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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:PRKDC-SPIDR

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PRKDC-SPIDR
FusionPDB ID: 68845
FusionGDB2.0 ID: 68845
HgeneTgene
Gene symbol

PRKDC

SPIDR

Gene ID

5591

23514

Gene nameprotein kinase, DNA-activated, catalytic subunitscaffold protein involved in DNA repair
SynonymsDNA-PKC|DNA-PKcs|DNAPK|DNAPKc|DNPK1|HYRC|HYRC1|IMD26|XRCC7|p350KIAA0146
Cytomap

8q11.21

8q11.21

Type of geneprotein-codingprotein-coding
DescriptionDNA-dependent protein kinase catalytic subunitDNA-PK catalytic subunithyper-radiosensitivity of murine scid mutation, complementing 1p460protein kinase, DNA-activated, catalytic polypeptideDNA repair-scaffolding proteinscaffolding protein involved in DNA repair
Modification date2020032220200320
UniProtAcc.

Q14159

Main function of 5'-partner protein: FUNCTION: Plays a role in DNA double-strand break (DBS) repair via homologous recombination (HR). Serves as a scaffolding protein that helps to promote the recruitment of DNA-processing enzymes like the helicase BLM and recombinase RAD51 to site of DNA damage, and hence contributes to maintain genomic integrity. {ECO:0000269|PubMed:23509288, ECO:0000269|PubMed:23754376}.
Ensembl transtripts involved in fusion geneENST idsENST00000314191, ENST00000338368, 
ENST00000523565, 
ENST00000521214, 
ENST00000297423, ENST00000517693, 
ENST00000518060, ENST00000518074, 
ENST00000541342, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score24 X 28 X 10=672019 X 18 X 7=2394
# samples 2822
** MAII scorelog2(28/6720*10)=-4.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(22/2394*10)=-3.44384772341884
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: PRKDC [Title/Abstract] AND SPIDR [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PRKDC [Title/Abstract] AND SPIDR [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PRKDC(48706851)-SPIDR(48508373), # samples:1
PRKDC(48730011)-SPIDR(48508373), # samples:1
PRKDC(48839754)-SPIDR(48508373), # samples:1
PRKDC(48746757)-SPIDR(48191858), # samples:1
SPIDR(48353104)-PRKDC(48686938), # samples:1
Anticipated loss of major functional domain due to fusion event.PRKDC-SPIDR 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.
PRKDC-SPIDR 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.
PRKDC-SPIDR 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.
PRKDC-SPIDR 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.
SPIDR-PRKDC 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.
SPIDR-PRKDC 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.
PRKDC-SPIDR seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
PRKDC-SPIDR seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PRKDC-SPIDR seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
PRKDC-SPIDR seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgenePRKDC

