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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:CCDC141-GMPS

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CCDC141-GMPS
FusionPDB ID: 13638
FusionGDB2.0 ID: 13638
HgeneTgene
Gene symbol

CCDC141

GMPS

Gene ID

285025

8833

Gene namecoiled-coil domain containing 141guanine monophosphate synthase
SynonymsCAMDIGATD7
Cytomap

2q31.2

3q25.31

Type of geneprotein-codingprotein-coding
Descriptioncoiled-coil domain-containing protein 141coiled-coil protein associated with myosin II and DISC1GMP synthase [glutamine-hydrolyzing]GMP synthaseGMP synthetaseMLL/GMPS fusion proteinglutamine amidotransferaseguanine monophosphate synthetaseguanosine 5'-monophosphate synthasetesticular tissue protein Li 82
Modification date2020031320200313
UniProtAcc

Q6ZP82

Main function of 5'-partner protein: FUNCTION: Plays a critical role in radial migration and centrosomal function. {ECO:0000250|UniProtKB:A2AST1}.

P49915

Main function of 5'-partner protein: FUNCTION: Involved in the de novo synthesis of guanine nucleotides which are not only essential for DNA and RNA synthesis, but also provide GTP, which is involved in a number of cellular processes important for cell division.
Ensembl transtripts involved in fusion geneENST idsENST00000409284, ENST00000420890, 
ENST00000295723, ENST00000480419, 
ENST00000295920, ENST00000476145, 
ENST00000496455, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 3 X 1=98 X 7 X 6=336
# samples 311
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(11/336*10)=-1.6109577092541
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CCDC141 [Title/Abstract] AND GMPS [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CCDC141 [Title/Abstract] AND GMPS [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CCDC141(179912011)-GMPS(155611305), # samples:1
Anticipated loss of major functional domain due to fusion event.CCDC141-GMPS 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.
CCDC141-GMPS 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.
CCDC141-GMPS 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.
CCDC141-GMPS 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
TgeneGMPS

GO:0006177

GMP biosynthetic process

8089153



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/chr2:179912011/chr3:155611305)
- 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 CCDC141 (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 GMPS (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)
ENST00000420890CCDC141chr2179912011-ENST00000496455GMPSchr3155611305+87323431182397759
ENST00000409284CCDC141chr2179912011-ENST00000496455GMPSchr3155611305+87323431182397759

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
ENST00000420890ENST00000496455CCDC141chr2179912011-GMPSchr3155611305+0.0003603970.99963963
ENST00000409284ENST00000496455CCDC141chr2179912011-GMPSchr3155611305+0.0003603970.99963963

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 CCDC141-GMPS

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CCDC141chr2179912011GMPSchr315561130534373KKLLHDHELLLAKLKLENAGGDLKDG

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Potential FusionNeoAntigen Information of CCDC141-GMPS 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.
CCDC141-GMPS_179912011_155611305.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)
CCDC141-GMPSchr2179912011chr3155611305343HLA-B18:01HELLLAKL0.99810.9533614
CCDC141-GMPSchr2179912011chr3155611305343HLA-B08:01LLLAKLKL0.99810.7503816
CCDC141-GMPSchr2179912011chr3155611305343HLA-B47:01HELLLAKL0.99460.7694614
CCDC141-GMPSchr2179912011chr3155611305343HLA-B39:13HELLLAKL0.91550.9813614
CCDC141-GMPSchr2179912011chr3155611305343HLA-B14:02DHELLLAKL0.99550.5914514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B14:01DHELLLAKL0.99550.5914514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B08:09LAKLKLENA0.99540.86181019
CCDC141-GMPSchr2179912011chr3155611305343HLA-B39:01DHELLLAKL0.9820.9264514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B38:02DHELLLAKL0.98030.9591514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B38:01DHELLLAKL0.97760.9465514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B39:06DHELLLAKL0.91760.7684514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B38:01HDHELLLAKL0.64410.9411414
CCDC141-GMPSchr2179912011chr3155611305343HLA-B38:01LHDHELLLAKL0.99960.9637314
CCDC141-GMPSchr2179912011chr3155611305343HLA-B38:01DHELLLAKLKL0.95940.8947516
CCDC141-GMPSchr2179912011chr3155611305343HLA-B39:09DHELLLAKL0.98640.5956514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B39:05DHELLLAKL0.97570.9096514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B39:12DHELLLAKL0.97510.9315514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B14:03DHELLLAKL0.52410.8022514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B44:10HELLLAKLKL0.80820.6012616
CCDC141-GMPSchr2179912011chr3155611305343HLA-B40:04HELLLAKL0.99960.7577614
CCDC141-GMPSchr2179912011chr3155611305343HLA-B18:06HELLLAKL0.99830.9637614
CCDC141-GMPSchr2179912011chr3155611305343HLA-B18:08HELLLAKL0.99830.9419614
CCDC141-GMPSchr2179912011chr3155611305343HLA-B08:18LLLAKLKL0.99810.7503816
CCDC141-GMPSchr2179912011chr3155611305343HLA-B18:05HELLLAKL0.99810.9533614
CCDC141-GMPSchr2179912011chr3155611305343HLA-B18:03HELLLAKL0.99640.9493614
CCDC141-GMPSchr2179912011chr3155611305343HLA-B18:11HELLLAKL0.98530.9469614
CCDC141-GMPSchr2179912011chr3155611305343HLA-B41:03HELLLAKL0.98040.8106614
CCDC141-GMPSchr2179912011chr3155611305343HLA-B39:31DHELLLAKL0.98230.9266514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B38:05DHELLLAKL0.97760.9465514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B39:11DHELLLAKL0.67730.8474514
CCDC141-GMPSchr2179912011chr3155611305343HLA-B08:12ELLLAKLKL0.57760.9469716
CCDC141-GMPSchr2179912011chr3155611305343HLA-B40:04HELLLAKLKL0.96670.7253616
CCDC141-GMPSchr2179912011chr3155611305343HLA-B38:05HDHELLLAKL0.64410.9411414
CCDC141-GMPSchr2179912011chr3155611305343HLA-B38:05LHDHELLLAKL0.99960.9637314
CCDC141-GMPSchr2179912011chr3155611305343HLA-B38:05DHELLLAKLKL0.95940.8947516

