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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:ARAP1-FADD

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ARAP1-FADD
FusionPDB ID: 5757
FusionGDB2.0 ID: 5757
HgeneTgene
Gene symbol

ARAP1

FADD

Gene ID

116985

8772

Gene nameArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1Fas associated via death domain
SynonymsCENTD2GIG3|MORT1
Cytomap

11q13.4

11q13.3

Type of geneprotein-codingprotein-coding
Descriptionarf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 1ARF-GAP, RHO-GAP, ankyrin repeat, and pleckstrin homology domains-containing protein 1centaurin-delta-2cnt-d2FAS-associated death domain proteinFas (TNFRSF6)-associated via death domainFas-associating death domain-containing proteinFas-associating protein with death domaingrowth-inhibiting gene 3 proteinmediator of receptor-induced toxicity
Modification date2020031320200313
UniProtAcc

Q96P48

Main function of 5'-partner protein: FUNCTION: Phosphatidylinositol 3,4,5-trisphosphate-dependent GTPase-activating protein that modulates actin cytoskeleton remodeling by regulating ARF and RHO family members. Is activated by phosphatidylinositol 3,4,5-trisphosphate (PtdIns(3,4,5)P3) binding. Can be activated by phosphatidylinositol 3,4-bisphosphate (PtdIns(3,4,5)P2) binding, albeit with lower efficiency. Has a preference for ARF1 and ARF5 (By similarity). {ECO:0000250, ECO:0000269|PubMed:11804590}.

Q13158

Main function of 5'-partner protein: FUNCTION: Apoptotic adaptor molecule that recruits caspase-8 or caspase-10 to the activated Fas (CD95) or TNFR-1 receptors. The resulting aggregate called the death-inducing signaling complex (DISC) performs caspase-8 proteolytic activation. Active caspase-8 initiates the subsequent cascade of caspases mediating apoptosis. Involved in interferon-mediated antiviral immune response, playing a role in the positive regulation of interferon signaling. {ECO:0000269|PubMed:16762833, ECO:0000269|PubMed:19118384, ECO:0000269|PubMed:20935634, ECO:0000269|PubMed:21109225}.
Ensembl transtripts involved in fusion geneENST idsENST00000393609, ENST00000334211, 
ENST00000359373, ENST00000393605, 
ENST00000426523, ENST00000429686, 
ENST00000455638, ENST00000495878, 
ENST00000301838, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score15 X 15 X 9=20255 X 2 X 4=40
# samples 176
** MAII scorelog2(17/2025*10)=-3.57431525652165
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/40*10)=0.584962500721156
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Fusion gene context

PubMed: ARAP1 [Title/Abstract] AND FADD [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ARAP1 [Title/Abstract] AND FADD [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ARAP1(72412694)-FADD(70052239), # samples:3
Anticipated loss of major functional domain due to fusion event.ARAP1-FADD 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.
ARAP1-FADD 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.
ARAP1-FADD 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.
ARAP1-FADD 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.
ARAP1-FADD seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ARAP1-FADD seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted 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
HgeneARAP1

GO:0043547

positive regulation of GTPase activity

11804590

TgeneFADD

GO:0032757

positive regulation of interleukin-8 production

16127453

TgeneFADD

GO:0032760

positive regulation of tumor necrosis factor production

16127453

TgeneFADD

GO:0036462

TRAIL-activated apoptotic signaling pathway

21785459

TgeneFADD

GO:0043065

positive regulation of apoptotic process

11821383

TgeneFADD

GO:0045862

positive regulation of proteolysis

18387192

TgeneFADD

GO:0045944

positive regulation of transcription by RNA polymerase II

16127453

TgeneFADD

GO:0097190

apoptotic signaling pathway

11101870

TgeneFADD

GO:0097191

extrinsic apoptotic signaling pathway

21785459

TgeneFADD

GO:0097202

activation of cysteine-type endopeptidase activity

18387192



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/chr11:72412694/chr11:70052239)
- 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 ARAP1 (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 FADD (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)
ENST00000359373ARAP1chr1172412694-ENST00000301838FADDchr1170052239+441231548103494894
ENST00000455638ARAP1chr1172412694-ENST00000301838FADDchr1170052239+3560230202642880
ENST00000393605ARAP1chr1172412694-ENST00000301838FADDchr1170052239+339621385442478644
ENST00000334211ARAP1chr1172412694-ENST00000301838FADDchr1170052239+356023025102642710
ENST00000426523ARAP1chr1172412694-ENST00000301838FADDchr1170052239+323019721802312710
ENST00000429686ARAP1chr1172412694-ENST00000301838FADDchr1170052239+304717891802129649

