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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:FAT1-ACSL1 (FusionGDB2 ID:29448)

Fusion Gene Summary for FAT1-ACSL1

check button Fusion gene summary
Fusion gene informationFusion gene name: FAT1-ACSL1
Fusion gene ID: 29448
HgeneTgene
Gene symbol

FAT1

ACSL1

Gene ID

2195

2180

Gene nameFAT atypical cadherin 1acyl-CoA synthetase long chain family member 1
SynonymsCDHF7|CDHR8|FAT|ME5|hFat1ACS1|FACL1|FACL2|LACS|LACS1|LACS2
Cytomap

4q35.2

4q35.1

Type of geneprotein-codingprotein-coding
Descriptionprotocadherin Fat 1FAT tumor suppressor 1cadherin ME5cadherin family member 7cadherin-related family member 8cadherin-related tumor suppressor homologprotein fat homologlong-chain-fatty-acid--CoA ligase 1LACS 1LACS 2acyl-CoA synthetase 1arachidonate--CoA ligasefatty-acid-Coenzyme A ligase, long-chain 1fatty-acid-Coenzyme A ligase, long-chain 2lignoceroyl-CoA synthaselong-chain acyl-CoA synthetase 1long-chain acy
Modification date2020031320200313
UniProtAcc

Q14517

P33121

Ensembl transtripts involved in fusion geneENST00000441802, ENST00000512347, 
ENST00000281455, ENST00000437665, 
ENST00000504342, ENST00000504900, 
ENST00000507295, ENST00000513317, 
ENST00000515030, ENST00000454703, 
Fusion gene scores* DoF score16 X 17 X 8=21763 X 3 X 3=27
# samples 203
** MAII scorelog2(20/2176*10)=-3.44360665147561
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: FAT1 [Title/Abstract] AND ACSL1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFAT1(187627716)-ACSL1(185724700), # samples:2
FAT1(187627717)-ACSL1(185724700), # samples:2
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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
TgeneACSL1

GO:0001676

long-chain fatty acid metabolic process

22022213|24269233

TgeneACSL1

GO:0008610

lipid biosynthetic process

21242590

TgeneACSL1

GO:0044539

long-chain fatty acid import

22022213


check buttonFusion gene breakpoints across FAT1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across ACSL1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4HNSCTCGA-CN-4722-01AFAT1chr4

187627717

-ACSL1chr4

185724700

-
ChimerDB4HNSCTCGA-CN-4722FAT1chr4

187627716

-ACSL1chr4

185724700

-
ChimerDB4HNSCTCGA-CN-4722FAT1chr4

187627717

-ACSL1chr4

185724700

-


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Fusion Gene ORF analysis for FAT1-ACSL1

check button 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.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5CDS-5UTRENST00000441802ENST00000281455FAT1chr4

187627716

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000281455FAT1chr4

187627717

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000437665FAT1chr4

187627716

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000437665FAT1chr4

187627717

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000504342FAT1chr4

187627716

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000504342FAT1chr4

187627717

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000504900FAT1chr4

187627716

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000504900FAT1chr4

187627717

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000507295FAT1chr4

187627716

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000507295FAT1chr4

187627717

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000513317FAT1chr4

187627716

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000513317FAT1chr4

187627717

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000515030FAT1chr4

187627716

-ACSL1chr4

185724700

-
5CDS-5UTRENST00000441802ENST00000515030FAT1chr4

187627717

-ACSL1chr4

185724700

-
5CDS-intronENST00000441802ENST00000454703FAT1chr4

187627716

-ACSL1chr4

185724700

-
5CDS-intronENST00000441802ENST00000454703FAT1chr4

187627717

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000281455FAT1chr4

187627716

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000281455FAT1chr4

187627717

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000437665FAT1chr4

187627716

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000437665FAT1chr4

187627717

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000504342FAT1chr4

187627716

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000504342FAT1chr4

187627717

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000504900FAT1chr4

187627716

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000504900FAT1chr4

187627717

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000507295FAT1chr4

187627716

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000507295FAT1chr4

187627717

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000513317FAT1chr4

187627716

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000513317FAT1chr4

187627717

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000515030FAT1chr4

187627716

-ACSL1chr4

185724700

-
intron-5UTRENST00000512347ENST00000515030FAT1chr4

187627717

-ACSL1chr4

185724700

-
intron-intronENST00000512347ENST00000454703FAT1chr4

187627716

-ACSL1chr4

185724700

-
intron-intronENST00000512347ENST00000454703FAT1chr4

187627717

-ACSL1chr4

185724700

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF 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.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for FAT1-ACSL1


check buttonFusionAI 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.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution 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.

check buttonDistribution 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 FAT1-ACSL1


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:187627716/:185724700)
- 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.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FAT1

Q14517

ACSL1

P33121

FUNCTION: [Protocadherin Fat 1]: Plays an essential role for cellular polarization, directed cell migration and modulating cell-cell contact. {ECO:0000250}.FUNCTION: Catalyzes the conversion of long-chain fatty acids to their active form acyl-CoAs for both synthesis of cellular lipids, and degradation via beta-oxidation (PubMed:24269233, PubMed:22633490, PubMed:21242590). Preferentially uses palmitoleate, oleate and linoleate (PubMed:24269233). Preferentially activates arachidonate than epoxyeicosatrienoic acids (EETs) or hydroxyeicosatrienoic acids (HETEs) (By similarity). {ECO:0000250|UniProtKB:P18163, ECO:0000269|PubMed:21242590, ECO:0000269|PubMed:22633490, ECO:0000269|PubMed:24269233}.

check buttonRetention 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

download page


* 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.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for FAT1-ACSL1


check button 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 FAT1-ACSL1


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for FAT1-ACSL1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for FAT1-ACSL1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource