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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:KCMF1-PRKDC

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: KCMF1-PRKDC
FusionPDB ID: 41325
FusionGDB2.0 ID: 41325
HgeneTgene
Gene symbol

KCMF1

PRKDC

Gene ID

56888

5591

Gene namepotassium channel modulatory factor 1protein kinase, DNA-activated, catalytic subunit
SynonymsDEBT91|FIGC|PCMF|ZZZ1DNA-PKC|DNA-PKcs|DNAPK|DNAPKc|DNPK1|HYRC|HYRC1|IMD26|XRCC7|p350
Cytomap

2p11.2

8q11.21

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase KCMF1FGF-induced in gastric cancerFGF-induced ubiquitin-protein ligase in gastric cancersRING-type E3 ubiquitin transferase KCMF1ZZ-type zinc finger-containing protein 1differentially expressed in branching tubulogenesis 9DNA-dependent protein kinase catalytic subunitDNA-PK catalytic subunithyper-radiosensitivity of murine scid mutation, complementing 1p460protein kinase, DNA-activated, catalytic polypeptide
Modification date2020031320200322
UniProtAcc

Q9P0J7

Main function of 5'-partner protein: FUNCTION: Has intrinsic E3 ubiquitin ligase activity and promotes ubiquitination. {ECO:0000269|PubMed:15581609}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000409785, ENST00000523565, 
ENST00000314191, ENST00000338368, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score14 X 12 X 7=117618 X 20 X 5=1800
# samples 1819
** MAII scorelog2(18/1176*10)=-2.70781924850669
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(19/1800*10)=-3.24392558288609
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: KCMF1 [Title/Abstract] AND PRKDC [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: KCMF1 [Title/Abstract] AND PRKDC [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)KCMF1(85255179)-PRKDC(48772320), # samples:3
Anticipated loss of major functional domain due to fusion event.KCMF1-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.
KCMF1-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.
KCMF1-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.
KCMF1-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.
KCMF1-PRKDC seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
KCMF1-PRKDC seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
KCMF1-PRKDC seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
KCMF1-PRKDC seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
KCMF1-PRKDC seems lost the major protein functional domain in Tgene partner, which is a kinase 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
TgenePRKDC

GO:0002218

activation of innate immune response

28712728

TgenePRKDC

GO:0006468

protein phosphorylation

26237645

TgenePRKDC

GO:0006974

cellular response to DNA damage stimulus

26237645

TgenePRKDC

GO:0018105

peptidyl-serine phosphorylation

15194694|19303849

TgenePRKDC

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/chr2:85255179/chr8:48772320)
- 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 KCMF1 (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 PRKDC (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)
ENST00000409785KCMF1chr285255179+ENST00000338368PRKDCchr848772320-784454335967782139
ENST00000409785KCMF1chr285255179+ENST00000314191PRKDCchr848772320-793754335968712170

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
ENST00000409785ENST00000338368KCMF1chr285255179+PRKDCchr848772320-0.000875350.9991247
ENST00000409785ENST00000314191KCMF1chr285255179+PRKDCchr848772320-0.0006178980.999382

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 KCMF1-PRKDC

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
KCMF1chr285255179PRKDCchr84877232054361DHPMQCILTRVDFDGPSYMSSLSYLA

