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Fusion Protein:NUP98-MLXIP |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: NUP98-MLXIP | FusionPDB ID: 61126 | FusionGDB2.0 ID: 61126 | Hgene | Tgene | Gene symbol | NUP98 | MLXIP | Gene ID | 4928 | 22877 |
| Gene name | nucleoporin 98 and 96 precursor | MLX interacting protein | |
| Synonyms | ADIR2|NUP196|NUP96|Nup98-96 | MIR|MONDOA|bHLHe36 | |
| Cytomap | 11p15.4 | 12q24.31 | |
| Type of gene | protein-coding | protein-coding | |
| Description | nuclear pore complex protein Nup98-Nup96nuclear pore complex protein Nup98GLFG-repeat containing nucleoporinNUP98/PHF23 fusion 2 proteinNup98-Nup96nucleoporin 96nucleoporin 98kDnucleoporin 98kDa | MLX-interacting proteinMlx interactorclass E basic helix-loop-helix protein 36transcriptional activator MondoA | |
| Modification date | 20200313 | 20200329 | |
| UniProtAcc | P52948 | Q9NP71 | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000324932, ENST00000355260, ENST00000359171, ENST00000397004, ENST00000397007, ENST00000488828, | ENST00000377037, ENST00000535996, ENST00000538698, ENST00000319080, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 35 X 37 X 11=14245 | 11 X 11 X 6=726 |
| # samples | 31 | 12 | |
| ** MAII score | log2(31/14245*10)=-5.52204359593698 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(12/726*10)=-2.59693514238723 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context (manual curation of fusion genes in FusionPDB) | PubMed: NUP98 [Title/Abstract] AND MLXIP [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | NUP98(3789811)-MLXIP(122611803), # samples:3 | ||
| Anticipated loss of major functional domain due to fusion event. | NUP98-MLXIP 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. NUP98-MLXIP 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. NUP98-MLXIP 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. NUP98-MLXIP 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. NUP98-MLXIP seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF. NUP98-MLXIP seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. NUP98-MLXIP seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF. NUP98-MLXIP seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. NUP98-MLXIP seems lost the major protein functional domain in Tgene partner, which is a transcription factor 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 |
| Tgene | MLXIP | GO:0045944 | positive regulation of transcription by RNA polymerase II | 11073985 |
| Fusion gene breakpoints across NUP98 (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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| Fusion gene breakpoints across MLXIP (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
| Fusion gene information from FusionGDB2.0. |
| 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. |
| Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| ChimerDB4 | UCEC | TCGA-D1-A3DG-01A | NUP98 | chr11 | 3789811 | - | MLXIP | chr12 | 122611803 | + |
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Fusion ORF Analysis |
| Fusion information from ORFfinder translation from full-length transcript sequence from FusionPDB. |
| 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) |
| ENST00000359171 | NUP98 | chr11 | 3789811 | - | ENST00000319080 | MLXIP | chr12 | 122611803 | + | 9251 | 1369 | 1376 | 3715 | 779 |
| 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 |
| ENST00000359171 | ENST00000319080 | NUP98 | chr11 | 3789811 | - | MLXIP | chr12 | 122611803 | + | 0.005780425 | 0.99421954 |
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Fusion Amino Acid Sequences |
| 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 >61126_61126_1_NUP98-MLXIP_NUP98_chr11_3789811_ENST00000359171_MLXIP_chr12_122611803_ENST00000319080_length(amino acids)=779AA_BP= MVSPKWKNFKGLKLQWRDKIRLNNAIWRAWYMQYLEKRKNPVCHFVTPLDGSVDVDEHRRPEAITTEGKYWKSRIEIVIREYHKWRTYFK KRLQQHKDEDLSSLVQDDDMLYWHKHGDGWKTPVPMEEDPLLDTDMLMSEFSDTLFSTLSSHQPVAWPNPREIAHLGNADMIQPGLIPLQ PNLDFMDTFEPFQDLFSSSRSIFGSMLPASASAPVPDPNNPPAQESILPTTALPTVSLPDSLIAPPTAPSLAHMDEQGCEHTSRTEDPFI QPTDFGPSEPPLSVPQPFLPVFTMPLLSPSPAPPPISPVLPLVPPPATALNPPAPPTFHQPQKFAGVNKAPSVITHTASATLTHDAPATT FSQSQGLVITTHHPAPSAAPCGLALSPVTRPPQPRLTFVHPKPVSLTGGRPKQPHKIVPAPKPEPVSLVLKNARIAPAAFSGQPQAVIMT SGPLKREGMLASTVSQSNVVIAPAAIARAPGVPEFHSSILVTDLGHGTSSPPAPVSRLFPSTAQDPLGKGEQVPLHGGSPQVTVTGPSRD CPNSGQASPCASEQSPSPQSPQNNCSGKSDPKNVAALKNRQMKHISAEQKRRFNIKMCFDMLNSLISNNSKLTSHAITLQKTVEYITKLQ QERGQMQEEARRLREEIEELNATIISCQQLLPATGVPVTRRQFDHMKDMFDEYVKTRTLQNWKFWIFSIIIKPLFESFKGMVSTSSLEEL -------------------------------------------------------------- |
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Fusion Protein Functional Features |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr11:3789811/chr12:122611803) - 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 |
| NUP98 | MLXIP |
| 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}. | FUNCTION: Transcriptional repressor. Binds to the canonical and non-canonical E box sequences 5'-CACGTG-3' (By similarity). {ECO:0000250}. |
| 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. |
| - 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 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000324932 | - | 8 | 33 | 1_156 | 316.0 | 1801.0 | Region | Note=FG repeats 1 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000355260 | - | 8 | 32 | 1_156 | 316.0 | 1727.0 | Region | Note=FG repeats 1 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000397004 | - | 8 | 20 | 1_156 | 316.0 | 921.0 | Region | Note=FG repeats 1 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000397007 | - | 8 | 20 | 1_156 | 316.0 | 938.0 | Region | Note=FG repeats 1 |
| Tgene | MLXIP | chr11:3789811 | chr12:122611803 | ENST00000319080 | 0 | 17 | 719_769 | 137.66666666666666 | 920.0 | Domain | bHLH | |
| Tgene | MLXIP | chr11:3789811 | chr12:122611803 | ENST00000538698 | 0 | 9 | 719_769 | 0 | 527.0 | Domain | bHLH | |
| Tgene | MLXIP | chr11:3789811 | chr12:122611803 | ENST00000319080 | 0 | 17 | 322_445 | 137.66666666666666 | 920.0 | Region | Transactivation domain | |
| Tgene | MLXIP | chr11:3789811 | chr12:122611803 | ENST00000319080 | 0 | 17 | 769_790 | 137.66666666666666 | 920.0 | Region | Note=Leucine-zipper | |
| Tgene | MLXIP | chr11:3789811 | chr12:122611803 | ENST00000538698 | 0 | 9 | 322_445 | 0 | 527.0 | Region | Transactivation domain | |
| Tgene | MLXIP | chr11:3789811 | chr12:122611803 | ENST00000538698 | 0 | 9 | 73_327 | 0 | 527.0 | Region | Required for cytoplasmic localization | |
| Tgene | MLXIP | chr11:3789811 | chr12:122611803 | ENST00000538698 | 0 | 9 | 769_790 | 0 | 527.0 | Region | Note=Leucine-zipper |
| - 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 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000324932 | - | 8 | 33 | 7_480 | 316.0 | 1801.0 | Compositional bias | Note=Gly/Thr-rich |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000324932 | - | 8 | 33 | 890_894 | 316.0 | 1801.0 | Compositional bias | Note=Poly-Glu |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000355260 | - | 8 | 32 | 7_480 | 316.0 | 1727.0 | Compositional bias | Note=Gly/Thr-rich |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000355260 | - | 8 | 32 | 890_894 | 316.0 | 1727.0 | Compositional bias | Note=Poly-Glu |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000397004 | - | 8 | 20 | 7_480 | 316.0 | 921.0 | Compositional bias | Note=Gly/Thr-rich |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000397004 | - | 8 | 20 | 890_894 | 316.0 | 921.0 | Compositional bias | Note=Poly-Glu |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000397007 | - | 8 | 20 | 7_480 | 316.0 | 938.0 | Compositional bias | Note=Gly/Thr-rich |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000397007 | - | 8 | 20 | 890_894 | 316.0 | 938.0 | Compositional bias | Note=Poly-Glu |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000324932 | - | 8 | 33 | 738_880 | 316.0 | 1801.0 | Domain | Peptidase S59 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000355260 | - | 8 | 32 | 738_880 | 316.0 | 1727.0 | Domain | Peptidase S59 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000397004 | - | 8 | 20 | 738_880 | 316.0 | 921.0 | Domain | Peptidase S59 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000397007 | - | 8 | 20 | 738_880 | 316.0 | 938.0 | Domain | Peptidase S59 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000324932 | - | 8 | 33 | 214_480 | 316.0 | 1801.0 | Region | Note=FG repeats 2 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000355260 | - | 8 | 32 | 214_480 | 316.0 | 1727.0 | Region | Note=FG repeats 2 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000397004 | - | 8 | 20 | 214_480 | 316.0 | 921.0 | Region | Note=FG repeats 2 |
| Hgene | NUP98 | chr11:3789811 | chr12:122611803 | ENST00000397007 | - | 8 | 20 | 214_480 | 316.0 | 938.0 | Region | Note=FG repeats 2 |
| Tgene | MLXIP | chr11:3789811 | chr12:122611803 | ENST00000319080 | 0 | 17 | 73_327 | 137.66666666666666 | 920.0 | Region | Required for cytoplasmic localization |
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Fusion Protein-Protein Interaction |
| 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 from validated records (BIOGRID-3.4.160) |
| Gene | PPI interactors |
| NUP98 | MOB1A, PARP11, QRICH2, TPR, NUP88, CREBBP, EP300, NUP133, Rae1, KPNB1, RAE1, TNPO2, CRM1, KAP104, NXF1, TNPO1, USP7, NPM1, PTTG1, APC, HDAC1, tat, NUP82, NUP159, Nup188, Nup98, Nup107, Nup214, SIRT7, NUP107, RAPGEF3, rev, NUMA1, ECT2, CSNK2A1, HNRNPUL1, LMNA, HDAC8, HDAC11, FBXO6, ARFGEF2, CDC73, PAF1, CDC37, CUL7, OBSL1, EED, MAPK8, COMTD1, SEC13, PNKD, NUP43, CLEC11A, RNF166, UNK, NUP54, NUP85, SEH1L, XPO5, KRAS, IFI16, NUP160, NUP35, B9D2, UBE2I, NUPL1, NUP153, PIM2, NUDT21, NCBP2, CHMP4B, GTF2H5, Ranbp2, Ube2i, Ssna1, Rcc1, Xpo1, Kifc1, Nup155, FOXI2, FOXL1, FOXQ1, FAF1, C11orf30, DUSP13, SPAST, FAM136A, UXS1, CD70, VASN, TRIM25, G3BP1, ORF10, CDC27, ANAPC4, ANAPC10, MAD2L1, CDC20, FZR1, PIN1, CTNNB1, TGFB1, NKX2-1, ESR2, NUP155, EZH2, DCPS, CDK9, DYNLT1, TOMM20, KIAA1429, DISC1, NR2C2, AGRN, HIST1H4A, PTPMT1, ORF6, BIRC3, LMBR1L, FAM105A, PLEKHA4, TTC9, HIST1H2BH, HIST3H3, M, nsp16, nsp4, nsp6, ORF7b, GLE1, NEK4, CIT, KIF14, KIF20A, PRC1, ARHGEF19, MYO9A, PTPN1, SEC61B, NFX1, HULC, NUPR1, BRD4, LGALS9, DYRK1A, NUP37, DDX58, CKAP4, DERL1, EMD, HSD17B11, HSD3B7, LMNB1, LRRC59, METTL7A, NUP50, REEP5, SEC62, SSR1, STIM1, SYNE3, TMPO, WDR5, NAA40, OCIAD1, CADPS, TACSTD2, RGPD1, TPST2, CD40, SLFN11, FBXO32, RCHY1, SIRT6, ETV6, |
| Protein-protein interactors based on sequence similarity (STRING) |
| Gene | STRING network |
| NUP98 |  |
| MLXIP |
| - Retained interactions in fusion protein (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost interactions due to fusion (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs to NUP98-MLXIP |
| Drugs used for this fusion-positive patient. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to NUP98-MLXIP |
| Diseases that have this fusion gene. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Disease | Source | PMID |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | NUP98 | C0002871 | Anemia | 1 | CTD_human |
| Hgene | NUP98 | C0023467 | Leukemia, Myelocytic, Acute | 1 | CTD_human |
| Hgene | NUP98 | C0024312 | Lymphopenia | 1 | CTD_human |
| Hgene | NUP98 | C0026998 | Acute Myeloid Leukemia, M1 | 1 | CTD_human |
| Hgene | NUP98 | C0027947 | Neutropenia | 1 | CTD_human |
| Hgene | NUP98 | C1879321 | Acute Myeloid Leukemia (AML-M2) | 1 | CTD_human |
| Hgene | NUP98 | C2930974 | Acute erythroleukemia | 1 | CTD_human |
| Hgene | NUP98 | C2930975 | Acute erythroleukemia - M6a subtype | 1 | CTD_human |
| Hgene | NUP98 | C2930976 | Acute myeloid leukemia FAB-M6 | 1 | CTD_human |
| Hgene | NUP98 | C2930977 | Acute erythroleukemia - M6b subtype | 1 | CTD_human |
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