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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:CEP350-GPR161 (FusionGDB2 ID:HG9857TG23432)

Fusion Gene Summary for CEP350-GPR161

check button Fusion gene summary
Fusion gene informationFusion gene name: CEP350-GPR161
Fusion gene ID: hg9857tg23432
HgeneTgene
Gene symbol

CEP350

GPR161

Gene ID

9857

23432

Gene namecentrosomal protein 350G protein-coupled receptor 161
SynonymsCAP350|GM133RE2
Cytomap('CEP350')('GPR161')

1q25.2

1q24.2

Type of geneprotein-codingprotein-coding
Descriptioncentrosome-associated protein 350centrosomal protein 350kDaG-protein coupled receptor 161G-protein coupled receptor RE2
Modification date2020031320200313
UniProtAcc.

Q8N6U8

Ensembl transtripts involved in fusion geneENST00000367607, ENST00000490141, 
Fusion gene scores* DoF score11 X 10 X 8=8804 X 3 X 4=48
# samples 134
** MAII scorelog2(13/880*10)=-2.75899190049621
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CEP350 [Title/Abstract] AND GPR161 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCEP350(179924277)-GPR161(168074132), # samples:4
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


check button Fusion gene information
* 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
ChimerDB4PRADTCGA-EJ-5518-01ACEP350chr1

179924277

-GPR161chr1

168074132

-
ChimerDB4PRADTCGA-EJ-5518-01ACEP350chr1

179924277

+GPR161chr1

168074132

-
ChimerDB4PRADTCGA-EJ-5518CEP350chr1

179924277

+GPR161chr1

168074132

-


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Fusion Gene ORF analysis for CEP350-GPR161

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
5UTR-5UTRENST00000367607ENST00000271357CEP350chr1

179924277

+GPR161chr1

168074132

-
5UTR-5UTRENST00000367607ENST00000361697CEP350chr1

179924277

+GPR161chr1

168074132

-
5UTR-5UTRENST00000367607ENST00000367835CEP350chr1

179924277

+GPR161chr1

168074132

-
5UTR-5UTRENST00000367607ENST00000367838CEP350chr1

179924277

+GPR161chr1

168074132

-
5UTR-intronENST00000367607ENST00000367836CEP350chr1

179924277

+GPR161chr1

168074132

-
5UTR-intronENST00000367607ENST00000485232CEP350chr1

179924277

+GPR161chr1

168074132

-
5UTR-intronENST00000367607ENST00000537209CEP350chr1

179924277

+GPR161chr1

168074132

-
5UTR-intronENST00000367607ENST00000539777CEP350chr1

179924277

+GPR161chr1

168074132

-
5UTR-intronENST00000367607ENST00000546300CEP350chr1

179924277

+GPR161chr1

168074132

-
intron-5UTRENST00000490141ENST00000271357CEP350chr1

179924277

+GPR161chr1

168074132

-
intron-5UTRENST00000490141ENST00000361697CEP350chr1

179924277

+GPR161chr1

168074132

-
intron-5UTRENST00000490141ENST00000367835CEP350chr1

179924277

+GPR161chr1

168074132

-
intron-5UTRENST00000490141ENST00000367838CEP350chr1

179924277

+GPR161chr1

168074132

-
intron-intronENST00000490141ENST00000367836CEP350chr1

179924277

+GPR161chr1

168074132

-
intron-intronENST00000490141ENST00000485232CEP350chr1

179924277

+GPR161chr1

168074132

-
intron-intronENST00000490141ENST00000537209CEP350chr1

179924277

+GPR161chr1

168074132

-
intron-intronENST00000490141ENST00000539777CEP350chr1

179924277

+GPR161chr1

168074132

-
intron-intronENST00000490141ENST00000546300CEP350chr1

179924277

+GPR161chr1

168074132

-

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 CEP350-GPR161


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 CEP350-GPR161


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/:179924277/:168074132)
- 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
.GPR161

Q8N6U8

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: Key negative regulator of Shh signaling, which promotes the processing of GLI3 into GLI3R during neural tube development. Recruited by TULP3 and the IFT-A complex to primary cilia and acts as a regulator of the PKA-dependent basal repression machinery in Shh signaling by increasing cAMP levels, leading to promote the PKA-dependent processing of GLI3 into GLI3R and repress the Shh signaling. In presence of SHH, it is removed from primary cilia and is internalized into recycling endosomes, preventing its activity and allowing activation of the Shh signaling. Its ligand is unknown (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 CEP350-GPR161


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 CEP350-GPR161


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 CEP350-GPR161


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 CEP350-GPR161


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC4053775Pituitary stalk interruption syndrome1GENOMICS_ENGLAND;ORPHANET