|
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:ATF7-EXOC4 (FusionGDB2 ID:7464) |
Fusion Gene Summary for ATF7-EXOC4 |
Fusion gene summary |
Fusion gene information | Fusion gene name: ATF7-EXOC4 | Fusion gene ID: 7464 | Hgene | Tgene | Gene symbol | ATF7 | EXOC4 | Gene ID | 11016 | 60412 |
Gene name | activating transcription factor 7 | exocyst complex component 4 | |
Synonyms | ATFA | SEC8|SEC8L1|Sec8p | |
Cytomap | 12q13.13 | 7q33 | |
Type of gene | protein-coding | protein-coding | |
Description | cyclic AMP-dependent transcription factor ATF-7transcription factor ATF-A | exocyst complex component 4SEC8-like 1exocyst complex component Sec8 | |
Modification date | 20200313 | 20200320 | |
UniProtAcc | P17544 | Q96A65 | |
Ensembl transtripts involved in fusion gene | ENST00000328463, ENST00000415113, ENST00000420353, ENST00000456903, ENST00000548118, ENST00000548446, ENST00000591397, ENST00000546661, | ENST00000460346, ENST00000393161, ENST00000541309, ENST00000545148, ENST00000253861, ENST00000539845, | |
Fusion gene scores | * DoF score | 12 X 11 X 10=1320 | 35 X 25 X 10=8750 |
# samples | 18 | 39 | |
** MAII score | log2(18/1320*10)=-2.87446911791614 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(39/8750*10)=-4.48773698785744 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ATF7 [Title/Abstract] AND EXOC4 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | ATF7(53994737)-EXOC4(133502078), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | ATF7-EXOC4 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. ATF7-EXOC4 seems lost the major protein functional domain in Hgene 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 | ATF7 | GO:0006355 | regulation of transcription, DNA-templated | 8288576 |
Fusion gene breakpoints across ATF7 (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 EXOC4 (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 | STAD | TCGA-CD-A48C-01A | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Top |
Fusion Gene ORF analysis for ATF7-EXOC4 |
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-3UTR | ENST00000328463 | ENST00000460346 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-3UTR | ENST00000415113 | ENST00000460346 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-3UTR | ENST00000420353 | ENST00000460346 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-3UTR | ENST00000456903 | ENST00000460346 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-3UTR | ENST00000548118 | ENST00000460346 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-3UTR | ENST00000548446 | ENST00000460346 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-3UTR | ENST00000591397 | ENST00000460346 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000328463 | ENST00000393161 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000328463 | ENST00000541309 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000328463 | ENST00000545148 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000415113 | ENST00000393161 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000415113 | ENST00000541309 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000415113 | ENST00000545148 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000420353 | ENST00000393161 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000420353 | ENST00000541309 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000420353 | ENST00000545148 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000456903 | ENST00000393161 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000456903 | ENST00000541309 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000456903 | ENST00000545148 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000548118 | ENST00000393161 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000548118 | ENST00000541309 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000548118 | ENST00000545148 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000548446 | ENST00000393161 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000548446 | ENST00000541309 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000548446 | ENST00000545148 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000591397 | ENST00000393161 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000591397 | ENST00000541309 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
5CDS-intron | ENST00000591397 | ENST00000545148 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000328463 | ENST00000253861 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000328463 | ENST00000539845 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000415113 | ENST00000253861 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000415113 | ENST00000539845 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000420353 | ENST00000253861 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000420353 | ENST00000539845 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000456903 | ENST00000253861 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000456903 | ENST00000539845 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000548118 | ENST00000253861 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000548118 | ENST00000539845 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000548446 | ENST00000253861 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000548446 | ENST00000539845 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000591397 | ENST00000253861 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
Frame-shift | ENST00000591397 | ENST00000539845 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
intron-3CDS | ENST00000546661 | ENST00000253861 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
intron-3CDS | ENST00000546661 | ENST00000539845 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
intron-3UTR | ENST00000546661 | ENST00000460346 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
intron-intron | ENST00000546661 | ENST00000393161 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
intron-intron | ENST00000546661 | ENST00000541309 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
intron-intron | ENST00000546661 | ENST00000545148 | ATF7 | chr12 | 53994737 | - | EXOC4 | chr7 | 133502078 | + |
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 |
Top |
Fusion Genomic Features for ATF7-EXOC4 |
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) |
ATF7 | chr12 | 53994736 | - | EXOC4 | chr7 | 133502077 | + | 8.63E-06 | 0.9999914 |
ATF7 | chr12 | 53994736 | - | EXOC4 | chr7 | 133502077 | + | 8.63E-06 | 0.9999914 |
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. |
Top |
Fusion Protein Features for ATF7-EXOC4 |
Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:53994737/:133502078) - 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. |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
ATF7 | EXOC4 |
FUNCTION: Stress-responsive chromatin regulator that plays a role in various biological processes including innate immunological memory, adipocyte differentiation or telomerase regulation (PubMed:29490055). In absence of stress, contributes to the formation of heterochromatin and heterochromatin-like structure by recruiting histone H3K9 tri- and di-methyltransferases thus silencing the transcription of target genes such as STAT1 in adipocytes, or genes involved in innate immunity in macrophages and adipocytes (By similarity). Stress induces ATF7 phosphorylation that disrupts interactions with histone methyltransferase and enhances the association with coactivators containing histone acetyltransferase and/or histone demethylase, leading to disruption of the heterochromatin-like structure and subsequently transcriptional activation (By similarity). In response to TNF-alpha, which is induced by various stresses, phosphorylated ATF7 and telomerase are released from telomeres leading to telomere shortening (PubMed:29490055). Plays also a role in maintaining epithelial regenerative capacity and protecting against cell death during intestinal epithelial damage and repair (By similarity). {ECO:0000250|UniProtKB:Q8R0S1, ECO:0000269|PubMed:29490055}.; FUNCTION: [Isoform 4]: Acts as a dominant repressor of the E-selectin/NF-ELAM1/delta-A promoter.; FUNCTION: [Isoform 5]: Acts as a negative regulator, inhibiting both ATF2 and ATF7 transcriptional activities. It may exert these effects by sequestrating in the cytoplasm the Thr-53 phosphorylating kinase, preventing activation. {ECO:0000269|PubMed:21858082}. | FUNCTION: Component of the exocyst complex involved in the docking of exocytic vesicles with fusion sites on the plasma membrane. {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 |
Top |
Fusion Gene Sequence for ATF7-EXOC4 |
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. |
Top |
Fusion Gene PPI Analysis for ATF7-EXOC4 |
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 |
Top |
Related Drugs for ATF7-EXOC4 |
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 |
Top |
Related Diseases for ATF7-EXOC4 |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |