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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:RNF213-AKAP8L (FusionGDB2 ID:74960) |
Fusion Gene Summary for RNF213-AKAP8L |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: RNF213-AKAP8L | Fusion gene ID: 74960 | Hgene | Tgene | Gene symbol | RNF213 | AKAP8L | Gene ID | 57674 | 26993 |
| Gene name | ring finger protein 213 | A-kinase anchoring protein 8 like | |
| Synonyms | ALO17|C17orf27|KIAA1618|MYMY2|MYSTR|NET57 | HA95|HAP95|NAKAP|NAKAP95 | |
| Cytomap | 17q25.3 | 19p13.12 | |
| Type of gene | protein-coding | protein-coding | |
| Description | E3 ubiquitin-protein ligase RNF213ALK lymphoma oligomerization partner on chromosome 17RING-type E3 ubiquitin transferase RNF213mysterin | A-kinase anchor protein 8-likeA kinase (PRKA) anchor protein 8-likeAKAP8-like proteinhelicase A-binding protein 95 kDahomologous to AKAP95 proteinneighbor of A-kinase anchoring protein 95neighbor of AKAP95testis tissue sperm-binding protein Li 90mP | |
| Modification date | 20200313 | 20200313 | |
| UniProtAcc | . | Q9ULX6 | |
| Ensembl transtripts involved in fusion gene | ENST00000336301, ENST00000508628, ENST00000582970, ENST00000319921, ENST00000427003, ENST00000456466, | ENST00000595879, ENST00000397410, ENST00000595465, | |
| Fusion gene scores | * DoF score | 34 X 32 X 16=17408 | 9 X 7 X 8=504 |
| # samples | 41 | 11 | |
| ** MAII score | log2(41/17408*10)=-5.40798274174489 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(11/504*10)=-2.19592020997526 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: RNF213 [Title/Abstract] AND AKAP8L [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint | RNF213(78332279)-AKAP8L(15521405), # samples:2 | ||
| Anticipated loss of major functional domain due to fusion event. | RNF213-AKAP8L seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF. RNF213-AKAP8L seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. RNF213-AKAP8L 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 |
| Hgene | RNF213 | GO:0016567 | protein ubiquitination | 21799892 |
| Hgene | RNF213 | GO:0051260 | protein homooligomerization | 24658080|26126547 |
| Hgene | RNF213 | GO:0051865 | protein autoubiquitination | 21799892 |
| Tgene | AKAP8L | GO:0006397 | mRNA processing | 17594903 |
| Tgene | AKAP8L | GO:0010793 | regulation of mRNA export from nucleus | 11402034 |
| Tgene | AKAP8L | GO:0045944 | positive regulation of transcription by RNA polymerase II | 11884601 |
| Fusion gene breakpoints across RNF213 (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 AKAP8L (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 |
| ChimerDB4 | UCEC | TCGA-EY-A4KR-01A | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
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Fusion Gene ORF analysis for RNF213-AKAP8L |
| 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 | ENST00000336301 | ENST00000595879 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| 5CDS-intron | ENST00000508628 | ENST00000595879 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| 5CDS-intron | ENST00000582970 | ENST00000595879 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| Frame-shift | ENST00000336301 | ENST00000397410 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| Frame-shift | ENST00000336301 | ENST00000595465 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| Frame-shift | ENST00000508628 | ENST00000397410 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| Frame-shift | ENST00000508628 | ENST00000595465 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| Frame-shift | ENST00000582970 | ENST00000397410 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| Frame-shift | ENST00000582970 | ENST00000595465 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| intron-3CDS | ENST00000319921 | ENST00000397410 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| intron-3CDS | ENST00000319921 | ENST00000595465 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| intron-3CDS | ENST00000427003 | ENST00000397410 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| intron-3CDS | ENST00000427003 | ENST00000595465 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| intron-3CDS | ENST00000456466 | ENST00000397410 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| intron-3CDS | ENST00000456466 | ENST00000595465 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| intron-intron | ENST00000319921 | ENST00000595879 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| intron-intron | ENST00000427003 | ENST00000595879 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| intron-intron | ENST00000456466 | ENST00000595879 | RNF213 | chr17 | 78332279 | + | AKAP8L | chr19 | 15521405 | - |
| 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 RNF213-AKAP8L |
| 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 RNF213-AKAP8L |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:78332279/:15521405) - 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 |
| . | AKAP8L |
| FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. | FUNCTION: Could play a role in constitutive transport element (CTE)-mediated gene expression by association with DHX9. Increases CTE-dependent nuclear unspliced mRNA export (PubMed:10748171, PubMed:11402034). Proposed to target PRKACA to the nucleus but does not seem to be implicated in the binding of regulatory subunit II of PKA (PubMed:10761695, PubMed:11884601). May be involved in nuclear envelope breakdown and chromatin condensation. May be involved in anchoring nuclear membranes to chromatin in interphase and in releasing membranes from chromating at mitosis (PubMed:11034899). May regulate the initiation phase of DNA replication when associated with TMPO isoform Beta (PubMed:12538639). Required for cell cycle G2/M transition and histone deacetylation during mitosis. In mitotic cells recruits HDAC3 to the vicinity of chromatin leading to deacetylation and subsequent phosphorylation at 'Ser-10' of histone H3; in this function seems to act redundantly with AKAP8 (PubMed:16980585). May be involved in regulation of pre-mRNA splicing (PubMed:17594903). {ECO:0000269|PubMed:10748171, ECO:0000269|PubMed:11034899, ECO:0000269|PubMed:11402034, ECO:0000269|PubMed:11884601, ECO:0000269|PubMed:12538639, ECO:0000269|PubMed:16980585, ECO:0000305|PubMed:10761695}.; FUNCTION: (Microbial infection) In case of EBV infection, may target PRKACA to EBNA-LP-containing nuclear sites to modulate transcription from specific promoters. {ECO:0000269|PubMed:11884601}.; FUNCTION: (Microbial infection) Can synergize with DHX9 to activate the CTE-mediated gene expression of type D retroviruses. {ECO:0000269|PubMed:11402034}.; FUNCTION: (Microbial infection) In case of HIV-1 infection, involved in the DHX9-promoted annealing of host tRNA(Lys3) to viral genomic RNA as a primer in reverse transcription; in vitro negatively regulates DHX9 annealing activity. {ECO:0000269|PubMed:25034436}. |
| 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 RNF213-AKAP8L |
| 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 RNF213-AKAP8L |
| 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 RNF213-AKAP8L |
| 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 RNF213-AKAP8L |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
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