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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:ZFP36-OAZ1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ZFP36-OAZ1
FusionPDB ID: 101060
FusionGDB2.0 ID: 101060
HgeneTgene
Gene symbol

ZFP36

OAZ1

Gene ID

7538

4946

Gene nameZFP36 ring finger proteinornithine decarboxylase antizyme 1
SynonymsG0S24|GOS24|NUP475|RNF162A|TIS11|TTP|zfp-36AZ1|AZI|OAZ
Cytomap

19q13.2

19p13.3

Type of geneprotein-codingprotein-coding
DescriptionmRNA decay activator protein ZFP36G0/G1 switch regulatory protein 24growth factor-inducible nuclear protein NUP475tristetraprolintristetraprolinezinc finger protein 36 homologzinc finger protein 36, C3H type, homologzinc finger protein, C3H type, 3ornithine decarboxylase antizyme 1ODC-Azantizyme 1
Modification date2020031320200313
UniProtAcc

Q07352

.
Ensembl transtripts involved in fusion geneENST idsENST00000248673, ENST00000594045, 
ENST00000597629, 
ENST00000322297, 
ENST00000582888, ENST00000583542, 
ENST00000588673, ENST00000602676, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 6 X 7=42014 X 9 X 8=1008
# samples 1015
** MAII scorelog2(10/420*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/1008*10)=-2.74846123300404
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: ZFP36 [Title/Abstract] AND OAZ1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ZFP36(39897568)-OAZ1(2271384), # samples:1
Anticipated loss of major functional domain due to fusion event.ZFP36-OAZ1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
ZFP36-OAZ1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
ZFP36-OAZ1 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
ZFP36-OAZ1 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
ZFP36-OAZ1 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
ZFP36-OAZ1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* 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
HgeneZFP36

GO:0000288

nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay

23644599

HgeneZFP36

GO:0006402

mRNA catabolic process

10330172|10751406|11782475|20221403

HgeneZFP36

GO:0009611

response to wounding

27182009

HgeneZFP36

GO:0031086

nuclear-transcribed mRNA catabolic process, deadenylation-independent decay

11279239

HgeneZFP36

GO:0032680

regulation of tumor necrosis factor production

15014438

HgeneZFP36

GO:0042594

response to starvation

15014438

HgeneZFP36

GO:0043488

regulation of mRNA stability

9703499|11719186|15687258|20702587

HgeneZFP36

GO:0044344

cellular response to fibroblast growth factor stimulus

20166898

HgeneZFP36

GO:0045647

negative regulation of erythrocyte differentiation

20702587

HgeneZFP36

GO:0060213

positive regulation of nuclear-transcribed mRNA poly(A) tail shortening

10330172

HgeneZFP36

GO:0061158

3'-UTR-mediated mRNA destabilization

9703499|11719186|15687258|20221403|27193233

HgeneZFP36

GO:0070935

3'-UTR-mediated mRNA stabilization

15014438

HgeneZFP36

GO:0071222

cellular response to lipopolysaccharide

14766228

HgeneZFP36

GO:0071356

cellular response to tumor necrosis factor

20166898

HgeneZFP36

GO:0071364

cellular response to epidermal growth factor stimulus

20166898

HgeneZFP36

GO:0071385

cellular response to glucocorticoid stimulus

20166898

HgeneZFP36

GO:0097011

cellular response to granulocyte macrophage colony-stimulating factor stimulus

20166898

HgeneZFP36

GO:1900153

positive regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay

12748283

HgeneZFP36

GO:1901835

positive regulation of deadenylation-independent decapping of nuclear-transcribed mRNA

16364915

TgeneOAZ1

GO:0045732

positive regulation of protein catabolic process

17900240


check buttonFusion gene breakpoints across ZFP36 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across OAZ1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4HNSCTCGA-CR-5250-01AZFP36chr19

39897568

+OAZ1chr19

2271384

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000594045ZFP36chr1939897568+ENST00000588673OAZ1chr192271384+789181258722154

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
ENST00000594045ENST00000588673ZFP36chr1939897568+OAZ1chr192271384+0.9182740.081726

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>101060_101060_1_ZFP36-OAZ1_ZFP36_chr19_39897568_ENST00000594045_OAZ1_chr19_2271384_ENST00000588673_length(amino acids)=154AA_BP=
MKIPGGRGNSQRDHNLSANLFYSDDRLNVTEELTSNDKTRILNVQSRLTDAKRINWRTVLSGGSLYIEIPGGALPEGSKDSFAVLLEFAE

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr19:39897568/chr19:2271384)
- 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
ZFP36

