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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:ATF4-FAT3 (FusionGDB2 ID:7426) |
Fusion Gene Summary for ATF4-FAT3 |
Fusion gene summary |
Fusion gene information | Fusion gene name: ATF4-FAT3 | Fusion gene ID: 7426 | Hgene | Tgene | Gene symbol | ATF4 | FAT3 | Gene ID | 468 | 120114 |
Gene name | activating transcription factor 4 | FAT atypical cadherin 3 | |
Synonyms | CREB-2|CREB2|TAXREB67|TXREB | CDHF15|CDHR10|hFat3 | |
Cytomap | 22q13.1 | 11q14.3 | |
Type of gene | protein-coding | protein-coding | |
Description | cyclic AMP-dependent transcription factor ATF-4DNA-binding protein TAXREB67cAMP response element-binding protein 2cAMP-dependent transcription factor ATF-4cAMP-responsive element-binding protein 2cyclic AMP-responsive element-binding protein 2tax-re | protocadherin Fat 3FAT tumor suppressor homolog 3cadherin family member 15cadherin-related family member 10 | |
Modification date | 20200329 | 20200313 | |
UniProtAcc | P18848 | Q8TDW7 | |
Ensembl transtripts involved in fusion gene | ENST00000337304, ENST00000396680, ENST00000404241, | ENST00000298047, ENST00000409404, ENST00000525166, ENST00000541502, ENST00000489716, ENST00000533797, | |
Fusion gene scores | * DoF score | 10 X 11 X 3=330 | 11 X 11 X 4=484 |
# samples | 11 | 11 | |
** MAII score | log2(11/330*10)=-1.58496250072116 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(11/484*10)=-2.13750352374993 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ATF4 [Title/Abstract] AND FAT3 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | ATF4(39918643)-FAT3(92086534), # 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 | ATF4 | GO:0034976 | response to endoplasmic reticulum stress | 19061639 |
Hgene | ATF4 | GO:0045893 | positive regulation of transcription, DNA-templated | 15775988|18940792 |
Hgene | ATF4 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 11478948|15775988|18940792 |
Hgene | ATF4 | GO:1990440 | positive regulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress | 12871976 |
Fusion gene breakpoints across ATF4 (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 FAT3 (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 | AI611026 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
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Fusion Gene ORF analysis for ATF4-FAT3 |
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-3CDS | ENST00000337304 | ENST00000298047 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000337304 | ENST00000409404 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000337304 | ENST00000525166 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000337304 | ENST00000541502 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000396680 | ENST00000298047 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000396680 | ENST00000409404 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000396680 | ENST00000525166 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000396680 | ENST00000541502 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000404241 | ENST00000298047 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000404241 | ENST00000409404 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000404241 | ENST00000525166 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-3CDS | ENST00000404241 | ENST00000541502 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-intron | ENST00000337304 | ENST00000489716 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-intron | ENST00000337304 | ENST00000533797 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-intron | ENST00000396680 | ENST00000489716 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-intron | ENST00000396680 | ENST00000533797 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-intron | ENST00000404241 | ENST00000489716 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
3UTR-intron | ENST00000404241 | ENST00000533797 | ATF4 | chr22 | 39918643 | - | FAT3 | chr11 | 92086534 | - |
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 ATF4-FAT3 |
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 ATF4-FAT3 |
Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:39918643/:92086534) - 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 |
ATF4 | FAT3 |
FUNCTION: Transcription factor that binds the cAMP response element (CRE) (consensus: 5'-GTGACGT[AC][AG]-3') and acts both as a regulator of normal metabolic and redox processes, and as a master transcription factor during the integrated stress response (ISR) (PubMed:1847461, PubMed:16682973, PubMed:31444471, PubMed:32132707). Binds to asymmetric CRE's as a heterodimer and to palindromic CRE's as a homodimer (By similarity). Core effector of the ISR, which is required for adaptation to various stress, such as endoplasmic reticulum (ER) stress, amino acid starvation, mitochondrial stress or oxidative stress (PubMed:32132707). During the ISR, ATF4 protein is translated in response to eIF-2-alpha/EIF2S1 phosphorylation caused by stress, and acts as a master transcription factor of stress-responsive genes in order to promote cell recovery (PubMed:32132707). Protects cells against metabolic consequences of ER oxidation by promoting expression of genes linked to amino acid sufficiency and resistance to oxidative stress (By similarity). Regulates the induction of DDIT3/CHOP and asparagine synthetase (ASNS) in response to amino acid deprivation or endoplasmic reticulum (ER) stress (PubMed:11960987). Together with DDIT3/CHOP, mediates ER-mediated cell death by promoting expression of genes involved in cellular amino acid metabolic processes, mRNA translation and the unfolded protein response (UPR) in response to ER stress (By similarity). ATF4 and DDIT3/CHOP activate the transcription of TRIB3 and promote ER stress-induced neuronal cell-death by regulating the expression of BBC3/PUMA (PubMed:15775988, PubMed:18940792). During ER stress response, activates the transcription of NLRP1, possibly in concert with other factors (PubMed:26086088). Activates expression of genes required to promote cell recovery in response to mitochondrial stress (PubMed:32132706, PubMed:32132707). Independently of the ISR, also required for normal metabolic processes: plays a key role in embryonic lens formation, fetal liver hematopoiesis, bone development and synaptic plasticity (By similarity). Acts as a regulator of osteoblast differentiation in response to phosphorylation by RPS6KA3/RSK2: phosphorylation in osteoblasts enhances transactivation activity and promotes expression of osteoblast-specific genes and post-transcriptionally regulates the synthesis of Type I collagen, the main constituent of the bone matrix (PubMed:15109498). Cooperates with FOXO1 in osteoblasts to regulate glucose homeostasis through suppression of beta-cell production and decrease in insulin production (By similarity). Activates transcription of SIRT4 (By similarity). Regulates the circadian expression of the core clock component PER2 and the serotonin transporter SLC6A4 (By similarity). Binds in a circadian time-dependent manner to the cAMP response elements (CRE) in the SLC6A4 and PER2 promoters and periodically activates the transcription of these genes (By similarity). Mainly acts as a transcriptional activator in cellular stress adaptation, but it can also act as a transcriptional repressor: acts as a regulator of synaptic plasticity by repressing transcription, thereby inhibiting induction and maintenance of long-term memory (By similarity). Regulates synaptic functions via interaction with DISC1 in neurons, which inhibits ATF4 transcription factor activity by disrupting ATF4 dimerization and DNA-binding (PubMed:31444471). {ECO:0000250|UniProtKB:Q06507, ECO:0000269|PubMed:11960987, ECO:0000269|PubMed:15109498, ECO:0000269|PubMed:15775988, ECO:0000269|PubMed:16682973, ECO:0000269|PubMed:1847461, ECO:0000269|PubMed:18940792, ECO:0000269|PubMed:26086088, ECO:0000269|PubMed:31444471, ECO:0000269|PubMed:32132706, ECO:0000269|PubMed:32132707}.; FUNCTION: (Microbial infection) Binds to a Tax-responsive enhancer element in the long terminal repeat of HTLV-I. {ECO:0000269|PubMed:1847461}. | FUNCTION: May play a role in the interactions between neurites derived from specific subsets of neurons during development. {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 ATF4-FAT3 |
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 ATF4-FAT3 |
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 ATF4-FAT3 |
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 ATF4-FAT3 |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |