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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:KCTD20-JARID2 (FusionGDB2 ID:41638)

Fusion Gene Summary for KCTD20-JARID2

check button Fusion gene summary
Fusion gene informationFusion gene name: KCTD20-JARID2
Fusion gene ID: 41638
HgeneTgene
Gene symbol

KCTD20

JARID2

Gene ID

222658

3720

Gene namepotassium channel tetramerization domain containing 20jumonji and AT-rich interaction domain containing 2
SynonymsC6orf69|dJ108K11.3JMJ
Cytomap

6p21.31

6p22.3

Type of geneprotein-codingprotein-coding
DescriptionBTB/POZ domain-containing protein KCTD20potassium channel tetramerisation domain containing 20protein Jumonjijumonji homologjumonji, AT rich interactive domain 2jumonji-like proteinjumonji/ARID domain-containing protein 2
Modification date2020031320200313
UniProtAcc

Q7Z5Y7

Q92833

Ensembl transtripts involved in fusion geneENST00000373731, ENST00000449081, 
ENST00000536244, ENST00000544295, 
ENST00000474988, 
ENST00000397311, 
ENST00000474854, ENST00000541660, 
ENST00000341776, 
Fusion gene scores* DoF score9 X 3 X 8=2166 X 6 X 3=108
# samples 106
** MAII scorelog2(10/216*10)=-1.11103131238874
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KCTD20 [Title/Abstract] AND JARID2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointKCTD20(36438034)-JARID2(15374348), # samples:3
Anticipated loss of major functional domain due to fusion event.KCTD20-JARID2 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
KCTD20-JARID2 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* 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 KCTD20 (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 JARID2 (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
ChimerDB4BRCATCGA-D8-A27H-01AKCTD20chr6

36438034

-JARID2chr6

15374348

+
ChimerDB4BRCATCGA-D8-A27H-01AKCTD20chr6

36438034

+JARID2chr6

15374348

+


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Fusion Gene ORF analysis for KCTD20-JARID2

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-5UTRENST00000373731ENST00000397311KCTD20chr6

36438034

+JARID2chr6

15374348

+
5CDS-5UTRENST00000449081ENST00000397311KCTD20chr6

36438034

+JARID2chr6

15374348

+
5CDS-intronENST00000373731ENST00000474854KCTD20chr6

36438034

+JARID2chr6

15374348

+
5CDS-intronENST00000373731ENST00000541660KCTD20chr6

36438034

+JARID2chr6

15374348

+
5CDS-intronENST00000449081ENST00000474854KCTD20chr6

36438034

+JARID2chr6

15374348

+
5CDS-intronENST00000449081ENST00000541660KCTD20chr6

36438034

+JARID2chr6

15374348

+
5UTR-3CDSENST00000536244ENST00000341776KCTD20chr6

36438034

+JARID2chr6

15374348

+
5UTR-3CDSENST00000544295ENST00000341776KCTD20chr6

36438034

+JARID2chr6

15374348

+
5UTR-5UTRENST00000536244ENST00000397311KCTD20chr6

36438034

+JARID2chr6

15374348

+
5UTR-5UTRENST00000544295ENST00000397311KCTD20chr6

36438034

+JARID2chr6

15374348

+
5UTR-intronENST00000536244ENST00000474854KCTD20chr6

36438034

+JARID2chr6

15374348

+
5UTR-intronENST00000536244ENST00000541660KCTD20chr6

36438034

+JARID2chr6

15374348

+
5UTR-intronENST00000544295ENST00000474854KCTD20chr6

36438034

+JARID2chr6

15374348

+
5UTR-intronENST00000544295ENST00000541660KCTD20chr6

36438034

+JARID2chr6

15374348

+
Frame-shiftENST00000373731ENST00000341776KCTD20chr6

36438034

+JARID2chr6

15374348

+
Frame-shiftENST00000449081ENST00000341776KCTD20chr6

36438034

+JARID2chr6

15374348

+
intron-3CDSENST00000474988ENST00000341776KCTD20chr6

36438034

+JARID2chr6

15374348

+
intron-5UTRENST00000474988ENST00000397311KCTD20chr6

36438034

+JARID2chr6

15374348

+
intron-intronENST00000474988ENST00000474854KCTD20chr6

36438034

+JARID2chr6

15374348

+
intron-intronENST00000474988ENST00000541660KCTD20chr6

36438034

+JARID2chr6

15374348

+

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 KCTD20-JARID2


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)
KCTD20chr636438034+JARID2chr615374347+2.35E-081
KCTD20chr636438034+JARID2chr615374347+2.35E-081

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 KCTD20-JARID2


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/:36438034/:15374348)
- 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
KCTD20

Q7Z5Y7

JARID2

Q92833

FUNCTION: Promotes the phosphorylation of AKT family members. {ECO:0000250|UniProtKB:Q8CDD8}.FUNCTION: Regulator of histone methyltransferase complexes that plays an essential role in embryonic development, including heart and liver development, neural tube fusion process and hematopoiesis (PubMed:20075857). Acts as an accessory subunit for the core PRC2 (Polycomb repressive complex 2) complex, which mediates histone H3K27 (H3K27me3) trimethylation on chromatin (PubMed:20075857, PubMed:29499137, PubMed:31959557). Binds DNA and mediates the recruitment of the PRC2 complex to target genes in embryonic stem cells, thereby playing a key role in stem cell differentiation and normal embryonic development (PubMed:20075857). In cardiac cells, it is required to repress expression of cyclin-D1 (CCND1) by activating methylation of 'Lys-9' of histone H3 (H3K9me) by the GLP1/EHMT1 and G9a/EHMT2 histone methyltransferases (By similarity). Also acts as a transcriptional repressor of ANF via its interaction with GATA4 and NKX2-5 (By similarity). Participates in the negative regulation of cell proliferation signaling (By similarity). Does not have histone demethylase activity (By similarity). {ECO:0000250|UniProtKB:Q62315, ECO:0000269|PubMed:20075857, ECO:0000269|PubMed:29499137, ECO:0000269|PubMed:31959557}.

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 KCTD20-JARID2


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 KCTD20-JARID2


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 KCTD20-JARID2


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 KCTD20-JARID2


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