FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:SMYD2-KCNK2 (FusionGDB2 ID:84357)

Fusion Gene Summary for SMYD2-KCNK2

check button Fusion gene summary
Fusion gene informationFusion gene name: SMYD2-KCNK2
Fusion gene ID: 84357
HgeneTgene
Gene symbol

SMYD2

KCNK2

Gene ID

56950

3776

Gene nameSET and MYND domain containing 2potassium two pore domain channel subfamily K member 2
SynonymsHSKM-B|KMT3C|ZMYND14K2p2.1|TPKC1|TREK|TREK-1|TREK1|hTREK-1c|hTREK-1e
Cytomap

1q32.3

1q41

Type of geneprotein-codingprotein-coding
DescriptionN-lysine methyltransferase SMYD2SET and MYND domain-containing protein 2histone methyltransferase SMYD2lysine N-methyltransferase 3Czinc finger, MYND domain containing 14potassium channel subfamily K member 2K2P2.1 potassium channelTREK-1 K(+) channel subunitTWIK-related potassium channel 1outward rectifying potassium channel protein TREK-1potassium channel subfamily k member 2 variant 1potassium channel subfamily k
Modification date2020032020200313
UniProtAcc.

O95069

Ensembl transtripts involved in fusion geneENST00000491455, ENST00000366957, 
ENST00000415093, 
ENST00000391894, 
ENST00000391895, ENST00000444842, 
Fusion gene scores* DoF score10 X 7 X 7=4902 X 3 X 2=12
# samples 113
** MAII scorelog2(11/490*10)=-2.15527822547791
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SMYD2 [Title/Abstract] AND KCNK2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSMYD2(214454770)-KCNK2(215259711), # samples:2
Anticipated loss of major functional domain due to fusion event.SMYD2-KCNK2 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
SMYD2-KCNK2 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
SMYD2-KCNK2 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
HgeneSMYD2

GO:0018026

peptidyl-lysine monomethylation

17108971|20870719


check buttonFusion gene breakpoints across SMYD2 (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 KCNK2 (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
ChimerDB4OVTCGA-29-1783-01ASMYD2chr1

214454770

+KCNK2chr1

215259711

+
ChimerDB4OVTCGA-29-1783SMYD2chr1

214454770

+KCNK2chr1

215259710

+


Top

Fusion Gene ORF analysis for SMYD2-KCNK2

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
3UTR-3CDSENST00000491455ENST00000391894SMYD2chr1

214454770

+KCNK2chr1

215259711

+
3UTR-3CDSENST00000491455ENST00000391894SMYD2chr1

214454770

+KCNK2chr1

215259710

+
3UTR-3CDSENST00000491455ENST00000391895SMYD2chr1

214454770

+KCNK2chr1

215259711

+
3UTR-3CDSENST00000491455ENST00000391895SMYD2chr1

214454770

+KCNK2chr1

215259710

+
3UTR-3CDSENST00000491455ENST00000444842SMYD2chr1

214454770

+KCNK2chr1

215259711

+
3UTR-3CDSENST00000491455ENST00000444842SMYD2chr1

214454770

+KCNK2chr1

215259710

+
Frame-shiftENST00000366957ENST00000391894SMYD2chr1

214454770

+KCNK2chr1

215259711

+
Frame-shiftENST00000366957ENST00000391894SMYD2chr1

214454770

+KCNK2chr1

215259710

+
Frame-shiftENST00000366957ENST00000391895SMYD2chr1

214454770

+KCNK2chr1

215259711

+
Frame-shiftENST00000366957ENST00000391895SMYD2chr1

214454770

+KCNK2chr1

215259710

+
Frame-shiftENST00000366957ENST00000444842SMYD2chr1

214454770

+KCNK2chr1

215259711

+
Frame-shiftENST00000366957ENST00000444842SMYD2chr1

214454770

+KCNK2chr1

215259710

+
Frame-shiftENST00000415093ENST00000391894SMYD2chr1

214454770

+KCNK2chr1

215259711

+
Frame-shiftENST00000415093ENST00000391894SMYD2chr1

214454770

+KCNK2chr1

215259710

+
Frame-shiftENST00000415093ENST00000391895SMYD2chr1

214454770

+KCNK2chr1

215259711

+
Frame-shiftENST00000415093ENST00000391895SMYD2chr1

214454770

+KCNK2chr1

215259710

+
Frame-shiftENST00000415093ENST00000444842SMYD2chr1

214454770

+KCNK2chr1

215259711

+
Frame-shiftENST00000415093ENST00000444842SMYD2chr1

214454770

+KCNK2chr1

215259710

+

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

Top

Fusion Genomic Features for SMYD2-KCNK2


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)
SMYD2chr1214454770+KCNK2chr1215259710+1.93E-070.99999976
SMYD2chr1214454770+KCNK2chr1215259710+1.93E-070.99999976
SMYD2chr1214454770+KCNK2chr1215259710+1.93E-070.99999976
SMYD2chr1214454770+KCNK2chr1215259710+1.93E-070.99999976

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%

Top

Fusion Protein Features for SMYD2-KCNK2


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/:214454770/:215259711)
- 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
.KCNK2

O95069

FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Ion channel that contributes to passive transmembrane potassium transport (PubMed:23169818). Reversibly converts between a voltage-insensitive potassium leak channel and a voltage-dependent outward rectifying potassium channel in a phosphorylation-dependent manner (PubMed:11319556). In astrocytes, forms mostly heterodimeric potassium channels with KCNK1, with only a minor proportion of functional channels containing homodimeric KCNK2. In astrocytes, the heterodimer formed by KCNK1 and KCNK2 is required for rapid glutamate release in response to activation of G-protein coupled receptors, such as F2R and CNR1 (By similarity). {ECO:0000250|UniProtKB:P97438, ECO:0000269|PubMed:10784345, ECO:0000269|PubMed:11319556, ECO:0000269|PubMed:23169818}.; FUNCTION: [Isoform 4]: Does not display channel activity but reduces the channel activity of isoform 1 and isoform 2 and reduces cell surface expression of isoform 2. {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


Top

Fusion Gene Sequence for SMYD2-KCNK2


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.

Top

Fusion Gene PPI Analysis for SMYD2-KCNK2


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


Top

Related Drugs for SMYD2-KCNK2


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

Top

Related Diseases for SMYD2-KCNK2


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