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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:KCNK1-UCHL5

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: KCNK1-UCHL5
FusionPDB ID: 41468
FusionGDB2.0 ID: 41468
HgeneTgene
Gene symbol

KCNK1

UCHL5

Gene ID

3775

51377

Gene namepotassium two pore domain channel subfamily K member 1ubiquitin C-terminal hydrolase L5
SynonymsDPK|HOHO|K2P1|K2p1.1|KCNO1|TWIK-1|TWIK1CGI-70|INO80R|UCH-L5|UCH37
Cytomap

1q42.2

1q31.2

Type of geneprotein-codingprotein-coding
Descriptionpotassium channel subfamily K member 1inward rectifying potassium channel protein TWIK-1potassium channel K2P1potassium channel KCNO1potassium channel, two pore domain subfamily K, member 1potassium inwardly-rectifying channel, subfamily K, member 1ubiquitin carboxyl-terminal hydrolase isozyme L5INO80 complex subunit Rubiquitin C-terminal hydrolase UCH37ubiquitin carboxyl-terminal esterase L5ubiquitin carboxyl-terminal hydrolase L5ubiquitin thioesterase L5
Modification date2020032020200329
UniProtAcc

Q96T54

.
Ensembl transtripts involved in fusion geneENST idsENST00000366621, ENST00000366620, 
ENST00000472190, 
ENST00000367452, 
ENST00000483156, ENST00000530098, 
ENST00000367448, ENST00000367449, 
ENST00000367451, ENST00000367454, 
ENST00000367455, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 2 X 3=184 X 3 X 4=48
# samples 34
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
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 (manual curation of fusion genes in FusionPDB)

PubMed: KCNK1 [Title/Abstract] AND UCHL5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)KCNK1(233750272)-UCHL5(193020947), # samples:1
Anticipated loss of major functional domain due to fusion event.KCNK1-UCHL5 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
KCNK1-UCHL5 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
KCNK1-UCHL5 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
KCNK1-UCHL5 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
KCNK1-UCHL5 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
KCNK1-UCHL5 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
KCNK1-UCHL5 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
HgeneKCNK1

GO:0035725

sodium ion transmembrane transport

21653227

HgeneKCNK1

GO:0071805

potassium ion transmembrane transport

21653227|22282804

TgeneUCHL5

GO:0016579

protein deubiquitination

18922472


check buttonFusion gene breakpoints across KCNK1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across UCHL5 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4STADTCGA-HU-8238-01AKCNK1chr1

233750272

+UCHL5chr1

193020947

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000366621KCNK1chr1233750272+ENST00000367455UCHL5chr1193020947-55385231411436431
ENST00000366621KCNK1chr1233750272+ENST00000367454UCHL5chr1193020947-20265231411433430
ENST00000366621KCNK1chr1233750272+ENST00000367451UCHL5chr1193020947-17045231411514457
ENST00000366621KCNK1chr1233750272+ENST00000367449UCHL5chr1193020947-18055231411397418

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
ENST00000366621ENST00000367455KCNK1chr1233750272+UCHL5chr1193020947-0.0001798670.9998202
ENST00000366621ENST00000367454KCNK1chr1233750272+UCHL5chr1193020947-0.0009288640.9990711
ENST00000366621ENST00000367451KCNK1chr1233750272+UCHL5chr1193020947-0.0035984240.99640155
ENST00000366621ENST00000367449KCNK1chr1233750272+UCHL5chr1193020947-0.0012850930.9987149

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>41468_41468_1_KCNK1-UCHL5_KCNK1_chr1_233750272_ENST00000366621_UCHL5_chr1_193020947_ENST00000367449_length(amino acids)=418AA_BP=127
MALAAAVEKMLQSLAGSSCVRLVERHRSAWCFGFLVLGYLLYLVFGAVVFSSVELPYEDLLRQELRKLKRRFLEEHECLSEQQLEQFLGR
VLEASNYGVSVLSNASGNWNWDFTSALFFASTVLSTTGCRGAQVEEIWSLEPENFEKLKPVHGLIFLFKWQPGEEPAGSVVQDSRLDTIF
FAKQVINNACATQAIVSVLLNCTHQDVHLGETLSEFKEFSQSFDAAMKGLALSNSDVIRQVHNSFARQQMFEFDTKTSAKEEDAFHFVSY
VPVNGRLYELDGLREGPIDLGACNQDDWISAVRPVIEKRIQKYSEGEIRFNLMAIVSDRKMIYEQKIAELQRQLAEEPMDTDQGNSMLSA