Q07352

.
FUNCTION: Zinc-finger RNA-binding protein that destabilizes several cytoplasmic AU-rich element (ARE)-containing mRNA transcripts by promoting their poly(A) tail removal or deadenylation, and hence provide a mechanism for attenuating protein synthesis (PubMed:12198173, PubMed:15538381, PubMed:15467755, PubMed:17030608, PubMed:19179481, PubMed:20702587, PubMed:24700863, PubMed:25106868, PubMed:25014217, PubMed:26542173). Acts as a 3'-untranslated region (UTR) ARE mRNA-binding adapter protein to communicate signaling events to the mRNA decay machinery (PubMed:15687258). Functions by recruiting the CCR4-NOT deadenylase complex and components of the cytoplasmic RNA decay machinery to the bound ARE-containing mRNAs, and hence promotes ARE-mediated mRNA deadenylation and decay processes (PubMed:15687258, PubMed:18326031, PubMed:25106868). Induces also the degradation of ARE-containing mRNAs even in absence of poly(A) tail (By similarity). Binds to 3'-UTR ARE of numerous mRNAs (PubMed:12198173, PubMed:15538381, PubMed:15467755, PubMed:17030608, PubMed:19179481, PubMed:20702587, PubMed:24700863, PubMed:25106868, PubMed:25014217, PubMed:26542173). Positively regulates early adipogenesis by promoting ARE-mediated mRNA decay of immediate early genes (IEGs) (By similarity). Promotes ARE-mediated mRNA decay of mineralocorticoid receptor NR3C2 mRNA in response to hypertonic stress (PubMed:24700863). Negatively regulates hematopoietic/erythroid cell differentiation by promoting ARE-mediated mRNA decay of the transcription factor STAT5B mRNA (PubMed:20702587). Positively regulates monocyte/macrophage cell differentiation by promoting ARE-mediated mRNA decay of the cyclin-dependent kinase CDK6 mRNA (PubMed:26542173). Promotes degradation of ARE-containing pluripotency-associated mRNAs in embryonic stem cells (ESCs), such as NANOG, through a fibroblast growth factor (FGF)-induced MAPK-dependent signaling pathway, and hence attenuates ESC self-renewal and positively regulates mesendoderm differentiation (By similarity). May play a role in mediating pro-apoptotic effects in malignant B-cells by promoting ARE-mediated mRNA decay of BCL2 mRNA (PubMed:25014217). In association with ZFP36L2 maintains quiescence on developing B lymphocytes by promoting ARE-mediated decay of several mRNAs encoding cell cycle regulators that help B cells progress through the cell cycle, and hence ensuring accurate variable-diversity-joining (VDJ) recombination and functional immune cell formation (By similarity). Together with ZFP36L2 is also necessary for thymocyte development and prevention of T-cell acute lymphoblastic leukemia (T-ALL) transformation by promoting ARE-mediated mRNA decay of the oncogenic transcription factor NOTCH1 mRNA (By similarity). Participates in the delivery of target ARE-mRNAs to processing bodies (PBs) (PubMed:17369404). In addition to its cytosolic mRNA-decay function, plays a role in the regulation of nuclear mRNA 3'-end processing; modulates mRNA 3'-end maturation efficiency of the DLL4 mRNA through binding with an ARE embedded in a weak noncanonical polyadenylation (poly(A)) signal in endothelial cells (PubMed:21832157). Also involved in the regulation of stress granule (SG) and P-body (PB) formation and fusion (PubMed:15967811). Plays a role in vasculogenesis and endocardial development (By similarity). Plays a role in the regulation of keratinocyte proliferation, differentiation and apoptosis (PubMed:27182009). Plays a role in myoblast cell differentiation (By similarity). {ECO:0000250|UniProtKB:P17431, ECO:0000250|UniProtKB:P23950, ECO:0000269|PubMed:12198173, ECO:0000269|PubMed:15467755, ECO:0000269|PubMed:15538381, ECO:0000269|PubMed:15687258, ECO:0000269|PubMed:15967811, ECO:0000269|PubMed:17030608, ECO:0000269|PubMed:17369404, ECO:0000269|PubMed:18326031, ECO:0000269|PubMed:19179481, ECO:0000269|PubMed:20702587, ECO:0000269|PubMed:21832157, ECO:0000269|PubMed:24700863, ECO:0000269|PubMed:25014217, ECO:0000269|PubMed:25106868, ECO:0000269|PubMed:26542173, ECO:0000269|PubMed:27182009}.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+12100_3268.0327.0RegionNecessary for localization of ARE-containing mRNAs to processing bodies (PBs)
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+12174_3268.0327.0RegionNecessary for mRNA decay activation
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+121_1008.0327.0RegionNecessary and sufficient for the association with mRNA decay enzymes and mRNA decay activation
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+121_158.0327.0RegionNecessary for nuclear export
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+121_1748.0327.0RegionNecessary for localization of ARE-containing mRNAs to processing bodies (PBs)
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+1295_1688.0327.0RegionNecessary for nuclear localization
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+1297_1738.0327.0RegionNecessary for RNA-binding
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+12198_2028.0327.0RepeatNote=P-P-P-P-G
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+12219_2238.0327.0RepeatNote=P-P-P-P-G
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+1271_758.0327.0RepeatNote=P-P-P-P-G
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+12103_1318.0327.0Zinc fingerC3H1-type 1
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+12141_1698.0327.0Zinc fingerC3H1-type 2


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
ZFP36
OAZ1


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
HgeneZFP36chr19:39897568chr19:2271384ENST00000248673+12312_3268.0327.0CNOT1


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Related Drugs to ZFP36-OAZ1


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to ZFP36-OAZ1


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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