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 | Fusion Gene Summary |
| Fusion Gene ORF analysis |
| Fusion Genomic Features |
| Fusion Protein Features |
| Fusion Gene Sequence |
| Fusion Gene PPI analysis |
| Related Drugs |
| Related Diseases |
Fusion gene:ADD3-NUP98 (FusionGDB2 ID:HG120TG4928) |
Fusion Gene Summary for ADD3-NUP98 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: ADD3-NUP98 | Fusion gene ID: hg120tg4928 | Hgene | Tgene | Gene symbol | ADD3 | NUP98 | Gene ID | 120 | 4928 |
| Gene name | adducin 3 | nucleoporin 98 and 96 precursor | |
| Synonyms | ADDL|CPSQ3 | ADIR2|NUP196|NUP96|Nup98-96 | |
| Cytomap | ('ADD3')('NUP98') 10q25.1-q25.2 | 11p15.4 | |
| Type of gene | protein-coding | protein-coding | |
| Description | gamma-adducinadducin 3 (gamma)adducin-like protein 70 | nuclear pore complex protein Nup98-Nup96nuclear pore complex protein Nup98GLFG-repeat containing nucleoporinNUP98/PHF23 fusion 2 proteinNup98-Nup96nucleoporin 96nucleoporin 98kDnucleoporin 98kDa | |
| Modification date | 20200313 | 20200313 | |
| UniProtAcc | Q9UEY8 | P52948 | |
| Ensembl transtripts involved in fusion gene | ENST00000277900, ENST00000356080, ENST00000360162, ENST00000497125, | ENST00000497125, ENST00000277900, ENST00000356080, ENST00000360162, | |
| Fusion gene scores | * DoF score | 13 X 10 X 5=650 | 17 X 18 X 10=3060 |
| # samples | 14 | 18 | |
| ** MAII score | log2(14/650*10)=-2.21501289097085 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(18/3060*10)=-4.08746284125034 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: ADD3 [Title/Abstract] AND NUP98 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint | |||
| Anticipated loss of major functional domain due to fusion event. | ADD3-NUP98 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. ADD3-NUP98 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF. ADD3-NUP98 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. ADD3-NUP98 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF. NUP98-ADD3 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF. NUP98-ADD3 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. NUP98-ADD3 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF. NUP98-ADD3 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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) |
| Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Partner | Gene | GO ID | GO term | PubMed ID |
| Fusion gene information * 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. |
| Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| ChimerKB3 | . | . | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
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Fusion Gene ORF analysis for ADD3-NUP98 |
| Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
| ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| 5CDS-intron | ENST00000277900 | ENST00000488828 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| 5CDS-intron | ENST00000356080 | ENST00000488828 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| 5CDS-intron | ENST00000360162 | ENST00000488828 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000277900 | ENST00000324932 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000277900 | ENST00000355260 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000277900 | ENST00000359171 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000277900 | ENST00000397004 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000277900 | ENST00000397007 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000356080 | ENST00000324932 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000356080 | ENST00000355260 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000356080 | ENST00000359171 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000356080 | ENST00000397004 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000356080 | ENST00000397007 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000360162 | ENST00000324932 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000360162 | ENST00000355260 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000360162 | ENST00000359171 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000360162 | ENST00000397004 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| Frame-shift | ENST00000360162 | ENST00000397007 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| intron-3CDS | ENST00000497125 | ENST00000324932 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| intron-3CDS | ENST00000497125 | ENST00000355260 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| intron-3CDS | ENST00000497125 | ENST00000359171 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| intron-3CDS | ENST00000497125 | ENST00000397004 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| intron-3CDS | ENST00000497125 | ENST00000397007 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| intron-intron | ENST00000497125 | ENST00000488828 | ADD3 | chr10 | 111886261 | + | NUP98 | chr11 | 3774638 | - |