--------------------------------------------------------------

>41468_41468_2_KCNK1-UCHL5_KCNK1_chr1_233750272_ENST00000366621_UCHL5_chr1_193020947_ENST00000367451_length(amino acids)=457AA_BP=127
MALAAAVEKMLQSLAGSSCVRLVERHRSAWCFGFLVLGYLLYLVFGAVVFSSVELPYEDLLRQELRKLKRRFLEEHECLSEQQLEQFLGR
VLEASNYGVSVLSNASGNWNWDFTSALFFASTVLSTTGCRGAQVEEIWSLEPENFEKLKPVHGLIFLFKWQPGEEPAGSVVQDSRLDTIF
FAKQVINNACATQAIVSVLLNCTHQDVHLGETLSEFKEFSQSFDAAMKGLALSNSDVIRQVHNSFARQQMFEFDTKTSAKEEDAFHFVSY
VPVNGRLYELDGLREGPIDLGACNQDDWISAVRPVIEKRIQKDGFSPCCPGWSQTPELKPSACLDLPKWYSEGEIRFNLMAIVSDRKMIY
EQKIAELQRQLAEEPMDTDQGNSMLSAIQSEVAKNQMLIEEEVQKLKRYKIENIRRKHNYLPFIMELLKTLAEHQQLIPLVEKAKEKQNA

--------------------------------------------------------------

>41468_41468_3_KCNK1-UCHL5_KCNK1_chr1_233750272_ENST00000366621_UCHL5_chr1_193020947_ENST00000367454_length(amino acids)=430AA_BP=127
MALAAAVEKMLQSLAGSSCVRLVERHRSAWCFGFLVLGYLLYLVFGAVVFSSVELPYEDLLRQELRKLKRRFLEEHECLSEQQLEQFLGR
VLEASNYGVSVLSNASGNWNWDFTSALFFASTVLSTTGCRGAQVEEIWSLEPENFEKLKPVHGLIFLFKWQPGEEPAGSVVQDSRLDTIF
FAKQVINNACATQAIVSVLLNCTHQDVHLGETLSEFKEFSQSFDAAMKGLALSNSDVIRQVHNSFARQQMFEFDTKTSAKEEDAFHFVSY
VPVNGRLYELDGLREGPIDLGACNQDDWISAVRPVIEKRIQKYSEGEIRFNLMAIVSDRKMIYEQKIAELQRQLAEEPMDTDQGNSMLSA

--------------------------------------------------------------

>41468_41468_4_KCNK1-UCHL5_KCNK1_chr1_233750272_ENST00000366621_UCHL5_chr1_193020947_ENST00000367455_length(amino acids)=431AA_BP=127
MALAAAVEKMLQSLAGSSCVRLVERHRSAWCFGFLVLGYLLYLVFGAVVFSSVELPYEDLLRQELRKLKRRFLEEHECLSEQQLEQFLGR
VLEASNYGVSVLSNASGNWNWDFTSALFFASTVLSTTGCRGAQVEEIWSLEPENFEKLKPVHGLIFLFKWQPGEEPAGSVVQDSRLDTIF
FAKQVINNACATQAIVSVLLNCTHQDVHLGETLSEFKEFSQSFDAAMKGLALSNSDVIRQVHNSFARQQMFEFDTKTSAKEEDAFHFVSY
VPVNGRLYELDGLREGPIDLGACNQDDWISAVRPVIEKRIQKYSEGEIRFNLMAIVSDRKMIYEQKIAELQRQLAEEEPMDTDQGNSMLS

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr1:233750272/chr1:193020947)
- 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
KCNK1

Q96T54

.
FUNCTION: Outward rectifying potassium channel. Produces rapidly activating and non-inactivating outward rectifier K(+) currents.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13104_116118.33333333333333337.0IntramembraneHelical%3B Name%3DPore helix 1
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+131_20118.33333333333333337.0Topological domainCytoplasmic
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+1342_103118.33333333333333337.0Topological domainExtracellular
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+1321_41118.33333333333333337.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13212_224118.33333333333333337.0IntramembraneHelical%3B Name%3DPore helix 2
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13225_231118.33333333333333337.0IntramembraneOntology_term=ECO:0000269
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13117_122118.33333333333333337.0RegionSelectivity filter 1
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13225_230118.33333333333333337.0RegionSelectivity filter 2
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13293_299118.33333333333333337.0RegionImportant for intracellular retention in recycling endosomes
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13123_132118.33333333333333337.0Topological domainExtracellular
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13157_181118.33333333333333337.0Topological domainCytoplasmic
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13203_211118.33333333333333337.0Topological domainExtracellular
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13232_243118.33333333333333337.0Topological domainExtracellular
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13268_336118.33333333333333337.0Topological domainCytoplasmic
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13133_156118.33333333333333337.0TransmembraneHelical
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13182_202118.33333333333333337.0TransmembraneHelical
HgeneKCNK1chr1:233750272chr1:193020947ENST00000366621+13244_267118.33333333333333337.0TransmembraneHelical


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
KCNK1
UCHL5


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to KCNK1-UCHL5


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to KCNK1-UCHL5


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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