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Potential FusionNeoAntigen Information of KCMF1-PRKDC 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.
KCMF1-PRKDC_85255179_48772320.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)
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:25RVDFDGPSY0.94210.9662918
KCMF1-PRKDCchr285255179chr848772320543HLA-B35:08RVDFDGPSY0.88710.9125918
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:02RVDFDGPSY0.86730.9709918
KCMF1-PRKDCchr285255179chr848772320543HLA-B47:01VDFDGPSYM0.64220.73441019
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:05TRVDFDGPSY0.99980.7501818
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:04TRVDFDGPSY0.99970.7617818
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:16RVDFDGPSYM0.91070.967919
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:18TRVDFDGPSY0.90990.7928818
KCMF1-PRKDCchr285255179chr848772320543HLA-A30:08RVDFDGPSYM0.79740.8627919
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:04TRVDFDGPSYM10.7818819
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:05TRVDFDGPSYM10.7545819
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:07TRVDFDGPSYM10.7252819
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:18TRVDFDGPSYM0.99910.8439819
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:07DFDGPSYM0.99980.76211119
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:10DFDGPSYM0.99970.75191119
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:14DFDGPSYM0.97540.74981119
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:05RVDFDGPSY0.88130.9401918
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:21RVDFDGPSY0.86750.9456918
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:31RVDFDGPSY0.77070.9444918
KCMF1-PRKDCchr285255179chr848772320543HLA-C05:09RVDFDGPSYM10.9523919
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:07RVDFDGPSYM10.8516919
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:10RVDFDGPSYM10.8293919
KCMF1-PRKDCchr285255179chr848772320543HLA-C08:15RVDFDGPSYM0.99990.9726919
KCMF1-PRKDCchr285255179chr848772320543HLA-C15:04RVDFDGPSYM0.99880.9564919
KCMF1-PRKDCchr285255179chr848772320543HLA-C15:06RVDFDGPSYM0.99840.9602919
KCMF1-PRKDCchr285255179chr848772320543HLA-C01:30FDGPSYMSSL0.99830.96681222
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:03TRVDFDGPSY0.99820.7673818
KCMF1-PRKDCchr285255179chr848772320543HLA-C01:17FDGPSYMSSL0.99810.95891222
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:95TRVDFDGPSY0.99750.536818
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:06RVDFDGPSYM0.99730.9347919
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:27TRVDFDGPSY0.99580.9282818
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:19TRVDFDGPSY0.99360.6887818
KCMF1-PRKDCchr285255179chr848772320543HLA-C02:06RVDFDGPSYM0.99060.9663919
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:67TRVDFDGPSY0.98740.9366818
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:80TRVDFDGPSY0.98740.9366818
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:10TRVDFDGPSY0.98730.9628818
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:46TRVDFDGPSY0.9870.8616818
KCMF1-PRKDCchr285255179chr848772320543HLA-C08:04RVDFDGPSYM0.98070.9782919
KCMF1-PRKDCchr285255179chr848772320543HLA-C08:13RVDFDGPSYM0.98070.9782919
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:04RVDFDGPSYM0.92130.977919
KCMF1-PRKDCchr285255179chr848772320543HLA-C08:03RVDFDGPSYM0.84520.9841919
KCMF1-PRKDCchr285255179chr848772320543HLA-C12:16TRVDFDGPSY0.83380.937818
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:27TRVDFDGPSYM10.9484819
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:07DFDGPSYMSSL10.73371122
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:14TRVDFDGPSYM10.7135819
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:10DFDGPSYMSSL10.73071122
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:95TRVDFDGPSYM10.6524819
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:05TRVDFDGPSYM0.99990.9581819
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:13TRVDFDGPSYM0.99990.9467819
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:29TRVDFDGPSYM0.99990.9237819
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:46TRVDFDGPSYM0.99980.915819
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:19TRVDFDGPSYM0.99980.808819
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:10TRVDFDGPSYM0.99980.9729819
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:03TRVDFDGPSYM0.99970.7734819
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:80TRVDFDGPSYM0.99960.9536819
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:67TRVDFDGPSYM0.99960.9536819
KCMF1-PRKDCchr285255179chr848772320543HLA-C12:16TRVDFDGPSYM0.99940.948819
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:01DFDGPSYM0.99980.76211119
KCMF1-PRKDCchr285255179chr848772320543HLA-C18:01DFDGPSYM0.99970.76531119
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:04DFDGPSYM0.98580.90341119
KCMF1-PRKDCchr285255179chr848772320543HLA-B18:11VDFDGPSY0.96210.93791018
KCMF1-PRKDCchr285255179chr848772320543HLA-B18:04VDFDGPSY0.9420.9561018
KCMF1-PRKDCchr285255179chr848772320543HLA-B18:08VDFDGPSY0.92670.79341018
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:39RVDFDGPSY0.93710.9173918
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:20RVDFDGPSY0.89520.9649918
KCMF1-PRKDCchr285255179chr848772320543HLA-B35:28RVDFDGPSY0.82510.9668918
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:50RVDFDGPSY0.80710.9225918
KCMF1-PRKDCchr285255179chr848772320543HLA-B35:20RVDFDGPSY0.74830.9682918
KCMF1-PRKDCchr285255179chr848772320543HLA-C03:02RVDFDGPSY0.3570.9809918
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:03RVDFDGPSYM10.8806919
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:01RVDFDGPSYM10.8516919
KCMF1-PRKDCchr285255179chr848772320543HLA-C05:01RVDFDGPSYM10.9523919
KCMF1-PRKDCchr285255179chr848772320543HLA-C08:02RVDFDGPSYM0.99990.9726919
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:10TRVDFDGPSY0.99970.8722818
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:08TRVDFDGPSY0.99970.6435818
KCMF1-PRKDCchr285255179chr848772320543HLA-C01:03FDGPSYMSSL0.99930.93631222
KCMF1-PRKDCchr285255179chr848772320543HLA-C15:09RVDFDGPSYM0.99880.9564919
KCMF1-PRKDCchr285255179chr848772320543HLA-C01:02FDGPSYMSSL0.99850.95671222
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:01TRVDFDGPSY0.99750.5475818
KCMF1-PRKDCchr285255179chr848772320543HLA-C15:05RVDFDGPSYM0.99670.9182919
KCMF1-PRKDCchr285255179chr848772320543HLA-C02:02RVDFDGPSYM0.99650.9807919
KCMF1-PRKDCchr285255179chr848772320543HLA-C02:10RVDFDGPSYM0.99650.9807919
KCMF1-PRKDCchr285255179chr848772320543HLA-C15:02RVDFDGPSYM0.99490.9307919
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:02TRVDFDGPSY0.98740.9366818
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:22TRVDFDGPSY0.98210.5683818
KCMF1-PRKDCchr285255179chr848772320543HLA-C17:01RVDFDGPSYM0.97310.9799919
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:73RVDFDGPSYM0.90660.9599919
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:54TRVDFDGPSY0.90050.8857818
KCMF1-PRKDCchr285255179chr848772320543HLA-B07:13RVDFDGPSYM0.89770.892919
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:30RVDFDGPSYM0.85680.9471919
KCMF1-PRKDCchr285255179chr848772320543HLA-C08:01RVDFDGPSYM0.84520.9841919
KCMF1-PRKDCchr285255179chr848772320543HLA-B15:68TRVDFDGPSY0.83690.6615818
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:01TRVDFDGPSYM10.6767819
KCMF1-PRKDCchr285255179chr848772320543HLA-C18:01DFDGPSYMSSL10.73261122
KCMF1-PRKDCchr285255179chr848772320543HLA-C04:01DFDGPSYMSSL10.73371122
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:08TRVDFDGPSYM10.6882819
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:09TRVDFDGPSYM10.7413819
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:06TRVDFDGPSYM10.7836819
KCMF1-PRKDCchr285255179chr848772320543HLA-B27:10TRVDFDGPSYM10.8769819
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:22TRVDFDGPSYM0.99980.64819
KCMF1-PRKDCchr285255179chr848772320543HLA-C06:08TRVDFDGPSYM0.99970.9875819
KCMF1-PRKDCchr285255179chr848772320543HLA-C07:02TRVDFDGPSYM0.99960.9536819
KCMF1-PRKDCchr285255179chr848772320543HLA-C06:17TRVDFDGPSYM0.99870.9898819
KCMF1-PRKDCchr285255179chr848772320543HLA-C06:02TRVDFDGPSYM0.99870.9898819

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Potential FusionNeoAntigen Information of KCMF1-PRKDC 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 KCMF1-PRKDC

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
3821ILTRVDFDGPSYMSKCMF1PRKDCchr285255179chr848772320543

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of KCMF1-PRKDC

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-B14:023BVN3821ILTRVDFDGPSYMS-6.01316-6.12656
HLA-B14:023BVN3821ILTRVDFDGPSYMS-3.92858-4.96388
HLA-B52:013W393821ILTRVDFDGPSYMS-5.92102-6.95632
HLA-B52:013W393821ILTRVDFDGPSYMS-4.84472-4.95812
HLA-A24:025HGA3821ILTRVDFDGPSYMS-8.26357-9.29887
HLA-A24:025HGA3821ILTRVDFDGPSYMS-7.03366-7.14706
HLA-B44:053DX83821ILTRVDFDGPSYMS-6.13971-6.25311
HLA-B44:053DX83821ILTRVDFDGPSYMS-5.20728-6.24258
HLA-A02:016TDR3821ILTRVDFDGPSYMS-5.28864-5.40204

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Vaccine Design for the FusionNeoAntigens of KCMF1-PRKDC

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
KCMF1-PRKDCchr285255179chr8487723201018VDFDGPSYTAGATTTTGATGGTCCTTCCTATA
KCMF1-PRKDCchr285255179chr8487723201019VDFDGPSYMTAGATTTTGATGGTCCTTCCTATATGT
KCMF1-PRKDCchr285255179chr8487723201119DFDGPSYMATTTTGATGGTCCTTCCTATATGT
KCMF1-PRKDCchr285255179chr8487723201122DFDGPSYMSSLATTTTGATGGTCCTTCCTATATGTCTTCCCTGT
KCMF1-PRKDCchr285255179chr8487723201222FDGPSYMSSLTTGATGGTCCTTCCTATATGTCTTCCCTGT
KCMF1-PRKDCchr285255179chr848772320818TRVDFDGPSYCAAGGGTAGATTTTGATGGTCCTTCCTATA
KCMF1-PRKDCchr285255179chr848772320819TRVDFDGPSYMCAAGGGTAGATTTTGATGGTCCTTCCTATATGT
KCMF1-PRKDCchr285255179chr848772320918RVDFDGPSYGGGTAGATTTTGATGGTCCTTCCTATA
KCMF1-PRKDCchr285255179chr848772320919RVDFDGPSYMGGGTAGATTTTGATGGTCCTTCCTATATGT

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 KCMF1-PRKDC

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
BRCAKCMF1-PRKDCchr285255179ENST00000409785chr848772320ENST00000314191TCGA-EW-A1P4-01A

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Potential target of CAR-T therapy development for KCMF1-PRKDC

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 KCMF1-PRKDC

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 KCMF1-PRKDC

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