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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:C19orf48-CCDC9 (FusionGDB2 ID:HG84798TG26093)

Fusion Gene Summary for C19orf48-CCDC9

check button Fusion gene summary
Fusion gene informationFusion gene name: C19orf48-CCDC9
Fusion gene ID: hg84798tg26093
HgeneTgene
Gene symbol

C19orf48

CCDC9

Gene ID

84798

26093

Gene namechromosome 19 open reading frame 48coiled-coil domain containing 9
Synonyms--
Cytomap('C19orf48')('CCDC9')

19q13.33

19q13.32

Type of geneprotein-codingprotein-coding
Descriptionuncharacterized protein C19orf48multidrug resistance-related proteincoiled-coil domain-containing protein 9
Modification date2020032020200313
UniProtAcc

Q6RUI8

Q9Y3X0

Ensembl transtripts involved in fusion geneENST00000345523, ENST00000391812, 
ENST00000595794, ENST00000596655, 
ENST00000598463, 
Fusion gene scores* DoF score12 X 11 X 5=6605 X 6 X 4=120
# samples 157
** MAII scorelog2(15/660*10)=-2.13750352374993
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/120*10)=-0.777607578663552
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: C19orf48 [Title/Abstract] AND CCDC9 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointC19orf48(51305474)-CCDC9(47759780), # 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


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-KK-A8IC-01AC19orf48chr19

51305474

-CCDC9chr19

47759780

+


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Fusion Gene ORF analysis for C19orf48-CCDC9

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-3UTRENST00000345523ENST00000601154C19orf48chr19

51305474

-CCDC9chr19

47759780

+
5UTR-3UTRENST00000391812ENST00000601154C19orf48chr19

51305474

-CCDC9chr19

47759780

+
5UTR-3UTRENST00000595794ENST00000601154C19orf48chr19

51305474

-CCDC9chr19

47759780

+
5UTR-3UTRENST00000596655ENST00000601154C19orf48chr19

51305474

-CCDC9chr19

47759780

+
5UTR-3UTRENST00000598463ENST00000601154C19orf48chr19

51305474

-CCDC9chr19

47759780

+
5UTR-5UTRENST00000345523ENST00000221922C19orf48chr19

51305474

-CCDC9chr19

47759780

+
5UTR-5UTRENST00000391812ENST00000221922C19orf48chr19

51305474

-CCDC9chr19

47759780

+
5UTR-5UTRENST00000595794ENST00000221922C19orf48chr19

51305474

-CCDC9chr19

47759780

+
5UTR-5UTRENST00000596655ENST00000221922C19orf48chr19

51305474

-CCDC9chr19

47759780

+
5UTR-5UTRENST00000598463ENST00000221922C19orf48chr19

51305474

-CCDC9chr19

47759780

+

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 C19orf48-CCDC9


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)
C19orf48chr1951305473-CCDC9chr1947759779+9.35E-070.99999905
C19orf48chr1951305473-CCDC9chr1947759779+9.35E-070.99999905


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.
genomic feature of top 1%

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Fusion Protein Features for C19orf48-CCDC9


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/:51305474/:47759780)
- 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
C19orf48

Q6RUI8

CCDC9

Q9Y3X0


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 C19orf48-CCDC9


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 C19orf48-CCDC9


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 C19orf48-CCDC9


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 C19orf48-CCDC9


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource