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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:ARHGEF11-CIT

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ARHGEF11-CIT
FusionPDB ID: 6194
FusionGDB2.0 ID: 6194
HgeneTgene
Gene symbol

ARHGEF11

CIT

Gene ID

9826

79947

Gene nameRho guanine nucleotide exchange factor 11dehydrodolichyl diphosphate synthase subunit
SynonymsGTRAP48|PDZ-RHOGEFCIT|CPT|DEDSM|DS|HDS|RP59|hCIT
Cytomap

1q23.1

1p36.11

Type of geneprotein-codingprotein-coding
Descriptionrho guanine nucleotide exchange factor 11Rho guanine exchange factor (GEF) 11Rho guanine nucleotide exchange factor (GEF) 11RhoA-specific guanine nucleotide exchange factorRhoGEF glutamate transport modulatorglutamate transporter EAAT4-associated prodehydrodolichyl diphosphate synthase complex subunit DHDDScis-IPTasecis-isoprenyltransferasecis-prenyl transferasecis-prenyltransferase subunit hCITdedol-PP synthasedehydrodolichyl diphosphate syntase complex subunit DHDDSepididymis tissue protein
Modification date2020031320200313
UniProtAcc

O15085

Main function of 5'-partner protein: FUNCTION: May play a role in the regulation of RhoA GTPase by guanine nucleotide-binding alpha-12 (GNA12) and alpha-13 (GNA13). Acts as guanine nucleotide exchange factor (GEF) for RhoA GTPase and may act as GTPase-activating protein (GAP) for GNA12 and GNA13. Involved in neurotrophin-induced neurite outgrowth. {ECO:0000269|PubMed:21670212}.

Q96RK1

Main function of 5'-partner protein: FUNCTION: Acts as transcriptional coactivator for TFAP2/AP-2. Enhances estrogen-dependent transactivation mediated by estrogen receptors. May function as an inhibitor of transactivation by HIF1A by disrupting HIF1A interaction with CREBBP. May be involved in regulation of gene expression during development and differentiation of blood cells, endothelial cells and mammary epithelial cells. {ECO:0000269|PubMed:11744733, ECO:0000269|PubMed:15342390}.
Ensembl transtripts involved in fusion geneENST idsENST00000361409, ENST00000368194, 
ENST00000315174, ENST00000487682, 
ENST00000537607, ENST00000261833, 
ENST00000392521, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 5 X 7=3854 X 4 X 4=64
# samples 145
** MAII scorelog2(14/385*10)=-1.4594316186373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/64*10)=-0.356143810225275
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ARHGEF11 [Title/Abstract] AND CIT [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ARHGEF11 [Title/Abstract] AND CIT [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ARHGEF11(157014090)-CIT(120173162), # samples:1
Anticipated loss of major functional domain due to fusion event.ARHGEF11-CIT 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.
ARHGEF11-CIT 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.
ARHGEF11-CIT 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.
ARHGEF11-CIT 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
HgeneARHGEF11

GO:0007186

G protein-coupled receptor signaling pathway

15755723

HgeneARHGEF11

GO:0007266

Rho protein signal transduction

10026210

HgeneARHGEF11

GO:0045893

positive regulation of transcription, DNA-templated

10026210

TgeneCIT

GO:0006489

dolichyl diphosphate biosynthetic process

28842490



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/chr1:157014090/chr12:120173162)
- 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 ARHGEF11 (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 CIT (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)
ENST00000368194ARHGEF11chr1157014090-ENST00000392521CITchr12120173162-6766107290143231140
ENST00000368194ARHGEF11chr1157014090-ENST00000261833CITchr12120173162-6765107290143231140
ENST00000361409ARHGEF11chr1157014090-ENST00000392521CITchr12120173162-646977560440261140
ENST00000361409ARHGEF11chr1157014090-ENST00000261833CITchr12120173162-646877560440261140

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
ENST00000368194ENST00000392521ARHGEF11chr1157014090-CITchr12120173162-0.0028825880.9971174
ENST00000368194ENST00000261833ARHGEF11chr1157014090-CITchr12120173162-0.0028911440.9971089
ENST00000361409ENST00000392521ARHGEF11chr1157014090-CITchr12120173162-0.0022997540.9977003
ENST00000361409ENST00000261833ARHGEF11chr1157014090-CITchr12120173162-0.0023062730.9976937

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 ARHGEF11-CIT

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ARHGEF11chr1157014090CITchr12120173162107257RNHECKVTPEYRQVITDLEEQLNQLT
ARHGEF11chr1157014090CITchr1212017316277557RNHECKVTPEYRQVITDLEEQLNQLT

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Potential FusionNeoAntigen Information of ARHGEF11-CIT 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.
ARHGEF11-CIT_157014090_120173162.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)
ARHGEF11-CITchr1157014090chr12120173162775HLA-A30:08KVTPEYRQV0.87480.7861514
ARHGEF11-CITchr1157014090chr12120173162775HLA-A02:21KVTPEYRQV0.78890.646514
ARHGEF11-CITchr1157014090chr12120173162775HLA-B13:02KVTPEYRQV0.23190.9029514
ARHGEF11-CITchr1157014090chr12120173162775HLA-B48:01RQVITDLEEQL0.99610.84921122
ARHGEF11-CITchr1157014090chr12120173162775HLA-B13:01RQVITDLEEQL0.95240.97871122
ARHGEF11-CITchr1157014090chr12120173162775HLA-B39:13RQVITDLEEQL0.89150.97111122
ARHGEF11-CITchr1157014090chr12120173162775HLA-C07:05YRQVITDL0.99950.94381018
ARHGEF11-CITchr1157014090chr12120173162775HLA-C07:27YRQVITDL0.99920.94451018
ARHGEF11-CITchr1157014090chr12120173162775HLA-B39:12YRQVITDL0.99860.84941018
ARHGEF11-CITchr1157014090chr12120173162775HLA-C01:17VTPEYRQV0.98110.9711614
ARHGEF11-CITchr1157014090chr12120173162775HLA-B51:08TPEYRQVI0.97290.5211715
ARHGEF11-CITchr1157014090chr12120173162775HLA-C12:16YRQVITDL0.94070.96051018
ARHGEF11-CITchr1157014090chr12120173162775HLA-C01:30VTPEYRQV0.93520.9815614
ARHGEF11-CITchr1157014090chr12120173162775HLA-C15:06KVTPEYRQV0.99770.766514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C15:04KVTPEYRQV0.99640.7587514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C06:03VTPEYRQVI0.89110.989615
ARHGEF11-CITchr1157014090chr12120173162775HLA-C12:04KVTPEYRQV0.88940.99514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C06:03KVTPEYRQV0.88560.9899514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C12:04VTPEYRQVI0.88490.9882615
ARHGEF11-CITchr1157014090chr12120173162775HLA-C01:17VTPEYRQVI0.86880.9564615
ARHGEF11-CITchr1157014090chr12120173162775HLA-C01:30VTPEYRQVI0.74740.9732615
ARHGEF11-CITchr1157014090chr12120173162775HLA-C02:06KVTPEYRQV0.53250.946514
ARHGEF11-CITchr1157014090chr12120173162775HLA-B48:03RQVITDLEEQL0.96120.62981122
ARHGEF11-CITchr1157014090chr12120173162775HLA-B42:01TPEYRQVITDL0.93030.6505718
ARHGEF11-CITchr1157014090chr12120173162775HLA-C01:03VTPEYRQV0.99230.975614
ARHGEF11-CITchr1157014090chr12120173162775HLA-C01:02VTPEYRQV0.98130.97614
ARHGEF11-CITchr1157014090chr12120173162775HLA-C06:17YRQVITDL0.93860.99371018
ARHGEF11-CITchr1157014090chr12120173162775HLA-C06:02YRQVITDL0.93860.99371018
ARHGEF11-CITchr1157014090chr12120173162775HLA-C15:02KVTPEYRQV0.99860.7576514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C15:05KVTPEYRQV0.99810.8448514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C15:09KVTPEYRQV0.99640.7587514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C16:02KVTPEYRQV0.9880.9862514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C03:17VTPEYRQVI0.97410.9631615
ARHGEF11-CITchr1157014090chr12120173162775HLA-C01:03VTPEYRQVI0.90850.952615
ARHGEF11-CITchr1157014090chr12120173162775HLA-C01:02VTPEYRQVI0.88080.9543615
ARHGEF11-CITchr1157014090chr12120173162775HLA-A30:01KVTPEYRQV0.87560.8782514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C06:17KVTPEYRQV0.83560.9897514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C06:02KVTPEYRQV0.83560.9897514
ARHGEF11-CITchr1157014090chr12120173162775HLA-A02:14KVTPEYRQV0.79010.5702514
ARHGEF11-CITchr1157014090chr12120173162775HLA-A02:06KVTPEYRQV0.78890.646514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C16:02VTPEYRQVI0.77630.9882615
ARHGEF11-CITchr1157014090chr12120173162775HLA-C06:08KVTPEYRQV0.4270.9887514
ARHGEF11-CITchr1157014090chr12120173162775HLA-C14:03EYRQVITDL0.23620.9191918
ARHGEF11-CITchr1157014090chr12120173162775HLA-C14:02EYRQVITDL0.23620.9191918
ARHGEF11-CITchr1157014090chr12120173162775HLA-B40:12RQVITDLEEQL0.96120.62981122
ARHGEF11-CITchr1157014090chr12120173162775HLA-B40:21RQVITDLEEQL0.95280.75091122
ARHGEF11-CITchr1157014090chr12120173162775HLA-B39:02RQVITDLEEQL0.95240.97041122
ARHGEF11-CITchr1157014090chr12120173162775HLA-B40:49RQVITDLEEQL0.94240.61121122

