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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:ARHGAP23-HECTD4 (FusionGDB2 ID:6002)

Fusion Gene Summary for ARHGAP23-HECTD4

check button Fusion gene summary
Fusion gene informationFusion gene name: ARHGAP23-HECTD4
Fusion gene ID: 6002
HgeneTgene
Gene symbol

ARHGAP23

HECTD4

Gene ID

57636

283450

Gene nameRho GTPase activating protein 23HECT domain E3 ubiquitin protein ligase 4
Synonyms-C12ord51|C12orf51|HEEL|POTAGE
Cytomap

17q12

12q24.13

Type of geneprotein-codingprotein-coding
Descriptionrho GTPase-activating protein 23rho-type GTPase-activating protein 23probable E3 ubiquitin-protein ligase HECTD4AF-1 specific protein phosphataseHECT domain containing E3 ubiquitin protein ligase 4HECT domain-containing protein 4HECT-type E3 ubiquitin transferase HECTD4probable E3 ubiquitin-protein ligase C12orf51tra
Modification date2020031320200313
UniProtAcc

Q9P227

Q9Y4D8

Ensembl transtripts involved in fusion geneENST00000431231, ENST00000437668, 
ENST00000443378, ENST00000582409, 
ENST00000549141, ENST00000377560, 
ENST00000430131, ENST00000550722, 
Fusion gene scores* DoF score13 X 12 X 10=156012 X 13 X 8=1248
# samples 1413
** MAII scorelog2(14/1560*10)=-3.47804729680464
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/1248*10)=-3.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ARHGAP23 [Title/Abstract] AND HECTD4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointARHGAP23(36625863)-HECTD4(112631311), # samples:1
Anticipated loss of major functional domain due to fusion event.ARHGAP23-HECTD4 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* 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 buttonFusion gene breakpoints across ARHGAP23 (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 HECTD4 (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
ChiTaRS5.0N/ABE700195ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-


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Fusion Gene ORF analysis for ARHGAP23-HECTD4

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-intronENST00000431231ENST00000549141ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
5CDS-intronENST00000437668ENST00000549141ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
5CDS-intronENST00000443378ENST00000549141ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
Frame-shiftENST00000431231ENST00000377560ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
Frame-shiftENST00000431231ENST00000430131ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
Frame-shiftENST00000431231ENST00000550722ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
Frame-shiftENST00000437668ENST00000377560ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
Frame-shiftENST00000437668ENST00000430131ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
Frame-shiftENST00000437668ENST00000550722ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
Frame-shiftENST00000443378ENST00000377560ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
Frame-shiftENST00000443378ENST00000430131ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
Frame-shiftENST00000443378ENST00000550722ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
intron-3CDSENST00000582409ENST00000377560ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
intron-3CDSENST00000582409ENST00000430131ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
intron-3CDSENST00000582409ENST00000550722ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-
intron-intronENST00000582409ENST00000549141ARHGAP23chr17

36625863

+HECTD4chr12

112631311

-

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 ARHGAP23-HECTD4


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 ARHGAP23-HECTD4


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/:36625863/:112631311)
- 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
ARHGAP23

Q9P227

HECTD4

Q9Y4D8

FUNCTION: GTPase activator for the Rho-type GTPases by converting them to an inactive GDP-bound state. {ECO:0000250}.FUNCTION: E3 ubiquitin-protein ligase which accepts ubiquitin from an E2 ubiquitin-conjugating enzyme in the form of a thioester and then directly transfers the ubiquitin to targeted substrates. {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 ARHGAP23-HECTD4


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 ARHGAP23-HECTD4


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 ARHGAP23-HECTD4


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 ARHGAP23-HECTD4


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