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
ENST00000359373ENST00000301838ARAP1chr1172412694-FADDchr1170052239+0.0041113990.99588865
ENST00000455638ENST00000301838ARAP1chr1172412694-FADDchr1170052239+0.0054326470.9945674
ENST00000393605ENST00000301838ARAP1chr1172412694-FADDchr1170052239+0.0047976120.9952024
ENST00000334211ENST00000301838ARAP1chr1172412694-FADDchr1170052239+0.0032532450.9967468
ENST00000426523ENST00000301838ARAP1chr1172412694-FADDchr1170052239+0.0054144980.9945856
ENST00000429686ENST00000301838ARAP1chr1172412694-FADDchr1170052239+0.0061609080.9938391

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 ARAP1-FADD

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ARAP1chr1172412694FADDchr11700522391789536SAGKLLQDRRAREDLCAAFNVICDNV
ARAP1chr1172412694FADDchr11700522391972597SAGKLLQDRRAREDLCAAFNVICDNV
ARAP1chr1172412694FADDchr11700522392138531SAGKLLQDRRAREDLCAAFNVICDNV
ARAP1chr1172412694FADDchr11700522392302597SAGKLLQDRRAREDLCAAFNVICDNV
ARAP1chr1172412694FADDchr11700522392302767SAGKLLQDRRAREDLCAAFNVICDNV
ARAP1chr1172412694FADDchr11700522393154781SAGKLLQDRRAREDLCAAFNVICDNV

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Potential FusionNeoAntigen Information of ARAP1-FADD 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.
ARAP1-FADD_72412694_70052239.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)
ARAP1-FADDchr1172412694chr11700522392302HLA-B27:02AREDLCAAF0.9630.58221019
ARAP1-FADDchr1172412694chr11700522392302HLA-B27:04AREDLCAAF0.95120.781019
ARAP1-FADDchr1172412694chr11700522392302HLA-B15:18AREDLCAAF0.35860.7521019
ARAP1-FADDchr1172412694chr11700522392302HLA-B27:04RRAREDLCAAF0.99990.7014819
ARAP1-FADDchr1172412694chr11700522392302HLA-B27:07RRAREDLCAAF0.99950.5998819
ARAP1-FADDchr1172412694chr11700522392302HLA-B39:08REDLCAAF0.89270.86011119
ARAP1-FADDchr1172412694chr11700522392302HLA-C07:27AREDLCAAF0.9270.94811019
ARAP1-FADDchr1172412694chr11700522392302HLA-C07:95AREDLCAAF0.92580.70421019
ARAP1-FADDchr1172412694chr11700522392302HLA-C07:46AREDLCAAF0.79290.89841019
ARAP1-FADDchr1172412694chr11700522392302HLA-C07:80AREDLCAAF0.77880.94381019
ARAP1-FADDchr1172412694chr11700522392302HLA-C07:67AREDLCAAF0.77880.94381019
ARAP1-FADDchr1172412694chr11700522392302HLA-C07:19AREDLCAAF0.76760.79081019
ARAP1-FADDchr1172412694chr11700522392302HLA-C07:10AREDLCAAF0.760.95231019
ARAP1-FADDchr1172412694chr11700522392302HLA-C12:16AREDLCAAF0.03230.96421019
ARAP1-FADDchr1172412694chr11700522392302HLA-B27:03RRAREDLCAAF0.99620.6464819
ARAP1-FADDchr1172412694chr11700522392302HLA-B27:06AREDLCAAF0.97150.79311019
ARAP1-FADDchr1172412694chr11700522392302HLA-B27:08AREDLCAAF0.96470.71661019
ARAP1-FADDchr1172412694chr11700522392302HLA-C07:01AREDLCAAF0.94710.66471019
ARAP1-FADDchr1172412694chr11700522392302HLA-B27:09AREDLCAAF0.93630.8081019
ARAP1-FADDchr1172412694chr11700522392302HLA-B39:31AREDLCAAF0.850.88831019
ARAP1-FADDchr1172412694chr11700522392302HLA-C07:02AREDLCAAF0.77880.94381019
ARAP1-FADDchr1172412694chr11700522392302HLA-C07:17AREDLCAAF0.77180.95171019
ARAP1-FADDchr1172412694chr11700522392302HLA-B27:08RRAREDLCAAF0.99990.5232819
ARAP1-FADDchr1172412694chr11700522392302HLA-B27:09RRAREDLCAAF0.99950.6176819

