1028872434chr1026855890564HLA-B13:02AITQAKLQMQI0.76470.7635314
WAC-APBB1IPchr1028872434chr1026855890648HLA-C08:15DADKKPAL10.92121119
WAC-APBB1IPchr1028872434chr1026855890648HLA-B14:03DADKKPAL0.99960.77871119
WAC-APBB1IPchr1028872434chr1026855890648HLA-B14:03SDADKKPAL0.95870.74551019
WAC-APBB1IPchr1028872434chr1026855890648HLA-B39:08SDADKKPAL0.90250.64911019
WAC-APBB1IPchr1028872434chr1026855890564HLA-B15:04TQAKLQMQI0.83720.8616514
WAC-APBB1IPchr1028872434chr1026855890564HLA-C02:06TQAKLQMQI0.6790.9384514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B39:08TQAKLQMQI0.61880.8981514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B51:07TQAKLQMQI0.21650.7846514
WAC-APBB1IPchr1028872434chr1026855890648HLA-C05:09TSDADKKPAL10.9378919
WAC-APBB1IPchr1028872434chr1026855890648HLA-C08:15TSDADKKPAL0.99990.9415919
WAC-APBB1IPchr1028872434chr1026855890648HLA-C08:02DADKKPAL10.92121119
WAC-APBB1IPchr1028872434chr1026855890564HLA-B15:24TQAKLQMQI0.95290.8136514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B15:73TQAKLQMQI0.8960.9428514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B15:30TQAKLQMQI0.85010.9386514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B39:02TQAKLQMQI0.66260.9274514
WAC-APBB1IPchr1028872434chr1026855890648HLA-B39:02SDADKKPAL0.66120.78111019
WAC-APBB1IPchr1028872434chr1026855890564HLA-B38:05TQAKLQMQI0.65260.951514
WAC-APBB1IPchr1028872434chr1026855890564HLA-B40:21TQAKLQMQI0.52010.595514
WAC-APBB1IPchr1028872434chr1026855890648HLA-C05:01TSDADKKPAL10.9378919
WAC-APBB1IPchr1028872434chr1026855890648HLA-C08:02TSDADKKPAL0.99990.9415919

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Potential FusionNeoAntigen Information of WAC-APBB1IP 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 WAC-APBB1IP

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
6991PSKTSDADKKPALGWACAPBB1IPchr1028872434chr1026855890648
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
7141QAKLQMQIRSQPSGWACAPBB1IPchr1028872434chr1026855890564

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of WAC-APBB1IP

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-B14:023BVN6991PSKTSDADKKPALG-7.15543-7.26883
HLA-B14:023BVN6991PSKTSDADKKPALG-4.77435-5.80965
HLA-B52:013W396991PSKTSDADKKPALG-6.80875-6.92215
HLA-B52:013W396991PSKTSDADKKPALG-4.20386-5.23916
HLA-A11:014UQ26991PSKTSDADKKPALG-7.5194-8.5547
HLA-A11:014UQ26991PSKTSDADKKPALG-6.9601-7.0735
HLA-A24:025HGA6991PSKTSDADKKPALG-7.52403-7.63743
HLA-A24:025HGA6991PSKTSDADKKPALG-5.82433-6.85963
HLA-B27:056PYJ6991PSKTSDADKKPALG-3.28285-4.31815
HLA-B44:053DX86991PSKTSDADKKPALG-5.91172-6.94702
HLA-B44:053DX86991PSKTSDADKKPALG-4.24346-4.35686
HLA-B14:023BVN7141QAKLQMQIRSQPSG-7.9962-8.1096
HLA-B14:023BVN7141QAKLQMQIRSQPSG-5.70842-6.74372
HLA-B52:013W397141QAKLQMQIRSQPSG-6.83737-6.95077
HLA-B52:013W397141QAKLQMQIRSQPSG-4.4836-5.5189
HLA-A11:014UQ27141QAKLQMQIRSQPSG-10.0067-10.1201
HLA-A11:014UQ27141QAKLQMQIRSQPSG-9.03915-10.0745
HLA-A24:025HGA7141QAKLQMQIRSQPSG-6.56204-6.67544
HLA-A24:025HGA7141QAKLQMQIRSQPSG-5.42271-6.45801
HLA-B44:053DX87141QAKLQMQIRSQPSG-7.85648-8.89178
HLA-B44:053DX87141QAKLQMQIRSQPSG-5.3978-5.5112
HLA-A02:016TDR7141QAKLQMQIRSQPSG-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of WAC-APBB1IP

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
WAC-APBB1IPchr1028872434chr10268558901019SDADKKPALTCAGATGCAGATAAGAAGCCAGCCCTC
WAC-APBB1IPchr1028872434chr10268558901119DADKKPALGATGCAGATAAGAAGCCAGCCCTC
WAC-APBB1IPchr1028872434chr1026855890314AITQAKLQMQIAGCAATAACCCAAGCAAAACTTCAGATGCAGAT
WAC-APBB1IPchr1028872434chr1026855890414ITQAKLQMQIAATAACCCAAGCAAAACTTCAGATGCAGAT
WAC-APBB1IPchr1028872434chr1026855890514TQAKLQMQIAACCCAAGCAAAACTTCAGATGCAGAT
WAC-APBB1IPchr1028872434chr1026855890919TSDADKKPALACTTCAGATGCAGATAAGAAGCCAGCCCTC

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 WAC-APBB1IP

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
BRCAWAC-APBB1IPchr1028872434ENST00000347934chr1026855890ENST00000376236TCGA-E9-A1NA-01A
BRCAWAC-APBB1IPchr1028872434ENST00000375646chr1026855890ENST00000376236TCGA-E9-A1NA-01A

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Potential target of CAR-T therapy development for WAC-APBB1IP

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 WAC-APBB1IP

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 WAC-APBB1IP

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