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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:CCDC132-CDH1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CCDC132-CDH1
FusionPDB ID: 13625
FusionGDB2.0 ID: 98460
HgeneTgene
Gene symbol

CCDC132

CDH1

Gene ID

55610

51343

Gene nameVPS50 subunit of EARP/GARPII complexfizzy and cell division cycle 20 related 1
SynonymsCCDC132|VPS54LCDC20C|CDH1|FZR|FZR2|HCDH|HCDH1
Cytomap

7q21.2-q21.3

19p13.3

Type of geneprotein-codingprotein-coding
DescriptionsyndetinEARP/GARPII complex subunit VPS50VPS50, EARP/GARPII complex subunitcoiled-coil domain containing 132coiled-coil domain-containing protein 132fizzy-related protein homologCDC20 homolog 1CDC20-like 1bCDC20-like protein 1cdh1/Hct1 homologfizzy/cell division cycle 20 related 1
Modification date2020031320200313
UniProtAcc.

Q9H159

Main function of 5'-partner protein: FUNCTION: Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types.
Ensembl transtripts involved in fusion geneENST idsENST00000305866, ENST00000317751, 
ENST00000535481, ENST00000541136, 
ENST00000544910, ENST00000251739, 
ENST00000474412, 
ENST00000562836, 
ENST00000261769, ENST00000422392, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score2 X 2 X 2=819 X 20 X 5=1900
# samples 323
** MAII scorelog2(3/8*10)=1.90689059560852log2(23/1900*10)=-3.04629365227394
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CCDC132 [Title/Abstract] AND CDH1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CCDC132 [Title/Abstract] AND CDH1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CCDC132(92940584)-CDH1(68862077), # samples:2
CDH1(68857529)-CCDC132(92952923), # samples:2
Anticipated loss of major functional domain due to fusion event.CCDC132-CDH1 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.
CCDC132-CDH1 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.
CCDC132-CDH1 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.
CCDC132-CDH1 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.
CDH1-CCDC132 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.
CDH1-CCDC132 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
HgeneCCDC132

GO:0032456

endocytic recycling

25799061

TgeneCDH1

GO:0031145

anaphase-promoting complex-dependent catabolic process

18662541|21596315

TgeneCDH1

GO:0072425

signal transduction involved in G2 DNA damage checkpoint

18662541

TgeneCDH1

GO:1904668

positive regulation of ubiquitin protein ligase activity

11459826



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/chr7:92940584/chr16:68862077)
- 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 CCDC132 (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 CDH1 (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)
ENST00000305866CCDC132chr792940584+ENST00000261769CDH1chr1668862076+451719831282467779
ENST00000305866CCDC132chr792940584+ENST00000422392CDH1chr1668862076+250519831282467779
ENST00000541136CCDC132chr792940584+ENST00000261769CDH1chr1668862076+438418502412334697
ENST00000541136CCDC132chr792940584+ENST00000422392CDH1chr1668862076+237218502412334697
ENST00000544910CCDC132chr792940584+ENST00000261769CDH1chr1668862076+451919852202469749
ENST00000544910CCDC132chr792940584+ENST00000422392CDH1chr1668862076+250719852202469749
ENST00000535481CCDC132chr792940584+ENST00000261769CDH1chr1668862076+36381104891588499
ENST00000535481CCDC132chr792940584+ENST00000422392CDH1chr1668862076+16261104891588499
ENST00000317751CCDC132chr792940584+ENST00000261769CDH1chr1668862076+44741940852424779
ENST00000317751CCDC132chr792940584+ENST00000422392CDH1chr1668862076+24621940852424779
ENST00000305866CCDC132chr792940584+ENST00000261769CDH1chr1668862077+451719831282467779
ENST00000305866CCDC132chr792940584+ENST00000422392CDH1chr1668862077+250519831282467779
ENST00000541136CCDC132chr792940584+ENST00000261769CDH1chr1668862077+438418502412334697
ENST00000541136CCDC132chr792940584+ENST00000422392CDH1chr1668862077+237218502412334697
ENST00000544910CCDC132chr792940584+ENST00000261769CDH1chr1668862077+451919852202469749
ENST00000544910CCDC132chr792940584+ENST00000422392CDH1chr1668862077+250719852202469749
ENST00000535481CCDC132chr792940584+ENST00000261769CDH1chr1668862077+36381104891588499
ENST00000535481CCDC132chr792940584+ENST00000422392CDH1chr1668862077+16261104891588499
ENST00000317751CCDC132chr792940584+ENST00000261769CDH1chr1668862077+44741940852424779
ENST00000317751CCDC132chr792940584+ENST00000422392CDH1chr1668862077+24621940852424779

