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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:COMMD4-ABHD2 (FusionGDB2 ID:18523)

Fusion Gene Summary for COMMD4-ABHD2

check button Fusion gene summary
Fusion gene informationFusion gene name: COMMD4-ABHD2
Fusion gene ID: 18523
HgeneTgene
Gene symbol

COMMD4

ABHD2

Gene ID

54939

11057

Gene nameCOMM domain containing 4abhydrolase domain containing 2, acylglycerol lipase
Synonyms-HS1-2|LABH2|PHPS1-2
Cytomap

15q24.2

15q26.1

Type of geneprotein-codingprotein-coding
DescriptionCOMM domain-containing protein 4monoacylglycerol lipase ABHD22-arachidonoylglycerol hydrolaseabhydrolase domain containing 2abhydrolase domain-containing protein 2acetylesterasealpha/beta hydrolase domain containing protein 2lung alpha/beta hydrolase 2progesterone-sensitive lipas
Modification date2020031320200313
UniProtAcc.

P08910

Ensembl transtripts involved in fusion geneENST00000561662, ENST00000267935, 
ENST00000338995, ENST00000564815, 
ENST00000567195, ENST00000562789, 
ENST00000352732, ENST00000355100, 
ENST00000565973, ENST00000562254, 
Fusion gene scores* DoF score2 X 2 X 2=811 X 11 X 4=484
# samples 213
** MAII scorelog2(2/8*10)=1.32192809488736log2(13/484*10)=-1.89649542424614
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: COMMD4 [Title/Abstract] AND ABHD2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCOMMD4(75628433)-ABHD2(89656955), # 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
TgeneABHD2

GO:0032570

response to progesterone

26989199

TgeneABHD2

GO:0043401

steroid hormone mediated signaling pathway

26989199

TgeneABHD2

GO:0046464

acylglycerol catabolic process

26989199

TgeneABHD2

GO:0048240

sperm capacitation

26989199


check buttonFusion gene breakpoints across COMMD4 (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 ABHD2 (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
ChimerDB4STADTCGA-BR-4292COMMD4chr15

75628433

+ABHD2chr15

89656955

+


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Fusion Gene ORF analysis for COMMD4-ABHD2

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-5UTRENST00000561662ENST00000352732COMMD4chr15

75628433

+ABHD2chr15

89656955

+
3UTR-5UTRENST00000561662ENST00000355100COMMD4chr15

75628433

+ABHD2chr15

89656955

+
3UTR-5UTRENST00000561662ENST00000565973COMMD4chr15

75628433

+ABHD2chr15

89656955

+
3UTR-intronENST00000561662ENST00000562254COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000267935ENST00000352732COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000267935ENST00000355100COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000267935ENST00000565973COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000338995ENST00000352732COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000338995ENST00000355100COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000338995ENST00000565973COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000564815ENST00000352732COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000564815ENST00000355100COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000564815ENST00000565973COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000567195ENST00000352732COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000567195ENST00000355100COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-5UTRENST00000567195ENST00000565973COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-intronENST00000267935ENST00000562254COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-intronENST00000338995ENST00000562254COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-intronENST00000564815ENST00000562254COMMD4chr15

75628433

+ABHD2chr15

89656955

+
5CDS-intronENST00000567195ENST00000562254COMMD4chr15

75628433

+ABHD2chr15

89656955

+
intron-5UTRENST00000562789ENST00000352732COMMD4chr15

75628433

+ABHD2chr15

89656955

+
intron-5UTRENST00000562789ENST00000355100COMMD4chr15

75628433

+ABHD2chr15

89656955

+
intron-5UTRENST00000562789ENST00000565973COMMD4chr15

75628433

+ABHD2chr15

89656955

+
intron-intronENST00000562789ENST00000562254COMMD4chr15

75628433

+ABHD2chr15

89656955

+

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 COMMD4-ABHD2


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)
COMMD4chr1575628433+ABHD2chr1589656955+6.67E-060.9999933
COMMD4chr1575628433+ABHD2chr1589656955+6.67E-060.9999933

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.
genomic feature of top 1%

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Fusion Protein Features for COMMD4-ABHD2


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/:75628433/:89656955)
- 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
.ABHD2

P08910

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: Progesterone-dependent acylglycerol lipase that catalyzes hydrolysis of endocannabinoid arachidonoylglycerol (AG) from cell membrane (PubMed:26989199). Acts as a progesterone receptor: progesterone-binding activates the acylglycerol lipase activity, mediating degradation of 1-arachidonoylglycerol (1AG) and 2-arachidonoylglycerol (2AG) to glycerol and arachidonic acid (AA) (PubMed:26989199). Also displays an ester hydrolase activity against acetyl ester, butanoate ester and hexadecanoate ester (PubMed:27247428). Plays a key role in sperm capacitation in response to progesterone by mediating degradation of 2AG, an inhibitor of the sperm calcium channel CatSper, leading to calcium influx via CatSper and sperm activation (PubMed:26989199). May also play a role in smooth muscle cells migration (By similarity). {ECO:0000250|UniProtKB:Q9QXM0, ECO:0000269|PubMed:26989199, ECO:0000269|PubMed:27247428}.

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 COMMD4-ABHD2


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 COMMD4-ABHD2


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 COMMD4-ABHD2


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 COMMD4-ABHD2


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