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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:NCOA3-GGT7 (FusionGDB2 ID:HG8202TG2686)

Fusion Gene Summary for NCOA3-GGT7

check button Fusion gene summary
Fusion gene informationFusion gene name: NCOA3-GGT7
Fusion gene ID: hg8202tg2686
HgeneTgene
Gene symbol

NCOA3

GGT7

Gene ID

8202

2686

Gene namenuclear receptor coactivator 3gamma-glutamyltransferase 7
SynonymsACTR|AIB-1|AIB1|CAGH16|CTG26|KAT13B|RAC3|SRC-3|SRC3|TNRC14|TNRC16|TRAM-1|bHLHe42|pCIPD20S101|GGT4|GGTL3|GGTL5
Cytomap('NCOA3')('GGT7')

20q13.12

20q11.22

Type of geneprotein-codingprotein-coding
Descriptionnuclear receptor coactivator 3CBP-interacting proteinamplified in breast cancer 1 proteinclass E basic helix-loop-helix protein 42receptor-associated coactivator 3steroid receptor coactivator protein 3thyroid hormone receptor activator molecule 1glutathione hydrolase 7GGT 7gamma-glutamyltransferase 4gamma-glutamyltransferase-like 3gamma-glutamyltransferase-like 5gamma-glutamyltranspeptidase 7gamma-glutamyltranspeptidase-like 3
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000341724, ENST00000371997, 
ENST00000371998, ENST00000372004, 
ENST00000497292, 
Fusion gene scores* DoF score27 X 14 X 11=41584 X 4 X 3=48
# samples 355
** MAII scorelog2(35/4158*10)=-3.57046293102604
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/48*10)=0.0588936890535686
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: NCOA3 [Title/Abstract] AND GGT7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNCOA3(46130763)-GGT7(33451351), # samples:2
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
HgeneNCOA3

GO:0045944

positive regulation of transcription by RNA polymerase II

9267036

HgeneNCOA3

GO:0071392

cellular response to estradiol stimulus

15831516



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
ChimerDB4LUSCTCGA-6A-AB49-01ANCOA3chr20

46130763

-GGT7chr20

33451351

-
ChimerDB4LUSCTCGA-6A-AB49-01ANCOA3chr20

46130763

+GGT7chr20

33451351

-


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Fusion Gene ORF analysis for NCOA3-GGT7

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-3CDSENST00000341724ENST00000336431NCOA3chr20

46130763

+GGT7chr20

33451351

-
5UTR-3CDSENST00000371997ENST00000336431NCOA3chr20

46130763

+GGT7chr20

33451351

-
5UTR-3CDSENST00000371998ENST00000336431NCOA3chr20

46130763

+GGT7chr20

33451351

-
5UTR-3CDSENST00000372004ENST00000336431NCOA3chr20

46130763

+GGT7chr20

33451351

-
5UTR-intronENST00000341724ENST00000469018NCOA3chr20

46130763

+GGT7chr20

33451351

-
5UTR-intronENST00000371997ENST00000469018NCOA3chr20

46130763

+GGT7chr20

33451351

-
5UTR-intronENST00000371998ENST00000469018NCOA3chr20

46130763

+GGT7chr20

33451351

-
5UTR-intronENST00000372004ENST00000469018NCOA3chr20

46130763

+GGT7chr20

33451351

-
intron-3CDSENST00000497292ENST00000336431NCOA3chr20

46130763

+GGT7chr20

33451351

-
intron-intronENST00000497292ENST00000469018NCOA3chr20

46130763

+GGT7chr20

33451351

-

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 NCOA3-GGT7


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)


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Fusion Protein Features for NCOA3-GGT7


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/:46130763/:33451351)
- 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


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Fusion Gene Sequence for NCOA3-GGT7


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 NCOA3-GGT7


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 NCOA3-GGT7


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 NCOA3-GGT7


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNCOA3C0023418leukemia2CTD_human
HgeneNCOA3C0033578Prostatic Neoplasms2CTD_human
HgeneNCOA3C0376358Malignant neoplasm of prostate2CTD_human
HgeneNCOA3C0001418Adenocarcinoma1CTD_human
HgeneNCOA3C0004114Astrocytoma1CTD_human
HgeneNCOA3C0005967Bone neoplasms1CTD_human
HgeneNCOA3C0006142Malignant neoplasm of breast1CTD_human
HgeneNCOA3C0007131Non-Small Cell Lung Carcinoma1CTD_human
HgeneNCOA3C0007137Squamous cell carcinoma1CTD_human
HgeneNCOA3C0205641Adenocarcinoma, Basal Cell1CTD_human
HgeneNCOA3C0205642Adenocarcinoma, Oxyphilic1CTD_human
HgeneNCOA3C0205643Carcinoma, Cribriform1CTD_human
HgeneNCOA3C0205644Carcinoma, Granular Cell1CTD_human
HgeneNCOA3C0205645Adenocarcinoma, Tubular1CTD_human
HgeneNCOA3C0205768Subependymal Giant Cell Astrocytoma1CTD_human
HgeneNCOA3C0279530Malignant Bone Neoplasm1CTD_human
HgeneNCOA3C0280783Juvenile Pilocytic Astrocytoma1CTD_human
HgeneNCOA3C0280785Diffuse Astrocytoma1CTD_human
HgeneNCOA3C0334579Anaplastic astrocytoma1CTD_human
HgeneNCOA3C0334580Protoplasmic astrocytoma1CTD_human
HgeneNCOA3C0334581Gemistocytic astrocytoma1CTD_human
HgeneNCOA3C0334582Fibrillary Astrocytoma1CTD_human
HgeneNCOA3C0334583Pilocytic Astrocytoma1CTD_human
HgeneNCOA3C0338070Childhood Cerebral Astrocytoma1CTD_human
HgeneNCOA3C0547065Mixed oligoastrocytoma1CTD_human
HgeneNCOA3C0678222Breast Carcinoma1CTD_human
HgeneNCOA3C0750935Cerebral Astrocytoma1CTD_human
HgeneNCOA3C0750936Intracranial Astrocytoma1CTD_human
HgeneNCOA3C1257931Mammary Neoplasms, Human1CTD_human
HgeneNCOA3C1458155Mammary Neoplasms1CTD_human
HgeneNCOA3C1704230Grade I Astrocytoma1CTD_human
HgeneNCOA3C4704874Mammary Carcinoma, Human1CTD_human