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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:ATP9A-NFATC2 (FusionGDB2 ID:8284) |
Fusion Gene Summary for ATP9A-NFATC2 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: ATP9A-NFATC2 | Fusion gene ID: 8284 | Hgene | Tgene | Gene symbol | ATP9A | NFATC2 | Gene ID | 10079 | 4773 |
| Gene name | ATPase phospholipid transporting 9A (putative) | nuclear factor of activated T cells 2 | |
| Synonyms | ATPIIA | NFAT1|NFATP | |
| Cytomap | 20q13.2 | 20q13.2 | |
| Type of gene | protein-coding | protein-coding | |
| Description | probable phospholipid-transporting ATPase IIAATPase type IV, phospholipid-transporting (P-type),(putative)ATPase, class II, type 9Aphospholipid-transporting ATPase IIA | nuclear factor of activated T-cells, cytoplasmic 2NF-ATc2NFAT pre-existing subunitNFAT transcription complex, preexisting componentT cell transcription factor NFAT1nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2nuclear fact | |
| Modification date | 20200313 | 20200329 | |
| UniProtAcc | O75110 | Q8NCF5 | |
| Ensembl transtripts involved in fusion gene | ENST00000311637, ENST00000338821, ENST00000402822, ENST00000477492, | ENST00000371564, ENST00000396009, ENST00000414705, ENST00000609507, ENST00000609943, ENST00000610033, | |
| Fusion gene scores | * DoF score | 15 X 13 X 10=1950 | 10 X 12 X 6=720 |
| # samples | 16 | 12 | |
| ** MAII score | log2(16/1950*10)=-3.60733031374961 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(12/720*10)=-2.58496250072116 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: ATP9A [Title/Abstract] AND NFATC2 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint | ATP9A(50344281)-NFATC2(50078782), # samples:1 NFATC2(50071085)-ATP9A(50292747), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | NFATC2-ATP9A seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF. NFATC2-ATP9A seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. NFATC2-ATP9A seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF. NFATC2-ATP9A seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF. NFATC2-ATP9A seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. NFATC2-ATP9A seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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 | NFATC2 | GO:0016477 | cell migration | 21871017 |
| Tgene | NFATC2 | GO:0045893 | positive regulation of transcription, DNA-templated | 15790681 |
| Tgene | NFATC2 | GO:1905064 | negative regulation of vascular smooth muscle cell differentiation | 23853098 |
| Fusion gene breakpoints across ATP9A (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
| Fusion gene breakpoints across NFATC2 (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
| 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 |
| ChiTaRS5.0 | N/A | EC528351 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
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Fusion Gene ORF analysis for ATP9A-NFATC2 |
| 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 |
| intron-intron | ENST00000311637 | ENST00000371564 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000311637 | ENST00000396009 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000311637 | ENST00000414705 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000311637 | ENST00000609507 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000311637 | ENST00000609943 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000311637 | ENST00000610033 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000338821 | ENST00000371564 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000338821 | ENST00000396009 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000338821 | ENST00000414705 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000338821 | ENST00000609507 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000338821 | ENST00000609943 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000338821 | ENST00000610033 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000402822 | ENST00000371564 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000402822 | ENST00000396009 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000402822 | ENST00000414705 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000402822 | ENST00000609507 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000402822 | ENST00000609943 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000402822 | ENST00000610033 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000477492 | ENST00000371564 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000477492 | ENST00000396009 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000477492 | ENST00000414705 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000477492 | ENST00000609507 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000477492 | ENST00000609943 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| intron-intron | ENST00000477492 | ENST00000610033 | ATP9A | chr20 | 50344281 | - | NFATC2 | chr20 | 50078782 | - |
| 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 ATP9A-NFATC2 |
| 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) |
| Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page. |
| Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page. |
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Fusion Protein Features for ATP9A-NFATC2 |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:50344281/:50078782) - 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 |
| ATP9A | NFATC2 |
| FUNCTION: Plays a role in regulating membrane trafficking of cargo proteins, namely endosome to plasma membrane recycling and endosome to trans-Golgi network retrograde transport (PubMed:27733620, PubMed:30213940). In complex with MON2 and DOP1B, regulates SNX3 retromer-mediated endosomal sorting of WLS, a transporter of Wnt morphogens in developing tissues. Participates in the formation of endosomal carriers that direct WLS trafficking back to Golgi, away from lysosomal degradation (PubMed:30213940). Appears to be implicated in intercellular communication by negatively regulating the release of exosomes (PubMed:30947313). The flippase activity towards membrane lipids and its role in membrane asymmetry remains to be proved (PubMed:30947313). {ECO:0000269|PubMed:27733620, ECO:0000269|PubMed:30213940, ECO:0000269|PubMed:30947313}. | FUNCTION: In T-helper 2 (Th2) cells, regulates the magnitude of NFAT-driven transcription of a specific subset of cytokine genes, including IL3, IL4, IL5 and IL13, but not IL2. Recruits PRMT1 to the IL4 promoter; this leads to enhancement of histone H4 'Arg-3'-methylation and facilitates subsequent histone acetylation at the IL4 locus, thus promotes robust cytokine expression (By similarity). Down-regulates formation of poly-SUMO chains by UBE2I/UBC9 (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. |
| - 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 ATP9A-NFATC2 |
| 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 ATP9A-NFATC2 |
| 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 ATP9A-NFATC2 |
| 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 ATP9A-NFATC2 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
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