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Potential FusionNeoAntigen Information of ARHGEF11-CIT 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.
ARHGEF11-CIT_157014090_120173162.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)
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0401VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0403VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0405VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0405TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0405KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0405PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0407VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0407TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0407KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0409VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0409TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0409KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0409PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0411VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0411TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0411KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0417VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0417TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0417KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0417PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0419VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0424VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0424TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0424KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0424PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0429VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0429TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0429KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0429PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0430VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0430TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0430KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0430PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0433VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0435VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0435TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0438VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0438TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0439VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0441VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0443VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0445VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0445TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0445KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0445PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0446VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0447VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0447TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0448VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0448TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0448KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0448PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0449VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0449TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0450VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0450TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0451VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0451TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0452VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0454VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0457VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0457TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0457KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0457PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0459VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0459TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0460VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0461VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0462VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0462TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0462KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0462PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0463VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0464VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0464TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0467VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0469VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0469TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0469KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0471VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0474VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0474TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0476VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0477VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0477TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0477KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0477PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0480VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0480TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0480KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0480PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0482VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0482TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0482KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0483VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0483TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0483KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0483PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0484VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0484TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0484KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0484PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0485VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0486VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0486TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0486KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0487VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0487TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0487KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0487PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0488VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0489VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0489TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0489KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0489PEYRQVITDLEEQLN823
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0491VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0491TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0491KVTPEYRQVITDLEE520
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0805VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0818VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0818TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0829VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0829TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0840VTPEYRQVITDLEEQ621
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0840TPEYRQVITDLEEQL722
ARHGEF11-CITchr1157014090chr12120173162775DRB1-0908VTPEYRQVITDLEEQ621

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Fusion breakpoint peptide structures of ARHGEF11-CIT

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
10322VTPEYRQVITDLEEARHGEF11CITchr1157014090chr12120173162775

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ARHGEF11-CIT

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-B14:023BVN10322VTPEYRQVITDLEE-7.15543-7.26883
HLA-B14:023BVN10322VTPEYRQVITDLEE-4.77435-5.80965
HLA-B52:013W3910322VTPEYRQVITDLEE-6.80875-6.92215
HLA-B52:013W3910322VTPEYRQVITDLEE-4.20386-5.23916
HLA-A11:014UQ210322VTPEYRQVITDLEE-7.5194-8.5547
HLA-A11:014UQ210322VTPEYRQVITDLEE-6.9601-7.0735
HLA-A24:025HGA10322VTPEYRQVITDLEE-7.52403-7.63743
HLA-A24:025HGA10322VTPEYRQVITDLEE-5.82433-6.85963
HLA-B27:056PYJ10322VTPEYRQVITDLEE-3.28285-4.31815
HLA-B44:053DX810322VTPEYRQVITDLEE-5.91172-6.94702
HLA-B44:053DX810322VTPEYRQVITDLEE-4.24346-4.35686
HLA-B35:011A1N10322VTPEYRQVITDLEE-5.9251-6.0385
HLA-B35:011A1N10322VTPEYRQVITDLEE-4.80237-5.83767

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Vaccine Design for the FusionNeoAntigens of ARHGEF11-CIT

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
ARHGEF11-CITchr1157014090chr121201731621018YRQVITDLTATAGACAGGTAATCACAGACCTG
ARHGEF11-CITchr1157014090chr121201731621122RQVITDLEEQLAGACAGGTAATCACAGACCTGGAGGAGCAGCTA
ARHGEF11-CITchr1157014090chr12120173162514KVTPEYRQVAAGGTTACCCCAGAGTATAGACAGGTA
ARHGEF11-CITchr1157014090chr12120173162614VTPEYRQVGTTACCCCAGAGTATAGACAGGTA
ARHGEF11-CITchr1157014090chr12120173162615VTPEYRQVIGTTACCCCAGAGTATAGACAGGTAATC
ARHGEF11-CITchr1157014090chr12120173162715TPEYRQVIACCCCAGAGTATAGACAGGTAATC
ARHGEF11-CITchr1157014090chr12120173162718TPEYRQVITDLACCCCAGAGTATAGACAGGTAATCACAGACCTG
ARHGEF11-CITchr1157014090chr12120173162918EYRQVITDLGAGTATAGACAGGTAATCACAGACCTG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ARHGEF11-CITchr1157014090chr12120173162520KVTPEYRQVITDLEEAAGGTTACCCCAGAGTATAGACAGGTAATCACAGACCTGGAGGAG
ARHGEF11-CITchr1157014090chr12120173162621VTPEYRQVITDLEEQGTTACCCCAGAGTATAGACAGGTAATCACAGACCTGGAGGAGCAG
ARHGEF11-CITchr1157014090chr12120173162722TPEYRQVITDLEEQLACCCCAGAGTATAGACAGGTAATCACAGACCTGGAGGAGCAGCTA
ARHGEF11-CITchr1157014090chr12120173162823PEYRQVITDLEEQLNCCAGAGTATAGACAGGTAATCACAGACCTGGAGGAGCAGCTAAAC

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Information of the samples that have these potential fusion neoantigens of ARHGEF11-CIT

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
OVARHGEF11-CITchr1157014090ENST00000361409chr12120173162ENST00000261833TCGA-09-0369

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Potential target of CAR-T therapy development for ARHGEF11-CIT

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 ARHGEF11-CIT

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 ARHGEF11-CIT

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