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Potential FusionNeoAntigen Information of CCDC141-GMPS 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 CCDC141-GMPS

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
3303HELLLAKLKLENAGCCDC141GMPSchr2179912011chr3155611305343

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CCDC141-GMPS

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-B14:023BVN3303HELLLAKLKLENAG-7.15543-7.26883
HLA-B14:023BVN3303HELLLAKLKLENAG-4.77435-5.80965
HLA-B52:013W393303HELLLAKLKLENAG-6.80875-6.92215
HLA-B52:013W393303HELLLAKLKLENAG-4.20386-5.23916
HLA-A11:014UQ23303HELLLAKLKLENAG-7.5194-8.5547
HLA-A11:014UQ23303HELLLAKLKLENAG-6.9601-7.0735
HLA-A24:025HGA3303HELLLAKLKLENAG-7.52403-7.63743
HLA-A24:025HGA3303HELLLAKLKLENAG-5.82433-6.85963
HLA-B27:056PYJ3303HELLLAKLKLENAG-3.28285-4.31815
HLA-B44:053DX83303HELLLAKLKLENAG-5.91172-6.94702
HLA-B44:053DX83303HELLLAKLKLENAG-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of CCDC141-GMPS

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
CCDC141-GMPSchr2179912011chr31556113051019LAKLKLENAAAGCTCAAGCTGGAGAATGCTGGAGGA
CCDC141-GMPSchr2179912011chr3155611305314LHDHELLLAKLGATCATGAACTTCTTTTGGCCAAGCTCAAGCTG
CCDC141-GMPSchr2179912011chr3155611305414HDHELLLAKLCATGAACTTCTTTTGGCCAAGCTCAAGCTG
CCDC141-GMPSchr2179912011chr3155611305514DHELLLAKLGAACTTCTTTTGGCCAAGCTCAAGCTG
CCDC141-GMPSchr2179912011chr3155611305516DHELLLAKLKLGAACTTCTTTTGGCCAAGCTCAAGCTGGAGAAT
CCDC141-GMPSchr2179912011chr3155611305614HELLLAKLCTTCTTTTGGCCAAGCTCAAGCTG
CCDC141-GMPSchr2179912011chr3155611305616HELLLAKLKLCTTCTTTTGGCCAAGCTCAAGCTGGAGAAT
CCDC141-GMPSchr2179912011chr3155611305716ELLLAKLKLCTTTTGGCCAAGCTCAAGCTGGAGAAT
CCDC141-GMPSchr2179912011chr3155611305816LLLAKLKLTTGGCCAAGCTCAAGCTGGAGAAT

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 CCDC141-GMPS

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
N/ACCDC141-GMPSchr2179912011ENST00000409284chr3155611305ENST00000496455AU132130

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Potential target of CAR-T therapy development for CCDC141-GMPS

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 CCDC141-GMPS

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 CCDC141-GMPS

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