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Potential FusionNeoAntigen Information of ARAP1-FADD 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.
ARAP1-FADD_72412694_70052239.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)
ARAP1-FADDchr1172412694chr11700522392302DRB1-0301SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0301AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0303SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0305SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0307SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0307AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0310SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0313SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0313AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0315SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0315AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0318SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0318AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0320SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0320AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0322SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0322AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0324SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0326SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0328SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0328AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0330SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0330AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0332SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0332AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0334SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0334AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0336SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0336AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0340SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0344SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0344AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0346SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0346AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0348SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0348AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0350SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0350AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0352SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0352AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0354SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-0354AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-0840SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1107SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1107AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-1303SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1303AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-13101SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-13101AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-1310SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1310AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-1333SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1333AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-1338SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1365SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1366SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1381SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1381AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-1388SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1388AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-1389SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1389AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-1390SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1390AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-1394SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1394AGKLLQDRRAREDLC116
ARAP1-FADDchr1172412694chr11700522392302DRB1-1395SAGKLLQDRRAREDL015
ARAP1-FADDchr1172412694chr11700522392302DRB1-1395AGKLLQDRRAREDLC116

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Fusion breakpoint peptide structures of ARAP1-FADD

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
7195QDRRAREDLCAAFNARAP1FADDchr1172412694chr11700522392302

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ARAP1-FADD

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-B14:023BVN7195QDRRAREDLCAAFN-7.63753-7.75093
HLA-B14:023BVN7195QDRRAREDLCAAFN-4.36349-5.39879
HLA-B52:013W397195QDRRAREDLCAAFN-6.74822-6.86162
HLA-B52:013W397195QDRRAREDLCAAFN-4.96916-6.00446
HLA-A24:025HGA7195QDRRAREDLCAAFN-8.26666-9.30196
HLA-A24:025HGA7195QDRRAREDLCAAFN-7.6208-7.7342
HLA-B27:036PZ57195QDRRAREDLCAAFN0.0420189-0.993281
HLA-B44:053DX87195QDRRAREDLCAAFN-5.06122-5.17462
HLA-B44:053DX87195QDRRAREDLCAAFN-4.87073-5.90603

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Vaccine Design for the FusionNeoAntigens of ARAP1-FADD

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
ARAP1-FADDchr1172412694chr11700522391019AREDLCAAFCCCGGGAAGACCTGTGTGCAGCATTTA
ARAP1-FADDchr1172412694chr11700522391119REDLCAAFGGGAAGACCTGTGTGCAGCATTTA
ARAP1-FADDchr1172412694chr1170052239819RRAREDLCAAFGCCGGGCCCGGGAAGACCTGTGTGCAGCATTTA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ARAP1-FADDchr1172412694chr1170052239015SAGKLLQDRRAREDLCTGCCGGCAAGCTGCTACAGGACCGCCGGGCCCGGGAAGACCTGT
ARAP1-FADDchr1172412694chr1170052239116AGKLLQDRRAREDLCCCGGCAAGCTGCTACAGGACCGCCGGGCCCGGGAAGACCTGTGTG

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Information of the samples that have these potential fusion neoantigens of ARAP1-FADD

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
LUADARAP1-FADDchr1172412694ENST00000334211chr1170052239ENST00000301838TCGA-44-A4SU-01A

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Potential target of CAR-T therapy development for ARAP1-FADD

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 ARAP1-FADD

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 ARAP1-FADD

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