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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:CCSER1-HERC3 (FusionGDB2 ID:14256)

Fusion Gene Summary for CCSER1-HERC3

check button Fusion gene summary
Fusion gene informationFusion gene name: CCSER1-HERC3
Fusion gene ID: 14256
HgeneTgene
Gene symbol

CCSER1

HERC3

Gene ID

401145

8916

Gene namecoiled-coil serine rich protein 1HECT and RLD domain containing E3 ubiquitin protein ligase 3
SynonymsFAM190A-
Cytomap

4q22.1

4q22.1

Type of geneprotein-codingprotein-coding
Descriptionserine-rich coiled-coil domain-containing protein 1family with sequence similarity 190, member Aprotein FAM190Aprobable E3 ubiquitin-protein ligase HERC3HECT domain and RCC1-like domain-containing protein 3HECT-type E3 ubiquitin transferase HERC3hect domain and RLD 3
Modification date2020031320200313
UniProtAcc

Q9C0I3

Q15034

Ensembl transtripts involved in fusion geneENST00000509176, ENST00000333691, 
ENST00000432775, ENST00000504150, 
ENST00000402738, ENST00000264345, 
ENST00000407637, ENST00000543130, 
ENST00000601319, 
Fusion gene scores* DoF score16 X 13 X 7=14564 X 4 X 3=48
# samples 184
** MAII scorelog2(18/1456*10)=-3.01594154386902
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CCSER1 [Title/Abstract] AND HERC3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCCSER1(91048982)-HERC3(89599115), # 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)

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

check buttonFusion gene breakpoints across CCSER1 (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 HERC3 (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
ChimerDB4UCECTCGA-EY-A1GX-01ACCSER1chr4

91048982

+HERC3chr4

89599115

+


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Fusion Gene ORF analysis for CCSER1-HERC3

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
5UTR-3CDSENST00000509176ENST00000402738CCSER1chr4

91048982

+HERC3chr4

89599115

+
5UTR-intronENST00000509176ENST00000264345CCSER1chr4

91048982

+HERC3chr4

89599115

+
5UTR-intronENST00000509176ENST00000407637CCSER1chr4

91048982

+HERC3chr4

89599115

+
5UTR-intronENST00000509176ENST00000543130CCSER1chr4

91048982

+HERC3chr4

89599115

+
5UTR-intronENST00000509176ENST00000601319CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-3CDSENST00000333691ENST00000402738CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-3CDSENST00000432775ENST00000402738CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-3CDSENST00000504150ENST00000402738CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000333691ENST00000264345CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000333691ENST00000407637CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000333691ENST00000543130CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000333691ENST00000601319CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000432775ENST00000264345CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000432775ENST00000407637CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000432775ENST00000543130CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000432775ENST00000601319CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000504150ENST00000264345CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000504150ENST00000407637CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000504150ENST00000543130CCSER1chr4

91048982

+HERC3chr4

89599115

+
intron-intronENST00000504150ENST00000601319CCSER1chr4

91048982

+HERC3chr4

89599115

+

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 CCSER1-HERC3


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)
CCSER1chr491048982+HERC3chr489599114+3.92E-050.9999608
CCSER1chr491048982+HERC3chr489599114+3.92E-050.9999608

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.
genomic feature of top 1%

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Fusion Protein Features for CCSER1-HERC3


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/:91048982/:89599115)
- 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
CCSER1

Q9C0I3

HERC3

Q15034

FUNCTION: E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. {ECO:0000250}.

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 CCSER1-HERC3


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 CCSER1-HERC3


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 CCSER1-HERC3


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 CCSER1-HERC3


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