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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:CLIC5-RBM10 (FusionGDB2 ID:HG53405TG8241)

Fusion Gene Summary for CLIC5-RBM10

check button Fusion gene summary
Fusion gene informationFusion gene name: CLIC5-RBM10
Fusion gene ID: hg53405tg8241
HgeneTgene
Gene symbol

CLIC5

RBM10

Gene ID

53405

8241

Gene namechloride intracellular channel 5RNA binding motif protein 10
SynonymsDFNB102|DFNB103|MST130|MSTP130DXS8237E|GPATC9|GPATCH9|S1-1|TARPS|ZRANB5
Cytomap('CLIC5')('RBM10')

6p21.1

Xp11.3

Type of geneprotein-codingprotein-coding
Descriptionchloride intracellular channel protein 5RNA-binding protein 10RNA-binding protein S1-1epididymis secretory sperm binding proteing patch domain-containing protein 9
Modification date2020031320200313
UniProtAcc

Q9NZA1

.
Ensembl transtripts involved in fusion geneENST00000185206, ENST00000339561, 
ENST00000486570, ENST00000544153, 
Fusion gene scores* DoF score6 X 7 X 2=842 X 2 X 1=4
# samples 72
** MAII scorelog2(7/84*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: CLIC5 [Title/Abstract] AND RBM10 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCLIC5(45874302)-RBM10(47018749), # 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
HgeneCLIC5

GO:0006821

chloride transport

10793131



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/ABI494946CLIC5chr6

45874302

-RBM10chrX

47018749

+


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Fusion Gene ORF analysis for CLIC5-RBM10

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-intronENST00000185206ENST00000329236CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000185206ENST00000345781CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000185206ENST00000377604CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000185206ENST00000478410CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000339561ENST00000329236CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000339561ENST00000345781CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000339561ENST00000377604CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000339561ENST00000478410CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000486570ENST00000329236CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000486570ENST00000345781CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000486570ENST00000377604CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000486570ENST00000478410CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000544153ENST00000329236CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000544153ENST00000345781CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000544153ENST00000377604CLIC5chr6

45874302

-RBM10chrX

47018749

+
intron-intronENST00000544153ENST00000478410CLIC5chr6

45874302

-RBM10chrX

47018749

+

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 CLIC5-RBM10


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 CLIC5-RBM10


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/:45874302/:47018749)
- 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
CLIC5

Q9NZA1

.
FUNCTION: Required for normal hearing (PubMed:24781754). It is necessary for the formation of stereocilia in the inner ear and normal development of the organ of Corti (By similarity). Can insert into membranes and form poorly selective ion channels that may also transport chloride ions. May play a role in the regulation of transepithelial ion absorption and secretion. Is required for the development and/or maintenance of the proper glomerular endothelial cell and podocyte architecture (PubMed:15184393, PubMed:18028448, PubMed:20335315). Plays a role in formation of the lens suture in the eye, which is important for normal optical properties of the lens (By similarity). {ECO:0000250|UniProtKB:Q8BXK9, ECO:0000269|PubMed:15184393, ECO:0000269|PubMed:18028448, ECO:0000269|PubMed:20335315, ECO:0000269|PubMed:24781754}.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 CLIC5-RBM10


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 CLIC5-RBM10


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 CLIC5-RBM10


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 CLIC5-RBM10


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCLIC5C1846647DEAFNESS, AUTOSOMAL RECESSIVE (disorder)3CLINGEN
HgeneCLIC5C4015050DEAFNESS, AUTOSOMAL RECESSIVE 1031CTD_human;GENOMICS_ENGLAND
TgeneC1839463TARP syndrome4CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneC0008925Cleft Palate1GENOMICS_ENGLAND
TgeneC0152427Polydactyly1GENOMICS_ENGLAND