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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:PTPN23-KLHL18 (FusionGDB2 ID:70252)

Fusion Gene Summary for PTPN23-KLHL18

check button Fusion gene summary
Fusion gene informationFusion gene name: PTPN23-KLHL18
Fusion gene ID: 70252
HgeneTgene
Gene symbol

PTPN23

KLHL18

Gene ID

25930

23276

Gene nameprotein tyrosine phosphatase non-receptor type 23kelch like family member 18
SynonymsHD-PTP|HDPTP|PTP-TD14-
Cytomap

3p21.31

3p21.31

Type of geneprotein-codingprotein-coding
Descriptiontyrosine-protein phosphatase non-receptor type 23his domain-containing protein tyrosine phosphataseprotein tyrosine phosphatase TD14kelch-like protein 18
Modification date2020031320200313
UniProtAcc.

O94889

Ensembl transtripts involved in fusion geneENST00000265562, ENST00000431726, 
ENST00000455924, ENST00000483201, 
ENST00000232766, 
Fusion gene scores* DoF score11 X 5 X 9=4954 X 4 X 5=80
# samples 145
** MAII scorelog2(14/495*10)=-1.82200169802201
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PTPN23 [Title/Abstract] AND KLHL18 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPTPN23(47422670)-KLHL18(47371441), # samples:2
Anticipated loss of major functional domain due to fusion event.PTPN23-KLHL18 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PTPN23-KLHL18 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
PTPN23-KLHL18 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
TgeneKLHL18

GO:0016567

protein ubiquitination

23213400


check buttonFusion gene breakpoints across PTPN23 (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 KLHL18 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4LIHCTCGA-DD-A1EK-01APTPN23chr3

47422670

-KLHL18chr3

47371441

+
ChimerDB4LIHCTCGA-DD-A1EK-01APTPN23chr3

47422670

+KLHL18chr3

47371441

+
ChimerDB4LUADTCGA-55-A48Y-01APTPN23chr3

47437707

-KLHL18chr3

47361143

+


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Fusion Gene ORF analysis for PTPN23-KLHL18

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-intronENST00000265562ENST00000455924PTPN23chr3

47437707

-KLHL18chr3

47361143

+
5CDS-intronENST00000265562ENST00000483201PTPN23chr3

47422670

+KLHL18chr3

47371441

+
5CDS-intronENST00000265562ENST00000483201PTPN23chr3

47437707

-KLHL18chr3

47361143

+
5UTR-3CDSENST00000431726ENST00000232766PTPN23chr3

47422670

+KLHL18chr3

47371441

+
5UTR-3CDSENST00000431726ENST00000232766PTPN23chr3

47437707

-KLHL18chr3

47361143

+
5UTR-3CDSENST00000431726ENST00000455924PTPN23chr3

47422670

+KLHL18chr3

47371441

+
5UTR-intronENST00000431726ENST00000455924PTPN23chr3

47437707

-KLHL18chr3

47361143

+
5UTR-intronENST00000431726ENST00000483201PTPN23chr3

47422670

+KLHL18chr3

47371441

+
5UTR-intronENST00000431726ENST00000483201PTPN23chr3

47437707

-KLHL18chr3

47361143

+
Frame-shiftENST00000265562ENST00000232766PTPN23chr3

47422670

+KLHL18chr3

47371441

+
Frame-shiftENST00000265562ENST00000455924PTPN23chr3

47422670

+KLHL18chr3

47371441

+
In-frameENST00000265562ENST00000232766PTPN23chr3

47437707

-KLHL18chr3

47361143

+

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 PTPN23-KLHL18


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)
PTPN23chr347422670+KLHL18chr347371440+1.87E-121
PTPN23chr347422670+KLHL18chr347371440+1.87E-121

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.
genomic feature

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 PTPN23-KLHL18


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/chr3:47422670/chr3:47371441)
- 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
.KLHL18

O94889

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: Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complex required for mitotic progression and cytokinesis (PubMed:23213400). The BCR(KLHL18) E3 ubiquitin ligase complex mediates the ubiquitination of AURKA leading to its activation at the centrosome which is required for initiating mitotic entry (PubMed:23213400). Regulates light-and dark-dependent alpha-transducin localization changes in rod photoreceptors through UNC119 ubiquitination and degradation (By similarity). Preferentially ubiquitinates the unphosphorylated form of UNC119 over the phosphorylated form (By similarity). In the presence of UNC119, under dark-adapted conditions alpha-transducin mislocalizes from the outer segment to the inner part of rod photoreceptors which leads to decreased photoreceptor damage caused by light (By similarity). {ECO:0000250|UniProtKB:E9Q4F2, ECO:0000269|PubMed:23213400}.

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
TgeneKLHL18chr3:47437707chr3:47361143ENST00000232766010140_24243575.0DomainNote=BACK
TgeneKLHL18chr3:47437707chr3:47361143ENST0000023276601066_10543575.0DomainBTB
TgeneKLHL18chr3:47437707chr3:47361143ENST00000232766010289_33643575.0RepeatNote=Kelch 1
TgeneKLHL18chr3:47437707chr3:47361143ENST00000232766010337_38343575.0RepeatNote=Kelch 2
TgeneKLHL18chr3:47437707chr3:47361143ENST00000232766010384_43043575.0RepeatNote=Kelch 3
TgeneKLHL18chr3:47437707chr3:47361143ENST00000232766010432_47743575.0RepeatNote=Kelch 4
TgeneKLHL18chr3:47437707chr3:47361143ENST00000232766010479_52443575.0RepeatNote=Kelch 5
TgeneKLHL18chr3:47437707chr3:47361143ENST00000232766010525_57143575.0RepeatNote=Kelch 6

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225550_623531637.0Coiled coilOntology_term=ECO:0000255
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-2251509_1573531637.0Compositional biasNote=Pro-rich
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225716_1108531637.0Compositional biasNote=Pro-rich
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-2251192_1452531637.0DomainTyrosine-protein phosphatase
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-2258_394531637.0DomainBRO1
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225770_1130531637.0RegionNote=His
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225953_964531637.0RegionNote=6 X 2 AA approximate tandem repeats of P-Q
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225250_283531637.0RepeatNote=TPR 1
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225374_407531637.0RepeatNote=TPR 2
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225953_954531637.0RepeatNote=1
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225955_956531637.0RepeatNote=2
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225957_958531637.0RepeatNote=3
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225959_960531637.0RepeatNote=4
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225961_962531637.0RepeatNote=5
HgenePTPN23chr3:47437707chr3:47361143ENST00000265562-225963_964531637.0RepeatNote=6


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Fusion Gene Sequence for PTPN23-KLHL18


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 PTPN23-KLHL18


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 PTPN23-KLHL18


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 PTPN23-KLHL18


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