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
ENST00000305866ENST00000261769CCDC132chr792940584+CDH1chr1668862076+0.0005274440.99947256
ENST00000305866ENST00000422392CCDC132chr792940584+CDH1chr1668862076+0.0013695690.9986304
ENST00000541136ENST00000261769CCDC132chr792940584+CDH1chr1668862076+0.0005646810.99943525
ENST00000541136ENST00000422392CCDC132chr792940584+CDH1chr1668862076+0.0010344490.9989655
ENST00000544910ENST00000261769CCDC132chr792940584+CDH1chr1668862076+0.0008498580.99915016
ENST00000544910ENST00000422392CCDC132chr792940584+CDH1chr1668862076+0.0018844380.99811554
ENST00000535481ENST00000261769CCDC132chr792940584+CDH1chr1668862076+0.0005606590.9994393
ENST00000535481ENST00000422392CCDC132chr792940584+CDH1chr1668862076+0.0009372220.99906284
ENST00000317751ENST00000261769CCDC132chr792940584+CDH1chr1668862076+0.0005214990.9994785
ENST00000317751ENST00000422392CCDC132chr792940584+CDH1chr1668862076+0.0013338070.99866617
ENST00000305866ENST00000261769CCDC132chr792940584+CDH1chr1668862077+0.0005274440.99947256
ENST00000305866ENST00000422392CCDC132chr792940584+CDH1chr1668862077+0.0013695690.9986304
ENST00000541136ENST00000261769CCDC132chr792940584+CDH1chr1668862077+0.0005646810.99943525
ENST00000541136ENST00000422392CCDC132chr792940584+CDH1chr1668862077+0.0010344490.9989655
ENST00000544910ENST00000261769CCDC132chr792940584+CDH1chr1668862077+0.0008498580.99915016
ENST00000544910ENST00000422392CCDC132chr792940584+CDH1chr1668862077+0.0018844380.99811554
ENST00000535481ENST00000261769CCDC132chr792940584+CDH1chr1668862077+0.0005606590.9994393
ENST00000535481ENST00000422392CCDC132chr792940584+CDH1chr1668862077+0.0009372220.99906284
ENST00000317751ENST00000261769CCDC132chr792940584+CDH1chr1668862077+0.0005214990.9994785
ENST00000317751ENST00000422392CCDC132chr792940584+CDH1chr1668862077+0.0013338070.99866617

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 CCDC132-CDH1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CCDC132chr792940584CDH1chr16688620761104338ILTNTTLNVIRLVVLILLLLLFLRRR
CCDC132chr792940584CDH1chr16688620761850536ILTNTTLNVIRLVVLILLLLLFLRRR
CCDC132chr792940584CDH1chr16688620761940618ILTNTTLNVIRLVVLILLLLLFLRRR
CCDC132chr792940584CDH1chr16688620761983618ILTNTTLNVIRLVVLILLLLLFLRRR
CCDC132chr792940584CDH1chr16688620761985588ILTNTTLNVIRLVVLILLLLLFLRRR
CCDC132chr792940584CDH1chr16688620771104338ILTNTTLNVIRLVVLILLLLLFLRRR
CCDC132chr792940584CDH1chr16688620771850536ILTNTTLNVIRLVVLILLLLLFLRRR
CCDC132chr792940584CDH1chr16688620771940618ILTNTTLNVIRLVVLILLLLLFLRRR
CCDC132chr792940584CDH1chr16688620771983618ILTNTTLNVIRLVVLILLLLLFLRRR
CCDC132chr792940584CDH1chr16688620771985588ILTNTTLNVIRLVVLILLLLLFLRRR

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Potential FusionNeoAntigen Information of CCDC132-CDH1 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.
CCDC132-CDH1_92940584_68862076.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)
CCDC132-CDH1chr792940584chr16688620761983HLA-B27:05IRLVVLILL0.99970.8154918
CCDC132-CDH1chr792940584chr16688620761983HLA-B27:04IRLVVLILL0.99960.5542918
CCDC132-CDH1chr792940584chr16688620761983HLA-B08:01LNVIRLVVL0.99020.7203615
CCDC132-CDH1chr792940584chr16688620761983HLA-A02:17RLVVLILLL0.88850.50871019
CCDC132-CDH1chr792940584chr16688620761983HLA-B27:14IRLVVLILL0.99970.6719918
CCDC132-CDH1chr792940584chr16688620761983HLA-C07:05IRLVVLILL0.99860.9246918
CCDC132-CDH1chr792940584chr16688620761983HLA-B27:03IRLVVLILL0.98270.8453918
CCDC132-CDH1chr792940584chr16688620761983HLA-B08:12NVIRLVVL0.9870.547715
CCDC132-CDH1chr792940584chr16688620761983HLA-B27:08IRLVVLILL0.99970.615918
CCDC132-CDH1chr792940584chr16688620761983HLA-B27:06IRLVVLILL0.99960.5033918
CCDC132-CDH1chr792940584chr16688620761983HLA-B27:10IRLVVLILL0.99960.7785918
CCDC132-CDH1chr792940584chr16688620761983HLA-B27:09IRLVVLILL0.99890.7311918
CCDC132-CDH1chr792940584chr16688620761983HLA-B08:18LNVIRLVVL0.99020.7203615
CCDC132-CDH1chr792940584chr16688620761983HLA-C06:08IRLVVLILL0.92040.9841918
CCDC132-CDH1chr792940584chr16688620761983HLA-C06:17IRLVVLILL0.37040.9914918
CCDC132-CDH1chr792940584chr16688620761983HLA-C06:02IRLVVLILL0.37040.9914918

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Potential FusionNeoAntigen Information of CCDC132-CDH1 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 CCDC132-CDH1

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
5359LNVIRLVVLILLLLCCDC132CDH1chr792940584chr16688620761983

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CCDC132-CDH1

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-B14:023BVN5359LNVIRLVVLILLLL-7.15543-7.26883
HLA-B14:023BVN5359LNVIRLVVLILLLL-4.77435-5.80965
HLA-B52:013W395359LNVIRLVVLILLLL-6.80875-6.92215
HLA-B52:013W395359LNVIRLVVLILLLL-4.20386-5.23916
HLA-A11:014UQ25359LNVIRLVVLILLLL-7.5194-8.5547
HLA-A11:014UQ25359LNVIRLVVLILLLL-6.9601-7.0735
HLA-A24:025HGA5359LNVIRLVVLILLLL-7.52403-7.63743
HLA-A24:025HGA5359LNVIRLVVLILLLL-5.82433-6.85963
HLA-B27:056PYJ5359LNVIRLVVLILLLL-3.28285-4.31815
HLA-B44:053DX85359LNVIRLVVLILLLL-5.91172-6.94702
HLA-B44:053DX85359LNVIRLVVLILLLL-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of CCDC132-CDH1

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
CCDC132-CDH1chr792940584chr16688620761019RLVVLILLLGACTTGTTGTTCTGATTCTGCTGCTCT
CCDC132-CDH1chr792940584chr1668862076615LNVIRLVVLTGAACGTCATAAGACTTGTTGTTCTGA
CCDC132-CDH1chr792940584chr1668862076715NVIRLVVLACGTCATAAGACTTGTTGTTCTGA
CCDC132-CDH1chr792940584chr1668862076918IRLVVLILLTAAGACTTGTTGTTCTGATTCTGCTGC

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 CCDC132-CDH1

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
BRCACCDC132-CDH1chr792940584ENST00000305866chr1668862076ENST00000261769TCGA-AO-A12E

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Potential target of CAR-T therapy development for CCDC132-CDH1

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 CCDC132-CDH1

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 CCDC132-CDH1

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