GO:0002218

activation of innate immune response

28712728

HgenePRKDC

GO:0006468

protein phosphorylation

26237645

HgenePRKDC

GO:0006974

cellular response to DNA damage stimulus

26237645

HgenePRKDC

GO:0018105

peptidyl-serine phosphorylation

15194694|19303849

HgenePRKDC

GO:2001034

positive regulation of double-strand break repair via nonhomologous end joining

26237645

TgeneSPIDR

GO:0006974

cellular response to DNA damage stimulus

23509288

TgeneSPIDR

GO:0010569

regulation of double-strand break repair via homologous recombination

23754376

TgeneSPIDR

GO:0031334

positive regulation of protein complex assembly

23509288

TgeneSPIDR

GO:0070202

regulation of establishment of protein localization to chromosome

23509288

TgeneSPIDR

GO:0071479

cellular response to ionizing radiation

23509288|23754376

TgeneSPIDR

GO:0072711

cellular response to hydroxyurea

23509288

TgeneSPIDR

GO:0072757

cellular response to camptothecin

23509288



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/chr8:48706851/chr8:48508373)
- 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 PRKDC (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 SPIDR (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)
ENST00000338368PRKDCchr848706851-ENST00000297423SPIDRchr848508373+132311072457123744105
ENST00000338368PRKDCchr848706851-ENST00000518074SPIDRchr848508373+124551072457124374126
ENST00000338368PRKDCchr848706851-ENST00000541342SPIDRchr848508373+124361072457123744105
ENST00000314191PRKDCchr848706851-ENST00000297423SPIDRchr848508373+132311072457123744105
ENST00000314191PRKDCchr848706851-ENST00000518074SPIDRchr848508373+124551072457124374126
ENST00000314191PRKDCchr848706851-ENST00000541342SPIDRchr848508373+124361072457123744105
ENST00000338368PRKDCchr848730011-ENST00000297423SPIDRchr848508373+12118961157112613734
ENST00000338368PRKDCchr848730011-ENST00000518074SPIDRchr848508373+11342961157113243755
ENST00000338368PRKDCchr848730011-ENST00000541342SPIDRchr848508373+11323961157112613734
ENST00000314191PRKDCchr848730011-ENST00000297423SPIDRchr848508373+12118961157112613734
ENST00000314191PRKDCchr848730011-ENST00000518074SPIDRchr848508373+11342961157113243755
ENST00000314191PRKDCchr848730011-ENST00000541342SPIDRchr848508373+11323961157112613734

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
ENST00000338368ENST00000297423PRKDCchr848706851-SPIDRchr848508373+0.0004228830.9995771
ENST00000338368ENST00000518074PRKDCchr848706851-SPIDRchr848508373+0.0003584520.99964154
ENST00000338368ENST00000541342PRKDCchr848706851-SPIDRchr848508373+0.0005464690.9994535
ENST00000314191ENST00000297423PRKDCchr848706851-SPIDRchr848508373+0.0004228830.9995771
ENST00000314191ENST00000518074PRKDCchr848706851-SPIDRchr848508373+0.0003584520.99964154
ENST00000314191ENST00000541342PRKDCchr848706851-SPIDRchr848508373+0.0005464690.9994535
ENST00000338368ENST00000297423PRKDCchr848730011-SPIDRchr848508373+0.0002671940.9997328
ENST00000338368ENST00000518074PRKDCchr848730011-SPIDRchr848508373+0.0005569460.999443
ENST00000338368ENST00000541342PRKDCchr848730011-SPIDRchr848508373+0.000347910.99965215
ENST00000314191ENST00000297423PRKDCchr848730011-SPIDRchr848508373+0.0002671940.9997328
ENST00000314191ENST00000518074PRKDCchr848730011-SPIDRchr848508373+0.0005569460.999443
ENST00000314191ENST00000541342PRKDCchr848730011-SPIDRchr848508373+0.000347910.99965215

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 PRKDC-SPIDR

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PRKDCchr848706851SPIDRchr848508373107243555DTSTGHKNKEFVARQKLIIPSGSCPV
PRKDCchr848730011SPIDRchr84850837396113184MDPMNIWDDIITNRQKLIIPSGSCPV

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Potential FusionNeoAntigen Information of PRKDC-SPIDR 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.
PRKDC-SPIDR_48706851_48508373.msa
PRKDC-SPIDR_48730011_48508373.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)
PRKDC-SPIDRchr848706851chr84850837310724HLA-B13:01KEFVARQKL0.98870.6872817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B44:03KEFVARQKL0.97770.9658817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B50:02KEFVARQKL0.85280.5629817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B45:01KEFVARQKL0.7640.7805817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B18:01KEFVARQKL0.68030.8866817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B41:01KEFVARQKL0.38990.7158817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B39:13KEFVARQKL0.1280.8819817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B50:01KEFVARQKL0.05770.6808817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B27:14ARQKLIIPS0.99750.61081221
PRKDC-SPIDRchr848706851chr84850837310724HLA-B73:01ARQKLIIPS0.95950.55621221
PRKDC-SPIDRchr848706851chr84850837310724HLA-B39:08KEFVARQKL0.19510.718817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B40:04KEFVARQKL0.99430.6346817
PRKDC-SPIDRchr848706851chr84850837310724HLA-C15:02FVARQKLII0.98780.66361019
PRKDC-SPIDRchr848706851chr84850837310724HLA-B44:13KEFVARQKL0.97770.9658817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B44:07KEFVARQKL0.97770.9658817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B44:26KEFVARQKL0.97770.9658817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B18:05KEFVARQKL0.68030.8866817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B18:11KEFVARQKL0.61570.8471817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B39:02KEFVARQKL0.1550.8893817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B48:02KEFVARQKL0.1280.8286817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B15:68KEFVARQKL0.1050.5418817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B15:54KEFVARQKL0.09590.7682817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B50:05KEFVARQKL0.05770.6808817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B50:04KEFVARQKL0.05770.6808817
PRKDC-SPIDRchr848706851chr84850837310724HLA-B15:53KEFVARQKL0.03020.7884817
PRKDC-SPIDRchr848730011chr8485083739611HLA-C15:06ITNRQKLII0.99350.85581019
PRKDC-SPIDRchr848730011chr8485083739611HLA-B73:01NRQKLIIPS0.98660.54761221
PRKDC-SPIDRchr848730011chr8485083739611HLA-A25:01DIITNRQKL0.99570.8604817
PRKDC-SPIDRchr848730011chr8485083739611HLA-C15:02ITNRQKLII0.99360.82931019
PRKDC-SPIDRchr848730011chr8485083739611HLA-C15:05ITNRQKLII0.99350.86551019
PRKDC-SPIDRchr848730011chr8485083739611HLA-B08:12DIITNRQKL0.61470.5093817

