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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: 27091

FusionGeneSummary for PIAS4_ZNF787

check button Fusion gene summary
Fusion gene informationFusion gene name: PIAS4_ZNF787
Fusion gene ID: 27091
HgeneTgene
Gene symbol

PIAS4

ZNF787

Gene ID

51588

126208

Gene nameprotein inhibitor of activated STAT 4zinc finger protein 787
SynonymsPIAS-gamma|PIASY|Piasg|ZMIZ6TIP20
Cytomap

19p13.3

19q13.43

Type of geneprotein-codingprotein-coding
DescriptionE3 SUMO-protein ligase PIAS4RING-type E3 ubiquitin transferase PIAS4protein inhibitor of activated STAT protein 4protein inhibitor of activated STAT protein PIASyprotein inhibitor of activated STAT protein gammazinc finger, MIZ-type containing 6zinc finger protein 787TTF-I-interacting peptide 20transcription termination factor I interacting peptide 20
Modification date2018052220180519
UniProtAcc

Q8N2W9

Q6DD87

Ensembl transtripts involved in fusion geneENST00000262971, ENST00000596144, 
ENST00000270459, ENST00000587279, 
Fusion gene scores* DoF score6 X 5 X 5=1502 X 2 X 2=8
# samples 62
** MAII scorelog2(6/150*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: PIAS4 [Title/Abstract] AND ZNF787 [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
HgenePIAS4

GO:0016925

protein sumoylation

18579533

HgenePIAS4

GO:0033235

positive regulation of protein sumoylation

17696781|21965678

HgenePIAS4

GO:0045892

negative regulation of transcription, DNA-templated

11248056


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
TCGARVSARCTCGA-3B-A9HX-01APIAS4chr19

4033578

+ZNF787chr19

56614596

-
* 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-5UTRENST00000262971ENST00000270459PIAS4chr19

4033578

+ZNF787chr19

56614596

-
5CDS-5UTRENST00000262971ENST00000587279PIAS4chr19

4033578

+ZNF787chr19

56614596

-
intron-5UTRENST00000596144ENST00000270459PIAS4chr19

4033578

+ZNF787chr19

56614596

-
intron-5UTRENST00000596144ENST00000587279PIAS4chr19

4033578

+ZNF787chr19

56614596

-

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FusionProtFeatures for PIAS4_ZNF787


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PIAS4

Q8N2W9

ZNF787

Q6DD87

Functions as an E3-type small ubiquitin-like modifier(SUMO) ligase, stabilizing the interaction between UBE2I and thesubstrate, and as a SUMO-tethering factor. Plays a crucial role asa transcriptional coregulation in various cellular pathways,including the STAT pathway, the p53/TP53 pathway, the Wnt pathwayand the steroid hormone signaling pathway. Involved in genesilencing. Mediates sumoylation of CEBPA, PARK7, HERC2, MYB, TCF4and RNF168. In Wnt signaling, represses LEF1 and enhances TCF4transcriptional activities through promoting their sumoylations.Enhances the sumoylation of MTA1 and may participate in itsparalog-selective sumoylation. {ECO:0000269|PubMed:12511558,ECO:0000269|PubMed:12631292, ECO:0000269|PubMed:12727872,ECO:0000269|PubMed:15831457, ECO:0000269|PubMed:15976810,ECO:0000269|PubMed:21965678, ECO:0000269|PubMed:22508508}. 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 PIAS4_ZNF787


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 PIAS4_ZNF787


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
PIAS4LEF1, SMAD7, CALCOCO2, SMAD6, SMAD2, SMAD3, SMAD4, AR, ETS1, ZMIZ2, TP53BP1, BRCA1, PARP1, TCF4, SMAD1, CEBPD, TRIM27, HDAC1, HDAC2, SATB1, TRIM32, TGM2, KNTC1, ZW10, PRKCZ, HERC2, MDC1, ELAVL1, VHL, IKBKG, ERBB4, HTT, SUMO2, TADA3, BARD1, TCERG1, CLK1, GADD45G, UBE2K, IMMT, CHD3, IMPDH2, KPNB1, MAGEH1, NEFL, MAP1LC3A, LRIF1, PRPF40A, PTN, SH3GL3, TP53, VIM, ZHX1, SERBP1, PLAG1, TICAM1, IRF3, IRF7, SKIL, ZNF512B, PDE4DIP, PHGDH, OPTN, IL15RA, PHF11, KRT18, FTH1, ALDOA, ESRRA, LAMP2, OAZ1, SERPINA5, UBE2I, BTAF1, PIAS2, HNRNPUL1, MPRIP, ACTN1, MECOM, SUMO1, PDE4A, PDE4D, HIC1, HNF4A, TOP2A, CA10, EIF5B, REV1, AREL1, FANCAZNF787PTEN, FMNL1, IL7R, SOX2, MOV10, RNF2, BMI1, P4HA3, PNLIP, TRIM25


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 PIAS4_ZNF787


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 PIAS4_ZNF787


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