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Center for Computational Systems Medicine level2
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein Structure

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pLDDT scores

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Ramachandran Plot of Fusion Protein Structure

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:ARID3A-MORC2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ARID3A-MORC2
FusionPDB ID: 6448
FusionGDB2.0 ID: 6448
HgeneTgene
Gene symbol

ARID3A

MORC2

Gene ID

1820

22880

Gene nameAT-rich interaction domain 3AMORC family CW-type zinc finger 2
SynonymsBRIGHT|DRIL1|DRIL3|E2FBP1CMT2Z|ZCW3|ZCWCC1
Cytomap

19p13.3

22q12.2

Type of geneprotein-codingprotein-coding
DescriptionAT-rich interactive domain-containing protein 3AARID domain-containing 3AARID domain-containing protein 3AAT rich interactive domain 3A (BRIGHT- like) proteinAT rich interactive domain 3A (BRIGHT-like)B-cell regulator of IgH transcriptionE2F-bindingATPase MORC2zinc finger CW-type coiled-coil domain protein 1
Modification date2020031320200313
UniProtAcc

Q99856

Q9Y6X9

Ensembl transtripts involved in fusion geneENST idsENST00000263620, ENST00000592216, 
ENST00000469915, ENST00000215862, 
ENST00000397641, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 6 X 6=2525 X 5 X 5=125
# samples 85
** MAII scorelog2(8/252*10)=-1.65535182861255
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/125*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: ARID3A [Title/Abstract] AND MORC2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ARID3A(929896)-MORC2(31328756), # samples:4
Anticipated loss of major functional domain due to fusion event.ARID3A-MORC2 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.
ARID3A-MORC2 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.
ARID3A-MORC2 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.
ARID3A-MORC2 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
TgeneMORC2

GO:0006338

chromatin remodeling

23260667

TgeneMORC2

GO:0006974

cellular response to DNA damage stimulus

23260667

TgeneMORC2

GO:0045814

negative regulation of gene expression, epigenetic

28581500|29211708

TgeneMORC2

GO:0090309

positive regulation of methylation-dependent chromatin silencing

28581500|29211708


check buttonFusion gene breakpoints across ARID3A (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 MORC2 (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 Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4UCECTCGA-EY-A2ON-01AARID3Achr19

929895

+MORC2chr22

31328755

-
ChimerDB4UCECTCGA-EY-A2ON-01AARID3Achr19

929896

-MORC2chr22

31328756

-
ChimerDB4UCECTCGA-EY-A2ON-01AARID3Achr19

929896

+MORC2chr22

31328756

-
ChimerDB4UCECTCGA-EY-A2ONARID3Achr19

929896

+MORC2chr22

31328756

-


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Fusion ORF Analysis


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)
ENST00000263620ARID3Achr19929896+ENST00000397641MORC2chr2231328756-29456951861271361
ENST00000263620ARID3Achr19929896+ENST00000215862MORC2chr2231328756-14646951861271361
ENST00000263620ARID3Achr19929895+ENST00000397641MORC2chr2231328755-29456951861271361
ENST00000263620ARID3Achr19929895+ENST00000215862MORC2chr2231328755-14646951861271361

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
ENST00000263620ENST00000397641ARID3Achr19929896+MORC2chr2231328756-0.0014374520.9985625
ENST00000263620ENST00000215862ARID3Achr19929896+MORC2chr2231328756-0.0037537190.9962463
ENST00000263620ENST00000397641ARID3Achr19929895+MORC2chr2231328755-0.0014374520.9985625
ENST00000263620ENST00000215862ARID3Achr19929895+MORC2chr2231328755-0.0037537190.9962463

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>6448_6448_1_ARID3A-MORC2_ARID3A_chr19_929895_ENST00000263620_MORC2_chr22_31328755_ENST00000215862_length(amino acids)=361AA_BP=170
MHCPGSPAAPTLQCGRAPSPQGPPPPPTPSARGGGGGGGGGGPGRRAMKLQAVMETLLQRQQRARQELEARQQLPPDPPAAPPGRARAAP
DEDREPESARMQRAQMAALAAMRAAAAGLGHPASPGGSEDGPPGSEEEDAAREGTPGSPGRGREGPGEEHFEDMASDEDMVEKGSEDVRL
MKPPSPEHQSLDTQQEGGEEEVGPVAQQAIAVAEPSTSECLRIEPDTTALSTNHETIDLLVQILRNCLRYFLPPSFPISKKQLSAMNSDE
LISFPLKEYFKQYEVGLQNLCNSYQSRADSRAKASEESLRTSERKLRETEEKLQKLRTNIVALLQKVQEDIDINTDDELDAYIEDLITKG

--------------------------------------------------------------

>6448_6448_2_ARID3A-MORC2_ARID3A_chr19_929895_ENST00000263620_MORC2_chr22_31328755_ENST00000397641_length(amino acids)=361AA_BP=170
MHCPGSPAAPTLQCGRAPSPQGPPPPPTPSARGGGGGGGGGGPGRRAMKLQAVMETLLQRQQRARQELEARQQLPPDPPAAPPGRARAAP
DEDREPESARMQRAQMAALAAMRAAAAGLGHPASPGGSEDGPPGSEEEDAAREGTPGSPGRGREGPGEEHFEDMASDEDMVEKGSEDVRL
MKPPSPEHQSLDTQQEGGEEEVGPVAQQAIAVAEPSTSECLRIEPDTTALSTNHETIDLLVQILRNCLRYFLPPSFPISKKQLSAMNSDE
LISFPLKEYFKQYEVGLQNLCNSYQSRADSRAKASEESLRTSERKLRETEEKLQKLRTNIVALLQKVQEDIDINTDDELDAYIEDLITKG

--------------------------------------------------------------

>6448_6448_3_ARID3A-MORC2_ARID3A_chr19_929896_ENST00000263620_MORC2_chr22_31328756_ENST00000215862_length(amino acids)=361AA_BP=170
MHCPGSPAAPTLQCGRAPSPQGPPPPPTPSARGGGGGGGGGGPGRRAMKLQAVMETLLQRQQRARQELEARQQLPPDPPAAPPGRARAAP
DEDREPESARMQRAQMAALAAMRAAAAGLGHPASPGGSEDGPPGSEEEDAAREGTPGSPGRGREGPGEEHFEDMASDEDMVEKGSEDVRL
MKPPSPEHQSLDTQQEGGEEEVGPVAQQAIAVAEPSTSECLRIEPDTTALSTNHETIDLLVQILRNCLRYFLPPSFPISKKQLSAMNSDE
LISFPLKEYFKQYEVGLQNLCNSYQSRADSRAKASEESLRTSERKLRETEEKLQKLRTNIVALLQKVQEDIDINTDDELDAYIEDLITKG

--------------------------------------------------------------

>6448_6448_4_ARID3A-MORC2_ARID3A_chr19_929896_ENST00000263620_MORC2_chr22_31328756_ENST00000397641_length(amino acids)=361AA_BP=170
MHCPGSPAAPTLQCGRAPSPQGPPPPPTPSARGGGGGGGGGGPGRRAMKLQAVMETLLQRQQRARQELEARQQLPPDPPAAPPGRARAAP
DEDREPESARMQRAQMAALAAMRAAAAGLGHPASPGGSEDGPPGSEEEDAAREGTPGSPGRGREGPGEEHFEDMASDEDMVEKGSEDVRL
MKPPSPEHQSLDTQQEGGEEEVGPVAQQAIAVAEPSTSECLRIEPDTTALSTNHETIDLLVQILRNCLRYFLPPSFPISKKQLSAMNSDE
LISFPLKEYFKQYEVGLQNLCNSYQSRADSRAKASEESLRTSERKLRETEEKLQKLRTNIVALLQKVQEDIDINTDDELDAYIEDLITKG

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr19:929896/chr22:31328756)
- 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 buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ARID3A

