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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:PNCK-HCFC1 (FusionGDB2 ID:66703)

Fusion Gene Summary for PNCK-HCFC1

check button Fusion gene summary
Fusion gene informationFusion gene name: PNCK-HCFC1
Fusion gene ID: 66703
HgeneTgene
Gene symbol

PNCK

HCFC1

Gene ID

139728

3054

Gene namepregnancy up-regulated nonubiquitous CaM kinasehost cell factor C1
SynonymsBSTK3|CaMK1bCFF|HCF|HCF-1|HCF1|HFC1|MRX3|PPP1R89|VCAF
Cytomap

Xq28

Xq28

Type of geneprotein-codingprotein-coding
Descriptioncalcium/calmodulin-dependent protein kinase type 1BcaM kinase I betacaM kinase IBcaM-KI betacaMKI-betapregnancy up-regulated non-ubiquitously-expressed CaM kinasepregnancy upregulated non-ubiquitously expressed CaM kinasehost cell factor 1VP16-accessory proteinprotein phosphatase 1, regulatory subunit 89
Modification date2020032020200313
UniProtAcc.

Q9NWW0

Ensembl transtripts involved in fusion geneENST00000340888, ENST00000370142, 
ENST00000370145, ENST00000370150, 
ENST00000393831, ENST00000447676, 
ENST00000475172, 
ENST00000310441, 
ENST00000354233, ENST00000369984, 
ENST00000461098, 
Fusion gene scores* DoF score1 X 1 X 1=16 X 7 X 3=126
# samples 17
** MAII scorelog2(1/1*10)=3.32192809488736log2(7/126*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PNCK [Title/Abstract] AND HCFC1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPNCK(152952886)-HCFC1(153230177), # 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
TgeneHCFC1

GO:0006355

regulation of transcription, DNA-templated

12670868

TgeneHCFC1

GO:0010628

positive regulation of gene expression

21285374

TgeneHCFC1

GO:0043254

regulation of protein complex assembly

10675337

TgeneHCFC1

GO:0043981

histone H4-K5 acetylation

20018852

TgeneHCFC1

GO:0043982

histone H4-K8 acetylation

20018852

TgeneHCFC1

GO:0043984

histone H4-K16 acetylation

20018852

TgeneHCFC1

GO:0050821

protein stabilization

21285374


check buttonFusion gene breakpoints across PNCK (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 HCFC1 (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-C8-A12Q-01APNCKchrX

152952886

-HCFC1chrX

153230177

-


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Fusion Gene ORF analysis for PNCK-HCFC1

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
intron-3CDSENST00000340888ENST00000310441PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000340888ENST00000354233PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000340888ENST00000369984PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000370142ENST00000310441PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000370142ENST00000354233PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000370142ENST00000369984PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000370145ENST00000310441PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000370145ENST00000354233PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000370145ENST00000369984PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000370150ENST00000310441PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000370150ENST00000354233PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000370150ENST00000369984PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000393831ENST00000310441PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000393831ENST00000354233PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000393831ENST00000369984PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000447676ENST00000310441PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000447676ENST00000354233PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000447676ENST00000369984PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000475172ENST00000310441PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000475172ENST00000354233PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-3CDSENST00000475172ENST00000369984PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-intronENST00000340888ENST00000461098PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-intronENST00000370142ENST00000461098PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-intronENST00000370145ENST00000461098PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-intronENST00000370150ENST00000461098PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-intronENST00000393831ENST00000461098PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-intronENST00000447676ENST00000461098PNCKchrX

152952886

-HCFC1chrX

153230177

-
intron-intronENST00000475172ENST00000461098PNCKchrX

152952886

-HCFC1chrX

153230177

-

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 PNCK-HCFC1


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)

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.

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Fusion Protein Features for PNCK-HCFC1


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/:152952886/:153230177)
- 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
.HCFC1

Q9NWW0

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: Regulates HCFC1 activity by modulating its subcellular localization. Overexpression of HCFC1R1 leads to accumulation of HCFC1 in the cytoplasm. HCFC1R1-mediated export may provide the pool of cytoplasmic HCFC1 required for import of virion-derived VP16 into the nucleus. {ECO:0000269|PubMed:12235138}.

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 PNCK-HCFC1


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 PNCK-HCFC1


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 PNCK-HCFC1


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 PNCK-HCFC1


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