FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

leaf

Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

leaf

Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

leaf

Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:PRKDC-TOMM70A

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PRKDC-TOMM70A
FusionPDB ID: 68847
FusionGDB2.0 ID: 68847
HgeneTgene
Gene symbol

PRKDC

TOMM70A

Gene ID

5591

9868

Gene nameprotein kinase, DNA-activated, catalytic subunittranslocase of outer mitochondrial membrane 70
SynonymsDNA-PKC|DNA-PKcs|DNAPK|DNAPKc|DNPK1|HYRC|HYRC1|IMD26|XRCC7|p350TOMM70A|Tom70
Cytomap

8q11.21

3q12.2

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 polypeptidemitochondrial import receptor subunit TOM70mitochondrial precursor proteins import receptortranslocase of outer membrane 70 kDa subunittranslocase of outer mitochondrial membrane 70 homolog Atranslocase of outer mitochondrial membrane protein 70
Modification date2020032220200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000523565, ENST00000314191, 
ENST00000338368, 
ENST00000284320, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score24 X 28 X 10=67201 X 1 X 1=1
# samples 281
** MAII scorelog2(28/6720*10)=-4.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Fusion gene context

PubMed: PRKDC [Title/Abstract] AND TOMM70A [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: PRKDC [Title/Abstract] AND TOMM70A [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PRKDC(48868434)-TOMM70A(100092489), # samples:1
Anticipated loss of major functional domain due to fusion event.PRKDC-TOMM70A 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-TOMM70A 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
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



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/chr8:48868434/chr3:100092489)
- 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 TOMM70A (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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)
ENST00000338368PRKDCchr848868434-ENST00000284320TOMM70Achr3100092489-3189456571055332
ENST00000314191PRKDCchr848868434-ENST00000284320TOMM70Achr3100092489-3189456571055332

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
ENST00000338368ENST00000284320PRKDCchr848868434-TOMM70Achr3100092489-7.10E-050.99992895
ENST00000314191ENST00000284320PRKDCchr848868434-TOMM70Achr3100092489-7.10E-050.99992895

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

Top

Fusion Protein Breakpoint Sequences for PRKDC-TOMM70A

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
PRKDCchr848868434TOMM70Achr3100092489456133AKCKIPALDLLIKLKILLDQVEEAVA

Top

Potential FusionNeoAntigen Information of PRKDC-TOMM70A 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-TOMM70A_48868434_100092489.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-TOMM70Achr848868434chr3100092489456HLA-A02:22KLKILLDQV0.98850.66091221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B08:09DLLIKLKIL0.98260.5459817
PRKDC-TOMM70Achr848868434chr3100092489456HLA-A02:13KLKILLDQV0.97990.71391221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-A02:27KLKILLDQV0.97310.64971221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-A02:11KLKILLDQV0.96210.70871221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-A02:16KLKILLDQV0.96130.69861221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-A02:04KLKILLDQV0.93040.82461221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-A02:29KLKILLDQV0.8080.70441221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-A02:20KLKILLDQV0.79840.70741221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B13:02KLKILLDQV0.07480.94661221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B35:03IPALDLLIKL0.92310.5793414
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B35:02IPALDLLIKL0.77860.655414
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B35:04IPALDLLIKL0.77860.655414
PRKDC-TOMM70Achr848868434chr3100092489456HLA-C04:07ALDLLIKL10.7667614
PRKDC-TOMM70Achr848868434chr3100092489456HLA-C05:09ALDLLIKL10.9153614
PRKDC-TOMM70Achr848868434chr3100092489456HLA-C04:10ALDLLIKL10.7062614
PRKDC-TOMM70Achr848868434chr3100092489456HLA-C08:15ALDLLIKL0.99990.9584614
PRKDC-TOMM70Achr848868434chr3100092489456HLA-A02:05KLKILLDQV0.98850.55921221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B35:12IPALDLLIKL0.77860.655414
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B42:01IPALDLLIKL0.66230.622414
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B39:10IPALDLLIKL0.54970.6585414
PRKDC-TOMM70Achr848868434chr3100092489456HLA-C04:01ALDLLIKL10.7667614
PRKDC-TOMM70Achr848868434chr3100092489456HLA-C05:01ALDLLIKL10.9153614
PRKDC-TOMM70Achr848868434chr3100092489456HLA-C04:03ALDLLIKL10.825614
PRKDC-TOMM70Achr848868434chr3100092489456HLA-C08:02ALDLLIKL0.99990.9584614
PRKDC-TOMM70Achr848868434chr3100092489456HLA-A02:03KLKILLDQV0.99530.74511221
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B08:12DLLIKLKIL0.69060.5876817
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B35:13IPALDLLIKL0.9220.5996414
PRKDC-TOMM70Achr848868434chr3100092489456HLA-B35:09IPALDLLIKL0.77860.655414

