FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

leaf

Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

leaf

Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

leaf

Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:ANO1-CDC42BPG

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ANO1-CDC42BPG
FusionPDB ID: 4847
FusionGDB2.0 ID: 4847
HgeneTgene
Gene symbol

ANO1

CDC42BPG

Gene ID

55107

55561

Gene nameanoctamin 1CDC42 binding protein kinase gamma
SynonymsDOG1|ORAOV2|TAOS2|TMEM16ADMPK2|HSMDPKIN|KAPPA-200|MRCKG|MRCKgamma
Cytomap

11q13.3

11q13.1

Type of geneprotein-codingprotein-coding
Descriptionanoctamin-1Ca2+-activated Cl- channelanoctamin 1, calcium activated chloride channelcalcium activated chloride channeldiscovered on gastrointestinal stromal tumors protein 1oral cancer overexpressed 2transmembrane protein 16A (eight membrane-spanninserine/threonine-protein kinase MRCK gammaCDC42 binding protein kinase gamma (DMPK-like)DMPK-like gammaMRCK gammamyotonic dystrophy kinase-related CDC42-binding kinase gammamyotonic dystrophy protein kinase like proteinmyotonic dystrophy protein kin
Modification date2020031320200313
UniProtAcc

Q9NW15

Main function of 5'-partner protein: FUNCTION: Does not exhibit calcium-activated chloride channel (CaCC) activity. Can inhibit the activity of ANO1. {ECO:0000269|PubMed:20056604, ECO:0000269|PubMed:22946059}.

Q6DT37

Main function of 5'-partner protein: FUNCTION: May act as a downstream effector of CDC42 in cytoskeletal reorganization. Contributes to the actomyosin contractility required for cell invasion, through the regulation of MYPT1 and thus MLC2 phosphorylation (By similarity). {ECO:0000250|UniProtKB:Q5VT25, ECO:0000269|PubMed:15194684}.
Ensembl transtripts involved in fusion geneENST idsENST00000316296, ENST00000355303, 
ENST00000398543, ENST00000530676, 
ENST00000538023, ENST00000525494, 
ENST00000531349, 
ENST00000491280, 
ENST00000342711, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score20 X 18 X 9=32405 X 5 X 5=125
# samples 205
** MAII scorelog2(20/3240*10)=-4.01792190799726
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/125*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ANO1 [Title/Abstract] AND CDC42BPG [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ANO1 [Title/Abstract] AND CDC42BPG [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ANO1(69951894)-CDC42BPG(64606374), # samples:1
Anticipated loss of major functional domain due to fusion event.ANO1-CDC42BPG 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.
ANO1-CDC42BPG 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.
ANO1-CDC42BPG 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.
ANO1-CDC42BPG 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
HgeneANO1

GO:0006812

cation transport

22946059

TgeneCDC42BPG

GO:0006468

protein phosphorylation

15194684



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/chr11:69951894/chr11:64606374)
- 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 ANO1 (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 CDC42BPG (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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)
ENST00000355303ANO1chr1169951894-ENST00000342711CDC42BPGchr1164606374-5918105222148311536
ENST00000398543ANO1chr1169951894-ENST00000342711CDC42BPGchr1164606374-56627964945751508
ENST00000538023ANO1chr1169951894-ENST00000342711CDC42BPGchr1164606374-56627964945751508
ENST00000316296ANO1chr1169951894-ENST00000342711CDC42BPGchr1164606374-563476810545471480
ENST00000530676ANO1chr1169951894-ENST00000342711CDC42BPGchr1164606374-575488824946671472

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
ENST00000355303ENST00000342711ANO1chr1169951894-CDC42BPGchr1164606374-0.0049332320.99506676
ENST00000398543ENST00000342711ANO1chr1169951894-CDC42BPGchr1164606374-0.0037838110.99621624
ENST00000538023ENST00000342711ANO1chr1169951894-CDC42BPGchr1164606374-0.0037838110.99621624
ENST00000316296ENST00000342711ANO1chr1169951894-CDC42BPGchr1164606374-0.0040742060.9959258
ENST00000530676ENST00000342711ANO1chr1169951894-CDC42BPGchr1164606374-0.005776660.9942233

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

Top

Fusion Protein Breakpoint Sequences for ANO1-CDC42BPG

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ANO1chr1169951894CDC42BPGchr11646063741052277KDSFFDSKTRSTIDHLQFPPDVPDVP
ANO1chr1169951894CDC42BPGchr1164606374768221KDSFFDSKTRSTIDHLQFPPDVPDVP
ANO1chr1169951894CDC42BPGchr1164606374796249KDSFFDSKTRSTIDHLQFPPDVPDVP
ANO1chr1169951894CDC42BPGchr1164606374888213KDSFFDSKTRSTIDHLQFPPDVPDVP

Top

Potential FusionNeoAntigen Information of ANO1-CDC42BPG 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.
ANO1-CDC42BPG_69951894_64606374.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)
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B15:17STIDHLQF0.99820.84751018
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B15:16STIDHLQF0.99710.5741018
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:01RSTIDHLQF0.99770.9918918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B58:01RSTIDHLQF0.99490.9753918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B58:02RSTIDHLQF0.99460.9688918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-A30:08KTRSTIDHL0.99310.5807716
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B15:17RSTIDHLQF0.99110.969918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B15:16RSTIDHLQF0.99060.9485918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B15:17KTRSTIDHL0.98190.8796716
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B15:16KTRSTIDHL0.97770.67716
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:03RSTIDHLQF0.97410.9927918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:03KTRSTIDHL0.94240.9727716
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-A32:13RSTIDHLQF0.81840.9267918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B27:02TRSTIDHLQF10.6634818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B27:05TRSTIDHLQF10.9239818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B27:04TRSTIDHLQF0.99990.8022818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B27:07TRSTIDHLQF0.99970.6249818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:01KTRSTIDHLQF0.99990.9769718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B58:02KTRSTIDHLQF0.99970.8468718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B15:17KTRSTIDHLQF0.99960.8986718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:03KTRSTIDHLQF0.99940.9848718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B15:16KTRSTIDHLQF0.99940.7555718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B58:01KTRSTIDHLQF0.99920.918718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-A30:08KTRSTIDHLQF0.99020.5937718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C15:04STIDHLQF0.99970.80341018
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C03:14STIDHLQF0.99640.94321018
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C15:06KTRSTIDHL0.99050.8747716
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C15:04RSTIDHLQF0.97320.9329918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C03:14RSTIDHLQF0.81490.987918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C07:95TRSTIDHLQF0.99970.7442818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C07:19TRSTIDHLQF0.99930.6882818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B27:03TRSTIDHLQF0.99910.9366818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C07:46TRSTIDHLQF0.99860.8436818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C15:09STIDHLQF0.99970.80341018
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C03:02STIDHLQF0.99970.93821018
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C16:01STIDHLQF0.99710.9651018
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C16:02STIDHLQF0.99580.98631018
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C02:02STIDHLQF0.96190.87231018
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C02:10STIDHLQF0.96190.87231018
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:10RSTIDHLQF0.99770.9918918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:04RSTIDHLQF0.99540.7785918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B58:06RSTIDHLQF0.99330.9114918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-A30:01KTRSTIDHL0.9930.7918716
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C15:02KTRSTIDHL0.99260.8307716
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C15:05KTRSTIDHL0.99050.8456716
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B58:06KTRSTIDHL0.98640.7224716
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:02RSTIDHLQF0.97790.9621918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C15:09RSTIDHLQF0.97320.9329918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-A32:01RSTIDHLQF0.94490.9132918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:02KTRSTIDHL0.92220.7885716
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C16:01RSTIDHLQF0.7170.9845918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C16:02RSTIDHLQF0.58040.9944918
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B27:08TRSTIDHLQF10.822818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B27:10TRSTIDHLQF0.99990.9158818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B27:06TRSTIDHLQF0.99990.8204818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C07:01TRSTIDHLQF0.99980.6518818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B27:09TRSTIDHLQF0.99980.8861818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-C07:22TRSTIDHLQF0.99930.6345818
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:04KTRSTIDHLQF0.99990.6704718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:10KTRSTIDHLQF0.99990.9769718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B58:06KTRSTIDHLQF0.99980.7169718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-B57:02KTRSTIDHLQF0.99940.8877718
ANO1-CDC42BPGchr1169951894chr1164606374768HLA-A32:01KTRSTIDHLQF0.9970.8926718

Top

Potential FusionNeoAntigen Information of ANO1-CDC42BPG 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)

Top

Fusion breakpoint peptide structures of ANO1-CDC42BPG

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
8714SKTRSTIDHLQFPPANO1CDC42BPGchr1169951894chr1164606374768

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ANO1-CDC42BPG

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-B14:023BVN8714SKTRSTIDHLQFPP-7.15543-7.26883
HLA-B14:023BVN8714SKTRSTIDHLQFPP-4.77435-5.80965
HLA-B52:013W398714SKTRSTIDHLQFPP-6.80875-6.92215
HLA-B52:013W398714SKTRSTIDHLQFPP-4.20386-5.23916
HLA-A11:014UQ28714SKTRSTIDHLQFPP-7.5194-8.5547
HLA-A11:014UQ28714SKTRSTIDHLQFPP-6.9601-7.0735
HLA-A24:025HGA8714SKTRSTIDHLQFPP-7.52403-7.63743
HLA-A24:025HGA8714SKTRSTIDHLQFPP-5.82433-6.85963
HLA-B27:056PYJ8714SKTRSTIDHLQFPP-3.28285-4.31815
HLA-B44:053DX88714SKTRSTIDHLQFPP-5.91172-6.94702
HLA-B44:053DX88714SKTRSTIDHLQFPP-4.24346-4.35686

Top

Vaccine Design for the FusionNeoAntigens of ANO1-CDC42BPG

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
ANO1-CDC42BPGchr1169951894chr11646063741018STIDHLQFAGCACGATTGACCACCTGCAGTTC
ANO1-CDC42BPGchr1169951894chr1164606374716KTRSTIDHLAAAACCCGGAGCACGATTGACCACCTG
ANO1-CDC42BPGchr1169951894chr1164606374718KTRSTIDHLQFAAAACCCGGAGCACGATTGACCACCTGCAGTTC
ANO1-CDC42BPGchr1169951894chr1164606374818TRSTIDHLQFACCCGGAGCACGATTGACCACCTGCAGTTC
ANO1-CDC42BPGchr1169951894chr1164606374918RSTIDHLQFCGGAGCACGATTGACCACCTGCAGTTC

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

Top

Information of the samples that have these potential fusion neoantigens of ANO1-CDC42BPG

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
TGCTANO1-CDC42BPGchr1169951894ENST00000316296chr1164606374ENST00000342711TCGA-2G-AAGP-01A

Top

Potential target of CAR-T therapy development for ANO1-CDC42BPG

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

Top

Related Drugs to ANO1-CDC42BPG

check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

Top

Related Diseases to ANO1-CDC42BPG

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