Q99856

MORC2

Q9Y6X9

FUNCTION: Transcription factor which may be involved in the control of cell cycle progression by the RB1/E2F1 pathway and in B-cell differentiation. {ECO:0000269|PubMed:11812999, ECO:0000269|PubMed:12692263}.FUNCTION: Essential for epigenetic silencing by the HUSH (human silencing hub) complex. Recruited by HUSH to target site in heterochromatin, the ATPase activity and homodimerization are critical for HUSH-mediated silencing (PubMed:28581500, PubMed:29440755). Represses germ cell-related genes and L1 retrotransposons in collaboration with SETDB1 and the HUSH complex, the silencing is dependent of repressive epigenetic modifications, such as H3K9me3 mark. Silencing events often occur within introns of transcriptionally active genes, and lead to the down-regulation of host gene expression (PubMed:29211708). During DNA damage response, regulates chromatin remodeling through ATP hydrolysis. Upon DNA damage, is phosphorylated by PAK1, both colocalize to chromatin and induce H2AX expression. ATPase activity is required and dependent of phosphorylation by PAK1 and presence of DNA (PubMed:23260667). Recruits histone deacetylases, such as HDAC4, to promoter regions, causing local histone H3 deacetylation and transcriptional repression of genes such as CA9 (PubMed:20225202, PubMed:20110259). Exhibits a cytosolic function in lipogenesis, adipogenic differentiation, and lipid homeostasis by increasing the activity of ACLY, possibly preventing its dephosphorylation (PubMed:24286864). {ECO:0000269|PubMed:20110259, ECO:0000269|PubMed:20225202, ECO:0000269|PubMed:23260667, ECO:0000269|PubMed:24286864, ECO:0000269|PubMed:28581500, ECO:0000269|PubMed:29211708, ECO:0000269|PubMed:29440755}.

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, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

* Minus value of BPloci means that the break pointn is located before the CDS.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneARID3Achr19:929895chr22:31328755ENST00000263620+2967_70122.66666666666667594.0Compositional biasNote=Poly-Ala
HgeneARID3Achr19:929896chr22:31328756ENST00000263620+2967_70122.66666666666667594.0Compositional biasNote=Poly-Ala
TgeneMORC2chr19:929895chr22:31328755ENST000002158622227966_1016778.6666666666666971.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929895chr22:31328755ENST000003976412126966_1016840.66666666666661033.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929896chr22:31328756ENST000002158622227966_1016778.6666666666666971.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929896chr22:31328756ENST000003976412126966_1016840.66666666666661033.0Coiled coilOntology_term=ECO:0000255

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneARID3Achr19:929895chr22:31328755ENST00000263620+29424_445122.66666666666667594.0Compositional biasNote=Ala-rich
HgeneARID3Achr19:929895chr22:31328755ENST00000263620+29550_579122.66666666666667594.0Compositional biasNote=Gly-rich
HgeneARID3Achr19:929895chr22:31328755ENST00000263620+2989_157122.66666666666667594.0Compositional biasNote=Glu-rich
HgeneARID3Achr19:929896chr22:31328756ENST00000263620+29424_445122.66666666666667594.0Compositional biasNote=Ala-rich
HgeneARID3Achr19:929896chr22:31328756ENST00000263620+29550_579122.66666666666667594.0Compositional biasNote=Gly-rich
HgeneARID3Achr19:929896chr22:31328756ENST00000263620+2989_157122.66666666666667594.0Compositional biasNote=Glu-rich
HgeneARID3Achr19:929895chr22:31328755ENST00000263620+29238_330122.66666666666667594.0DomainARID
HgeneARID3Achr19:929895chr22:31328755ENST00000263620+29444_541122.66666666666667594.0DomainREKLES
HgeneARID3Achr19:929896chr22:31328756ENST00000263620+29238_330122.66666666666667594.0DomainARID
HgeneARID3Achr19:929896chr22:31328756ENST00000263620+29444_541122.66666666666667594.0DomainREKLES
HgeneARID3Achr19:929895chr22:31328755ENST00000263620+29119_156122.66666666666667594.0RegionNote=Acidic
HgeneARID3Achr19:929895chr22:31328755ENST00000263620+29445_488122.66666666666667594.0RegionImportant for nuclear localization
HgeneARID3Achr19:929895chr22:31328755ENST00000263620+29490_513122.66666666666667594.0RegionNote=Homodimerization
HgeneARID3Achr19:929895chr22:31328755ENST00000263620+29537_557122.66666666666667594.0RegionImportant for cytoplasmic localization
HgeneARID3Achr19:929896chr22:31328756ENST00000263620+29119_156122.66666666666667594.0RegionNote=Acidic
HgeneARID3Achr19:929896chr22:31328756ENST00000263620+29445_488122.66666666666667594.0RegionImportant for nuclear localization
HgeneARID3Achr19:929896chr22:31328756ENST00000263620+29490_513122.66666666666667594.0RegionNote=Homodimerization
HgeneARID3Achr19:929896chr22:31328756ENST00000263620+29537_557122.66666666666667594.0RegionImportant for cytoplasmic localization
TgeneMORC2chr19:929895chr22:31328755ENST000002158622227282_362778.6666666666666971.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929895chr22:31328755ENST000002158622227547_584778.6666666666666971.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929895chr22:31328755ENST000002158622227741_761778.6666666666666971.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929895chr22:31328755ENST000003976412126282_362840.66666666666661033.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929895chr22:31328755ENST000003976412126547_584840.66666666666661033.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929895chr22:31328755ENST000003976412126741_761840.66666666666661033.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929896chr22:31328756ENST000002158622227282_362778.6666666666666971.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929896chr22:31328756ENST000002158622227547_584778.6666666666666971.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929896chr22:31328756ENST000002158622227741_761778.6666666666666971.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929896chr22:31328756ENST000003976412126282_362840.66666666666661033.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929896chr22:31328756ENST000003976412126547_584840.66666666666661033.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929896chr22:31328756ENST000003976412126741_761840.66666666666661033.0Coiled coilOntology_term=ECO:0000255
TgeneMORC2chr19:929895chr22:31328755ENST00000215862222787_89778.6666666666666971.0Nucleotide bindingATP
TgeneMORC2chr19:929895chr22:31328755ENST00000215862222799_105778.6666666666666971.0Nucleotide bindingATP
TgeneMORC2chr19:929895chr22:31328755ENST00000397641212687_89840.66666666666661033.0Nucleotide bindingATP
TgeneMORC2chr19:929895chr22:31328755ENST00000397641212699_105840.66666666666661033.0Nucleotide bindingATP
TgeneMORC2chr19:929896chr22:31328756ENST00000215862222787_89778.6666666666666971.0Nucleotide bindingATP
TgeneMORC2chr19:929896chr22:31328756ENST00000215862222799_105778.6666666666666971.0Nucleotide bindingATP
TgeneMORC2chr19:929896chr22:31328756ENST00000397641212687_89840.66666666666661033.0Nucleotide bindingATP
TgeneMORC2chr19:929896chr22:31328756ENST00000397641212699_105840.66666666666661033.0Nucleotide bindingATP
TgeneMORC2chr19:929895chr22:31328755ENST000002158622227490_544778.6666666666666971.0Zinc fingerCW-type
TgeneMORC2chr19:929895chr22:31328755ENST000003976412126490_544840.66666666666661033.0Zinc fingerCW-type
TgeneMORC2chr19:929896chr22:31328756ENST000002158622227490_544778.6666666666666971.0Zinc fingerCW-type
TgeneMORC2chr19:929896chr22:31328756ENST000003976412126490_544840.66666666666661033.0Zinc fingerCW-type


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Fusion Protein Structures

check button PDB and CIF files of the predicted fusion proteins
* Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
Fusion protein PDB link (fusion AA seq ID in FusionPDB)HgeneHchrHbpHstrandTgeneTchrTbpTstrandAA seqLen(AA seq)
PDB file >>>710_ARID3A_929896_MORC2_31328756_ranked_0.pdbARID3A929895929896ENST00000215862MORC2chr2231328756-
MHCPGSPAAPTLQCGRAPSPQGPPPPPTPSARGGGGGGGGGGPGRRAMKLQAVMETLLQRQQRARQELEARQQLPPDPPAAPPGRARAAP
DEDREPESARMQRAQMAALAAMRAAAAGLGHPASPGGSEDGPPGSEEEDAAREGTPGSPGRGREGPGEEHFEDMASDEDMVEKGSEDVRL
MKPPSPEHQSLDTQQEGGEEEVGPVAQQAIAVAEPSTSECLRIEPDTTALSTNHETIDLLVQILRNCLRYFLPPSFPISKKQLSAMNSDE
LISFPLKEYFKQYEVGLQNLCNSYQSRADSRAKASEESLRTSERKLRETEEKLQKLRTNIVALLQKVQEDIDINTDDELDAYIEDLITKG
361


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pLDDT score distribution

check button pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
ARID3A_pLDDT.png
all structure
all structure
MORC2_pLDDT.png
all structure
all structure

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
all structure


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Ramachandran Plot of Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.
Fusion AA seq ID in FusionPDB and their Ramachandran plots

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Fusion Protein-Protein Interaction


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
ARID3A
MORC2


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to ARID3A-MORC2


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 ARID3A-MORC2


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