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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:FNTA-OVOL1 (FusionGDB2 ID:30882)

Fusion Gene Summary for FNTA-OVOL1

check button Fusion gene summary
Fusion gene informationFusion gene name: FNTA-OVOL1
Fusion gene ID: 30882
HgeneTgene
Gene symbol

FNTA

OVOL1

Gene ID

2339

5017

Gene namefarnesyltransferase, CAAX box, alphaovo like transcriptional repressor 1
SynonymsFPTA|PGGT1A|PTAR2HOVO1
Cytomap

8p11.21

11q13.1

Type of geneprotein-codingprotein-coding
Descriptionprotein farnesyltransferase/geranylgeranyltransferase type-1 subunit alphaFTase-alphaGGTase-I-alphafarnesyl-protein transferase alpha-subunitprotein prenyltransferase alpha subunit repeat containing 2ras proteins prenyltransferase subunit alphatype putative transcription factor Ovo-like 1ovo homolog-like 1ovo like zinc finger 1ovo-like 1(Drosophila)
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000302279, ENST00000342116, 
ENST00000524546, ENST00000529687, 
ENST00000335987, ENST00000531907, 
ENST00000532448, 
Fusion gene scores* DoF score9 X 10 X 4=3601 X 1 X 1=1
# samples 121
** MAII scorelog2(12/360*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: FNTA [Title/Abstract] AND OVOL1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFNTA(42911689)-OVOL1(65561502), # samples:3
Anticipated loss of major functional domain due to fusion event.FNTA-OVOL1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
FNTA-OVOL1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
FNTA-OVOL1 seems lost the major protein functional domain in Tgene partner, which is a transcription factor 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
HgeneFNTA

GO:0018343

protein farnesylation

16893176|19228685

HgeneFNTA

GO:0018344

protein geranylgeranylation

16893176

HgeneFNTA

GO:0090044

positive regulation of tubulin deacetylation

19228685

HgeneFNTA

GO:0090045

positive regulation of deacetylase activity

19228685


check buttonFusion gene breakpoints across FNTA (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 OVOL1 (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-A3IZ-01AFNTAchr8

42911689

+OVOL1chr11

65561502

+
ChimerDB4BRCATCGA-A7-A3IZ-01AFNTAchr8

42911689

+OVOL1chr11

65561502

+
ChimerDB4BRCATCGA-A7-A3IZ-01AFNTAchr8

42911689

-OVOL1chr11

65561502

+


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Fusion Gene ORF analysis for FNTA-OVOL1

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
Frame-shiftENST00000302279ENST00000335987FNTAchr8

42911689

+OVOL1chr11

65561502

+
5CDS-3UTRENST00000302279ENST00000531907FNTAchr8

42911689

+OVOL1chr11

65561502

+
5CDS-5UTRENST00000302279ENST00000532448FNTAchr8

42911689

+OVOL1chr11

65561502

+
Frame-shiftENST00000342116ENST00000335987FNTAchr8

42911689

+OVOL1chr11

65561502

+
5CDS-3UTRENST00000342116ENST00000531907FNTAchr8

42911689

+OVOL1chr11

65561502

+
5CDS-5UTRENST00000342116ENST00000532448FNTAchr8

42911689

+OVOL1chr11

65561502

+
3UTR-3CDSENST00000524546ENST00000335987FNTAchr8

42911689

+OVOL1chr11

65561502

+
3UTR-3UTRENST00000524546ENST00000531907FNTAchr8

42911689

+OVOL1chr11

65561502

+
3UTR-5UTRENST00000524546ENST00000532448FNTAchr8

42911689

+OVOL1chr11

65561502

+
intron-3CDSENST00000529687ENST00000335987FNTAchr8

42911689

+OVOL1chr11

65561502

+
intron-3UTRENST00000529687ENST00000531907FNTAchr8

42911689

+OVOL1chr11

65561502

+
intron-5UTRENST00000529687ENST00000532448FNTAchr8

42911689

+OVOL1chr11

65561502

+

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 FNTA-OVOL1


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)
FNTAchr842911689+OVOL1chr1165561501+7.04E-060.99999297
FNTAchr842911689+OVOL1chr1165561501+7.04E-060.99999297

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.

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Fusion Protein Features for FNTA-OVOL1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
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.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.
- 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 FNTA-OVOL1


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 FNTA-OVOL1


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 FNTA-OVOL1


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 FNTA-OVOL1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneOVOL1C0011615Dermatitis, Atopic1CTD_human
TgeneOVOL1C0086196Eczema, Infantile1CTD_human
TgeneOVOL1C0206711Pilomatrixoma1CTD_human