| ORFfinder result based on the fusion transcript sequence of in-frame fusion genes. |
| Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
| DeepORF 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. |
| Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
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Fusion Genomic Features for ADD3-NUP98 |
| FusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints. |
| Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
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Fusion Protein Features for ADD3-NUP98 |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:/:) - 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. |
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| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| ADD3 | NUP98 |
| FUNCTION: Membrane-cytoskeleton-associated protein that promotes the assembly of the spectrin-actin network. Plays a role in actin filament capping (PubMed:23836506). Binds to calmodulin. {ECO:0000269|PubMed:23836506}. | FUNCTION: Plays a role in the nuclear pore complex (NPC) assembly and/or maintenance. NUP98 and NUP96 are involved in the bidirectional transport across the NPC (PubMed:33097660). May anchor NUP153 and TPR to the NPC. In cooperation with DHX9, plays a role in transcription and alternative splicing activation of a subset of genes (PubMed:28221134). Involved in the localization of DHX9 in discrete intranuclear foci (GLFG-body) (PubMed:28221134). {ECO:0000269|PubMed:15229283, ECO:0000269|PubMed:33097660}.; FUNCTION: (Microbial infection) Interacts with HIV-1 capsid protein P24 and nucleocapsid protein P7 and may thereby promote the integration of the virus in the host nucleus (in vitro) (PubMed:23523133). Binding affinity to HIV-1 CA-NC complexes bearing the capsid change ASN-74-ASP is reduced (in vitro) (PubMed:23523133). {ECO:0000269|PubMed:23523133}. |
| Retention 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 * Minus value of BPloci means that the break pointn is located before the CDS. |
| - In-frame and retained protein feature among the 13 regional features. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
| - In-frame and not-retained protein feature among the 13 regional features. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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Fusion Gene Sequence for ADD3-NUP98 |
| For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
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Fusion Gene PPI Analysis for ADD3-NUP98 |
| Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in |
| Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160) |
| Hgene | Hgene's interactors | Tgene | Tgene's interactors |
| - Retained PPIs in in-frame fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost PPIs in in-frame fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
| - Retained PPIs, but lost function due to frame-shift fusion. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for ADD3-NUP98 |
| Drugs targeting genes involved in this fusion gene. (DrugBank Version 5.1.8 2021-05-08) |
| Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Related Diseases for ADD3-NUP98 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | ADD3 | C0005586 | Bipolar Disorder | 1 | CTD_human |
| Hgene | ADD3 | C0005587 | Depression, Bipolar | 1 | CTD_human |
| Hgene | ADD3 | C0007786 | Brain Ischemia | 1 | CTD_human |
| Hgene | ADD3 | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
| Hgene | ADD3 | C0024713 | Manic Disorder | 1 | CTD_human |
| Hgene | ADD3 | C0149504 | Encephalopathy, Toxic | 1 | CTD_human |
| Hgene | ADD3 | C0154659 | Toxic Encephalitis | 1 | CTD_human |
| Hgene | ADD3 | C0235032 | Neurotoxicity Syndromes | 1 | CTD_human |
| Hgene | ADD3 | C0338831 | Manic | 1 | CTD_human |
| Hgene | ADD3 | C0917798 | Cerebral Ischemia | 1 | CTD_human |
| Hgene | ADD3 | C2751938 | Cerebral Palsy, Spastic Quadriplegic, 1 | 1 | ORPHANET |
| Hgene | ADD3 | C4310767 | CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3 | 1 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
| Tgene | C0002871 | Anemia | 1 | CTD_human | |
| Tgene | C0023467 | Leukemia, Myelocytic, Acute | 1 | CTD_human | |
| Tgene | C0024312 | Lymphopenia | 1 | CTD_human | |
| Tgene | C0026998 | Acute Myeloid Leukemia, M1 | 1 | CTD_human | |
| Tgene | C0027947 | Neutropenia | 1 | CTD_human | |
| Tgene | C1879321 | Acute Myeloid Leukemia (AML-M2) | 1 | CTD_human | |
| Tgene | C2930974 | Acute erythroleukemia | 1 | CTD_human | |
| Tgene | C2930975 | Acute erythroleukemia - M6a subtype | 1 | CTD_human | |
| Tgene | C2930976 | Acute myeloid leukemia FAB-M6 | 1 | CTD_human | |
| Tgene | C2930977 | Acute erythroleukemia - M6b subtype | 1 | CTD_human |
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