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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:EXD2-FAM162A (FusionGDB2 ID:27865) |
Fusion Gene Summary for EXD2-FAM162A |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: EXD2-FAM162A | Fusion gene ID: 27865 | Hgene | Tgene | Gene symbol | EXD2 | FAM162A | Gene ID | 55218 | 26355 |
| Gene name | exonuclease 3'-5' domain containing 2 | family with sequence similarity 162 member A | |
| Synonyms | C14orf114|EXDL2 | C3orf28|E2IG5|HGTD-P | |
| Cytomap | 14q24.1 | 3q21.1 | |
| Type of gene | protein-coding | protein-coding | |
| Description | exonuclease 3'-5' domain-containing protein 23'-5' exoribonuclease EXD2exonuclease 3'-5' domain-like 2exonuclease 3'-5' domain-like-containing protein 2 | protein FAM162AE2-induced gene 5 proteinHIF-1 alpha-responsive proapoptotic moleculegrowth and transformation-dependent protein | |
| Modification date | 20200313 | 20200313 | |
| UniProtAcc | Q9NVH0 | Q96A26 | |
| Ensembl transtripts involved in fusion gene | ENST00000492815, ENST00000312994, ENST00000409018, ENST00000409014, ENST00000409242, ENST00000409949, ENST00000449989, ENST00000409675, | ENST00000232125, ENST00000477892, ENST00000469967, | |
| Fusion gene scores | * DoF score | 5 X 6 X 4=120 | 5 X 5 X 2=50 |
| # samples | 6 | 5 | |
| ** MAII score | log2(6/120*10)=-1 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(5/50*10)=0 | |
| Context | PubMed: EXD2 [Title/Abstract] AND FAM162A [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint | EXD2(69676499)-FAM162A(122128725), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | |||
| * 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 | EXD2 | GO:0000724 | double-strand break repair via homologous recombination | 26807646 |
| Hgene | EXD2 | GO:0000729 | DNA double-strand break processing | 26807646 |
| Hgene | EXD2 | GO:0006302 | double-strand break repair | 26807646 |
| Hgene | EXD2 | GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 26807646 |
| Tgene | FAM162A | GO:0006919 | activation of cysteine-type endopeptidase activity involved in apoptotic process | 15082785 |
| Tgene | FAM162A | GO:0043065 | positive regulation of apoptotic process | 15082785 |
| Tgene | FAM162A | GO:0071456 | cellular response to hypoxia | 15082785 |
| Tgene | FAM162A | GO:0090200 | positive regulation of release of cytochrome c from mitochondria | 15082785 |
| Fusion gene breakpoints across EXD2 (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 FAM162A (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 | BU565473 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
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Fusion Gene ORF analysis for EXD2-FAM162A |
| 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 |
| 3UTR-3UTR | ENST00000492815 | ENST00000232125 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 3UTR-3UTR | ENST00000492815 | ENST00000477892 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 3UTR-intron | ENST00000492815 | ENST00000469967 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5CDS-3UTR | ENST00000312994 | ENST00000232125 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5CDS-3UTR | ENST00000312994 | ENST00000477892 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5CDS-3UTR | ENST00000409018 | ENST00000232125 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5CDS-3UTR | ENST00000409018 | ENST00000477892 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5CDS-intron | ENST00000312994 | ENST00000469967 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5CDS-intron | ENST00000409018 | ENST00000469967 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-3UTR | ENST00000409014 | ENST00000232125 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-3UTR | ENST00000409014 | ENST00000477892 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-3UTR | ENST00000409242 | ENST00000232125 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-3UTR | ENST00000409242 | ENST00000477892 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-3UTR | ENST00000409949 | ENST00000232125 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-3UTR | ENST00000409949 | ENST00000477892 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-3UTR | ENST00000449989 | ENST00000232125 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-3UTR | ENST00000449989 | ENST00000477892 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-intron | ENST00000409014 | ENST00000469967 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-intron | ENST00000409242 | ENST00000469967 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-intron | ENST00000409949 | ENST00000469967 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 5UTR-intron | ENST00000449989 | ENST00000469967 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| intron-3UTR | ENST00000409675 | ENST00000232125 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| intron-3UTR | ENST00000409675 | ENST00000477892 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| intron-intron | ENST00000409675 | ENST00000469967 | EXD2 | chr14 | 69676499 | + | FAM162A | chr3 | 122128725 | + |
| 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 EXD2-FAM162A |
| 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 EXD2-FAM162A |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:69676499/:122128725) - 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 |
| EXD2 | FAM162A |
| FUNCTION: Exonuclease that has both 3'-5' exoribonuclease and exodeoxyribonuclease activities, depending on the divalent metal cation used as cofactor (PubMed:29335528, PubMed:31127291). In presence of Mg(2+), only shows 3'-5' exoribonuclease activity, while it shows both exoribonuclease and exodeoxyribonuclease activities in presence of Mn(2+) (PubMed:29335528, PubMed:31127291). Acts as an exoribonuclease in mitochondrion, possibly by regulating ATP production and mitochondrial translation (PubMed:29335528). Also involved in the response to DNA damage (PubMed:26807646, PubMed:31255466). Acts as 3'-5' exodeoxyribonuclease for double-strand breaks resection and efficient homologous recombination (PubMed:20603073, PubMed:26807646). Plays a key role in controlling the initial steps of chromosomal break repair, it is recruited to chromatin in a damage-dependent manner and functionally interacts with the MRN complex to accelerate resection through its 3'-5' exonuclease activity, which efficiently processes double-stranded DNA substrates containing nicks (PubMed:26807646). Also involved in response to replicative stress: recruited to stalled forks and is required to stabilize and restart stalled replication forks by restraining excessive fork regression, thereby suppressing their degradation (PubMed:31255466). {ECO:0000269|PubMed:20603073, ECO:0000269|PubMed:26807646, ECO:0000269|PubMed:29335528, ECO:0000269|PubMed:31127291, ECO:0000269|PubMed:31255466}. | FUNCTION: Proposed to be involved in regulation of apoptosis; the exact mechanism may differ between cell types/tissues (PubMed:15082785). May be involved in hypoxia-induced cell death of transformed cells implicating cytochrome C release and caspase activation (such as CASP9) and inducing mitochondrial permeability transition (PubMed:15082785). May be involved in hypoxia-induced cell death of neuronal cells probably by promoting release of AIFM1 from mitochondria to cytoplasm and its translocation to the nucleus; however, the involvement of caspases has been reported conflictingly (By similarity). {ECO:0000250|UniProtKB:Q9D6U8, ECO:0000269|PubMed:15082785}. |
| 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 EXD2-FAM162A |
| 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 EXD2-FAM162A |
| 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 EXD2-FAM162A |
| 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 EXD2-FAM162A |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
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