FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact
Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:CENPV-GNAS (FusionGDB2 ID:15745)

Fusion Gene Summary for CENPV-GNAS

check button Fusion gene summary
Fusion gene informationFusion gene name: CENPV-GNAS
Fusion gene ID: 15745
HgeneTgene
Gene symbol

CENPV

GNAS

Gene ID

201161

2778

Gene namecentromere protein VGNAS complex locus
Synonyms3110013H01Rik|CENP-V|PRR6|p30AHO|C20orf45|GNAS1|GPSA|GSA|GSP|NESP|PITA3|POH|SCG6|SgVI
Cytomap

17p11.2

20q13.32

Type of geneprotein-codingprotein-coding
Descriptioncentromere protein Vnuclear protein p30proline rich 6proline-rich protein 6protein ALEXprotein GNASprotein SCG6 (secretogranin VI)G protein subunit alpha Sadenylate cyclase-stimulating G alpha proteinalternative gene product encoded by XL-exonextra large alphas proteinguanine nucleotide binding protein (G protein), alpha
Modification date2020031320200329
UniProtAcc

Q7Z7K6

P63092

Ensembl transtripts involved in fusion geneENST00000299736, ENST00000476243, 
ENST00000313949, ENST00000371075, 
ENST00000371100, ENST00000464624, 
ENST00000265620, ENST00000306090, 
ENST00000306120, ENST00000354359, 
ENST00000371081, ENST00000371085, 
ENST00000371095, ENST00000371098, 
ENST00000371099, ENST00000371102, 
Fusion gene scores* DoF score3 X 3 X 2=18111 X 41 X 18=81918
# samples 3111
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0		log2(111/81918*10)=-6.20554891117303
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CENPV [Title/Abstract] AND GNAS [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCENPV(16253245)-GNAS(57478586), # 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
HgeneCENPV

GO:0001667

ameboidal-type cell migration

19930468


check buttonFusion gene breakpoints across CENPV (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 GNAS (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
ChimerDB4BRCATCGA-A7-A13F-01ACENPVchr17

16253245

-GNASchr20

57478586

+


Top

Fusion Gene ORF analysis for CENPV-GNAS

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-3UTRENST00000299736ENST00000313949CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-3UTRENST00000299736ENST00000371075CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-3UTRENST00000299736ENST00000371100CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-3UTRENST00000299736ENST00000464624CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-intronENST00000299736ENST00000265620CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-intronENST00000299736ENST00000306090CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-intronENST00000299736ENST00000306120CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-intronENST00000299736ENST00000354359CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-intronENST00000299736ENST00000371081CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-intronENST00000299736ENST00000371085CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-intronENST00000299736ENST00000371095CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-intronENST00000299736ENST00000371098CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-intronENST00000299736ENST00000371099CENPVchr17

16253245

-GNASchr20

57478586

+
5CDS-intronENST00000299736ENST00000371102CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-3UTRENST00000476243ENST00000313949CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-3UTRENST00000476243ENST00000371075CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-3UTRENST00000476243ENST00000371100CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-3UTRENST00000476243ENST00000464624CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-intronENST00000476243ENST00000265620CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-intronENST00000476243ENST00000306090CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-intronENST00000476243ENST00000306120CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-intronENST00000476243ENST00000354359CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-intronENST00000476243ENST00000371081CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-intronENST00000476243ENST00000371085CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-intronENST00000476243ENST00000371095CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-intronENST00000476243ENST00000371098CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-intronENST00000476243ENST00000371099CENPVchr17

16253245

-GNASchr20

57478586

+
5UTR-intronENST00000476243ENST00000371102CENPVchr17

16253245

-GNASchr20

57478586

+

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

Top

Fusion Genomic Features for CENPV-GNAS


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)
CENPVchr1716253244-GNASchr2057478582+2.34E-050.99997663
CENPVchr1716253244-GNASchr2057478582+2.34E-050.99997663

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%

Top

Fusion Protein Features for CENPV-GNAS


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/:16253245/:57478586)
- 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
CENPV

Q7Z7K6

GNAS

P63092

FUNCTION: Required for distribution of pericentromeric heterochromatin in interphase nuclei and for centromere formation and organization, chromosome alignment and cytokinesis. {ECO:0000269|PubMed:18772885}.FUNCTION: Guanine nucleotide-binding proteins (G proteins) function as transducers in numerous signaling pathways controlled by G protein-coupled receptors (GPCRs) (PubMed:17110384). Signaling involves the activation of adenylyl cyclases, resulting in increased levels of the signaling molecule cAMP (PubMed:26206488, PubMed:8702665). GNAS functions downstream of several GPCRs, including beta-adrenergic receptors (PubMed:21488135). Stimulates the Ras signaling pathway via RAPGEF2 (PubMed:12391161). {ECO:0000269|PubMed:12391161, ECO:0000269|PubMed:17110384, ECO:0000269|PubMed:21488135, ECO:0000269|PubMed:26206488, ECO:0000269|PubMed:8702665}.

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


Top

Fusion Gene Sequence for CENPV-GNAS


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.

Top

Fusion Gene PPI Analysis for CENPV-GNAS


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


Top

Related Drugs for CENPV-GNAS


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

Related Diseases for CENPV-GNAS


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