Top

Potential FusionNeoAntigen Information of PRKDC-TOMM70A 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-TOMM70A_48868434_100092489.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-TOMM70Achr848868434chr3100092489456DRB1-0422IKLKILLDQVEEAVA1126
PRKDC-TOMM70Achr848868434chr3100092489456DRB1-0422LIKLKILLDQVEEAV1025
PRKDC-TOMM70Achr848868434chr3100092489456DRB4-0104IKLKILLDQVEEAVA1126

Top

Fusion breakpoint peptide structures of PRKDC-TOMM70A

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
347ALDLLIKLKILLDQPRKDCTOMM70Achr848868434chr3100092489456

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of PRKDC-TOMM70A

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-B14:023BVN347ALDLLIKLKILLDQ-7.15543-7.26883
HLA-B14:023BVN347ALDLLIKLKILLDQ-4.77435-5.80965
HLA-B52:013W39347ALDLLIKLKILLDQ-6.80875-6.92215
HLA-B52:013W39347ALDLLIKLKILLDQ-4.20386-5.23916
HLA-A11:014UQ2347ALDLLIKLKILLDQ-7.5194-8.5547
HLA-A11:014UQ2347ALDLLIKLKILLDQ-6.9601-7.0735
HLA-A24:025HGA347ALDLLIKLKILLDQ-7.52403-7.63743
HLA-A24:025HGA347ALDLLIKLKILLDQ-5.82433-6.85963
HLA-B27:056PYJ347ALDLLIKLKILLDQ-3.28285-4.31815
HLA-B44:053DX8347ALDLLIKLKILLDQ-5.91172-6.94702
HLA-B44:053DX8347ALDLLIKLKILLDQ-4.24346-4.35686

Top

Vaccine Design for the FusionNeoAntigens of PRKDC-TOMM70A

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-TOMM70Achr848868434chr31000924891221KLKILLDQVAAGCTGAAAATACTCCTTGATCAAGTT
PRKDC-TOMM70Achr848868434chr3100092489414IPALDLLIKLATTCCAGCCCTGGACCTTCTTATTAAGCTG
PRKDC-TOMM70Achr848868434chr3100092489614ALDLLIKLGCCCTGGACCTTCTTATTAAGCTG
PRKDC-TOMM70Achr848868434chr3100092489817DLLIKLKILGACCTTCTTATTAAGCTGAAAATACTC

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-TOMM70Achr848868434chr31000924891025LIKLKILLDQVEEAVCTTATTAAGCTGAAAATACTCCTTGATCAAGTTGAAGAAGCAGTG
PRKDC-TOMM70Achr848868434chr31000924891126IKLKILLDQVEEAVAATTAAGCTGAAAATACTCCTTGATCAAGTTGAAGAAGCAGTGGCA

Top

Information of the samples that have these potential fusion neoantigens of PRKDC-TOMM70A

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
STADPRKDC-TOMM70Achr848868434ENST00000314191chr3100092489ENST00000284320TCGA-BR-8295-01A

Top

Potential target of CAR-T therapy development for PRKDC-TOMM70A

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

Top

Related Drugs to PRKDC-TOMM70A

check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

Top

Related Diseases to PRKDC-TOMM70A

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