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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:ARHGEF3-ACP6

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ARHGEF3-ACP6
FusionPDB ID: 6308
FusionGDB2.0 ID: 6308
HgeneTgene
Gene symbol

ARHGEF3

ACP6

Gene ID

50650

51205

Gene nameRho guanine nucleotide exchange factor 3acid phosphatase 6, lysophosphatidic
SynonymsGEF3|STA3|XPLNACPL1|LPAP|PACPL1
Cytomap

3p14.3

1q21.2

Type of geneprotein-codingprotein-coding
Descriptionrho guanine nucleotide exchange factor 359.8 kDA proteinRho guanine nucleotide exchange factor (GEF) 3RhoGEF proteinexchange factor found in platelets and leukemic and neuronal tissues, XPLNlysophosphatidic acid phosphatase type 6acid phosphatase-like protein 1
Modification date2020032720200313
UniProtAcc

Q8N4T4

Main function of 5'-partner protein: FUNCTION: Promotes cell proliferation. {ECO:0000269|PubMed:22327280}.

Q9NPH0

Main function of 5'-partner protein: FUNCTION: Hydrolyzes lysophosphatidic acid (LPA) containing a medium length fatty acid chain to the corresponding monoacylglycerol. Has highest activity with lysophosphatidic acid containing myristate (C14:0), monounsaturated oleate (C18:1) or palmitate (C16:0), and lower activity with C18:0 and C6:0 lysophosphatidic acid. {ECO:0000269|PubMed:10506173, ECO:0000269|PubMed:23807634}.
Ensembl transtripts involved in fusion geneENST idsENST00000338458, ENST00000496106, 
ENST00000498517, ENST00000296315, 
ENST00000413728, ENST00000495373, 
ENST00000497267, 
ENST00000392988, 
ENST00000460583, ENST00000369238, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score19 X 17 X 8=25842 X 2 X 2=8
# samples 233
** MAII scorelog2(23/2584*10)=-3.48990030374955
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/8*10)=1.90689059560852
Fusion gene context

PubMed: ARHGEF3 [Title/Abstract] AND ACP6 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ARHGEF3 [Title/Abstract] AND ACP6 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ARHGEF3(56916320)-ACP6(147131890), # samples:3
Anticipated loss of major functional domain due to fusion event.ARHGEF3-ACP6 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.
ARHGEF3-ACP6 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
TgeneACP6

GO:2001311

lysobisphosphatidic acid metabolic process

23807634



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/chr3:56916320/chr1:147131890)
- 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 ARHGEF3 (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 ACP6 (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)
ENST00000338458ARHGEF3chr356916320-ENST00000369238ACP6chr1147131890-65613021101369419
ENST00000496106ARHGEF3chr356916320-ENST00000369238ACP6chr1147131890-6485226821293403
ENST00000338458ARHGEF3chr356916319-ENST00000369238ACP6chr1147131890-65613021101369419
ENST00000496106ARHGEF3chr356916319-ENST00000369238ACP6chr1147131890-6485226821293403

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
ENST00000338458ENST00000369238ARHGEF3chr356916320-ACP6chr1147131890-0.0003262550.9996737
ENST00000496106ENST00000369238ARHGEF3chr356916320-ACP6chr1147131890-0.0002455730.99975437
ENST00000338458ENST00000369238ARHGEF3chr356916319-ACP6chr1147131890-0.0003262550.9996737
ENST00000496106ENST00000369238ARHGEF3chr356916319-ACP6chr1147131890-0.0002455730.99975437

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 ARHGEF3-ACP6

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ARHGEF3chr356916319ACP6chr114713189022648DEDAVSLCSLDISVEWNPQLLEVPPQ
ARHGEF3chr356916319ACP6chr114713189030264DEDAVSLCSLDISVEWNPQLLEVPPQ
ARHGEF3chr356916320ACP6chr114713189022648DEDAVSLCSLDISVEWNPQLLEVPPQ
ARHGEF3chr356916320ACP6chr114713189030264DEDAVSLCSLDISVEWNPQLLEVPPQ

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Potential FusionNeoAntigen Information of ARHGEF3-ACP6 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.
ARHGEF3-ACP6_56916319_147131890.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)
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B58:01SLDISVEW0.99020.9465816
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B58:01CSLDISVEW0.99920.9574716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:01CSLDISVEW0.99910.9878716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B58:02CSLDISVEW0.99810.9676716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:22SLCSLDISV0.99670.535514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B15:17CSLDISVEW0.99660.9744716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:27SLCSLDISV0.99580.6131514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:16SLCSLDISV0.99540.5053514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B15:16CSLDISVEW0.99480.9341716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:11SLCSLDISV0.99480.6948514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:67SLCSLDISV0.99440.672514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:30SLCSLDISV0.99440.672514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:24SLCSLDISV0.99440.672514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:60SLCSLDISV0.99430.628514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:19SLCSLDISV0.98860.5145514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B15:17ISVEWNPQL0.98690.92971120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:35SLCSLDISV0.98680.6959514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:04SLCSLDISV0.98660.7364514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:03CSLDISVEW0.98370.9927716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B15:16ISVEWNPQL0.98140.67521120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:29SLCSLDISV0.96880.6681514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:20SLCSLDISV0.960.6789514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:03ISVEWNPQL0.94310.96631120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A32:13CSLDISVEW0.87160.9619716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:21ISVEWNPQL0.7770.70871120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B52:01ISVEWNPQL0.7740.88341120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:01LCSLDISVEW0.99930.9913616
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B58:01LCSLDISVEW0.99820.9665616
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B58:02LCSLDISVEW0.99740.9768616
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B15:17LCSLDISVEW0.97860.9822616
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:03LCSLDISVEW0.97110.9952616
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B15:16LCSLDISVEW0.94010.9491616
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:01SLCSLDISVEW0.99960.984516
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B58:02SLCSLDISVEW0.99680.9532516
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B58:01SLCSLDISVEW0.99560.9387516
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:03SLCSLDISVEW0.99360.9901516
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A32:13SLCSLDISVEW0.98650.9717516
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B15:17SLCSLDISVEW0.98150.9609516
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C05:09SVEWNPQLL0.99990.8841221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C08:15SVEWNPQLL0.99980.95641221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:07ISVEWNPQL0.99960.97361120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:19ISVEWNPQL0.99950.98861120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:08ISVEWNPQL0.99950.90931120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C15:04ISVEWNPQL0.99940.89261120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C15:06ISVEWNPQL0.99940.91061120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C01:17SVEWNPQLL0.99870.91991221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C04:06ISVEWNPQL0.99860.92231120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C08:13ISVEWNPQL0.99480.96451120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C08:04ISVEWNPQL0.99480.96451120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:01SLCSLDISV0.99440.672514
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C04:06SVEWNPQLL0.97860.88081221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C06:03ISVEWNPQL0.94180.99211120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C12:04ISVEWNPQL0.93880.99441120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C12:12ISVEWNPQL0.93030.89931120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C08:04SVEWNPQLL0.9080.95231221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C08:13SVEWNPQLL0.9080.95231221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:14ISVEWNPQL0.85460.9811120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C08:03ISVEWNPQL0.85220.97861120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C08:03SVEWNPQLL0.75210.97971221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C02:06ISVEWNPQL0.55610.94711120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:02SLDISVEW0.9950.9175816
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C05:01SVEWNPQLL0.99990.8841221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C04:03SVEWNPQLL0.99990.83611221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C08:02SVEWNPQLL0.99980.95641221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C01:03SVEWNPQLL0.99980.88781221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:03ISVEWNPQL0.99950.98741120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:04ISVEWNPQL0.99950.98741120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C15:05ISVEWNPQL0.99940.89191120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C15:02ISVEWNPQL0.99940.861120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C15:09ISVEWNPQL0.99940.89261120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:04CSLDISVEW0.99920.9227716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:10CSLDISVEW0.99910.9878716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:02ISVEWNPQL0.99880.97721120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:05ISVEWNPQL0.99860.92531120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:17ISVEWNPQL0.99850.96971120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:02CSLDISVEW0.99740.9545716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B58:06CSLDISVEW0.9930.918716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:06ISVEWNPQL0.99180.98781120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C16:04ISVEWNPQL0.99120.97181120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B15:13CSLDISVEW0.97830.8554716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A32:01CSLDISVEW0.96170.9729716
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C16:02ISVEWNPQL0.9460.99151120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C12:03ISVEWNPQL0.92070.97631120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C03:06SVEWNPQLL0.89750.98531221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B35:13ISVEWNPQL0.88380.93851120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C08:01ISVEWNPQL0.85220.97861120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C16:01ISVEWNPQL0.84470.97451120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:14ISVEWNPQL0.78280.55281120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A02:06ISVEWNPQL0.7770.70871120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C08:01SVEWNPQLL0.75210.97971221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C17:01SVEWNPQLL0.6140.88591221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-C17:01ISVEWNPQL0.40530.90371120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B07:13SVEWNPQLL0.26450.80111221
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B07:13ISVEWNPQL0.04960.76541120
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:10LCSLDISVEW0.99930.9913616
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:04LCSLDISVEW0.99920.9154616
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:02LCSLDISVEW0.99520.9573616
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B58:06LCSLDISVEW0.98130.922616
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:10SLCSLDISVEW0.99960.984516
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:04SLCSLDISVEW0.99930.8656516
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B57:02SLCSLDISVEW0.99690.9552516
ARHGEF3-ACP6chr356916319chr1147131890302HLA-B58:06SLCSLDISVEW0.99410.8414516
ARHGEF3-ACP6chr356916319chr1147131890302HLA-A32:01SLCSLDISVEW0.98750.9554516

