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:ZSCAN30-PDXK (FusionGDB2 ID:103239)

Fusion Gene Summary for ZSCAN30-PDXK

check button Fusion gene summary
Fusion gene informationFusion gene name: ZSCAN30-PDXK
Fusion gene ID: 103239
HgeneTgene
Gene symbol

ZSCAN30

PDXK

Gene ID

100101467

8566

Gene namezinc finger and SCAN domain containing 30pyridoxal kinase
SynonymsZNF-WYM|ZNF397OS|ZNF917C21orf124|C21orf97|HEL-S-1a|HMSN6C|PKH|PNK|PRED79
Cytomap

18q12.2

21q22.3

Type of geneprotein-codingprotein-coding
Descriptionzinc finger and SCAN domain-containing protein 30ZNF397 opposite strandzinc finger protein 397 opposite strandzinc finger protein 397OSpyridoxal kinaseepididymis secretory sperm binding protein Li 1apyridoxal (pyridoxine, vitamin B6) kinasepyridoxamine kinasepyridoxine kinasevitamin B6 kinase
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000333206, ENST00000383091, 
ENST00000420878, ENST00000589178, 
ENST00000588832, ENST00000592278, 
ENST00000601405, 
ENST00000291565, 
ENST00000327574, ENST00000398081, 
ENST00000468090, ENST00000476313, 
ENST00000467908, 
Fusion gene scores* DoF score5 X 4 X 4=8011 X 7 X 8=616
# samples 513
** MAII scorelog2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/616*10)=-2.24441872766645
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZSCAN30 [Title/Abstract] AND PDXK [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointZSCAN30(32870048)-PDXK(45153950), # samples:1
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
TgenePDXK

GO:0042823

pyridoxal phosphate biosynthetic process

9099727|10987144|17766369


check buttonFusion gene breakpoints across ZSCAN30 (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 PDXK (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
ChimerDB4KIRCTCGA-BP-4784-01AZSCAN30chr18

32870048

-PDXKchr21

45153950

+


Top

Fusion Gene ORF analysis for ZSCAN30-PDXK

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
5UTR-3CDSENST00000333206ENST00000291565ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000333206ENST00000327574ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000333206ENST00000398081ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000333206ENST00000468090ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000383091ENST00000291565ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000383091ENST00000327574ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000383091ENST00000398081ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000383091ENST00000468090ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000420878ENST00000291565ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000420878ENST00000327574ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000420878ENST00000398081ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000420878ENST00000468090ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000589178ENST00000291565ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000589178ENST00000327574ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000589178ENST00000398081ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3CDSENST00000589178ENST00000468090ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3UTRENST00000333206ENST00000476313ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3UTRENST00000383091ENST00000476313ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3UTRENST00000420878ENST00000476313ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-3UTRENST00000589178ENST00000476313ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-intronENST00000333206ENST00000467908ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-intronENST00000383091ENST00000467908ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-intronENST00000420878ENST00000467908ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
5UTR-intronENST00000589178ENST00000467908ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000588832ENST00000291565ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000588832ENST00000327574ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000588832ENST00000398081ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000588832ENST00000468090ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000592278ENST00000291565ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000592278ENST00000327574ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000592278ENST00000398081ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000592278ENST00000468090ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000601405ENST00000291565ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000601405ENST00000327574ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000601405ENST00000398081ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3CDSENST00000601405ENST00000468090ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3UTRENST00000588832ENST00000476313ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3UTRENST00000592278ENST00000476313ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-3UTRENST00000601405ENST00000476313ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-intronENST00000588832ENST00000467908ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-intronENST00000592278ENST00000467908ZSCAN30chr18

32870048

-PDXKchr21

45153950

+
intron-intronENST00000601405ENST00000467908ZSCAN30chr18

32870048

-PDXKchr21

45153950

+

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 ZSCAN30-PDXK


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)
ZSCAN30chr1832870047-PDXKchr2145153949+0.868738650.13126135
ZSCAN30chr1832870047-PDXKchr2145153949+0.868738650.13126135

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 ZSCAN30-PDXK


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/:32870048/:45153950)
- 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


Top

Fusion Gene Sequence for ZSCAN30-PDXK


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 ZSCAN30-PDXK


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 ZSCAN30-PDXK


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 ZSCAN30-PDXK


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