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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:GPN1-CCNT2 (FusionGDB2 ID:34327)

Fusion Gene Summary for GPN1-CCNT2

check button Fusion gene summary
Fusion gene informationFusion gene name: GPN1-CCNT2
Fusion gene ID: 34327
HgeneTgene
Gene symbol

GPN1

CCNT2

Gene ID

11321

905

Gene nameGPN-loop GTPase 1cyclin T2
SynonymsATPBD1A|MBDIN|NTPBP|RPAP4|XAB1CYCT2
Cytomap

2p23.3

2q21.3

Type of geneprotein-codingprotein-coding
DescriptionGPN-loop GTPase 1ATP(GTP)-binding proteinMBD2-interacting proteinRNA polymerase II associated protein 4RNAPII-associated protein 4XPA binding protein 1, GTPasecyclin-T2SDS-stable vimentin-bound DNA fragment HEF42VIM22cyclin T2acyclin T2bsubunit of positive elongation transcription factor b
Modification date2020032820200313
UniProtAcc

Q9HCN4

O60583

Ensembl transtripts involved in fusion geneENST00000461249, ENST00000264718, 
ENST00000407583, ENST00000424214, 
ENST00000458167, ENST00000503738, 
ENST00000515877, ENST00000610189, 
ENST00000264157, ENST00000295238, 
ENST00000537343, 
Fusion gene scores* DoF score3 X 3 X 2=182 X 1 X 2=4
# samples 32
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/4*10)=2.32192809488736
Context

PubMed: GPN1 [Title/Abstract] AND CCNT2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGPN1(27862992)-CCNT2(135694411), # 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
TgeneCCNT2

GO:0019085

early viral transcription

21509660

TgeneCCNT2

GO:0019086

late viral transcription

21509660

TgeneCCNT2

GO:0045944

positive regulation of transcription by RNA polymerase II

15563843


check buttonFusion gene breakpoints across GPN1 (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 CCNT2 (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
ChimerDB4STADTCGA-BR-8364-01AGPN1chr2

27862992

+CCNT2chr2

135694411

+


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Fusion Gene ORF analysis for GPN1-CCNT2

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
3UTR-5UTRENST00000461249ENST00000264157GPN1chr2

27862992

+CCNT2chr2

135694411

+
3UTR-5UTRENST00000461249ENST00000295238GPN1chr2

27862992

+CCNT2chr2

135694411

+
3UTR-5UTRENST00000461249ENST00000537343GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000264718ENST00000264157GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000264718ENST00000295238GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000264718ENST00000537343GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000407583ENST00000264157GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000407583ENST00000295238GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000407583ENST00000537343GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000424214ENST00000264157GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000424214ENST00000295238GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000424214ENST00000537343GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000458167ENST00000264157GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000458167ENST00000295238GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000458167ENST00000537343GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000503738ENST00000264157GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000503738ENST00000295238GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000503738ENST00000537343GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000515877ENST00000264157GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000515877ENST00000295238GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000515877ENST00000537343GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000610189ENST00000264157GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000610189ENST00000295238GPN1chr2

27862992

+CCNT2chr2

135694411

+
5CDS-5UTRENST00000610189ENST00000537343GPN1chr2

27862992

+CCNT2chr2

135694411

+

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 GPN1-CCNT2


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)
GPN1chr227862992+CCNT2chr2135694410+4.95E-070.9999995
GPN1chr227862992+CCNT2chr2135694410+4.95E-070.9999995

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%

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Fusion Protein Features for GPN1-CCNT2


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/:27862992/:135694411)
- 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
GPN1

Q9HCN4

CCNT2

O60583

FUNCTION: Small GTPase required for proper nuclear import of RNA polymerase II (RNAPII) (PubMed:20855544, PubMed:21768307). May act at an RNAP assembly step prior to nuclear import (PubMed:21768307). Forms an interface between the RNA polymerase II enzyme and chaperone/scaffolding proteins, suggesting that it is required to connect RNA polymerase II to regulators of protein complex formation (PubMed:17643375). May be involved in nuclear localization of XPA (PubMed:11058119). {ECO:0000269|PubMed:17643375, ECO:0000269|PubMed:20855544, ECO:0000269|PubMed:21768307, ECO:0000305|PubMed:11058119}.FUNCTION: Regulatory subunit of the cyclin-dependent kinase pair (CDK9/cyclin T) complex, also called positive transcription elongation factor B (P-TEFB), which is proposed to facilitate the transition from abortive to production elongation by phosphorylating the CTD (carboxy-terminal domain) of the large subunit of RNA polymerase II (RNAP II) (PubMed:9499409, PubMed:15563843). The activity of this complex is regulated by binding with 7SK snRNA (PubMed:11713533). Plays a role during muscle differentiation; P-TEFB complex interacts with MYOD1; this tripartite complex promotes the transcriptional activity of MYOD1 through its CDK9-mediated phosphorylation and binds the chromatin of promoters and enhancers of muscle-specific genes; this event correlates with hyperphosphorylation of the CTD domain of RNA pol II (By similarity). In addition, enhances MYOD1-dependent transcription through interaction with PKN1 (PubMed:16331689). Involved in early embryo development (By similarity). {ECO:0000250|UniProtKB:Q7TQK0, ECO:0000269|PubMed:11713533, ECO:0000269|PubMed:15563843, ECO:0000269|PubMed:16331689, ECO:0000269|PubMed:9499409}.; FUNCTION: (Microbial infection) Promotes transcriptional activation of early and late herpes simplex virus 1/HHV-1 promoters. {ECO:0000269|PubMed:21509660}.

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 GPN1-CCNT2


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 GPN1-CCNT2


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 GPN1-CCNT2


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 GPN1-CCNT2


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