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Potential FusionNeoAntigen Information of ARHGEF3-ACP6 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 ARHGEF3-ACP6

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
4825LCSLDISVEWNPQLARHGEF3ACP6chr356916319chr1147131890302

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ARHGEF3-ACP6

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-B14:023BVN4825LCSLDISVEWNPQL-7.15543-7.26883
HLA-B14:023BVN4825LCSLDISVEWNPQL-4.77435-5.80965
HLA-B52:013W394825LCSLDISVEWNPQL-6.80875-6.92215
HLA-B52:013W394825LCSLDISVEWNPQL-4.20386-5.23916
HLA-A11:014UQ24825LCSLDISVEWNPQL-7.5194-8.5547
HLA-A11:014UQ24825LCSLDISVEWNPQL-6.9601-7.0735
HLA-A24:025HGA4825LCSLDISVEWNPQL-7.52403-7.63743
HLA-A24:025HGA4825LCSLDISVEWNPQL-5.82433-6.85963
HLA-B27:056PYJ4825LCSLDISVEWNPQL-3.28285-4.31815
HLA-B44:053DX84825LCSLDISVEWNPQL-5.91172-6.94702
HLA-B44:053DX84825LCSLDISVEWNPQL-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of ARHGEF3-ACP6

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
ARHGEF3-ACP6chr356916319chr11471318901120ISVEWNPQLATAAGTGTAGAGTGGAACCCCCAGCTA
ARHGEF3-ACP6chr356916319chr11471318901221SVEWNPQLLAGTGTAGAGTGGAACCCCCAGCTATTA
ARHGEF3-ACP6chr356916319chr1147131890514SLCSLDISVAGCCTTTGCAGTCTCGACATAAGTGTA
ARHGEF3-ACP6chr356916319chr1147131890516SLCSLDISVEWAGCCTTTGCAGTCTCGACATAAGTGTAGAGTGG
ARHGEF3-ACP6chr356916319chr1147131890616LCSLDISVEWCTTTGCAGTCTCGACATAAGTGTAGAGTGG
ARHGEF3-ACP6chr356916319chr1147131890716CSLDISVEWTGCAGTCTCGACATAAGTGTAGAGTGG
ARHGEF3-ACP6chr356916319chr1147131890816SLDISVEWAGTCTCGACATAAGTGTAGAGTGG

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 ARHGEF3-ACP6

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
BRCAARHGEF3-ACP6chr356916319ENST00000338458chr1147131890ENST00000369238TCGA-AO-A0J6

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Potential target of CAR-T therapy development for ARHGEF3-ACP6

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 ARHGEF3-ACP6

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 ARHGEF3-ACP6

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