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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:C6orf106-PRKCB

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: C6orf106-PRKCB
FusionPDB ID: 11915
FusionGDB2.0 ID: 11915
HgeneTgene
Gene symbol

C6orf106

PRKCB

Gene ID

64771

5579

Gene nameinflammation and lipid regulator with UBA-like and NBR1-like domainsprotein kinase C beta
SynonymsC6orf106|FP852|dJ391O22.4PKC-beta|PKCB|PKCI(2)|PKCbeta|PRKCB1|PRKCB2
Cytomap

6p21.31

16p12.2-p12.1

Type of geneprotein-codingprotein-coding
Descriptionprotein ILRUNinflammation and lipid regulator with UBA-like and NBR1-like domains proteinuncharacterized protein C6orf106protein kinase C beta typePKC-Bprotein kinase C, beta 1 polypeptide
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000374021, ENST00000374023, 
ENST00000374026, 
ENST00000482000, 
ENST00000498058, ENST00000303531, 
ENST00000321728, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 9 X 9=129620 X 15 X 13=3900
# samples 2125
** MAII scorelog2(21/1296*10)=-2.6256044852185
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(25/3900*10)=-3.96347412397489
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: C6orf106 [Title/Abstract] AND PRKCB [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: C6orf106 [Title/Abstract] AND PRKCB [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)C6orf106(34574331)-PRKCB(24043456), # samples:1
Anticipated loss of major functional domain due to fusion event.C6orf106-PRKCB 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.
C6orf106-PRKCB 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.
C6orf106-PRKCB 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.
C6orf106-PRKCB 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.
C6orf106-PRKCB seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
C6orf106-PRKCB seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
C6orf106-PRKCB seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
C6orf106-PRKCB seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
C6orf106-PRKCB seems lost the major protein functional domain in Tgene partner, which is a kinase due to the frame-shifted ORF.
C6orf106-PRKCB seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneC6orf106

GO:0043392

negative regulation of DNA binding

29802199

TgenePRKCB

GO:0010827

regulation of glucose transmembrane transport

25982116

TgenePRKCB

GO:0035408

histone H3-T6 phosphorylation

20228790



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/chr6:34574331/chr16:24043456)
- 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 C6orf106 (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 PRKCB (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)
ENST00000374023C6orf106chr634574331-ENST00000321728PRKCBchr1624043456+333111052022832876
ENST00000374023C6orf106chr634574331-ENST00000303531PRKCBchr1624043456+863411052022838878
ENST00000374026C6orf106chr634574331-ENST00000321728PRKCBchr1624043456+31459192142646810
ENST00000374026C6orf106chr634574331-ENST00000303531PRKCBchr1624043456+84489192142652812

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
ENST00000374023ENST00000321728C6orf106chr634574331-PRKCBchr1624043456+0.0010722840.99892765
ENST00000374023ENST00000303531C6orf106chr634574331-PRKCBchr1624043456+0.0005027190.9994973
ENST00000374026ENST00000321728C6orf106chr634574331-PRKCBchr1624043456+0.001587360.9984126
ENST00000374026ENST00000303531C6orf106chr634574331-PRKCBchr1624043456+0.0007089830.99929094

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 C6orf106-PRKCB

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
C6orf106chr634574331PRKCBchr16240434561105301SHANNLSVVTYSKDPRSKHKFKIHTY
C6orf106chr634574331PRKCBchr1624043456919235SHANNLSVVTYSKDPRSKHKFKIHTY

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Potential FusionNeoAntigen Information of C6orf106-PRKCB 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.
C6orf106-PRKCB_34574331_24043456.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)
C6orf106-PRKCBchr634574331chr16240434561105HLA-A30:08VTYSKDPRSK0.9740.6852818
C6orf106-PRKCBchr634574331chr16240434561105HLA-A30:08YSKDPRSKHK0.95670.55541020
C6orf106-PRKCBchr634574331chr16240434561105HLA-B58:02YSKDPRSKHKF0.99910.68081021
C6orf106-PRKCBchr634574331chr16240434561105HLA-C12:02YSKDPRSKH0.48330.88031019
C6orf106-PRKCBchr634574331chr16240434561105HLA-C12:03YSKDPRSKH0.19960.9171019
C6orf106-PRKCBchr634574331chr16240434561105HLA-A30:01VTYSKDPRSK0.97440.7591818
C6orf106-PRKCBchr634574331chr16240434561105HLA-A30:01YSKDPRSKHK0.95860.661020
C6orf106-PRKCBchr634574331chr16240434561105HLA-B58:06YSKDPRSKHKF0.99950.56931021

