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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:IFT52-INSC (FusionGDB2 ID:HG51098TG387755)

Fusion Gene Summary for IFT52-INSC

check button Fusion gene summary
Fusion gene informationFusion gene name: IFT52-INSC
Fusion gene ID: hg51098tg387755
HgeneTgene
Gene symbol

IFT52

INSC

Gene ID

51098

387755

Gene nameintraflagellar transport 52INSC spindle orientation adaptor protein
SynonymsC20orf9|CGI-53|NGD2|NGD5-
Cytomap('IFT52')('INSC')

20q13.12

11p15.2

Type of geneprotein-codingprotein-coding
Descriptionintraflagellar transport protein 52 homologprotein NGD5 homologprotein inscuteable homologinscuteable homologinscuteable spindle orientation adaptor protein
Modification date2020031520200313
UniProtAcc.

Q1MX18

Ensembl transtripts involved in fusion geneENST00000373030, ENST00000373039, 
ENST00000471199, 
Fusion gene scores* DoF score4 X 4 X 3=486 X 6 X 8=288
# samples 48
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/288*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: IFT52 [Title/Abstract] AND INSC [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointIFT52(42252594)-INSC(15218881), # 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
TgeneINSC

GO:0031647

regulation of protein stability

22074847



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/ACA489062IFT52chr20

42252594

+INSCchr11

15218881

-


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Fusion Gene ORF analysis for IFT52-INSC

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-intronENST00000373030ENST00000379554IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373030ENST00000379556IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373030ENST00000424273IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373030ENST00000447214IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373030ENST00000525218IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373030ENST00000528567IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373030ENST00000530161IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373039ENST00000379554IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373039ENST00000379556IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373039ENST00000424273IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373039ENST00000447214IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373039ENST00000525218IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373039ENST00000528567IFT52chr20

42252594

+INSCchr11

15218881

-
5CDS-intronENST00000373039ENST00000530161IFT52chr20

42252594

+INSCchr11

15218881

-
intron-intronENST00000471199ENST00000379554IFT52chr20

42252594

+INSCchr11

15218881

-
intron-intronENST00000471199ENST00000379556IFT52chr20

42252594

+INSCchr11

15218881

-
intron-intronENST00000471199ENST00000424273IFT52chr20

42252594

+INSCchr11

15218881

-
intron-intronENST00000471199ENST00000447214IFT52chr20

42252594

+INSCchr11

15218881

-
intron-intronENST00000471199ENST00000525218IFT52chr20

42252594

+INSCchr11

15218881

-
intron-intronENST00000471199ENST00000528567IFT52chr20

42252594

+INSCchr11

15218881

-
intron-intronENST00000471199ENST00000530161IFT52chr20

42252594

+INSCchr11

15218881

-

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 IFT52-INSC


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 IFT52-INSC


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/:42252594/:15218881)
- 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
.INSC

Q1MX18

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: May function as an adapter linking the Par3 complex to the GPSM1/GPSM2 complex (PubMed:16458856). Involved in spindle orientation during mitosis. May regulate cell proliferation and differentiation in the developing nervous system. May play a role in the asymmetric division of fibroblasts and participate in the process of stratification of the squamous epithelium (By similarity). {ECO:0000250|UniProtKB:Q3HNM7, ECO:0000305|PubMed:16458856}.

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 IFT52-INSC


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 IFT52-INSC


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 IFT52-INSC


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 IFT52-INSC


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneIFT52C4310718SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY4GENOMICS_ENGLAND;UNIPROT
HgeneIFT52C0432235CRANIOECTODERMAL DYSPLASIA 12ORPHANET
HgeneIFT52C0152427Polydactyly1GENOMICS_ENGLAND
HgeneIFT52C0238198Gastrointestinal Stromal Tumors1CTD_human
HgeneIFT52C3179349Gastrointestinal Stromal Sarcoma1CTD_human