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:CDC73-SWT1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CDC73-SWT1
FusionPDB ID: 14947
FusionGDB2.0 ID: 14947
HgeneTgene
Gene symbol

CDC73

SWT1

Gene ID

79577

54823

Gene namecell division cycle 73SWT1 RNA endoribonuclease homolog
SynonymsC1orf28|FIHP|HPTJT|HRPT1|HRPT2|HYXC1orf26|HsSwt1
Cytomap

1q31.2

1q25.3

Type of geneprotein-codingprotein-coding
DescriptionparafibrominFamilial isolated hyperparathyroidismPaf1/RNA polymerase II complex componentcell division cycle 73 Paf1/RNA polymerase II complex component-like proteincell division cycle 73, Paf1/RNA polymerase II complex component, homologcell divisiotranscriptional protein SWT1
Modification date2020031320200313
UniProtAcc

Q6P1J9

Main function of 5'-partner protein: FUNCTION: Tumor suppressor probably involved in transcriptional and post-transcriptional control pathways. May be involved in cell cycle progression through the regulation of cyclin D1/PRAD1 expression. Component of the PAF1 complex (PAF1C) which has multiple functions during transcription by RNA polymerase II and is implicated in regulation of development and maintenance of embryonic stem cell pluripotency. PAF1C associates with RNA polymerase II through interaction with POLR2A CTD non-phosphorylated and 'Ser-2'- and 'Ser-5'-phosphorylated forms and is involved in transcriptional elongation, acting both independently and synergistically with TCEA1 and in cooperation with the DSIF complex and HTATSF1. PAF1C is required for transcription of Hox and Wnt target genes. PAF1C is involved in hematopoiesis and stimulates transcriptional activity of KMT2A/MLL1; it promotes leukemogenesis through association with KMT2A/MLL1-rearranged oncoproteins, such as KMT2A/MLL1-MLLT3/AF9 and KMT2A/MLL1-MLLT1/ENL. PAF1C is involved in histone modifications such as ubiquitination of histone H2B and methylation on histone H3 'Lys-4' (H3K4me3). PAF1C recruits the RNF20/40 E3 ubiquitin-protein ligase complex and the E2 enzyme UBE2A or UBE2B to chromatin which mediate monoubiquitination of 'Lys-120' of histone H2B (H2BK120ub1); UB2A/B-mediated H2B ubiquitination is proposed to be coupled to transcription. PAF1C is involved in mRNA 3' end formation probably through association with cleavage and poly(A) factors. In case of infection by influenza A strain H3N2, PAF1C associates with viral NS1 protein, thereby regulating gene transcription. Connects PAF1C with the cleavage and polyadenylation specificity factor (CPSF) complex and the cleavage stimulation factor (CSTF) complex, and with Wnt signaling. Involved in polyadenylation of mRNA precursors. {ECO:0000269|PubMed:15580289, ECO:0000269|PubMed:15632063, ECO:0000269|PubMed:15923622, ECO:0000269|PubMed:16630820, ECO:0000269|PubMed:16989776, ECO:0000269|PubMed:19136632, ECO:0000269|PubMed:19952111, ECO:0000269|PubMed:20178742, ECO:0000269|PubMed:20541477, ECO:0000269|PubMed:21329879}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000367435, ENST00000477868, 
ENST00000367500, ENST00000367501, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 6 X 6=2883 X 3 X 3=27
# samples 83
** MAII scorelog2(8/288*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Fusion gene context

PubMed: CDC73 [Title/Abstract] AND SWT1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CDC73 [Title/Abstract] AND SWT1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CDC73(193205486)-SWT1(185153375), # samples:2
Anticipated loss of major functional domain due to fusion event.CDC73-SWT1 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.
CDC73-SWT1 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.
CDC73-SWT1 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.
CDC73-SWT1 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
HgeneCDC73

GO:0008285

negative regulation of cell proliferation

16989776

HgeneCDC73

GO:0010390

histone monoubiquitination

16307923

HgeneCDC73

GO:0030177

positive regulation of Wnt signaling pathway

16630820

HgeneCDC73

GO:0032968

positive regulation of transcription elongation from RNA polymerase II promoter

20178742

HgeneCDC73

GO:0033523

histone H2B ubiquitination

16307923

HgeneCDC73

GO:0045638

negative regulation of myeloid cell differentiation

20541477

HgeneCDC73

GO:0045944

positive regulation of transcription by RNA polymerase II

20178742

HgeneCDC73

GO:2000134

negative regulation of G1/S transition of mitotic cell cycle

16989776



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/chr1:193205486/chr1:185153375)
- 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 CDC73 (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 SWT1 (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)
ENST00000367435CDC73chr1193205486+ENST00000367501SWT1chr1185153375+33701601731651052
ENST00000367435CDC73chr1193205486+ENST00000367500SWT1chr1185153375+41281601731651052

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
ENST00000367435ENST00000367501CDC73chr1193205486+SWT1chr1185153375+0.000307010.99969304
ENST00000367435ENST00000367500CDC73chr1193205486+SWT1chr1185153375+0.0001698340.9998301

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 CDC73-SWT1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CDC73chr1193205486SWT1chr11851533751601532LPDGSPVDIFAKTNNTSDRKLLIVID

Top

Potential FusionNeoAntigen Information of CDC73-SWT1 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.
CDC73-SWT1_193205486_185153375.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)
CDC73-SWT1chr1193205486chr11851533751601HLA-A30:08KTNNTSDRK0.98260.68851120
CDC73-SWT1chr1193205486chr11851533751601HLA-A30:01KTNNTSDRK0.9830.84021120

Top

Potential FusionNeoAntigen Information of CDC73-SWT1 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.
CDC73-SWT1_193205486_185153375.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)
CDC73-SWT1chr1193205486chr11851533751601DRB1-0403PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0405PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0405VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0405SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0405DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0407PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0407VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0409PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0409VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0409SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0409DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0411PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0415PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0417PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0417VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0417SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0417DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0424PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0424VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0424SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0427PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0429PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0429VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0429SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0429DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0430PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0430VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0430SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0430DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0434PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0435PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0436PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0437PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0437SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0437VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0437GSPVDIFAKTNNTSD318
CDC73-SWT1chr1193205486chr11851533751601DRB1-0439PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0441PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0445PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0445VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0445SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0445DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0446PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0447PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0448PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0448VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0448SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0448DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0452PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0453PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0454PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0457PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0457VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0457SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0457DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0458PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0458SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0459PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0460PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0462PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0462VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0465PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0465SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0469PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0469VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0469SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0471PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0473PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0473SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0474PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0474VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0475PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0477PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0477VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0477SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0477DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0480PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0480VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0480SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0482PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0483PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0483VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0483SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0483DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0484PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0484VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0484SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0484DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0485PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0486PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0486VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0486SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0487PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0487VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0487SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0488PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0489PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0489VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-0489SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0489DIFAKTNNTSDRKLL722
CDC73-SWT1chr1193205486chr11851533751601DRB1-0491PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0802PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0804PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0804SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0809PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0813PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0813SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0815PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0815SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0820PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0821PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0828PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0828SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0829PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0830PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-0830SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-0831PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1130PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1141PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1167PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1167SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-1336PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1367PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1367SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-1367VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-1403PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1412PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1415PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1415SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-1424PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1440PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1457PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1457SPVDIFAKTNNTSDR419
CDC73-SWT1chr1193205486chr11851533751601DRB1-1457GSPVDIFAKTNNTSD318
CDC73-SWT1chr1193205486chr11851533751601DRB1-1457VDIFAKTNNTSDRKL621
CDC73-SWT1chr1193205486chr11851533751601DRB1-1467PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1477PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1484PVDIFAKTNNTSDRK520
CDC73-SWT1chr1193205486chr11851533751601DRB1-1489PVDIFAKTNNTSDRK520

Top

Fusion breakpoint peptide structures of CDC73-SWT1

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
9852VDIFAKTNNTSDRKCDC73SWT1chr1193205486chr11851533751601

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CDC73-SWT1

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-B14:023BVN9852VDIFAKTNNTSDRK-7.15543-7.26883
HLA-B14:023BVN9852VDIFAKTNNTSDRK-4.77435-5.80965
HLA-B52:013W399852VDIFAKTNNTSDRK-6.80875-6.92215
HLA-B52:013W399852VDIFAKTNNTSDRK-4.20386-5.23916
HLA-A11:014UQ29852VDIFAKTNNTSDRK-7.5194-8.5547
HLA-A11:014UQ29852VDIFAKTNNTSDRK-6.9601-7.0735
HLA-A24:025HGA9852VDIFAKTNNTSDRK-7.52403-7.63743
HLA-A24:025HGA9852VDIFAKTNNTSDRK-5.82433-6.85963
HLA-B27:056PYJ9852VDIFAKTNNTSDRK-3.28285-4.31815
HLA-B44:053DX89852VDIFAKTNNTSDRK-5.91172-6.94702
HLA-B44:053DX89852VDIFAKTNNTSDRK-4.24346-4.35686

Top

Vaccine Design for the FusionNeoAntigens of CDC73-SWT1

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
CDC73-SWT1chr1193205486chr11851533751120KTNNTSDRKCTAAAACAAATAATACTTCAGACAGAA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CDC73-SWT1chr1193205486chr1185153375318GSPVDIFAKTNNTSDATGGATCACCAGTTGATATATTTGCTAAAACAAATAATACTTCAG
CDC73-SWT1chr1193205486chr1185153375419SPVDIFAKTNNTSDRGATCACCAGTTGATATATTTGCTAAAACAAATAATACTTCAGACA
CDC73-SWT1chr1193205486chr1185153375520PVDIFAKTNNTSDRKCACCAGTTGATATATTTGCTAAAACAAATAATACTTCAGACAGAA
CDC73-SWT1chr1193205486chr1185153375621VDIFAKTNNTSDRKLCAGTTGATATATTTGCTAAAACAAATAATACTTCAGACAGAAAGC
CDC73-SWT1chr1193205486chr1185153375722DIFAKTNNTSDRKLLTTGATATATTTGCTAAAACAAATAATACTTCAGACAGAAAGCTTC

Top

Information of the samples that have these potential fusion neoantigens of CDC73-SWT1

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
SARCCDC73-SWT1chr1193205486ENST00000367435chr1185153375ENST00000367500TCGA-DX-A23R-01A

Top

Potential target of CAR-T therapy development for CDC73-SWT1

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 CDC73-SWT1

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

Top

Related Diseases to CDC73-SWT1

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