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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:ARPC4-GRM7

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ARPC4-GRM7
FusionPDB ID: 6815
FusionGDB2.0 ID: 6818
HgeneTgene
Gene symbol

ARPC4

GRM7

Gene ID

100526693

2917

Gene nameARPC4-TTLL3 readthroughglutamate metabotropic receptor 7
SynonymsARC20|ARPC4|p20-ARCGLUR7|GPRC1G|MGLU7|MGLUR7|PPP1R87
Cytomap

3p25.3

3p26.1

Type of geneprotein-codingprotein-coding
DescriptionARPC4-TTLL3 fusion proteinARPC4-TTLL3 read-through transcriptActin-related protein 2/3 complex subunit 4Arp2/3 complex 20 kDa subunitmetabotropic glutamate receptor 7glutamate receptor, metabotropic 7protein phosphatase 1, regulatory subunit 87
Modification date2020031320200313
UniProtAcc

P59998

Main function of 5'-partner protein: FUNCTION: Actin-binding component of the Arp2/3 complex, a multiprotein complex that mediates actin polymerization upon stimulation by nucleation-promoting factor (NPF) (PubMed:9230079). The Arp2/3 complex mediates the formation of branched actin networks in the cytoplasm, providing the force for cell motility (PubMed:9230079). In addition to its role in the cytoplasmic cytoskeleton, the Arp2/3 complex also promotes actin polymerization in the nucleus, thereby regulating gene transcription and repair of damaged DNA (PubMed:29925947). The Arp2/3 complex promotes homologous recombination (HR) repair in response to DNA damage by promoting nuclear actin polymerization, leading to drive motility of double-strand breaks (DSBs) (PubMed:29925947). {ECO:0000269|PubMed:29925947, ECO:0000269|PubMed:9230079}.

Q14831

Main function of 5'-partner protein: FUNCTION: G-protein coupled receptor for glutamate. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase. Signaling inhibits adenylate cyclase activity. {ECO:0000269|PubMed:9473604}.
Ensembl transtripts involved in fusion geneENST idsENST00000287613, ENST00000397261, 
ENST00000433034, ENST00000498623, 
ENST00000458641, ENST00000357716, 
ENST00000389336, ENST00000402647, 
ENST00000403881, ENST00000486284, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 3 X 3=2712 X 9 X 7=756
# samples 311
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(11/756*10)=-2.78088271069641
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ARPC4 [Title/Abstract] AND GRM7 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ARPC4 [Title/Abstract] AND GRM7 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ARPC4(9845697)-GRM7(7188139), # samples:2
Anticipated loss of major functional domain due to fusion event.ARPC4-GRM7 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.
ARPC4-GRM7 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
TgeneGRM7

GO:0007196

adenylate cyclase-inhibiting G protein-coupled glutamate receptor signaling pathway

9473604

TgeneGRM7

GO:0007268

chemical synaptic transmission

9473604



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/chr3:9845697/chr3:7188139)
- 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 ARPC4 (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 GRM7 (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)
ENST00000498623ARPC4chr39845697+ENST00000357716GRM7chr37188139+4043709462937963
ENST00000498623ARPC4chr39845697+ENST00000486284GRM7chr37188139+4152709462958970
ENST00000498623ARPC4chr39845697+ENST00000389336GRM7chr37188139+2942709462910954
ENST00000498623ARPC4chr39845697+ENST00000402647GRM7chr37188139+2959709462958971
ENST00000498623ARPC4chr39845697+ENST00000403881GRM7chr37188139+2926709462925960
ENST00000287613ARPC4chr39845697+ENST00000357716GRM7chr37188139+3850516392744901
ENST00000287613ARPC4chr39845697+ENST00000486284GRM7chr37188139+3959516392765908
ENST00000287613ARPC4chr39845697+ENST00000389336GRM7chr37188139+2749516392717892
ENST00000287613ARPC4chr39845697+ENST00000402647GRM7chr37188139+2766516392765908
ENST00000287613ARPC4chr39845697+ENST00000403881GRM7chr37188139+2733516392732897
ENST00000397261ARPC4chr39845697+ENST00000357716GRM7chr37188139+439910655643293909
ENST00000397261ARPC4chr39845697+ENST00000486284GRM7chr37188139+450810655643314916
ENST00000397261ARPC4chr39845697+ENST00000389336GRM7chr37188139+329810655643266900
ENST00000397261ARPC4chr39845697+ENST00000402647GRM7chr37188139+331510655643314916
ENST00000397261ARPC4chr39845697+ENST00000403881GRM7chr37188139+328210655643281905
ENST00000433034ARPC4chr39845697+ENST00000357716GRM7chr37188139+389756352791928
ENST00000433034ARPC4chr39845697+ENST00000486284GRM7chr37188139+400656352812935
ENST00000433034ARPC4chr39845697+ENST00000389336GRM7chr37188139+279656352764919
ENST00000433034ARPC4chr39845697+ENST00000402647GRM7chr37188139+281356352812936
ENST00000433034ARPC4chr39845697+ENST00000403881GRM7chr37188139+278056352779925

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
ENST00000498623ENST00000357716ARPC4chr39845697+GRM7chr37188139+0.0003894040.9996106
ENST00000498623ENST00000486284ARPC4chr39845697+GRM7chr37188139+0.0003250780.9996749
ENST00000498623ENST00000389336ARPC4chr39845697+GRM7chr37188139+0.0019177130.9980823
ENST00000498623ENST00000402647ARPC4chr39845697+GRM7chr37188139+0.0015055490.9984945
ENST00000498623ENST00000403881ARPC4chr39845697+GRM7chr37188139+0.0018893250.99811065
ENST00000287613ENST00000357716ARPC4chr39845697+GRM7chr37188139+0.0003668140.9996332
ENST00000287613ENST00000486284ARPC4chr39845697+GRM7chr37188139+0.0003102310.9996898
ENST00000287613ENST00000389336ARPC4chr39845697+GRM7chr37188139+0.0017563020.9982437
ENST00000287613ENST00000402647ARPC4chr39845697+GRM7chr37188139+0.0015318130.9984682
ENST00000287613ENST00000403881ARPC4chr39845697+GRM7chr37188139+0.0017257990.9982742
ENST00000397261ENST00000357716ARPC4chr39845697+GRM7chr37188139+0.0003862740.9996137
ENST00000397261ENST00000486284ARPC4chr39845697+GRM7chr37188139+0.0003105830.99968946
ENST00000397261ENST00000389336ARPC4chr39845697+GRM7chr37188139+0.0017199970.99828005
ENST00000397261ENST00000402647ARPC4chr39845697+GRM7chr37188139+0.0012411780.9987588
ENST00000397261ENST00000403881ARPC4chr39845697+GRM7chr37188139+0.0016630180.9983369
ENST00000433034ENST00000357716ARPC4chr39845697+GRM7chr37188139+0.0002956160.9997043
ENST00000433034ENST00000486284ARPC4chr39845697+GRM7chr37188139+0.0002357980.99976426
ENST00000433034ENST00000389336ARPC4chr39845697+GRM7chr37188139+0.0016066140.99839336
ENST00000433034ENST00000402647ARPC4chr39845697+GRM7chr37188139+0.0011987310.99880123
ENST00000433034ENST00000403881ARPC4chr39845697+GRM7chr37188139+0.001502690.99849737

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 ARPC4-GRM7

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ARPC4chr39845697GRM7chr371881391065167ARARIVAEEFLKNIPQISYASTAPEL
ARPC4chr39845697GRM7chr37188139516159ARARIVAEEFLKNIPQISYASTAPEL
ARPC4chr39845697GRM7chr37188139563186ARARIVAEEFLKNIPQISYASTAPEL
ARPC4chr39845697GRM7chr37188139709221ARARIVAEEFLKNIPQISYASTAPEL

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Potential FusionNeoAntigen Information of ARPC4-GRM7 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.
ARPC4-GRM7_9845697_7188139.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)
ARPC4-GRM7chr39845697chr37188139516HLA-B08:09FLKNIPQI0.97870.6105917
ARPC4-GRM7chr39845697chr37188139516HLA-B45:01AEEFLKNIP0.9960.8752615
ARPC4-GRM7chr39845697chr37188139516HLA-B50:02AEEFLKNIP0.99150.5489615
ARPC4-GRM7chr39845697chr37188139516HLA-B52:01VAEEFLKNI0.89460.9417514
ARPC4-GRM7chr39845697chr37188139516HLA-B15:25LKNIPQISY0.66350.86111019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:18LKNIPQISY0.53080.56731019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:03LKNIPQISY0.50920.61321019
ARPC4-GRM7chr39845697chr37188139516HLA-B41:01AEEFLKNIP0.49390.9192615
ARPC4-GRM7chr39845697chr37188139516HLA-B50:01AEEFLKNIP0.31480.5935615
ARPC4-GRM7chr39845697chr37188139516HLA-B15:01FLKNIPQISY0.99990.8786919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:25FLKNIPQISY0.99810.8488919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:02FLKNIPQISY0.99610.8637919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:03FLKNIPQISY0.87680.5561919
ARPC4-GRM7chr39845697chr37188139516HLA-A02:22FLKNIPQISYA0.99440.5107920
ARPC4-GRM7chr39845697chr37188139516HLA-A02:13FLKNIPQISYA0.9880.5262920
ARPC4-GRM7chr39845697chr37188139516HLA-A02:11FLKNIPQISYA0.9570.5124920
ARPC4-GRM7chr39845697chr37188139516HLA-B40:06AEEFLKNIP0.98990.5528615
ARPC4-GRM7chr39845697chr37188139516HLA-C07:46LKNIPQISY0.80210.75141019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:21LKNIPQISY0.60160.8581019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:07LKNIPQISY0.58480.63261019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:07FLKNIPQISY0.99980.5163919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:21FLKNIPQISY0.99540.8556919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:04FLKNIPQISY0.99150.8597919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:05FLKNIPQISY0.96050.7693919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:31FLKNIPQISY0.94330.7851919
ARPC4-GRM7chr39845697chr37188139516HLA-A02:03FLKNIPQI0.99330.7405917
ARPC4-GRM7chr39845697chr37188139516HLA-C07:17LKNIPQISY0.8080.96751019
ARPC4-GRM7chr39845697chr37188139516HLA-B18:06EEFLKNIPQ0.70760.9292716
ARPC4-GRM7chr39845697chr37188139516HLA-B15:39LKNIPQISY0.68460.73291019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:27LKNIPQISY0.66140.91341019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:12LKNIPQISY0.65570.91151019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:35LKNIPQISY0.58790.87191019
ARPC4-GRM7chr39845697chr37188139516HLA-B35:28LKNIPQISY0.52960.86161019
ARPC4-GRM7chr39845697chr37188139516HLA-B35:20LKNIPQISY0.52810.86851019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:50LKNIPQISY0.51150.92151019
ARPC4-GRM7chr39845697chr37188139516HLA-B48:02LKNIPQISY0.42010.84931019
ARPC4-GRM7chr39845697chr37188139516HLA-B50:05AEEFLKNIP0.31480.5935615
ARPC4-GRM7chr39845697chr37188139516HLA-B50:04AEEFLKNIP0.31480.5935615
ARPC4-GRM7chr39845697chr37188139516HLA-B15:53LKNIPQISY0.27730.88491019
ARPC4-GRM7chr39845697chr37188139516HLA-B18:04LKNIPQISY0.24360.9381019
ARPC4-GRM7chr39845697chr37188139516HLA-B18:06LKNIPQISY0.170.93231019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:54LKNIPQISY0.10940.87351019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:68LKNIPQISY0.07280.52821019
ARPC4-GRM7chr39845697chr37188139516HLA-B15:33FLKNIPQISY0.99990.8786919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:08FLKNIPQISY0.99990.8574919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:50FLKNIPQISY0.99990.9488919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:53FLKNIPQISY0.99990.8337919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:12FLKNIPQISY0.99990.9282919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:125FLKNIPQISY0.99990.8786919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:27FLKNIPQISY0.99990.8765919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:11FLKNIPQISY0.99990.8437919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:35FLKNIPQISY0.99990.8107919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:34FLKNIPQISY0.99990.8786919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:135FLKNIPQISY0.99990.8667919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:24FLKNIPQISY0.99970.8608919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:54FLKNIPQISY0.99890.8181919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:39FLKNIPQISY0.99780.6694919
ARPC4-GRM7chr39845697chr37188139516HLA-B15:20FLKNIPQISY0.96120.8475919
ARPC4-GRM7chr39845697chr37188139516HLA-B35:28FLKNIPQISY0.94310.8396919
ARPC4-GRM7chr39845697chr37188139516HLA-B35:20FLKNIPQISY0.93440.8526919
ARPC4-GRM7chr39845697chr37188139516HLA-A02:03FLKNIPQISYA0.99870.6498920

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Potential FusionNeoAntigen Information of ARPC4-GRM7 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.
ARPC4-GRM7_9845697_7188139.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)
ARPC4-GRM7chr39845697chr37188139516DRB1-0403KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0411KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0417KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0427KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0439KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0441KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0446KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0449KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0450KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0452KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0459KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0460KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0467KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0471KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0485KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0488KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-0491KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-1201EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1201AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1201VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1203EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1203AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1203VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1204EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1205EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1205AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1205VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1206EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1206AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1206VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1207EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1207AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1207VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1208EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1208AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1208VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1209EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1210EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1210AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1210VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1211EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1211AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1211VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1211EFLKNIPQISYASTA823
ARPC4-GRM7chr39845697chr37188139516DRB1-1212EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1212AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1212VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1212EFLKNIPQISYASTA823
ARPC4-GRM7chr39845697chr37188139516DRB1-1213EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1213AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1213VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1214EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1214AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1214VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1215EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1215AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1215VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1217EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1217AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1217VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1218EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1218AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1218VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1219EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1219AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1220EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1220AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1220VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1221EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1221AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1221VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1222EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1222AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1223EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB1-1223AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1223VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1367AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1367VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1410KNIPQISYASTAPEL1126
ARPC4-GRM7chr39845697chr37188139516DRB1-1447AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1447VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB1-1498AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB1-1498VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0202AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0202VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0202IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0202EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0205AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0205VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0205IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0205EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0209AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0209VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0210AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0210VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0210IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0210EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0211AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0211VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0211IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0211EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0212AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0212VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0212IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0212EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0213AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0213VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0213IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0213EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0214AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0214VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0214IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0215AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0215VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0215IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0215EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0216AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0216VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0216IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0217AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0217VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0217IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0217EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0218AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0218VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0218IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0218EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0219AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0219VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0219IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0219EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0220AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0220VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0220IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0220EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0221AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0221VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0222AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0222VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0222IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0222EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0223AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0223VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0223IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0223EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0225AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0225VAEEFLKNIPQISYA520
ARPC4-GRM7chr39845697chr37188139516DRB3-0225IVAEEFLKNIPQISY419
ARPC4-GRM7chr39845697chr37188139516DRB3-0225EEFLKNIPQISYAST722
ARPC4-GRM7chr39845697chr37188139516DRB3-0303AEEFLKNIPQISYAS621
ARPC4-GRM7chr39845697chr37188139516DRB3-0303VAEEFLKNIPQISYA520

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Fusion breakpoint peptide structures of ARPC4-GRM7

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
143AEEFLKNIPQISYAARPC4GRM7chr39845697chr37188139516

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ARPC4-GRM7

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-B14:023BVN143AEEFLKNIPQISYA-7.9962-8.1096
HLA-B14:023BVN143AEEFLKNIPQISYA-5.70842-6.74372
HLA-B52:013W39143AEEFLKNIPQISYA-6.83737-6.95077
HLA-B52:013W39143AEEFLKNIPQISYA-4.4836-5.5189
HLA-A11:014UQ2143AEEFLKNIPQISYA-10.0067-10.1201
HLA-A11:014UQ2143AEEFLKNIPQISYA-9.03915-10.0745
HLA-A24:025HGA143AEEFLKNIPQISYA-6.56204-6.67544
HLA-A24:025HGA143AEEFLKNIPQISYA-5.42271-6.45801
HLA-B44:053DX8143AEEFLKNIPQISYA-7.85648-8.89178
HLA-B44:053DX8143AEEFLKNIPQISYA-5.3978-5.5112
HLA-A02:016TDR143AEEFLKNIPQISYA-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of ARPC4-GRM7

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
ARPC4-GRM7chr39845697chr371881391019LKNIPQISYCTTAAGAATATCCCCCAGATTAGTTAT
ARPC4-GRM7chr39845697chr37188139514VAEEFLKNIGTGGCTGAAGAGTTCCTTAAGAATATC
ARPC4-GRM7chr39845697chr37188139615AEEFLKNIPGCTGAAGAGTTCCTTAAGAATATCCCC
ARPC4-GRM7chr39845697chr37188139716EEFLKNIPQGAAGAGTTCCTTAAGAATATCCCCCAG
ARPC4-GRM7chr39845697chr37188139917FLKNIPQITTCCTTAAGAATATCCCCCAGATT
ARPC4-GRM7chr39845697chr37188139919FLKNIPQISYTTCCTTAAGAATATCCCCCAGATTAGTTAT
ARPC4-GRM7chr39845697chr37188139920FLKNIPQISYATTCCTTAAGAATATCCCCCAGATTAGTTATGCA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ARPC4-GRM7chr39845697chr371881391126KNIPQISYASTAPELAAGAATATCCCCCAGATTAGTTATGCATCAACGGCACCCGAGCTA
ARPC4-GRM7chr39845697chr37188139419IVAEEFLKNIPQISYATTGTGGCTGAAGAGTTCCTTAAGAATATCCCCCAGATTAGTTAT
ARPC4-GRM7chr39845697chr37188139520VAEEFLKNIPQISYAGTGGCTGAAGAGTTCCTTAAGAATATCCCCCAGATTAGTTATGCA
ARPC4-GRM7chr39845697chr37188139621AEEFLKNIPQISYASGCTGAAGAGTTCCTTAAGAATATCCCCCAGATTAGTTATGCATCA
ARPC4-GRM7chr39845697chr37188139722EEFLKNIPQISYASTGAAGAGTTCCTTAAGAATATCCCCCAGATTAGTTATGCATCAACG
ARPC4-GRM7chr39845697chr37188139823EFLKNIPQISYASTAGAGTTCCTTAAGAATATCCCCCAGATTAGTTATGCATCAACGGCA

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Information of the samples that have these potential fusion neoantigens of ARPC4-GRM7

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
BRCAARPC4-GRM7chr39845697ENST00000287613chr37188139ENST00000357716TCGA-E9-A1RH-01A

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Potential target of CAR-T therapy development for ARPC4-GRM7

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
TgeneGRM7chr3:9845697chr3:7188139ENST00000357716010591_6150916.0TransmembraneHelical%3B Name%3D1
TgeneGRM7chr3:9845697chr3:7188139ENST00000357716010628_6480916.0TransmembraneHelical%3B Name%3D2
TgeneGRM7chr3:9845697chr3:7188139ENST00000357716010655_6750916.0TransmembraneHelical%3B Name%3D3
TgeneGRM7chr3:9845697chr3:7188139ENST00000357716010703_7230916.0TransmembraneHelical%3B Name%3D4
TgeneGRM7chr3:9845697chr3:7188139ENST00000357716010754_7750916.0TransmembraneHelical%3B Name%3D5
TgeneGRM7chr3:9845697chr3:7188139ENST00000357716010789_8100916.0TransmembraneHelical%3B Name%3D6
TgeneGRM7chr3:9845697chr3:7188139ENST00000357716010826_8500916.0TransmembraneHelical%3B Name%3D7
TgeneGRM7chr3:9845697chr3:7188139ENST00000389336010591_6150907.0TransmembraneHelical%3B Name%3D1
TgeneGRM7chr3:9845697chr3:7188139ENST00000389336010628_6480907.0TransmembraneHelical%3B Name%3D2
TgeneGRM7chr3:9845697chr3:7188139ENST00000389336010655_6750907.0TransmembraneHelical%3B Name%3D3
TgeneGRM7chr3:9845697chr3:7188139ENST00000389336010703_7230907.0TransmembraneHelical%3B Name%3D4
TgeneGRM7chr3:9845697chr3:7188139ENST00000389336010754_7750907.0TransmembraneHelical%3B Name%3D5
TgeneGRM7chr3:9845697chr3:7188139ENST00000389336010789_8100907.0TransmembraneHelical%3B Name%3D6
TgeneGRM7chr3:9845697chr3:7188139ENST00000389336010826_8500907.0TransmembraneHelical%3B Name%3D7
TgeneGRM7chr3:9845697chr3:7188139ENST00000402647010591_6150923.0TransmembraneHelical%3B Name%3D1
TgeneGRM7chr3:9845697chr3:7188139ENST00000402647010628_6480923.0TransmembraneHelical%3B Name%3D2
TgeneGRM7chr3:9845697chr3:7188139ENST00000402647010655_6750923.0TransmembraneHelical%3B Name%3D3
TgeneGRM7chr3:9845697chr3:7188139ENST00000402647010703_7230923.0TransmembraneHelical%3B Name%3D4
TgeneGRM7chr3:9845697chr3:7188139ENST00000402647010754_7750923.0TransmembraneHelical%3B Name%3D5
TgeneGRM7chr3:9845697chr3:7188139ENST00000402647010789_8100923.0TransmembraneHelical%3B Name%3D6
TgeneGRM7chr3:9845697chr3:7188139ENST00000402647010826_8500923.0TransmembraneHelical%3B Name%3D7
TgeneGRM7chr3:9845697chr3:7188139ENST00000403881010591_6150912.0TransmembraneHelical%3B Name%3D1
TgeneGRM7chr3:9845697chr3:7188139ENST00000403881010628_6480912.0TransmembraneHelical%3B Name%3D2
TgeneGRM7chr3:9845697chr3:7188139ENST00000403881010655_6750912.0TransmembraneHelical%3B Name%3D3
TgeneGRM7chr3:9845697chr3:7188139ENST00000403881010703_7230912.0TransmembraneHelical%3B Name%3D4
TgeneGRM7chr3:9845697chr3:7188139ENST00000403881010754_7750912.0TransmembraneHelical%3B Name%3D5
TgeneGRM7chr3:9845697chr3:7188139ENST00000403881010789_8100912.0TransmembraneHelical%3B Name%3D6
TgeneGRM7chr3:9845697chr3:7188139ENST00000403881010826_8500912.0TransmembraneHelical%3B Name%3D7
TgeneGRM7chr3:9845697chr3:7188139ENST00000486284011591_61501049.3333333333333TransmembraneHelical%3B Name%3D1
TgeneGRM7chr3:9845697chr3:7188139ENST00000486284011628_64801049.3333333333333TransmembraneHelical%3B Name%3D2
TgeneGRM7chr3:9845697chr3:7188139ENST00000486284011655_67501049.3333333333333TransmembraneHelical%3B Name%3D3
TgeneGRM7chr3:9845697chr3:7188139ENST00000486284011703_72301049.3333333333333TransmembraneHelical%3B Name%3D4
TgeneGRM7chr3:9845697chr3:7188139ENST00000486284011754_77501049.3333333333333TransmembraneHelical%3B Name%3D5
TgeneGRM7chr3:9845697chr3:7188139ENST00000486284011789_81001049.3333333333333TransmembraneHelical%3B Name%3D6
TgeneGRM7chr3:9845697chr3:7188139ENST00000486284011826_85001049.3333333333333TransmembraneHelical%3B Name%3D7

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 ARPC4-GRM7

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 ARPC4-GRM7

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