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Potential FusionNeoAntigen Information of PRKDC-SPIDR 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.
PRKDC-SPIDR_48706851_48508373.msa
PRKDC-SPIDR_48730011_48508373.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)
PRKDC-SPIDRchr848706851chr84850837310724DRB1-0837NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-0837KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1111NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1111KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1111HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1111KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1114NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1114KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1114HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1114KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1119NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1120NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1120KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1120HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1120KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1131NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1132NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1145NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1145KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1145HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1164NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1164KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1168NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1168KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1168HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1168KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1169NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1169KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1172NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1172KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1182NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1182KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1186NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1186KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1302NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1302KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1302HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1302KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-13100NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1316NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1316KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1323NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1323KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1323HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1323KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1329NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1329KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1329HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1329KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1331NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1331KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1331HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1331KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1334NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1334KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1334HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1334KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1336NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1336KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1336HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1336KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1338NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1338KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1338HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1339NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1339KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1339HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1339KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1341NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1341KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1346NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1363NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1363KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1363HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1363KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1365NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1365KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1365HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1373NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1373KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1373HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1373KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1374NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1374KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1374HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1374KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1382NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1396NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1396KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1396HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1397NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1397KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1397HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1397KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1399NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1399KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1399HKNKEFVARQKLIIP520
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1399KEFVARQKLIIPSGS823
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1403NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1424NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1440NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1442NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1442KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1453NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1463NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1463KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1467NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1467KNKEFVARQKLIIPS621
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1477NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1485NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848706851chr84850837310724DRB1-1498NKEFVARQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-0338WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-0338IWDDIITNRQKLIIP520
PRKDC-SPIDRchr848730011chr8485083739611DRB1-0338DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1102DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1102WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1103DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1116DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1116WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1121DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1121WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1136DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1148DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1148WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1155DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1155WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1159DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1163DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1165DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1165WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1170DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1170WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1176DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1185DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1301DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1301WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1304DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1304WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1308DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1308WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1315DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1317DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1317WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1319DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1319WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1320DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1322DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1322WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1324DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1327DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1331WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1331DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1331IWDDIITNRQKLIIP520
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1332DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1332WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1335DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1335WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1343DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1343WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1343IWDDIITNRQKLIIP520
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1348DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1348WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1351DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1351WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1352DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1352WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1353DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1353WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1354DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1354WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1354IWDDIITNRQKLIIP520
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1357DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1359DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1359WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1361DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1361WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1364DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1364WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1368DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1368WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1369DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1369WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1370DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1370WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1372DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1372WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1375DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1375WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1376DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1376WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1377WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1378DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1379DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1379WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1380DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1380WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1383DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1383WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1384DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1384WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1387DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1387WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1391DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1391WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1392DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1392WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1393DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1393WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1396WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1396DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1398DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1398WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1416DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1416WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1416IWDDIITNRQKLIIP520
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1428WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1438WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1438IWDDIITNRQKLIIP520
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1448WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1448IWDDIITNRQKLIIP520
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1449WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1450WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1450IWDDIITNRQKLIIP520
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1450DDIITNRQKLIIPSG722
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1455WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1470WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1493WDDIITNRQKLIIPS621
PRKDC-SPIDRchr848730011chr8485083739611DRB1-1493IWDDIITNRQKLIIP520

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Fusion breakpoint peptide structures of PRKDC-SPIDR

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
4452KNKEFVARQKLIIPPRKDCSPIDRchr848706851chr84850837310724
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
10431WDDIITNRQKLIIPPRKDCSPIDRchr848730011chr8485083739611

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PRKDC-SPIDR

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-B52:013W394452KNKEFVARQKLIIP-4.16556-4.16556
HLA-B44:053DX84452KNKEFVARQKLIIP-4.6351-4.6351
HLA-B14:023BVN10431WDDIITNRQKLIIP-7.9962-8.1096
HLA-B14:023BVN10431WDDIITNRQKLIIP-5.70842-6.74372
HLA-B52:013W3910431WDDIITNRQKLIIP-6.83737-6.95077
HLA-B52:013W3910431WDDIITNRQKLIIP-4.4836-5.5189
HLA-A11:014UQ210431WDDIITNRQKLIIP-10.0067-10.1201
HLA-A11:014UQ210431WDDIITNRQKLIIP-9.03915-10.0745
HLA-A24:025HGA10431WDDIITNRQKLIIP-6.56204-6.67544
HLA-A24:025HGA10431WDDIITNRQKLIIP-5.42271-6.45801
HLA-B44:053DX810431WDDIITNRQKLIIP-7.85648-8.89178
HLA-B44:053DX810431WDDIITNRQKLIIP-5.3978-5.5112
HLA-B35:011A1N10431WDDIITNRQKLIIP-6.27422-6.38762
HLA-B35:011A1N10431WDDIITNRQKLIIP-5.27424-6.30954
HLA-A02:016TDR10431WDDIITNRQKLIIP-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of PRKDC-SPIDR

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
PRKDC-SPIDRchr848706851chr8485083731019FVARQKLIITGTGGCAAGGCAAAAACTGATTATTCC
PRKDC-SPIDRchr848706851chr8485083731221ARQKLIIPSAAGGCAAAAACTGATTATTCCAAGTGG
PRKDC-SPIDRchr848706851chr848508373817KEFVARQKLGGAGTTTGTGGCAAGGCAAAAACTGAT
PRKDC-SPIDRchr848730011chr8485083731019ITNRQKLIICACAAATCGGCAAAAACTGATTATTCC
PRKDC-SPIDRchr848730011chr8485083731221NRQKLIIPSTCGGCAAAAACTGATTATTCCAAGTGG
PRKDC-SPIDRchr848730011chr848508373817DIITNRQKLCATCATCACAAATCGGCAAAAACTGAT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
PRKDC-SPIDRchr848706851chr848508373520HKNKEFVARQKLIIPTAAGAATAAGGAGTTTGTGGCAAGGCAAAAACTGATTATTCCAAG
PRKDC-SPIDRchr848706851chr848508373621KNKEFVARQKLIIPSGAATAAGGAGTTTGTGGCAAGGCAAAAACTGATTATTCCAAGTGG
PRKDC-SPIDRchr848706851chr848508373722NKEFVARQKLIIPSGTAAGGAGTTTGTGGCAAGGCAAAAACTGATTATTCCAAGTGGAAG
PRKDC-SPIDRchr848706851chr848508373823KEFVARQKLIIPSGSGGAGTTTGTGGCAAGGCAAAAACTGATTATTCCAAGTGGAAGTTG
PRKDC-SPIDRchr848730011chr848508373520IWDDIITNRQKLIIPCTGGGATGACATCATCACAAATCGGCAAAAACTGATTATTCCAAG
PRKDC-SPIDRchr848730011chr848508373621WDDIITNRQKLIIPSGGATGACATCATCACAAATCGGCAAAAACTGATTATTCCAAGTGG
PRKDC-SPIDRchr848730011chr848508373722DDIITNRQKLIIPSGTGACATCATCACAAATCGGCAAAAACTGATTATTCCAAGTGGAAG

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Information of the samples that have these potential fusion neoantigens of PRKDC-SPIDR

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
BRCAPRKDC-SPIDRchr848706851ENST00000314191chr848508373ENST00000297423TCGA-D8-A1XS-01A
CESCPRKDC-SPIDRchr848730011ENST00000314191chr848508373ENST00000297423TCGA-EA-A1QT-01A

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Potential target of CAR-T therapy development for PRKDC-SPIDR

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 PRKDC-SPIDR

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 PRKDC-SPIDR

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