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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:ABHD2-FANCI (FusionGDB2 ID:HG11057TG55215)

Fusion Gene Summary for ABHD2-FANCI

check button Fusion gene summary
Fusion gene informationFusion gene name: ABHD2-FANCI
Fusion gene ID: hg11057tg55215
HgeneTgene
Gene symbol

ABHD2

FANCI

Gene ID

11057

55215

Gene nameabhydrolase domain containing 2, acylglycerol lipaseFA complementation group I
SynonymsHS1-2|LABH2|PHPS1-2KIAA1794
Cytomap('ABHD2')('FANCI')

15q26.1

15q26.1

Type of geneprotein-codingprotein-coding
Descriptionmonoacylglycerol lipase ABHD22-arachidonoylglycerol hydrolaseabhydrolase domain containing 2abhydrolase domain-containing protein 2acetylesterasealpha/beta hydrolase domain containing protein 2lung alpha/beta hydrolase 2progesterone-sensitive lipasFanconi anemia group I proteinFanconi anemia complementation group I
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000352732, ENST00000355100, 
ENST00000565973, ENST00000562254, 
ENST00000562254, ENST00000352732, 
ENST00000355100, ENST00000565973, 
Fusion gene scores* DoF score10 X 10 X 5=5006 X 8 X 5=240
# samples 118
** MAII scorelog2(11/500*10)=-2.18442457113743
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/240*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

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

Most frequent breakpointABHD2(89736550)-FANCI(89790859), # samples:1
Anticipated loss of major functional domain due to fusion event.FANCI-ABHD2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
FANCI-ABHD2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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
HgeneABHD2

GO:0032570

response to progesterone

26989199

HgeneABHD2

GO:0043401

steroid hormone mediated signaling pathway

26989199

HgeneABHD2

GO:0046464

acylglycerol catabolic process

26989199

HgeneABHD2

GO:0048240

sperm capacitation

26989199

TgeneFANCI

GO:0031398

positive regulation of protein ubiquitination

18029348



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
ChimerDB4STADTCGA-HU-A4H8ABHD2chr15

89736550

+FANCIchr15

89790859

+


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Fusion Gene ORF analysis for ABHD2-FANCI

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-5UTRENST00000352732ENST00000300027ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000352732ENST00000310775ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000352732ENST00000451393ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000352732ENST00000567996ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000355100ENST00000300027ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000355100ENST00000310775ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000355100ENST00000451393ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000355100ENST00000567996ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000565973ENST00000300027ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000565973ENST00000310775ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000565973ENST00000451393ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-5UTRENST00000565973ENST00000567996ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-intronENST00000352732ENST00000566615ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-intronENST00000355100ENST00000566615ABHD2chr15

89736550

+FANCIchr15

89790859

+
5CDS-intronENST00000565973ENST00000566615ABHD2chr15

89736550

+FANCIchr15

89790859

+
intron-5UTRENST00000562254ENST00000300027ABHD2chr15

89736550

+FANCIchr15

89790859

+
intron-5UTRENST00000562254ENST00000310775ABHD2chr15

89736550

+FANCIchr15

89790859

+
intron-5UTRENST00000562254ENST00000451393ABHD2chr15

89736550

+FANCIchr15

89790859

+
intron-5UTRENST00000562254ENST00000567996ABHD2chr15

89736550

+FANCIchr15

89790859

+
intron-intronENST00000562254ENST00000566615ABHD2chr15

89736550

+FANCIchr15

89790859

+

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 ABHD2-FANCI


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)
ABHD2chr1589736550+FANCIchr1589790859+2.67E-060.9999974
ABHD2chr1589736550+FANCIchr1589790859+2.67E-060.9999974


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 ABHD2-FANCI


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/:89736550/:89790859)
- 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
..
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: 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 ABHD2-FANCI


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 ABHD2-FANCI


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 ABHD2-FANCI


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 ABHD2-FANCI


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC1836861FANCONI ANEMIA, COMPLEMENTATION GROUP I5CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneC0015625Fanconi Anemia4GENOMICS_ENGLAND
TgeneC0023465Acute monocytic leukemia1GENOMICS_ENGLAND
TgeneC0023467Leukemia, Myelocytic, Acute1GENOMICS_ENGLAND
TgeneC0030312Pancytopenia1GENOMICS_ENGLAND
TgeneC0265219Miller Dieker syndrome1GENOMICS_ENGLAND
TgeneC1855710Bone marrow hypocellularity1GENOMICS_ENGLAND
TgeneC2239176Liver carcinoma1CTD_human
TgeneC3463824MYELODYSPLASTIC SYNDROME1GENOMICS_ENGLAND
TgeneC4228778Abnormality of radial ray1GENOMICS_ENGLAND