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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:GSG1L-KCTD13 (FusionGDB2 ID:35021)

Fusion Gene Summary for GSG1L-KCTD13

check button Fusion gene summary
Fusion gene informationFusion gene name: GSG1L-KCTD13
Fusion gene ID: 35021
HgeneTgene
Gene symbol

GSG1L

KCTD13

Gene ID

146395

253980

Gene nameGSG1 likepotassium channel tetramerization domain containing 13
SynonymsPRO19651BACURD1|FKSG86|PDIP1|POLDIP1|hBACURD1
Cytomap

16p12.1

16p11.2

Type of geneprotein-codingprotein-coding
Descriptiongerm cell-specific gene 1-like proteinGSG1-like proteinKTSR5831BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 1BTB/POZ domain-containing protein KCTD13CTD-2574D22.4TNFAIP1-like proteinpolymerase delta-interacting protein 1potassium channel tetramerisation domain containing 13
Modification date2020031320200327
UniProtAcc

Q6UXU4

Q8WZ19

Ensembl transtripts involved in fusion geneENST00000380897, ENST00000380898, 
ENST00000395724, ENST00000447459, 
ENST00000569166, 
ENST00000561540, 
ENST00000568000, ENST00000568721, 
Fusion gene scores* DoF score2 X 2 X 2=84 X 4 X 3=48
# samples 24
** MAII scorelog2(2/8*10)=1.32192809488736log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GSG1L [Title/Abstract] AND KCTD13 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGSG1L(27992927)-KCTD13(29934510), # 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
TgeneKCTD13

GO:0016567

protein ubiquitination

19782033

TgeneKCTD13

GO:0043161

proteasome-mediated ubiquitin-dependent protein catabolic process

19782033


check buttonFusion gene breakpoints across GSG1L (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 KCTD13 (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
ChimerDB4LUSCTCGA-56-8629-01AGSG1Lchr16

27992927

-KCTD13chr16

29934510

+


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Fusion Gene ORF analysis for GSG1L-KCTD13

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-intronENST00000380897ENST00000561540GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000380897ENST00000568000GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000380897ENST00000568721GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000380898ENST00000561540GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000380898ENST00000568000GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000380898ENST00000568721GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000395724ENST00000561540GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000395724ENST00000568000GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000395724ENST00000568721GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000447459ENST00000561540GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000447459ENST00000568000GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000447459ENST00000568721GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000569166ENST00000561540GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000569166ENST00000568000GSG1Lchr16

27992927

-KCTD13chr16

29934510

+
intron-intronENST00000569166ENST00000568721GSG1Lchr16

27992927

-KCTD13chr16

29934510

+

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 GSG1L-KCTD13


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 GSG1L-KCTD13


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/:27992927/:29934510)
- 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
GSG1L

Q6UXU4

KCTD13

Q8WZ19

FUNCTION: As a component of the inner core of AMPAR complex, modifies AMPA receptor (AMPAR) gating. {ECO:0000250}.FUNCTION: Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex required for synaptic transmission (PubMed:19782033). The BCR(KCTD13) E3 ubiquitin ligase complex mediates the ubiquitination of RHOA, leading to its degradation by the proteasome (PubMed:19782033) Degradation of RHOA regulates the actin cytoskeleton and promotes synaptic transmission (By similarity). {ECO:0000250|UniProtKB:Q8BGV7, ECO:0000269|PubMed:19782033}.

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 GSG1L-KCTD13


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 GSG1L-KCTD13


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 GSG1L-KCTD13


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 GSG1L-KCTD13


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