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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:CCDC152-HP (FusionGDB2 ID:13685)

Fusion Gene Summary for CCDC152-HP

check button Fusion gene summary
Fusion gene informationFusion gene name: CCDC152-HP
Fusion gene ID: 13685
HgeneTgene
Gene symbol

CCDC152

HP

Gene ID

100129792

10395

Gene namecoiled-coil domain containing 152DLC1 Rho GTPase activating protein
SynonymsCH5400ARHGAP7|HP|STARD12|p122-RhoGAP
Cytomap

5p12

8p22

Type of geneprotein-codingprotein-coding
Descriptioncoiled-coil domain-containing protein 152rho GTPase-activating protein 7Rho-GTPase-activating protein 7START domain-containing protein 12StAR-related lipid transfer (START) domain containing 12deleted in liver cancer 1 proteindeleted in liver cancer 1 variant 2deleted in liver cancer varia
Modification date2020031320200313
UniProtAcc

Q4G0S7

P02790

Ensembl transtripts involved in fusion geneENST00000361970, ENST00000388827, 
ENST00000355906, ENST00000398131, 
ENST00000570083, ENST00000562526, 
ENST00000565574, ENST00000357763, 
ENST00000569639, 
Fusion gene scores* DoF score3 X 3 X 3=2714 X 11 X 3=462
# samples 313
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(13/462*10)=-1.8293812283876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CCDC152 [Title/Abstract] AND HP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCCDC152(42801243)-HP(72094658), # samples:2
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
TgeneHP

GO:0006915

apoptotic process

17292327

TgeneHP

GO:0006919

activation of cysteine-type endopeptidase activity involved in apoptotic process

17888903

TgeneHP

GO:0008285

negative regulation of cell proliferation

12545165|17932950

TgeneHP

GO:0030336

negative regulation of cell migration

17932950|19158340

TgeneHP

GO:0035307

positive regulation of protein dephosphorylation

17292327

TgeneHP

GO:0051497

negative regulation of stress fiber assembly

17932950

TgeneHP

GO:0051895

negative regulation of focal adhesion assembly

19158340

TgeneHP

GO:1900119

positive regulation of execution phase of apoptosis

17888903


check buttonFusion gene breakpoints across CCDC152 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across HP (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4LIHCTCGA-DD-A73C-01ACCDC152chr5

42801243

+HPchr16

72094658

+


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Fusion Gene ORF analysis for CCDC152-HP

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
3UTR-3CDSENST00000361970ENST00000355906CCDC152chr5

42801243

+HPchr16

72094658

+
3UTR-3CDSENST00000361970ENST00000398131CCDC152chr5

42801243

+HPchr16

72094658

+
3UTR-3CDSENST00000361970ENST00000570083CCDC152chr5

42801243

+HPchr16

72094658

+
3UTR-3UTRENST00000361970ENST00000562526CCDC152chr5

42801243

+HPchr16

72094658

+
3UTR-3UTRENST00000361970ENST00000565574CCDC152chr5

42801243

+HPchr16

72094658

+
3UTR-intronENST00000361970ENST00000357763CCDC152chr5

42801243

+HPchr16

72094658

+
3UTR-intronENST00000361970ENST00000569639CCDC152chr5

42801243

+HPchr16

72094658

+
intron-3CDSENST00000388827ENST00000355906CCDC152chr5

42801243

+HPchr16

72094658

+
intron-3CDSENST00000388827ENST00000398131CCDC152chr5

42801243

+HPchr16

72094658

+
intron-3CDSENST00000388827ENST00000570083CCDC152chr5

42801243

+HPchr16

72094658

+
intron-3UTRENST00000388827ENST00000562526CCDC152chr5

42801243

+HPchr16

72094658

+
intron-3UTRENST00000388827ENST00000565574CCDC152chr5

42801243

+HPchr16

72094658

+
intron-intronENST00000388827ENST00000357763CCDC152chr5

42801243

+HPchr16

72094658

+
intron-intronENST00000388827ENST00000569639CCDC152chr5

42801243

+HPchr16

72094658

+

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 CCDC152-HP


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)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

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.

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Fusion Protein Features for CCDC152-HP


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/:42801243/:72094658)
- 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
CCDC152

Q4G0S7

HP

P02790

FUNCTION: Binds heme and transports it to the liver for breakdown and iron recovery, after which the free hemopexin returns to the circulation.

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 CCDC152-HP


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 CCDC152-HP


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 CCDC152-HP


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 CCDC152-HP


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