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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:C1QTNF3-ESCO1 (FusionGDB2 ID:11433)

Fusion Gene Summary for C1QTNF3-ESCO1

check button Fusion gene summary
Fusion gene informationFusion gene name: C1QTNF3-ESCO1
Fusion gene ID: 11433
HgeneTgene
Gene symbol

C1QTNF3

ESCO1

Gene ID

114899

114799

Gene nameC1q and TNF related 3establishment of sister chromatid cohesion N-acetyltransferase 1
SynonymsC1ATNF3|CORCS|CORS|CORS-26|CORS26|CTRP3A930014I12Rik|CTF|ECO1|EFO1|ESO1
Cytomap

5p13.2

18q11.2

Type of geneprotein-codingprotein-coding
Descriptioncomplement C1q tumor necrosis factor-related protein 3C1q and tumor necrosis factor related protein 3cartonectincollagenous repeat-containing sequence 26 kDa proteincollagenous repeat-containing sequence of 26-kDasecretory protein CORS26N-acetyltransferase ESCO1CTF7 homolog 1ECO1 homolog 1EFO1pESO1 homolog 1N-acetyltransferase ESCO1 variant 2establishment factor-like protein 1establishment of cohesion 1 homolog 1hEFO1
Modification date2020032220200313
UniProtAcc

Q9BXJ4

Q5FWF5

Ensembl transtripts involved in fusion geneENST00000231338, ENST00000382065, 
ENST00000513065, 
ENST00000269214, 
ENST00000580101, 
Fusion gene scores* DoF score2 X 2 X 2=86 X 6 X 2=72
# samples 26
** MAII scorelog2(2/8*10)=1.32192809488736log2(6/72*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: C1QTNF3 [Title/Abstract] AND ESCO1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointC1QTNF3(34141926)-ESCO1(19154273), # samples:6
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
HgeneC1QTNF3

GO:0035356

cellular triglyceride homeostasis

20739398

HgeneC1QTNF3

GO:0045721

negative regulation of gluconeogenesis

20952387

HgeneC1QTNF3

GO:0050715

positive regulation of cytokine secretion

18421280

HgeneC1QTNF3

GO:0050728

negative regulation of inflammatory response

16213490

HgeneC1QTNF3

GO:0070165

positive regulation of adiponectin secretion

18421280

HgeneC1QTNF3

GO:0071638

negative regulation of monocyte chemotactic protein-1 production

20739398

HgeneC1QTNF3

GO:1900165

negative regulation of interleukin-6 secretion

16213490

HgeneC1QTNF3

GO:1901223

negative regulation of NIK/NF-kappaB signaling

16213490

TgeneESCO1

GO:0018394

peptidyl-lysine acetylation

27112597


check buttonFusion gene breakpoints across C1QTNF3 (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 ESCO1 (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
ChiTaRS5.0N/AAX184548C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-
ChiTaRS5.0N/AAX186211C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-
ChiTaRS5.0N/AAX187416C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-
ChiTaRS5.0N/AAX187584C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-
ChiTaRS5.0N/AAX188209C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-
ChiTaRS5.0N/AAX188317C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-


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Fusion Gene ORF analysis for C1QTNF3-ESCO1

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
intron-3CDSENST00000231338ENST00000269214C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-
intron-3CDSENST00000382065ENST00000269214C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-
intron-3CDSENST00000513065ENST00000269214C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-
intron-intronENST00000231338ENST00000580101C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-
intron-intronENST00000382065ENST00000580101C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-
intron-intronENST00000513065ENST00000580101C1QTNF3chr5

34141926

-ESCO1chr18

19154273

-

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 C1QTNF3-ESCO1


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 C1QTNF3-ESCO1


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/:34141926/:19154273)
- 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
C1QTNF3

Q9BXJ4

ESCO1

Q5FWF5

FUNCTION: Acetyltransferase required for the establishment of sister chromatid cohesion (PubMed:15958495, PubMed:18614053). Couples the processes of cohesion and DNA replication to ensure that only sister chromatids become paired together. In contrast to the structural cohesins, the deposition and establishment factors are required only during S phase. Acts by mediating the acetylation of cohesin component SMC3 (PubMed:18614053). {ECO:0000269|PubMed:14576321, ECO:0000269|PubMed:15958495, ECO:0000269|PubMed:18614053, ECO:0000269|PubMed:19907496, ECO:0000269|PubMed:27112597, ECO:0000269|PubMed:27803161}.

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 C1QTNF3-ESCO1


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 C1QTNF3-ESCO1


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 C1QTNF3-ESCO1


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 C1QTNF3-ESCO1


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