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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:OCRL-IFI16 (FusionGDB2 ID:HG4952TG3428)

Fusion Gene Summary for OCRL-IFI16

check button Fusion gene summary
Fusion gene informationFusion gene name: OCRL-IFI16
Fusion gene ID: hg4952tg3428
HgeneTgene
Gene symbol

OCRL

IFI16

Gene ID

4952

3428

Gene nameOCRL inositol polyphosphate-5-phosphataseinterferon gamma inducible protein 16
SynonymsDent-2|INPP5F|LOCR|NPHL2|OCRL-1|OCRL1IFNGIP1|PYHIN2
Cytomap('OCRL')('IFI16')

Xq26.1

1q23.1

Type of geneprotein-codingprotein-coding
Descriptioninositol polyphosphate 5-phosphatase OCRLLowe oculocerebrorenal syndrome proteininositol polyphosphate 5-phosphatase OCRL-1oculocerebrorenal syndrome of Lowephosphatidylinositol 3,4,5-triphosphate 5-phosphatasephosphatidylinositol polyphosphate 5-phogamma-interferon-inducible protein 16IFI16 beta isoforminterferon-gamma induced protein IFI 16interferon-inducible myeloid differentiation transcriptional activator
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000357121, ENST00000371113, 
ENST00000486673, 
Fusion gene scores* DoF score1 X 1 X 1=112 X 13 X 7=1092
# samples 115
** MAII scorelog2(1/1*10)=3.32192809488736log2(15/1092*10)=-2.86393845042397
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: OCRL [Title/Abstract] AND IFI16 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointOCRL(128684386)-IFI16(158990818), # 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
HgeneOCRL

GO:0043087

regulation of GTPase activity

12915445

TgeneIFI16

GO:0000122

negative regulation of transcription by RNA polymerase II

12894224|24413532

TgeneIFI16

GO:0002218

activation of innate immune response

21575908

TgeneIFI16

GO:0030224

monocyte differentiation

9766636

TgeneIFI16

GO:0032731

positive regulation of interleukin-1 beta production

21575908

TgeneIFI16

GO:0042149

cellular response to glucose starvation

21573174

TgeneIFI16

GO:0042771

intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator

14654789

TgeneIFI16

GO:0043392

negative regulation of DNA binding

22291595

TgeneIFI16

GO:0045071

negative regulation of viral genome replication

22291595

TgeneIFI16

GO:0045824

negative regulation of innate immune response

22046441

TgeneIFI16

GO:0045892

negative regulation of transcription, DNA-templated

9642285

TgeneIFI16

GO:0045944

positive regulation of transcription by RNA polymerase II

11146555

TgeneIFI16

GO:0051607

defense response to virus

21478870

TgeneIFI16

GO:0071479

cellular response to ionizing radiation

14654789

TgeneIFI16

GO:2000117

negative regulation of cysteine-type endopeptidase activity

22046441



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
ChiTaRS5.0N/AFN107964OCRLchrX

128684386

+IFI16chr1

158990818

+


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Fusion Gene ORF analysis for OCRL-IFI16

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
intron-intronENST00000357121ENST00000295809OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000357121ENST00000340979OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000357121ENST00000359709OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000357121ENST00000368131OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000357121ENST00000368132OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000357121ENST00000430894OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000357121ENST00000448393OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000371113ENST00000295809OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000371113ENST00000340979OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000371113ENST00000359709OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000371113ENST00000368131OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000371113ENST00000368132OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000371113ENST00000430894OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000371113ENST00000448393OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000486673ENST00000295809OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000486673ENST00000340979OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000486673ENST00000359709OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000486673ENST00000368131OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000486673ENST00000368132OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000486673ENST00000430894OCRLchrX

128684386

+IFI16chr1

158990818

+
intron-intronENST00000486673ENST00000448393OCRLchrX

128684386

+IFI16chr1

158990818

+

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 OCRL-IFI16


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 OCRL-IFI16


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/:128684386/:158990818)
- 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 OCRL-IFI16


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 OCRL-IFI16


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 OCRL-IFI16


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 OCRL-IFI16


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneOCRLC0028860Oculocerebrorenal Syndrome15CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneOCRLC1845167Dent Disease 25CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneOCRLC2713392Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency1CTD_human