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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 15529

FusionGeneSummary for GSK3A_ZSCAN5A

check button Fusion gene summary
Fusion gene informationFusion gene name: GSK3A_ZSCAN5A
Fusion gene ID: 15529
HgeneTgene
Gene symbol

GSK3A

ZSCAN5A

Gene ID

2931

79149

Gene nameglycogen synthase kinase 3 alphazinc finger and SCAN domain containing 5A
Synonyms-ZNF495|ZSCAN5
Cytomap

19q13.2

19q13.43

Type of geneprotein-codingprotein-coding
Descriptionglycogen synthase kinase-3 alphaGSK-3 alphaserine/threonine-protein kinase GSK3Azinc finger and SCAN domain-containing protein 5Azinc finger and SCAN domain containing 5zinc finger protein 495
Modification date2018052220180519
UniProtAcc

P49840

Q9BUG6

Ensembl transtripts involved in fusion geneENST00000222330, ENST00000398249, 
ENST00000587340, ENST00000254165, 
ENST00000587492, ENST00000391713, 
ENST00000592355, ENST00000591078, 
Fusion gene scores* DoF score7 X 5 X 5=1753 X 3 X 3=27
# samples 73
** MAII scorelog2(7/175*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: GSK3A [Title/Abstract] AND ZSCAN5A [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgeneGSK3A

GO:0006468

protein phosphorylation

11035810

HgeneGSK3A

GO:0018107

peptidyl-threonine phosphorylation

25897075


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGALDSARCTCGA-JV-A75J-01AGSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-intronENST00000222330ENST00000587340GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-intronENST00000222330ENST00000254165GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-intronENST00000222330ENST00000587492GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-intronENST00000222330ENST00000391713GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-intronENST00000222330ENST00000592355GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-5UTRENST00000222330ENST00000591078GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-intronENST00000398249ENST00000587340GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-intronENST00000398249ENST00000254165GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-intronENST00000398249ENST00000587492GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-intronENST00000398249ENST00000391713GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-intronENST00000398249ENST00000592355GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-
5CDS-5UTRENST00000398249ENST00000591078GSK3Achr19

42744107

-ZSCAN5Achr19

56786277

-

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FusionProtFeatures for GSK3A_ZSCAN5A


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GSK3A

P49840

ZSCAN5A

Q9BUG6

Constitutively active protein kinase that acts as anegative regulator in the hormonal control of glucose homeostasis,Wnt signaling and regulation of transcription factors andmicrotubules, by phosphorylating and inactivating glycogensynthase (GYS1 or GYS2), CTNNB1/beta-catenin, APC and AXIN1.Requires primed phosphorylation of the majority of its substrates.Contributes to insulin regulation of glycogen synthesis byphosphorylating and inhibiting GYS1 activity and hence glycogensynthesis. Regulates glycogen metabolism in liver, but not inmuscle. May also mediate the development of insulin resistance byregulating activation of transcription factors. In Wnt signaling,regulates the level and transcriptional activity of nuclearCTNNB1/beta-catenin. Facilitates amyloid precursor protein (APP)processing and the generation of APP-derived amyloid plaques foundin Alzheimer disease. May be involved in the regulation ofreplication in pancreatic beta-cells. Is necessary for theestablishment of neuronal polarity and axon outgrowth. Throughphosphorylation of the anti-apoptotic protein MCL1, may controlcell apoptosis in response to growth factors deprivation.{ECO:0000269|PubMed:12761548, ECO:0000269|PubMed:17229088}. May be involved in transcriptional regulation.

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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FusionGeneSequence for GSK3A_ZSCAN5A


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for GSK3A_ZSCAN5A


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
GSK3AAR, MYC, AKT1, AXIN1, YWHAG, HDAC6, EBNA1BP2, GLI3, CREB1, MAPT, PRKACA, PRKDC, HSP90AA1, PRKCA, PRKCB, PRKCG, PRKCH, PRKCD, DEAF1, SPICE1, MAP3K11, NBR1, VTA1, GSKIP, SPG21, ARHGEF11, KRBA1, FAM193B, PSMD1, AXIN2, PPP1R2, FRAT1, AKAP9, ZDHHC17, TRAK2, FCGR2B, PPP3CC, RCAN2, RICTOR, CTNNB1, RAE1, AIM1, CTNNA1, MDN1, POLR3B, FOXM1, PPP1CA, PPP1CB, PPP1CC, PPP3CB, RCAN1, SAMHD1, FBXO42, SRBD1, ARSG, BCL2L1, TRIM25ZSCAN5AAPP, EPHB4, HMGA1, MRPS12, ZMYM2, ZMYM4, IPO8, ZNF616, CDYL2, RCOR2, CSNK2A2, SCAND1, RCOR3, CSNK2A1, RCOR1, HDAC3, NCOR2, OBSL1, NCOR1, KDM1A, CSNK2B


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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RelatedDrugs for GSK3A_ZSCAN5A


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for GSK3A_ZSCAN5A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGSK3AC0005586Bipolar Disorder1CTD_human
HgeneGSK3AC0011581Depressive disorder1CTD_human
HgeneGSK3AC0036341Schizophrenia1CTD_human