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Potential FusionNeoAntigen Information of C6orf106-PRKCB 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.
C6orf106-PRKCB_34574331_24043456.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)
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0305VVTYSKDPRSKHKFK722
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0305SVVTYSKDPRSKHKF621
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0340VVTYSKDPRSKHKFK722
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0340SVVTYSKDPRSKHKF621
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0403LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0413LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0427LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0427NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0437LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0439LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0441LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0444LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0446LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0449LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0450LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0451LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0452LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0455LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0459LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0460LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0465LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0471LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0473LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0478LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0485LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-0488LSVVTYSKDPRSKHK520
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1102NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1116NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1121NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1136NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1165NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1170NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1179VVTYSKDPRSKHKFK722
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1301NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1309NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1309NNLSVVTYSKDPRSK318
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1315NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1317NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1317NNLSVVTYSKDPRSK318
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1320NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1322NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1327NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1327NNLSVVTYSKDPRSK318
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1335NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1337VVTYSKDPRSKHKFK722
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1351NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1352NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1357NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1359NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1361NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1364NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1368NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1369NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1371NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1371NNLSVVTYSKDPRSK318
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1378NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1379NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1380NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1383NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1387NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1391NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1392NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1398NLSVVTYSKDPRSKH419
C6orf106-PRKCBchr634574331chr16240434561105DRB1-1437NLSVVTYSKDPRSKH419

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Fusion breakpoint peptide structures of C6orf106-PRKCB

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
9173SVVTYSKDPRSKHKC6orf106PRKCBchr634574331chr16240434561105

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of C6orf106-PRKCB

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-B14:023BVN9173SVVTYSKDPRSKHK-7.9962-8.1096
HLA-B14:023BVN9173SVVTYSKDPRSKHK-5.70842-6.74372
HLA-B52:013W399173SVVTYSKDPRSKHK-6.83737-6.95077
HLA-B52:013W399173SVVTYSKDPRSKHK-4.4836-5.5189
HLA-A11:014UQ29173SVVTYSKDPRSKHK-10.0067-10.1201
HLA-A11:014UQ29173SVVTYSKDPRSKHK-9.03915-10.0745
HLA-A24:025HGA9173SVVTYSKDPRSKHK-6.56204-6.67544
HLA-A24:025HGA9173SVVTYSKDPRSKHK-5.42271-6.45801
HLA-B44:053DX89173SVVTYSKDPRSKHK-7.85648-8.89178
HLA-B44:053DX89173SVVTYSKDPRSKHK-5.3978-5.5112
HLA-A02:016TDR9173SVVTYSKDPRSKHK-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of C6orf106-PRKCB

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
C6orf106-PRKCBchr634574331chr16240434561019YSKDPRSKHTACAGTAAGGACCCCCGCAGCAAACAC
C6orf106-PRKCBchr634574331chr16240434561020YSKDPRSKHKTACAGTAAGGACCCCCGCAGCAAACACAAG
C6orf106-PRKCBchr634574331chr16240434561021YSKDPRSKHKFTACAGTAAGGACCCCCGCAGCAAACACAAGTTT
C6orf106-PRKCBchr634574331chr1624043456818VTYSKDPRSKGTGACTTACAGTAAGGACCCCCGCAGCAAA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
C6orf106-PRKCBchr634574331chr1624043456318NNLSVVTYSKDPRSKAACAACTTATCAGTAGTGACTTACAGTAAGGACCCCCGCAGCAAA
C6orf106-PRKCBchr634574331chr1624043456419NLSVVTYSKDPRSKHAACTTATCAGTAGTGACTTACAGTAAGGACCCCCGCAGCAAACAC
C6orf106-PRKCBchr634574331chr1624043456520LSVVTYSKDPRSKHKTTATCAGTAGTGACTTACAGTAAGGACCCCCGCAGCAAACACAAG
C6orf106-PRKCBchr634574331chr1624043456621SVVTYSKDPRSKHKFTCAGTAGTGACTTACAGTAAGGACCCCCGCAGCAAACACAAGTTT
C6orf106-PRKCBchr634574331chr1624043456722VVTYSKDPRSKHKFKGTAGTGACTTACAGTAAGGACCCCCGCAGCAAACACAAGTTTAAG

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Information of the samples that have these potential fusion neoantigens of C6orf106-PRKCB

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
Non-CancerC6orf106-PRKCBchr634574331ENST00000374023chr1624043456ENST0000030353161N

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Potential target of CAR-T therapy development for C6orf106-PRKCB

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 C6orf106-PRKCB

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 C6orf106-PRKCB

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