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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:PCK1-PCK1 (FusionGDB2 ID:HG5105TG5105)

Fusion Gene Summary for PCK1-PCK1

check button Fusion gene summary
Fusion gene informationFusion gene name: PCK1-PCK1
Fusion gene ID: hg5105tg5105
HgeneTgene
Gene symbol

PCK1

PCK1

Gene ID

5105

5105

Gene namephosphoenolpyruvate carboxykinase 1phosphoenolpyruvate carboxykinase 1
SynonymsPCKDC|PEPCK-C|PEPCK1|PEPCKCPCKDC|PEPCK-C|PEPCK1|PEPCKC
Cytomap('PCK1')('PCK1')

20q13.31

20q13.31

Type of geneprotein-codingprotein-coding
Descriptionphosphoenolpyruvate carboxykinase, cytosolic [GTP]PEP carboxykinasephosphoenolpyruvate carboxykinase 1 (soluble)phosphoenolpyruvate carboxykinase, cytosolicphosphoenolpyruvate carboxylasephosphopyruvate carboxylasephosphoenolpyruvate carboxykinase, cytosolic [GTP]PEP carboxykinasephosphoenolpyruvate carboxykinase 1 (soluble)phosphoenolpyruvate carboxykinase, cytosolicphosphoenolpyruvate carboxylasephosphopyruvate carboxylase
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000319441, ENST00000535860, 
ENST00000543666, 
ENST00000319441, 
ENST00000535860, ENST00000543666, 
Fusion gene scores* DoF score3 X 3 X 1=94 X 4 X 4=64
# samples 35
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/64*10)=-0.356143810225275
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PCK1 [Title/Abstract] AND PCK1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPCK1(56141455)-PCK1(56141388), # samples:3
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
HgenePCK1

GO:0006107

oxaloacetate metabolic process

30193097

HgenePCK1

GO:0006475

internal protein amino acid acetylation

20167786

HgenePCK1

GO:0032868

response to insulin

14764811

HgenePCK1

GO:0071333

cellular response to glucose stimulus

30193097

TgenePCK1

GO:0006107

oxaloacetate metabolic process

30193097

TgenePCK1

GO:0006475

internal protein amino acid acetylation

20167786

TgenePCK1

GO:0032868

response to insulin

14764811

TgenePCK1

GO:0071333

cellular response to glucose stimulus

30193097



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
ChiTaRS5.0N/AAA484379PCK1chr20

56141455

+PCK1chr20

56141388

-
ChiTaRS5.0N/AAA484525PCK1chr20

56141455

+PCK1chr20

56141388

-
ChiTaRS5.0N/AAA484533PCK1chr20

56141455

+PCK1chr20

56141388

-


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Fusion Gene ORF analysis for PCK1-PCK1

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-3UTRENST00000319441ENST00000319441PCK1chr20

56141455

+PCK1chr20

56141388

-
3UTR-intronENST00000319441ENST00000535860PCK1chr20

56141455

+PCK1chr20

56141388

-
3UTR-intronENST00000319441ENST00000543666PCK1chr20

56141455

+PCK1chr20

56141388

-
intron-3UTRENST00000535860ENST00000319441PCK1chr20

56141455

+PCK1chr20

56141388

-
intron-3UTRENST00000543666ENST00000319441PCK1chr20

56141455

+PCK1chr20

56141388

-
intron-intronENST00000535860ENST00000535860PCK1chr20

56141455

+PCK1chr20

56141388

-
intron-intronENST00000535860ENST00000543666PCK1chr20

56141455

+PCK1chr20

56141388

-
intron-intronENST00000543666ENST00000535860PCK1chr20

56141455

+PCK1chr20

56141388

-
intron-intronENST00000543666ENST00000543666PCK1chr20

56141455

+PCK1chr20

56141388

-

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 PCK1-PCK1


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)


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Fusion Protein Features for PCK1-PCK1


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/:56141455/:56141388)
- 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
..
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: 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}.

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 PCK1-PCK1


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 PCK1-PCK1


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 PCK1-PCK1


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 PCK1-PCK1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePCK1C0268194Phosphoenolpyruvate carboxykinase deficiency3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgenePCK1C2239176Liver carcinoma2CTD_human
HgenePCK1C0002152Alloxan Diabetes1CTD_human
HgenePCK1C0007570Celiac Disease1CTD_human
HgenePCK1C0011853Diabetes Mellitus, Experimental1CTD_human
HgenePCK1C0018801Heart failure1CTD_human
HgenePCK1C0018802Congestive heart failure1CTD_human
HgenePCK1C0023212Left-Sided Heart Failure1CTD_human
HgenePCK1C0023893Liver Cirrhosis, Experimental1CTD_human
HgenePCK1C0028754Obesity1CTD_human
HgenePCK1C0036341Schizophrenia1PSYGENET
HgenePCK1C0038433Streptozotocin Diabetes1CTD_human
HgenePCK1C0235527Heart Failure, Right-Sided1CTD_human
HgenePCK1C1959583Myocardial Failure1CTD_human
HgenePCK1C1961112Heart Decompensation1CTD_human
TgeneC0268194Phosphoenolpyruvate carboxykinase deficiency3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneC2239176Liver carcinoma2CTD_human
TgeneC0002152Alloxan Diabetes1CTD_human
TgeneC0007570Celiac Disease1CTD_human
TgeneC0011853Diabetes Mellitus, Experimental1CTD_human
TgeneC0018801Heart failure1CTD_human
TgeneC0018802Congestive heart failure1CTD_human
TgeneC0023212Left-Sided Heart Failure1CTD_human
TgeneC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneC0028754Obesity1CTD_human
TgeneC0036341Schizophrenia1PSYGENET
TgeneC0038433Streptozotocin Diabetes1CTD_human
TgeneC0235527Heart Failure, Right-Sided1CTD_human
TgeneC1959583Myocardial Failure1CTD_human
TgeneC1961112Heart Decompensation1CTD_human